Photoelectrochemical Homocoupling of Methane under Blue Light Irradiation
Source abstract
Abstract
Direct conversion of methane (CH4) into valuable chemicals with low-energy input is an important goal in the sustainable chemical industry. Herein, we report a photoelectrochemical activation of CH4 in the gas phase under visible light irradiation at room temperature. The proof-of-concept study revealed that homocoupling of CH4 to form ethane (C2H6) with high selectivity of 54% was induced by photogenerated holes over a tungsten trioxide (WO3) gas-diffusion photoanode coated with a proton-conducting ionomer in the presence of water vapor. The gas–electrolyte–solid triple-phase boundary enables the oxidation of the inert carbon–hydrogen bond of CH4, and the formation of carbon oxides and ethane with a carbon–carbon bond. The gas-phase photoelectrochemical system shows incident photon-to-current conversion efficiency of 11% under blue light at an applied voltage of 1.2 V. This work is also the first demonstration of a visible-light-driven hydrogen evolution from CH4. The hydrogen is separated from CH4 and oxidized products by a solid polymer electrolyte membrane.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Photocatalysis Techniques · Catalytic Processes in Materials Science · Electronic and Structural Properties of Oxides
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemical and Environmental Engineering, The University of Kitakyushu, Kitakyushu, Fukuoka 808-0135, Japan
Precursory Research for Embryonic Science and Technology (PRESTO), Japan Science and Technology Agency (JST), Kawaguchi, Saitama 332-0012, Japan
Department of Applied Chemistry, Kyushu Institute of Technology, Kitakyushu, Fukuoka 804-8550, Japan
Department of Applied Chemistry, Doshisha University, Kyotanabe, Kyoto 610-0321, Japan
Funding
Precursory Research for Embryonic Science and Technology
References (29)
Show source-provided references
1. 10.1126/science.125315010.1126/science.1253150 ↗
2. 10.1126/science.aag027410.1126/science.aag0274 ↗
3. 10.1021/acscatal.6b0108710.1021/acscatal.6b01087 ↗
4. 10.1021/acs.chemrev.6b0071510.1021/acs.chemrev.6b00715 ↗
5. 10.1039/c4cy00294f10.1039/c4cy00294f ↗
6. 10.1021/ar050194t10.1021/ar050194t ↗
7. 10.1007/s10563-014-9165-z10.1007/s10563-014-9165-z ↗
8. 10.1016/j.jcat.2008.05.02210.1016/j.jcat.2008.05.022 ↗
9. 10.1021/jp712029w10.1021/jp712029w ↗
10. 10.1016/j.apcatb.2016.11.03910.1016/j.apcatb.2016.11.039 ↗
11. 10.1039/C6CY02435A10.1039/C6CY02435A ↗
12. 10.1002/anie.20110232010.1002/anie.201102320 ↗
13. 10.1002/anie.20120004510.1002/anie.201200045 ↗
14. 10.1039/C7EE02951A10.1039/C7EE02951A ↗
15. 10.1021/ja500411910.1021/ja5004119 ↗
16. 10.1021/jp002232q10.1021/jp002232q ↗
17. 10.1016/j.matlet.2017.04.05110.1016/j.matlet.2017.04.051 ↗
18. Wagman D. D. · J. Phys. Chem. Ref. Data · 1982 · 11
19. 10.1021/acscentsci.8b0013010.1021/acscentsci.8b00130 ↗
20. 10.1039/c1ee01203g10.1039/c1ee01203g ↗
21. 10.1021/jp907367k10.1021/jp907367k ↗
22. 10.1016/j.elecom.2009.06.01910.1016/j.elecom.2009.06.019 ↗
23. 10.1039/C4RA05371K10.1039/C4RA05371K ↗
24. 10.1016/j.ijhydene.2016.07.23010.1016/j.ijhydene.2016.07.230 ↗
25. 10.1002/cssc.20180217810.1002/cssc.201802178 ↗
26. 10.3389/fchem.2018.0059810.3389/fchem.2018.00598 ↗
27. 10.1002/anie.20171094510.1002/anie.201710945 ↗
28. 10.1002/1097-4555(200006)31:6<451::AID-JRS528>3.0.CO;2-K10.1002/1097-4555(200006)31:6<451::AID-JRS528>3.0.CO;2-K ↗
29. 10.1002/anie.20180507910.1002/anie.201805079 ↗