An artificial photosynthetic system with CO2-reducing solar-to-fuel efficiency exceeding 20%

Abstract

Artificial photosynthetic systems store solar energy in chemical fuels via CO₂ reduction or renewable hydrogen evolution from water splitting. But only relatively moderate CO₂-reducing solar-to-fuel efficiency (η_STF < ca. 18%) was achieved previously even using the most active gold-based electrocatalyst for the CO₂ reduction reaction (CO₂RR), which is much lower than the current highest solar-to-hydrogen efficiency (η_STH = 30%). Here, we report a strategy based on a monolithic nanoporous silver-based membrane electrocatalyst (npm-Ag) to increase the density of active sites while breaking the three-phase diffusion-limit length of previous membrane electrodes, improving the effective thickness of the catalyst layer from tens of nanometers to several micrometers without any polymer additive. The npm-Ag showed exceptionally selective reduction of CO₂ to CO at low overpotentials (ca. 80%@40 millivolts, ca. 100%@90–290 millivolts). The catalyst also allowed a nearly full use of the photocurrent of the state-of-the-art solar cells and gave a projected maximum η_STF of ca. 25%. Combined with a NiFe-based O₂-evolving anode, a stable CO₂-reducing photosynthetic system with an η_STF of ca. 20.1% was demonstrated experimentally for 28 hours in the absence of a DC/DC converter.