Dijuan
Liang
*a,
Alexandre
Milovanoff
a,
Hyung Chul
Kim
b,
Robert
De Kleine
b,
James E.
Anderson
b,
I. Daniel
Posen
a and
Heather L.
MacLean
a
aDepartment of Civil & Mineral Engineering, University of Toronto, Toronto, Canada. E-mail: dijuan.liang@mail.utoronto.ca
bResearch and Innovation Center, Ford Motor Company, Dearborn, MI 48121, USA
First published on 29th May 2025
Mitigating greenhouse gas (GHG) emissions from light-duty vehicle (LDV) fleets cannot solely rely on battery electric vehicles (BEVs). This study focuses on a potential complementary solution: electrofuels (e-fuels, produced with electrolytic hydrogen and carbon dioxide) and specifically e-gasoline deployment in the U.S. as a drop-in fuel compatible with existing vehicles and fueling infrastructure. This study uses (1) fuel- and vehicle-level analyses to determine the energy and feedstock inputs that would enable e-gasoline to have lower GHG emissions than conventional gasoline or vehicle electrification and (2) fleet-level analysis to understand whether deploying e-gasoline in the U.S. LDV fleet can help reach 2015–2050 cumulative emission budgets under exogenous BEV deployment scenarios. For each scenario, we analyzed required e-gasoline production volumes and associated demands for feedstock, renewable electricity, and critical materials for water electrolyzers and electricity generation. The results show that e-gasoline GHG intensity is most sensitive to the GHG intensity of the electricity used for electrolysis. Deploying e-gasoline produced from fully renewable energy has the potential to assist the fleet in meeting climate targets. In the absence of other measures, slower deployment of BEVs or insufficient low-GHG intensity electricity for BEV charging increases the need for e-gasoline and an aggressive production ramp-up. When e-gasoline is produced through optimistic pathways (e.g., fuel-level GHG intensity as low as 7 g CO2-eq per MJ), meeting a 2 °C climate target would require a peak production of 17–400 billion L per year by ∼2040 depending on the BEV deployment scenario (requiring an estimated 2–45 times the 2023 U.S. carbon capture capacity, 60–1400 times the 2020 U.S. electrolytic hydrogen production, and 0.4–9 times the 2022 U.S. renewable electricity production). Without significant recycling of electrolyzer inputs, cumulative material demand could exceed global reserves of iridium, and place pressure on yttrium, nickel, and platinum reserves depending on the assumed electrolyzer technology. Mitigating GHG emissions from land passenger mobility cannot solely rely on BEVs and e-fuels; other complementary strategies based on vehicle efficiency, other low carbon fuels, trip avoidance, and modal shift must be considered.
Sustainability spotlightElectrofuels, especially drop-in ones (e.g., e-gasoline), may complement battery electric vehicles (BEVs) to help light-duty vehicle fleets meet climate targets. E-gasoline can have low greenhouse gas (GHG) emissions and is compatible with existing vehicles and fueling infrastructure. However, scale-up challenges make its mitigation potential unclear. This work evaluates whether e-gasoline can help the U.S. light-duty vehicle fleet meet 1.5 and 2 °C climate targets. We find that e-gasoline can assist in meeting climate targets, but associated resource use and the required deployment speed may create challenges, especially under a slow deployment of BEVs or an insufficient supply of low-GHG electricity for BEV charging. Our work aligns with the UN Sustainable Development Goals of climate action (SDG13) and affordable and clean energy (SDG7). |
Complementary solutions for ICEVs include improving fuel consumption, reducing vehicle weight, and switching to alternative lower GHG intensity fuels, such as lower GHG intensity biofuels or electrofuels (e-fuels).5 Electrofuels are hydrocarbon fuels derived from combining electrolytic hydrogen and captured CO2 through chemical synthesis.7 To produce low-GHG intensity e-fuels, low-GHG intensity feedstocks and energy sources are required.8,9 There are a number of feedstock and conversion pathways that are capable of producing a range of liquid and gaseous e-fuels, including methanol, methane, dimethyl ether, ammonia, gasoline, and diesel.8 With respect to the LDV fleet, drop-in e-fuels, i.e., those that have similar properties to gasoline (e-gasoline) or diesel (e-diesel), are potentially attractive for use in ICEVs, plug-in hybrid electric vehicles (PHEVs) and hybrid electric vehicles (HEVs), especially due to their compatibility with existing vehicles as well as distribution and refueling infrastructure.7,8,10,11
Despite the conceptual simplicity of using electricity to turn CO2 into hydrocarbons, e-fuels remain an emerging technology with unclear potential compared to other more mature alternative fuel options. Biofuels, for example, currently dominate the market for renewable liquid fuels12 and remain an important option for decarbonizing the transportation sector. While drop-in biofuels such as renewable gasoline and renewable diesel derived from biomass exist, the most common biofuels (e.g., bioethanol and biodiesel) are compatible only as low-level blends;13,14 biofuels also raise concerns about land use change15 and feedstock availability,16 thereby limiting their overall sustainable supply.17,18 In contrast, e-fuels require only a relatively generic set of globally available production inputs (primarily electricity and CO2), making them attractive to investigate as a potentially scalable alternative drop-in fuel for decarbonizing the LDV fleet.
Challenges of e-fuels include their currently limited production, projected high costs in the near term, uncertainty about the feasibility of their large-scale deployment, and potential competition from other sectors (e.g., aviation and heavy-duty vehicles), as well as requirements for these fuels to be produced with low environmental impacts including low GHG intensity. The first operating pilot facility to integrate all processes to produce e-gasoline began operation in Chile at the end of 202219 and the first commercial-scale facility in the U.S. is expected to begin operation in 2027.20
To provide insights into the GHG mitigation potential of e-fuels and their potential roles in helping LDV fleets meet climate targets, life cycle assessments (LCAs) are needed at the fuel, vehicle, and fleet levels along with an assessment of the feasibility of large-scale deployment (industry scale-up, timing, costs, etc.).
At the fuel level, LCAs of e-fuels have reported a wide range of GHG emission intensities (1.3–441 g CO2-eq per MJ for e-gasoline, e-diesel, or undifferentiated fuel mixtures),7,9,10,21–27 largely due to variations in the GHG intensities of the feedstock (CO2 sources) and energy sources (e.g., used in water electrolysis for hydrogen production and carbon capture). Studies have found that the most important parameter determining e-fuel GHG intensity is the GHG intensity of electricity, especially electricity used in water electrolysis.22,24 For example, Liu et al.24 estimated that an electricity emission factor of less than 139–144 g CO2-eq per kWh (well below that of even the most efficient unabated fossil fuel power plants27) would be needed for e-diesel using CO2 from direct air capture (DAC) to achieve a lower GHG intensity than conventional diesel.
Vehicle-level assessments are required to compare fuels or energy carriers used in distinct vehicles, e.g., e-gasoline in an ICEV or electricity in a BEV. GHG emissions per vehicle kilometer traveled (vkt) from using e-gasoline in an ICEV were reported to be higher than those from a BEV under low-carbon grids, if e-gasoline production and BEV charging rely on the same grid mix.7,28 A major contributor to this result is the much higher efficiency of the BEV compared to the ICEV.29 While the vehicle-level results suggest some challenges for e-fuels, their production facilities can be more easily located near low-GHG electricity generation (i.e., off-grid renewables) compared to charging all BEVs in the U.S. with low-GHG electricity, which would require the entire grid to be low-GHG.
Analyzing the GHG mitigation potential of large-scale deployment of fuel/vehicle options over time requires a dynamic fleet-level LCA, which considers fleet turnover and market shares of technologies. Some high-level system modeling studies have included e-fuels when simulating cost-minimal fuel/vehicle deployment in the U.S. and EU fleets to meet climate targets.30,31 These studies focused only on scenarios with high BEV and renewable electricity penetration levels and did not include life cycle emissions related to renewable electricity generation, vehicle manufacturing, and e-fuel production.30,31 Few LDV fleet-level LCAs have estimated the mitigation potential of the large-scale deployment of e-fuels.32–35 However, existing studies consider deploying BEVs and e-fuels as competing strategies instead of complementary strategies, and thus overlook potential interactions between BEV and e-fuel deployment (see a review of fleet-level studies in the ESI, Section 1.1†). To meet climate targets, the required contribution from e-fuels will be different depending on the mitigation gaps (i.e., the remaining emissions that must be mitigated to meet climate targets) under different BEV deployment scenarios and electricity sources used for charging BEVs and PHEVs. Given the uncertainty in projected BEV deployment, neglecting interactions between BEV and e-fuel deployment may lead to an incomplete evaluation of the mitigation potential of the large-scale deployment of e-fuels in the fleet.
Whether e-fuels could or should serve as a complementary strategy to BEVs to bridge the GHG mitigation gap depends not just on their fuel-, vehicle-, and fleet-level GHG intensities but also on the feasibility of their large-scale deployment (e.g., required industry growth rate, feedstock, energy, critical material requirements, and associated costs).
The required e-fuel industry growth rate could be high due to its early stage of development. The large-scale deployment of low-GHG e-fuels requires captured CO2, electrolytic hydrogen, and low-GHG electricity. Given that supply capacities of energy and feedstock are currently low36–38 and demands from other sectors are projected to be high,30 whether there will be sufficient energy and feedstock to produce e-fuels to bridge mitigation gaps is uncertain. Critical materials, such as platinum-group metals and rare-earth elements, are essential components in specific water electrolysis and renewable electricity technologies, both pivotal in the transition to clean energy and currently rely on supply chains with considerable geographical concentration.39 Due to the lack of fleet-level LCAs assessing the use of e-fuels in the LDV fleet and the associated feasibility, it remains unclear whether deploying e-fuels can bridge mitigation gaps in the fleet. As the U.S. LDV fleet is projected to be dominated by ICEVs until 2050 under current regulations,6 the demand for low-GHG drop-in e-fuels could be extensive if they are relied upon for meeting climate targets. We use the U.S. as a case study to explore the potential role of drop-in e-fuels (specifically e-gasoline) and associated scale-up challenges in mitigating LDV fleet GHG emissions.
The fuel-level LCAs estimate the GHG emissions from producing and combusting e-gasoline and compare them with conventional gasoline. E-gasoline production is then incorporated into the FLAME (Fleet Life Cycle Assessment and Material-Flow Estimation) model.5,40 The vehicle, automotive material flow, and LCA modules of FLAME are used to conduct vehicle-level LCAs which include embodied vehicle emissions. The vehicle-level GHG emissions from using e-gasoline in ICEVs-G, PHEVs, and HEVs are compared with those from using conventional gasoline in these vehicles and as well with BEVs. Both fuel- and vehicle-level LCAs include scenarios involving variations in e-gasoline production pathways and energy sources to explore the conditions required for an ICEV using e-gasoline to have lower GHG emissions than an ICEV using conventional gasoline or a BEV.
At the fleet level, the fleet module of FLAME is combined with the above modules to estimate the GHG emissions from the U.S. LDV fleet from 2015–2050 (although we focus on 2020–2050 for projected rather than historical results). We examine different mitigation scenarios based on assumptions about BEV deployment levels and the electricity sources used to charge BEVs and PHEVs (see “Section 2.3.3 BEV deployment scenarios” for more information). Overall, we aim to explore the potential of drop-in e-fuels (specifically e-gasoline) as a complementary mitigation solution. We estimate CO2 emission budgets for the U.S. LDV fleet to meet 1.5 and 2 °C climate targets to determine the mitigation gaps under various BEV deployment scenarios. The backcasting module in FLAME is used to estimate the required annual volumes of e-gasoline to bridge the mitigation gaps. The associated required industry growth rates and demands for feedstock, energy, and critical materials are then estimated to examine the feasibility of deploying the required volumes of e-gasoline. The following sections provide details on methods, data sources, and assumptions used in the LCAs.
For FT-gasoline, we modeled two production pathways: electrolysis-based and co-electrolysis-based production pathways (Fig. 2A and B). Both combine CO2 with H2 or water to produce syngas (a mixture of H2 and CO), and then pass syngas to FT synthesis to produce FT wax, which is hydrocracked into liquids and further refined and upgraded into FT-gasoline.9,22 The two pathways differ in the way they produce syngas. The electrolysis-based pathway includes electrolysis combined with a reverse water gas shift (RWGS) reaction.8,25 It first electrolyzes water through alkaline electrolysis (AEL) or proton exchange membrane (PEM) electrolysis to generate H2.8,43–45 Then the RWGS reaction combines H2 and CO2 to produce carbon monoxide (CO), which is blended with additional H2 to form syngas with an H2/CO molar ratio of 2:
1.21 We select AEL as the default water electrolysis technology for the electrolysis-based production pathway as it is the most mature technology.9,43,44 We also provide information on PEM electrolysis for the fuel-level result comparison with previous studies (in ESI Section 3.1†) and critical material analysis. The co-electrolysis-based pathway is represented by the solid oxide electrolyzer cell (SOEC) technology, a future production pathway that is expected to be more efficient and less GHG-intensive than the electrolysis-based pathway.9,22 It uses an SOEC to simultaneously electrolyze water and CO2 to generate syngas directly at typical operating temperatures of around 800–1000 °C.9,22,46 The syngas is further converted to FT-gasoline through the FT process, involving FT synthesis, hydrocracking, and product separation and upgrading. FT synthesis is a commercially mature stepwise polymerization reaction that was originally designed for converting fossil-based syngas into liquid fuels.21,47 For e-gasoline production, FT synthesis converts syngas produced from electrolytic H2 and captured CO2 into FT wax.9,21 The process is exothermic, and the released heat can meet the heat demand for both the RWGS reaction and SOEC;21,23 any surplus heat is treated as waste heat (i.e., no emission credits). The FT wax is hydrocracked with additional hydrogen input to yield a mixture of FT-fuels, a product slate of FT-gasoline, FT-diesel, and FT-kerosene.21 FT-gasoline needs to be further separated from the mixture and upgraded to improve the cold flow properties.21 FT-gasoline is mainly composed of paraffins and olefins.21,48 Estimates of the relative yield of e-gasoline vary across studies and across assumed process conditions (with example ranges from 26–37%21,27,46), requiring markets for the other products; from an LCA standpoint, using energy allocation, the exact mixture is moot as all products are assumed to have the same emissions intensity per MJ.
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Fig. 2 Production pathways for e-gasoline produced from carbon dioxide modeled in the study: (A) Fischer–Tropsch (FT) gasoline produced from the electrolysis-based pathway; (B) FT-gasoline produced from the co-electrolysis-based pathway; (C) Methanol-to-gasoline (MTG) gasoline produced from the electrolysis-based pathway. The dashed boxes represent all processes included in the FT or MTG process. SOEC: Solid Oxide Electrolyzer Cell; RWGS: Reverse Water Gas Shift reaction; MeOH: Methanol. Whether external heat is needed for carbon capture depends on the concentration of CO2 sources.27 |
For MTG-gasoline, we consider an electrolysis-based pathway (Fig. 2C). It combines electrolytic H2 and captured CO2 to produce methanol through methanol synthesis,11,21 a mature technology used commercially.49,50 Methanol is then passed to the MTG process to produce raw gasoline, which needs to be upgraded through hydrotreating to useable road fuel.11,21 The typical composition of MTG-gasoline is 50% paraffins, 20% olefins, and 30% aromatics.21 The MTG process is a technology that is specific for gasoline production and was developed by Exxon Mobil in the 1970s.41,51,52 The MTG technology has been applied at the HIF Haru Oni Demonstration Plant in Chile to produce 130000 L of e-gasoline per year19 and is expected to be applied in the HIF Matagorda eFuels Facility in the U.S. to produce 750 million L of e-gasoline per year by 2027.20
As using industrial CO2 to produce e-fuels eventually results in CO2 emissions during fuel combustion, it leads to the issue of how to allocate CO2 emissions between the industrial process and fuel combustion during vehicle use. Studies have attributed none, partial, or all CO2 emissions to e-fuel production.7,24 As we consider e-gasoline as carbon-neutral in terms of combustion, all CO2 emissions are allocated to the industrial process. The credit for the captured CO2 is allocated entirely to the purchaser of CO2, with no implicit emission benefit granted to the capture site.
Energy use for CO2 capture and compression depends on the CO2 source and the concentration. For industrial sources, high-concentration CO2 sources (e.g., natural gas processing) require less electricity than low-concentration CO2 sources (e.g., natural gas combined cycle power plants) (∼100 versus ∼330 kWh per t CO2).27 These numbers are indicative, but the exact values vary depending on the flue gas stream and the capture technology. DAC requires not only electricity (150–720 kWh per t CO2) but also heat (3.4–15 GJ per t CO2) to release concentrated CO2.27,56,57,59 The wide range of values derives from the various approaches (liquid solvent approach or solid sorbent approach) and the extent of heat integration.27,56,57,59 We utilize energy consumption data for capturing industrial flue gas and DAC from the Greenhouse Gases, Regulated Emissions, and Energy Use in Transportation (GREET) Model 2022.27 For industrial sources, we adopt data based on the use of the methyl diethanolamine (MDEA) CO2 removal process to capture flue gas from natural gas combined cycle power plants,60 which have been reported to have high carbon capture potential53 and projected to remain a major non-renewable electricity source in the U.S.6 For DAC, we adopt data on low-temperature adsorption-based DAC (solid sorbent approach) under current status as future technological improvements are uncertain and its temperature requirement (<100 °C)61 can be addressed by most renewable heat technologies, including solar thermal energy.62 The electricity demand for CO2 compression is calculated using the thermodynamic compression formula in ref. 60 and the outlet pressure is set to the default value of 2219 psia in GREET 2022.27 The choice of energy sources, especially the heat sources used in carbon capture, impacts the GHG emissions of e-fuels.22 Natural gas is a common heat source for DAC, while low-GHG electricity, industrial waste heat, solar thermal energy, and nuclear power are potentially less GHG-intensive sources.22,24 We consider three electricity sources (2022 U.S. grid electricity, solar PV, and wind power) and two heat sources (natural gas and solar thermal energy) for carbon capture (both industrial flue gas and DAC) to explore their impacts on the GHG intensity of e-gasoline.
# | Scenarioa | Production pathway | CO2 sourceb | Electricity sourcec | Heat sourced |
---|---|---|---|---|---|
a Scenarios are named according to the following rule: “production pathway” – “CO2 source” + “electricity source” + “heat source”. FT = Fischer–Tropsch; MTG = methanol-to-gasoline; ELE = electrolysis-based production pathway; COE = co-electrolysis-based production pathway; DAC = direct air capture; IND = post-combustion industrial flue gas; GRID = 2022 U.S. grid electricity; PV = solar PV; WIND = onshore wind power; NG = natural gas; ST = solar thermal energy; NA = not applicable. b For CO2 sources, DAC CO2 is CO2 captured from the atmosphere by the low-temperature adsorption-based approach, while IND CO2 is CO2 captured from the post-combustion flue gas from natural gas combined cycle power plants through the methyl diethanolamine (MDEA) approach. c For each scenario, the electricity source is assumed to be the same for all production steps (i.e., electrolysis/co-electrolysis, carbon capture & compression, syngas production, Fischer–Tropsch and methanol-to-gasoline processes). d External heat is only consumed for DAC but not for capturing industrial flue gas. NA = not applicable. | |||||
1 | FT-ELE-DAC + GRID + NG | FT + electrolysis | DAC | U.S. grid | Natural gas |
2 | FT-ELE-DAC + PV + NG | FT + electrolysis | DAC | Solar PV | Natural gas |
3 | FT-ELE-DAC + WIND + NG | FT + electrolysis | DAC | Wind | Natural gas |
4 | FT-ELE-DAC + PV + ST | FT + electrolysis | DAC | Solar PV | Solar thermal energy |
5 | FT-ELE-DAC + WIND + ST | FT + electrolysis | DAC | Wind | Solar thermal energy |
6 | FT-ELE-IND + GRID + NA | FT + electrolysis | IND | U.S. grid | NA |
7 | FT-ELE-IND + PV + NA | FT + electrolysis | IND | Solar PV | NA |
8 | FT-ELE-IND + WIND + NA | FT + electrolysis | IND | Wind | NA |
9 | FT-COE-DAC + GRID + NG | FT + co-electrolysis | DAC | U.S. grid | Natural gas |
10 | FT-COE-DAC + PV + NG | FT + co-electrolysis | DAC | Solar PV | Natural gas |
11 | FT-COE-DAC + WIND + NG | FT + co-electrolysis | DAC | Wind | Natural gas |
12 | FT-COE-DAC + PV + ST | FT + co-electrolysis | DAC | Solar PV | Solar thermal energy |
13 | FT-COE-DAC + WIND + ST | FT + co-electrolysis | DAC | Wind | Solar thermal energy |
14 | FT-COE-IND + GRID + NA | FT + co-electrolysis | IND | U.S. grid | NA |
15 | FT-COE-IND + PV + NA | FT + co-electrolysis | IND | Solar PV | NA |
16 | FT-COE-IND + WIND + NA | FT + co-electrolysis | IND | Wind | NA |
17 | MTG-ELE-DAC + GRID + NG | MTG + electrolysis | DAC | U.S. grid | Natural gas |
18 | MTG-ELE-DAC + PV + NG | MTG + electrolysis | DAC | Solar PV | Natural gas |
19 | MTG-ELE-DAC + WIND + NG | MTG + electrolysis | DAC | Wind | Natural gas |
20 | MTG-ELE-DAC + PV + ST | MTG + electrolysis | DAC | Solar PV | Solar thermal energy |
21 | MTG-ELE-DAC + WIND + ST | MTG + electrolysis | DAC | Wind | Solar thermal energy |
22 | MTG-ELE-IND + GRID + NA | MTG + electrolysis | IND | U.S. grid | NA |
23 | MTG-ELE-IND + PV + NA | MTG + electrolysis | IND | Solar PV | NA |
24 | MTG-ELE-IND + WIND + NA | MTG + electrolysis | IND | Wind | NA |
Parameter | Unit | Value | References | |
---|---|---|---|---|
a LHV: lower heating value; PV: photovoltaic; DAC: direct air capture; AEL: alkaline electrolysis; PEM: proton exchange membrane; RWGS: reverse water gas shift; SOEC: solid oxide electrolyzer cell; FT: Fischer–Tropsch; MTG: methanol-to-gasoline; MeOH: methanol. b U.S. electricity grid emissions factors estimated by using the emission factors of electricity from different sources in GREET 2022 and annual projected grid mix through 2050 in the Annual Energy Outlook (AEO) 2022.27,66 c We did not distinguish emission factors across sub-technologies of solar PV and wind power as the variations are relatively small when compared to emissions from U.S. grid electricity. We also note that there is substantial variability in the estimated intensity of low GHG sources; thus, although we draw emission factors from GREET 2022 based on solar PV and wind, these should be treated primarily as generic representations of low and ultra-low GHG power sources. | ||||
Lower heating value of e-gasoline | MJ/kg | 43.1 | 21 | |
Lower heating value of e-gasoline | MJ/L | 30.9 | 27 | |
GHG emission intensity of conventional gasoline | g CO2-eq/MJ LHV | 91 | 27 | |
Emission factor of 2022 U.S. grid electricityb | g CO2-eq/kWh | 438 | 27,66 | |
Emission factor of electricity from solar PVc | g CO2-eq/kWh | 39.2 | 27 | |
Emission factor of electricity from wind powerc | g CO2-eq/kWh | 10.4 | 27 | |
Emission factor of heat supply from natural gas | g CO2-eq/MJ heat | 75.4 | 22 | |
Emission factor of heat supply from solar thermal energy | g CO2-eq/MJ heat | 0.251 | 22 | |
CO2 capture & compression | Industrial flue gas capture: electricity consumption | kWh/kg CO2 | 0.34 | 27 |
Industrial flue gas capture: external heat consumption | MJ/kg CO2 | 0 | 27 | |
DAC: electricity consumption | kWh/kg CO2 | 0.72 | 27 | |
DAC: external heat consumption | MJ/kg CO2 | 14.88 | 27 | |
H2 production | AEL: electricity consumption | kWh/kg H2 | 50 | 21 |
PEM: electricity consumption | kWh/kg H2 | 48 | 42 | |
Syngas production | RWGS: electricity consumption | kWh/kg CO | 0.14 | 21 |
RWGS: H2 consumption | kg/kg CO | 0.07 | 21 | |
RWGS: CO2 consumption | kg/kg CO | 1.57 | 21 | |
SOEC: electricity consumption | kWh/kg syngas (CO![]() ![]() |
7.91 | 21 | |
SOEC: CO2 consumption | kg/kg syngas (CO![]() ![]() |
1.38 | 21 | |
Methanol synthesis | Electricity consumption | kWh/kg MeOH | 0.276 | 21 |
H2 consumption | kg/kg MeOH | 0.192 | 21 | |
CO2 consumption | kg/kg MeOH | 1.4 | 21 | |
FT process | CO consumption | kg/kg e-gasoline | 2.41 | 21 |
H2 consumption | kg/kg e-gasoline | 0.33 | 21 | |
Electricity consumption | kWh/kg e-gasoline | 0.193 | 21 | |
MTG process | Electricity consumption | kWh/kg e-gasoline | 0.196 | 21 |
MeOH consumption | kg/kg e-gasoline | 2.28 | 21 | |
H2 consumption | kg/kg e-gasoline | 0.001 | 21 | |
E-gasoline transportation & distribution | GHG emissions | kg CO2-eq/kg e-gasoline | 0.01 | 27 |
No | Fleet-level scenariob | E-gasoline production scenario c,d |
---|---|---|
a FLAME model: fleet life cycle assessment and material-flow estimation model. b Scenarios named “Mature production pathway” are represented by the electrolysis-based production pathway (Fischer–Tropsch + electrolysis), while scenarios named “Advanced production pathway” are represented by the co-electrolysis-based production pathway (Fischer–Tropsch + co-electrolysis). The “best-case” and “mid-case” are the scenarios with the lowest and median GHG intensities, respectively, under each combination of e-gasoline type, production pathway, and CO2 sources. c E-gasoline production scenarios are named using the following rule: “production pathway” – “CO2 source” + “electricity source” + “heat source”. FT = Fischer–Tropsch; ELE = electrolysis-based production pathway; COE = co-electrolysis-based production pathway; DAC = direct air capture; PV = solar PV; WIND = onshore wind power; ST = solar thermal energy. d For each scenario, the electricity source is the same for all production steps (i.e., electrolysis/co-electrolysis, carbon capture, syngas production, and Fischer–Tropsch process). | ||
1 | Mature production pathway best-case | FT-ELE-DAC + WIND + ST |
2 | Mature production pathway mid-case | FT-ELE-DAC + PV + ST |
3 | Advanced production pathway best-case | FT-COE-DAC + WIND + ST |
4 | Advanced production pathway mid-case | FT-COE-DAC + PV + ST |
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Fig. 3 2015–2050 U.S. light-duty vehicle (LDV) fleet cumulative greenhouse gas emissions versus CO2 emission budget under prospective future development. The renewable electricity in this figure is assumed to have zero embodied GHG emissions. The top three bars are reported as CO2-eq as they result from FLAME, which reports CO2 and non-CO2 GHGs, while the carbon budgets (bottom two bars) are reported as CO2 as they result from emission budgets of integrated assessment models that are reported as CO2 (see ESI Section 2.3† for details). |
To better understand these growth rates, we compare them with historical growth rates of the oil refining, biodiesel, and ethanol industries in the U.S. as well as with unconventional (very high) growth rates (e.g., World War II U.S. liberty ship deployment) in terms of emergence growth rates. The emergence growth rate is the maximum annual growth rate after the formative phase of the industry, which reflects the steepness of the logistic growth curve.71 It has been used as a unitless metric to measure how technology diffuses from the formative phase to the saturation phase.71 Although the demand for e-gasoline resulting from our model may not follow a logistic growth curve, the use of the emergence growth rate concept provides a basis for comparison against historical case studies (more in ESI Section 2.4†).
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Fig. 4 Fuel-level (well-to-wheel) GHG emission intensity of e-gasoline produced from various production pathways and conventional petroleum-derived gasoline. For energy sources on the y-axis, the first is the electricity source for all stages of e-gasoline production, while the second is the heat source for direct air capture (DAC) as industrial carbon capture does not require external heat. Emissions for e-gasoline include emissions from carbon capture, water electrolysis or co-electrolysis, syngas production, methanol synthesis, Fischer–Tropsch (FT) process, and methanol-to-gasoline (MTG) process. No direct emissions are assumed from the combustion of e-gasoline. Life cycle GHG emission intensity from conventional gasoline is 91 g CO2-eq per MJ,27 which includes emissions from fuel production and fuel combustion during vehicle use. The emission factor of U.S. grid electricity is 438 g CO2-eq per kWh for 2022. Error bars represent results using mass and energy balance from other data sources (details in ESI Sections 2.1 and 3.3†). ELE: electrolysis; COE: co-electrolysis; NG: natural gas; ST: Solar thermal; DAC: Direct Air Capture CO2; IND: Industrial flue gas CO2; T&D: Transportation & Distribution. |
As detailed in ESI Section 3.1,† our results generally fall within the ranges reported in the literature, with most variations due to differences in the assumed electricity mix and associated emissions; some key sources (e.g., GREET 202227) show higher emissions owing to higher H2 and CO2 input assumptions for the RWGS reaction. Such differences are explored in “Section 3.4 Sensitivity analysis”.
When U.S. grid electricity powers e-gasoline production, over 60% of fuel-level GHG emissions of e-gasoline are associated with electricity generation for electrolysis (or co-electrolysis), due to the high electricity demand from these processes. The remaining GHG emissions result mainly from carbon capture, especially emissions from heat generation from natural gas to power DAC in those pathways that include DAC. Employing low-GHG electricity for the electrolysis (or co-electrolysis) stage and a low-GHG heat source for DAC are generally necessary and sufficient conditions for e-gasoline to have lower GHG emission intensity than conventional gasoline. To be competitive with conventional gasoline, the electricity GHG intensity for electrolysis (or co-electrolysis) must be lower than 100–121 g CO2-eq per kWh (ESI Section 3.2†) when 2022 U.S. grid electricity is used for all other processes and DAC is heated with solar thermal energy. These break-even electricity GHG intensities increase to 139–159 g CO2-eq per kWh when we account for emissions from electricity used across the entire e-gasoline production chain (Fig. 5). The lower and upper ends of the range are associated with electrolysis- and co-electrolysis-based production pathways for FT-gasoline, respectively. They are close to previously reported break-even values of 144 g CO2-eq per kWh (ref. 24) or 116 g CO2-eq per kWh (ref. 10) (electrolysis + DAC with no heat input) and 143 g CO2-eq per kWh (ref. 10) (co-electrolysis + DAC with no heat input) between FT-fuels and conventional diesel. These break-even electricity GHG intensities are lower than U.S. grid electricity emission intensity in 2022 (438 g CO2-eq per kWh) and the projection by AEO 2022 for 2050 (316 g CO2-eq per kWh),27,66 indicating that e-gasoline produced using the projected U.S. grid would not mitigate GHG emissions compared to petroleum-derived gasoline.
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Fig. 5 Vehicle-level GHG emissions for different vehicle technologies (cars) and fuels produced from various production pathways, shown as a function of the emission factor of electricity. The results are for cars only (no light trucks). The figure includes Fischer–Tropsch (FT) gasoline produced from two production pathways (ELE: Electrolysis and COE: Co-electrolysis) and direct air capture (DAC) CO2 heated by solar thermal energy. FT-gasoline produced using industrial CO2 is removed from the figure as it is very close to the production pathway of using DAC CO2 heated by solar thermal energy. Vehicle-level GHG emissions include emissions from vehicle production, electricity generation, fuel production, vehicle use, and vehicle disposal. Contributions from each life stage are shown in ESI Section 3.4.† The emission factors of U.S. grid electricity are 438 g CO2-eq per kWh for the year 2022 and are projected to be 316 g CO2-eq per kWh by 2050.27,66 |
Well-to-wheel efficiency estimates energy losses during fuel production, fuel transportation & distribution, vehicle fueling, and fuel combustion during vehicle use.82 The higher well-to-wheel efficiency of BEVs (estimated as 64%) compared to those of HEVs or ICEVs-G using e-gasoline based on the various production processes (6–11% and 5–10%, respectively) (methods in ESI Section 2.2† and results in ESI Section 3.5†) indicates that e-gasoline is not an efficient way to ‘electrify’ LDVs. The low efficiencies of the e-gasoline vehicles result from the energy-intensive fuel production processes and the low vehicle efficiencies. The results presented in this section and shown in Fig. 5 are for cars, but results follow similar trends for light trucks. During fuel production and vehicle use phases, an ICEV-G using e-gasoline uses 1.3–1.6 kWh of electricity per vkt, while a BEV300 uses 0.21 kWh of electricity per vkt. If electricity from the same source is used for charging BEVs and producing e-gasoline, a BEV300 would have lower life cycle GHG emissions than an e-gasoline ICEV-G unless the electricity emission factor (for both BEV charging and e-fuel production) falls below 13–18 g CO2-eq per kWh. This occurs when the higher embodied emissions from manufacturing and disposing of BEVs compared to ICEVs-G (38 g CO2-eq per vkt vs. 19 g CO2-eq per vkt (ref. 5)) become a more significant relative contributor to total emissions when very low GHG electricity is used for fuel production. This scenario, however, is not realistic as it is unlikely that fuel cycle GHG emissions would reach such low levels without an associated decrease in vehicle cycle emissions. More plausible, however, is a scenario in which BEVs are charged with the 2022 U.S. grid average, while e-gasoline is produced with off-grid renewables; in this case, the breakeven grid intensity for e-gasoline (FT-gasoline produced from CO2 captured by DAC with solar thermal heat) is 68–78 g CO2-eq per kWh.
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Fig. 6 2020–2050 annual end-use demand for fuels from the U.S. light-duty vehicle fleet under various scenarios to meet 1.5 or 2 °C climate targets. The values in the figure are for fuel and energy carriers used during the vehicle operation stage only. Energy used for fuel production is not included. These fleet-level results correspond to Fischer–Tropsch gasoline produced from the electrolysis-based production pathway using direct air capture CO2 and powered by wind electricity and solar thermal heat. For other scenarios see ESI Section 3.7.† |
These absolute growth rates are converted to percentage emergence growth rates (see Section 2.5 and ESI Section 2.4†) and compared with other historical industries in Fig. 7. To meet climate targets, the lower BEV deployment scenarios require emergence growth rates lower than 50% per year, which are comparable to those of U.S. biodiesel and ethanol production (but ethanol and biodiesel growth slowed before reaching the large volumes required in most of our e-fuel scenarios). The high BEV deployment scenarios require emergence growth rates higher than 77% per year, close to the rate of U.S. nuclear weapon deployment. Meeting the 1.5 °C climate target under the high BEV with U.S. grid scenario would require the highest emergence growth rate (480% per year), substantially higher than that of World War II U.S. liberty ship deployment. These results are due to the lower long-term mitigation potential of e-gasoline under high electrification because of the smaller number of remaining vehicles that can use e-gasoline. As BEVs powered by U.S. grid electricity have higher emissions than vehicles powered by e-gasoline produced from renewable energy, it would be more difficult for the fleet to reduce emissions in the long run under the high BEV with U.S. grid scenario. Therefore, emissions would need to be reduced more quickly in the short run, requiring the highest deployment rate of e-gasoline. Such rapid growth of the e-gasoline industry required to meet climate targets is likely unrealistic. The extreme growth rates required in some scenarios are particularly noteworthy considering the narrow focus of this analysis (i.e., only U.S. LDVs); incorporating potential demand from other sectors (e.g., aviation, marine shipping, and heavy-duty vehicles) could pose further challenges for both the speed of scale-up required and the associated resource use discussed in Section 3.2.3.
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Fig. 7 Emergence growth rates of e-gasoline to meet 1.5 and 2 °C climate targets under various scenarios compared with historical industrial growth in the U.S. and examples of unconventional growth from the literature. These fleet-level results represent Fischer–Tropsch (FT) gasoline produced from the electrolysis-based production pathway using direct air capture CO2 powered by wind electricity and solar thermal heat. Carbon budgets consistent with 1.5 and 2 °C climate targets are included. Data on U.S. historical industrial growth (oil refinery, biodiesel, and ethanol) are obtained from ref. 84 and 85. Data on unconventional growth is obtained from ref. 71. Methods for calculating emergence growth rates are provided in ESI Section 2.4.† |
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Fig. 8 Peak annual demand for e-gasoline feedstock and energy carriers for the U.S. LDV fleet to meet climate targets. These fleet-level results correspond to Fischer–Tropsch gasoline produced from the electrolysis-based pathway using direct air capture CO2 and powered by wind electricity and solar thermal heat. The figure includes our model results for the U.S. LDV fleet (peak demand years range from 2033 to 2047) as well as high-level scoping estimates of feedstock and energy carrier demand to satisfy global e-fuel demand in 2035 (55% e-fuel share) and 2050 (100% e-fuel share). These demand estimates are compared with current (source data within the range from 2020–2023) and future U.S. and global production levels (2030 global data for CO2 and H2 and 2050 U.S. data for renewable electricity); data is from ref. 37, 38, 66, 86, 92 and 93. Detailed numeric results and results for alternative e-gasoline production pathways are shown in ESI Section 3.8.1.† |
Under the 2 °C BAU BEV with U.S. grid, high BEV with U.S. grid, and high BEV with RE scenarios, the peak annual demand for electrolytic hydrogen to produce e-gasoline is 140, 53, and 6 Mt, respectively. These peak demands are 60–1400 times the 2020 U.S. electrolytic hydrogen production (0.1 Mt),86 and two of three are higher than the 9 Mt per year from announced (as of 2023) U.S. low carbon H2 projects (green and blue hydrogen) by 2030.87 Assuming a focus on electrolytic hydrogen, the above demands would require newly installed capacities of 40, 36, and 4 GW per year on average before 2030 or cumulative newly installed capacities of 2000, 630, and 77 GW during 2022–2050, if AEL were the exclusive technology. Given that the 2030 planned global manufacturing capacity of water electrolyzers (based on existing announcements) is just over 130 GW per year,88 28–31% of this capacity would be required to produce hydrogen only for the U.S. LDV fleet when BEVs were charged with U.S. grid electricity. Considering the competitive demand for hydrogen in other sectors under net-zero strategies (e.g., 34–66 Mt in 2050 according to ref. 30), securing hydrogen supply for e-gasoline production could be challenging.
To produce the required volumes of e-gasoline under the 2 °C BAU BEV with U.S. grid, high BEV with U.S. grid, and high BEV with RE scenarios, 8200, 3000, and 350 TWh of low-GHG electricity, respectively, would be needed in the peak years. In the case of wind, this would require the newly installed generating capacities of 99, 28, and 3.5 GW per year or the cumulative newly installed capacities of 2900, 800, and 100 GW during 2022–2050, assuming that the capacity factor increases from 0.44 in 2022 to 0.48 in 2050.89 Under the less aggressive BEV deployment scenarios (BAU BEV with U.S. grid and high BEV with U.S. grid), these demands are 3 and 9 times the 2022 U.S. renewable electricity generation (913 TW h), respectively.38 These demands are of the same order of magnitude as those projected in the Princeton Net-Zero America E+ RE+ scenario, which assumed nearly 100% replacement of diesel, gasoline, jet fuel, and LPG with synthetic liquid fuels produced from hydrogen and CO2 by 2050 (ESI Section 3.8.2†).30 To further examine the renewable electricity demand for e-gasoline, the demands are compared to the AEO 2022 reference case, which is the projection of electricity supply under existing laws and policies.90 With the exception of the 2 °C high BEV with RE scenario, the peak renewable electricity demands in all our scenarios are higher than the projected renewable electricity supply in the AEO 2022 reference case, indicating that more aggressive expansion of renewable electricity generation would be needed to make e-gasoline a feasible solution under our scenarios.
As e-fuels are also attractive for other sectors (e.g., aviation and heavy-duty vehicles) and regions, competing demands would further increase the burden on supply growth in e-fuels and the required feedstock and energy carriers. We perform a high-level scoping estimate of global e-fuel demand by scaling our U.S. scenarios. Specifically, we benchmark against the 2 °C and BAU BEV with U.S. grid scenario, which results in approximately 55% of U.S. gasoline being replaced with e-fuel in 2035. This is similar to the projected e-fuel share (58%) in the peak year (2033) for the 2 °C and high BEV with U.S. grid scenario. Applying a similar 55% replacement rate for all global petroleum products (with e-gasoline) and natural gas (with e-methane) under the IEA World Energy Outlook 2024 Stated Policies scenario91 would require 3.2 trillion L of e-gasoline and 0.9 Gt of e-methane in 2035. This corresponds to a global e-gasoline & e-methane demand of 141 EJ, which would require 11 Gt of captured CO2, 1400 Mt of electrolytic H2, and 89 PWh of renewable electricity (e-methane production data from ref. 21). This would respectively require 228 times the current (2023) global amounts of captured CO2, 1010 times the current (2020) global electrolytic H2 production capacity, and 11 times the current (2021) global renewable electricity supply, as outlined in Fig. 8. These requirements are more aggressive than those estimated for U.S. LDVs by 2035 under the 2 °C and BAU BEV with U.S. grid scenario: 30, 722, and 5 times the current U.S. production of captured CO2, electrolytic H2, and renewable electricity, respectively. If we further extend the analysis to 2050 with a 100% e-fuel share, the global demand for feedstock and energy carriers in 2050 would be 1.7 times the 2035 levels. These numbers further illustrate the immense resource requirements and scale-up challenges that could be associated with an e-fuel focused decarbonization scenario.
Critical materials in water electrolyzers estimated to be in high demand from e-gasoline production are primarily determined by the assumed electrolyzer technology market share. To meet the 2 °C climate target, cumulative demands from 2020–2050 for most materials are estimated to be less than 10% of the 2021 global reserves despite material recovery assumptions, with the exception of iridium (Fig. 9). Iridium is a critical catalyst material for PEM electrolyzers and its current U.S. supply is dominated by imports.73 Under the high BEV with U.S. grid scenario, our results show that 140% and 290% of the 2021 global reserves of iridium would be needed if PEM electrolyzers were to have 50% and 100% of the market share, respectively, without material recovery. If 100% material recovery is assumed, the numbers would decrease to 11% and 22%. Under the 1.5 °C climate target, there are other materials whose cumulative demands may exceed 10% of global reserves without material recovery, including yttrium, nickel, and platinum, underscoring the importance of recycling and recovery to reduce supply chain risks. Further concerns arise from whether supply growth can keep pace with demand growth, especially given the long mine lead time, around 16 years from discovery to production.94 For example, to meet the 2 °C climate target under the high BEV with U.S. grid scenario, the annual average iridium demand by 2030 would need to be 7 times the 2021 U.S. consumption, assuming FT-gasoline production via PEM electrolysis. The fast growth rate could lead to a mismatch in timing between when critical materials are needed and when they could become available. Such challenges could potentially be mitigated, but only with sufficient advanced planning and lead time.
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Fig. 9 Cumulative demand from 2020 to 2050 for critical materials from water electrolyzers with 0% and 100% material recovery under the high BEV with U.S. grid scenario to meet the 2 °C climate target. These fleet-level results correspond to Fischer–Tropsch gasoline produced from wind electricity and CO2 captured by direct air capture heated by solar thermal energy. The top three panels represent scenarios with 100% of a certain electrolyzer technology, and the last panel represents a scenario with a 20% share of alkaline electrolyzer (AEL), 50% of proton exchange membrane (PEM), and 30% of solid oxide electrolyzer cells (SOECs). We include material use for water electrolyzers only for e-gasoline production but not for hydrogen production for fuel cell vehicles. Al: aluminum; Co: cobalt; Gd: gadolinium; Ir: iridium; La: lanthanum; Mn: manganese; Ni: nickel; Pt: platinum; Sm: Samarium; Ti: titanium; Y: yttrium; Zr: zirconium. Other scenarios are presented in ESI Section 3.9.1.† |
A sufficient supply of critical materials for associated renewable electricity generation is estimated to be less challenging. Even without material recovery, the cumulative demands for critical materials from wind turbines and solar panels from 2020 to 2050 are estimated to be similar to or less than 10% of the 2021 global reserves (ESI Section 3.9.2†).
As BEVs require critical materials for battery manufacturing, we adopt cumulative demands for aluminum, cobalt, lithium, manganese, and nickel under 0% and 90% material recovery for high BEV deployment scenarios from Tarabay et al.,81 which assumed 100% BEV sales by 2035 consistent with our study. For consistency with our previous work,5 GHG emission estimates assume the use of 100% lithium manganese oxide (LMO) cathodes, which introduces a minor inconsistency with the updated battery technology market shares that we use for calculating critical minerals: 71% nickel manganese cobalt oxide cathode (NMC 622), 25% lithium nickel cobalt aluminum oxide cathode (NCA), and 4% lithium iron phosphate cathode (LFP) from ref. 81. The use of LMO slightly underestimates the burdens of electric vehicle production. The resulting inconsistencies in the fleet-level GHG emissions and demand for e-gasoline to bridge mitigation gaps are expected to be minor given the relatively low contribution of battery production when BEVs are charged with U.S. grid electricity. Therefore, our emphasis is on the estimates to provide insight into the critical material demand arising from manufacturing the following products, i.e., electrolyzers, wind turbines and solar panels, and batteries. Under the high BEV with U.S. grid scenario, results show that the demands for cobalt, nickel, lithium, and iridium would exceed 10% of the 2021 global reserves to meet the 2 °C climate target even with 90–100% material recovery (Table S30†). Cobalt is the material of the highest concern, reported to use over 60% of the 2021 global reserves due to the high assumed market share of batteries containing cobalt. Cobalt, lithium, and nickel are predominantly associated with battery manufacturing, while iridium is exclusively linked to electrolyzer manufacturing (Fig. S16†).
The estimates of feedstock, energy requirements, and critical materials are based on near-term technologies, which may result in overestimates if future technological advancements occur. Additionally, there are uncertainties associated with variations in technology parameters reported in the literature (e.g., electrolyzer efficiency). Nevertheless, the results provide insights into the challenges associated with large-scale deployment of e-gasoline.
High e-fuel production costs for both FT-fuels and MTG-gasoline are likely to cause economic barriers for its large-scale deployment with reported production costs ranging from $0.72 to $8.3 per L ($0.02–0.27 per MJ)9,21,22,42,95,96 (methods in ESI Section 2.8† and results in ESI Section 3.10†), substantially higher than the average 2018–2022 production cost of conventional gasoline ($0.57 per L or $0.018 per MJ)97 (all values in 2022 USD). The wide range of production costs arises from variations in economic and production scenario assumptions. Economically, the production cost is mainly driven by the assumed prices of electricity and CO2. The lowest cost of $0.72 per L ($0.02 per MJ) is based on an electricity price of $0.05 per kWh and a CO2 price of $82 per t CO2,7 while the highest cost of $8.3 per L ($0.27 per MJ) assumes prices of $0.08 per kWh and $1600 per t CO2, respectively.42 For production scenarios, lower costs are associated with co-electrolysis due to higher production efficiency22,42 and with the utilization of industrial flue gas due to lower energy consumption.7,9,22,42,96
These variations lead to a range of carbon abatement costs (from $31 per t CO2 (ref. 7) to $11000 per t CO2 (ref. 22)). As the emitted GHGs from e-fuel production are dominated by CO2,27 we compare these abatement costs with the social cost of carbon to evaluate the social benefits of deploying e-fuels. For FT-fuels and MTG-gasoline whose carbon abatement costs are close to or lower than the 2020–2050 social cost of carbon ($140–540 per t CO2),98 they were reported to be produced using electricity with an emission factor of around 16–26 g CO2-eq per kWh and at a price below $0.08 per kWh.7 This suggests that it would be cost-beneficial to replace conventional gasoline with e-gasoline only when low-GHG and inexpensive electricity is used in its production. E-fuels should therefore be considered as a potential decarbonization strategy when drop-in fuels are required, but more cost-effective mitigation solutions such as biofuels,26 and demand-side reduction strategies99 are also worth considering as priority actions.
Although the possibility of low abatement costs offers incentives to replace conventional gasoline with e-gasoline, whether the industry would be motivated to scale up e-gasoline production is uncertain. In the 2 °C high BEV with U.S. grid scenario, the demand for e-gasoline is estimated to quickly grow by 0.4 EJ per year (12 billion L per year) before 2033 and then drop by 0.2 EJ per year (7 billion L per year) after 2033 on average. This is likely not reasonable and would be challenging for investors unless export markets could be developed, and/or production systems were flexible to produce products that would remain in high demand in the future, such as those possibly for other sectors (e.g., aviation) where electrification will be difficult.
Apart from climate impacts, e-fuel production and combustion are linked to other environmental and health risks, such as water depletion and air pollution. E-fuel production has been reported to involve high water consumption due to water losses in electricity generation and water electrolysis.27,33 Combusting e-gasoline in ICEVs-G results in tailpipe emissions of air pollutants, which are anticipated to be at similar levels to those from conventional gasoline; however there have been limited studies on this topic48,100 (ESI Section 3.11†). Tailpipe emissions of vehicles using e-gasoline are not expected to yield major air quality co-benefits when compared to measures such as direct electrification and travel demand reduction. Air pollutant emissions and other non-climate impacts should be further investigated in future work.
Returning to our default scenarios, we further investigate the annual and peak volumes of e-gasoline required for both electrolysis and co-electrolysis-based pathways, using either wind electricity (10 g CO2-eq per kWh) or solar electricity with slightly higher embodied emissions (39 g CO2-eq per kWh). The results are presented in ESI Section 3.7† and show minimal differences between the electrolysis and co-electrolysis-based pathways. In contrast, assuming higher life cycle emissions from renewable energy results in substantially higher required volumes of e-gasoline (Fig. 6) in peak years (up to 120% higher), depending on the underlying BEV deployment scenario and carbon budget. Bridging mitigation gaps with higher GHG intensity e-gasoline would be more challenging due to the higher required volumes.
Footnote |
† Electronic supplementary information (ESI) available. See DOI: https://doi.org/10.1039/d4su00654b |
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