Ka Yoon Shina,
Yujin Kimb,
Ali Mirzaei*c,
Hyoun Woo Kim*a and
Sang Sub Kim*b
aDivision of Materials Science and Engineering, Hanyang University, Seoul 04763, Republic of Korea. E-mail: hyounwoo@hanyang.ac.kr
bDepartment of Materials Science and Engineering, Inha University, Incheon 22212, Republic of Korea. E-mail: sangsub@inha.ac.kr
cDepartment of Materials Science and Engineering, Shiraz University of Technology, Shiraz 715557-13876, Islamic Republic of Iran. E-mail: mirzaei@sutech.ac.ir
First published on 12th May 2025
Correction for ‘Bimetal-decorated resistive gas sensors: a review’ by Ka Yoon Shin et al., J. Mater. Chem. C, 2025, https://doi.org/10.1039/D5TC00145E.
The correct form of eqn (3) is as follows:
O2−(ads) + e− → 2O−(ads) | (3) |
The correct version of Fig. 5 is as follows:
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Fig. 5 (a) and (b) Catalytic effect of noble metals for enhanced gas response of resistive gas sensors. |
The omitted paragraphs, and Tables 2 and 3, should appear immediately before the heading “Conclusions and outlook”, and should read as follows:
Table 2 summarizes the gas sensing performance of various bimetal-decorated resistive gas sensors. Overall, bimetal-decorated gas sensors have been successfully used for the detection of various gases such as H2, NO2, C3H6O, H2S, CH4, and CO gases. The optimal sensing temperature varies between RT to 400 °C depending on gas type, type of sensing material and type of bimetallic system. Response and recovery times also mainly depend on the sensing temperature; however, they are often short. Bimetal-decorated gas sensors generally have good long-term stability and show good stability at least up to 30 days after fabrication. Finally, detection limits down to ppb levels have been reported for bimetal-decorated gas sensors, showing their potential for the development of highly sensitive and reliable gas sensors.
Sensing material | Gas and conc./ppm | T (°C) | Response (Ra/Rg) or (Rg/Ra) | Response time (s)/recovery time (s) | Long-term stability (days) | Detection limit | Ref. |
---|---|---|---|---|---|---|---|
AuPd/SnO2 nanoparticles | H2 100 ppm | 150 | 72.8 | Not reported | 30 | Not reported | 58 |
AuPd/SnO2 nanorods | H2 100 ppm | 175 | 46.4 | 19/302 | 35 | Not reported | 59 |
AuPd/ZnO NWs | NO2 1 ppm | 100 | 94.2 | 35/30 | Not reported | Not reported | 60 |
AuPd/In2O3 porous spheres | C3H9N 100 ppm | 175 | 367.0 | 2/300 | Stable for 30 days | 300 ppb | 61 |
AuPd/WO3 hierarchical bundles | C4H10O 50 ppm | 200 | 91.0 | 8/12 | 20 | 1 ppm | 62 |
AuPd/WO3 nanorods | C3H6O 2 ppm | 300 | 12.0 | 5/3 | 56 | 100 ppb | 64 |
AuPd/SnO2 nanosheets | C3H6O 2 ppm | 250 | 6.6 | 4/6 (to 20 ppm acetone) | 40 | 45 ppb | 65 |
HCHO 2 ppm | 110 | 4.1 | Not reported | 40 | 30 ppb | ||
AuPd/WO3 nanospheres | C4H8O2 10 ppm | 250 | 400.0 | 8/4 | 30 | 100 ppb | 69 |
PdAu/W18O49 nanowires | H2S 50 ppm | 100 | 55.5 | 10/9 | 56 | Not reported | 72 |
CH4 1000 ppm | 320 | 7.8 | 25/15 | 56 | Not reported | ||
PdRu/SnO2 nanoclusters | C3H9N 100 ppm | 230 | 78.3 | 10/81 | 15 | 1 ppm | 74 |
AuPt/ZnO nanorods | H2 250 ppm | 130 | 157.4 | 115/not reported (RT) | Not reported | Not reported | 75 |
AuPt/ZnO nanowires | H2S 20 ppm | 300 | 17.7 | 17/151 | 30 | Not reported | 76 |
AuPt/ZnO nanoflowers | C7H8 50 ppm | 175 | 69.7 | 22/137 | 30 | 500 ppb | 77 |
AuPt/In2O3 nanofibers | O3 110 ppb | 90 | 10.3 | Not reported | 30 | 20 ppb | 78 |
C3H6O 50 ppm | 240 | 7.1 | Not reported | 30 | 500 ppb | ||
PtCu/WO3/H2O nanoplates | C3H6O 50 ppm | 280 | 204.9 | 3/8 | Not reported | 10 ppb | 79 |
PtNi3/WO3 nanoplates | HCOOH 100 ppm | 220 | 591.0 | 3/not reported | 60 | 500 ppb | 80 |
AuPt/Carbon nanofibers | H2 4 vol% | RT | 48% | 7/18 | 210 | Not reported | 81 |
Ni–Pt/CNF | H2 100 ppm | RT | 13% | 32/72 | Not reported | 10 ppb | 82 |
PtPd–WO3 NFs | C3H6O 1 ppm | 300 | 97.5 | 4.2/204 | Not reported | 1.07 ppb | 83 |
PtRh–WO3 NFs | C3H6O 1 ppm | 350 | 104.0 | 4/176 | Not reported | 0.3 ppb | |
PtPd/In2O3 nanoparticles | H2 100 ppm | RT | 29.8 | 58/200 | 30 | Not reported | 84 |
PdPt/ZnO nanorod clusters | H2 1% | 50 | 70% | 5/76 | Not reported | 0.2 ppm | 86 |
PdPt/SnO2 NWs | NO2 0.1 ppm | 300 | 880.0 | 13/9 | Not reported | Not reported | 89 |
PtPd/Ru-implanted WS2 nanosheets | C3H6O 50 ppm | 20 | 4.2 | 77/48 | Not reported | 1 ppb | 92 |
PdPt NOS-SnO2 | H2 1000 ppm | 50 | 75680 | 1/8 | 30 | 10 ppm | 93 |
PtPd/SnO2 multishell hollow microspheres | HCHO 1 ppm | 190 | 867% | 5/7 | 42 | 50 ppb | 94 |
PtPd/SnO2 nanosheets | CO 1 ppm | 100 | 6.5 | 5/4 | 60 | Not reported | 95 |
CH4 500 ppm | 320 | 3.1 | 5/4 | 60 | Not reported | ||
PtRu/Flower-like WO3 | C8H10 100 ppm | 170 | 261.0 | 2/329 | 14 | 1.97 ppm | 97 |
Ag6Au1/In2O3 nanoclusters | HCHO 5 ppm | 170 | 277.0 | 147/186 | 15 | 26 ppb | 98 |
AgPd/ZnO nanoplates | H2 500 ppm | 400 | 78.0 | 2/13 | 28 | 800 ppb | 99 |
AuAg/MWCNTs/WO3 | NO2 1000 ppb | RT | 1.995 (△R/Ra) (%) | 267/very slow recovery | 95 | 45 ppb | 100 |
Table 3 summarizes the selectivity and long-term stability of various bimetal-decorated gas sensors. The selectivity ratio of Au65Pd35 bimetallic decoration for the SnO2 gas sensor is 7.18, which is seven times higher than that of the pristine SnO2 sensor at 150 °C.58 While the optimal sensing temperature of the pristine ZnO sensor was 150 °C with a selectivity ratio of 3.15, AuPd bimetallic decoration decreased the sensing temperature to 100 °C and simultaneously increased the selectivity ratio to 14.95.60 For the pristine In2O3 sensor, which operated optimally at temperatures above 250 °C, AuPd bimetallic decoration reduced the sensing temperature to 175 °C, achieving a high selectivity ratio of 10.00.61 In addition, while the selectivity ratio of the pristine ZnO sensor was 1.00, PtAu bimetallic decoration increased the selectivity ratio to 14.70 at 130 °C.75 Similarly, for the pristine ZnO sensor with an optimal sensing temperature of 200 °C, AuPt bimetallic decoration reduced the sensing temperature to 175 °C, resulting in a high selectivity ratio of 10.00.77 Additionally, for a pristine WO3 sensor with an optimal sensing temperature of 300 °C, PtNi3 bimetallic decoration lowered the sensing temperature to 220 °C, achieving a selectivity ratio of 10.32.80 In particular, for the NOS PdPt/SnO2 sensor, the selectivity ratio was 1.87, while NOS Pd2Pt/SnO2 led to a dramatic increase in the selectivity ratio to 929.53 at 25 °C, achieved through an optimal Pd:
Pt atomic loading ratio. These results underscore the effectiveness of bimetallic catalysts in improving both the selectivity and operating temperature of resistive gas sensors, highlighting their potential for high-performance applications.
Bimetallic system | Sensing material | Selectivity to gas | Long-term stability (days) | Ref. |
---|---|---|---|---|
AuPd | SnO2 nanoparticles | H2 | 30 | 58 |
SnO2 nanorods | H2 | 35 | 59 | |
ZnO nanowires | NO2 | Not reported | 60 | |
In2O3 porous spheres | C3H9N | 30 | 61 | |
WO3 hierarchical bundles | C4H10O | 20 | 62 | |
WO3 nanorods | C3H6O | 35 | 64 | |
SnO2 nanosheets | C3H6O, HCHO | 40 | 65 | |
WO3 nanospheres | C4H8O2 | 30 | 69 | |
W18O49 nanowires | H2S, CH4 | 56 | 72 | |
PdRu | SnO2 nanoclusters | C3H9N | 15 | 74 |
AuPt | ZnO nanorods | H2 | Not reported | 75 |
ZnO nanowires | H2S | 30 | 76 | |
ZnO nanoflowers | C7H8 | 30 | 77 | |
In2O3 nanofibers | O3, C3H6O | 30 | 78 | |
Carbon nanofibers | H2 | 180 | 81 | |
PtCu | WO3/H2O hollow sphere | C3H6O | Not reported | 79 |
PtNi | WO3 nanoplates | HCOOH | 60 | 80 |
Carbon nanofibers | H2 | Not reported | 82 | |
PtRh | WO3 NFs | C3H6O | Not reported | 83 |
PtPd | WO3 NFs | C3H6O | Not reported | 83 |
In2O3 nanoparticles | H2 | 30 | 84 | |
ZnO nanorod | H2 | Not reported | 86 | |
SnO2 NWs | NO2 | Not reported | 89 | |
Ru-implanted WS2 nanosheets | C3H6O | Not reported | 92 | |
SnO2 | H2 | 30 | 93 | |
SnO2 multishell hollow microspheres | HCHO | 42 | 94 | |
SnO2 nanosheets | CO, CH4 | 60 | 95 | |
PtRu | Flower-like WO3 | C8H10 | 2 | 97 |
AuAg | In2O3 nanocluster | HCHO | 15 | 98 |
MWCNTs/WO3 | NO2 | 95 | 100 | |
AgPd | ZnO nanoplates | H2 | 4 | 99 |
The author contributions section should read as follows:
Author contributions
Ka Yoon Shin: conceptualization, writing – original draft; Yujin Kim: investigation, visualization; Ali Mirzaei: conceptualization, writing – original draft; Hyoun Woo Kim: supervision, validation; Sang Sub Kim: supervision, project administration, writing – review & editing.
The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.
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