Photoelectrochemical Homocoupling of Methane under Blue Light Irradiation
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 reve...
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Veröffentlicht in: | ACS energy letters 2019-02, Vol.4 (2), p.502-507 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | 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. |
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ISSN: | 2380-8195 2380-8195 |
DOI: | 10.1021/acsenergylett.8b02436 |