Efficient photoelectrochemical CO2 conversion for selective acetic acid production

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Amidst the development of photoelectrochemical(PEC)CO2 conversion toward practical application,the production of high-value chemicals beyond C1 compounds under mild conditions is greatly desired yet challenging.Here,through rational PEC device design by combining Au-loaded and N-doped TiO2 plate nanoarray photoanode with Zn-doped Cu2O dark cathode,efficient conversion of CO2 to CH3COOH has been achieved with an outstanding Faradaic efficiency up to 58.1%(91.5%carbon selectivity)at 0.5 V vs.Ag/AgCl.Temperature programmed desorption and in situ Raman spectra reveal that the Zn-dopant in Cu2O plays multiple roles in selective catalytic CO2 conversion,including local electronic structure manipulation and active site modification,which together promote the formation of intermediate*CH2/*CH3 for C-C coupling.Apart from that,it is also unveiled that the sufficient electron density pro-vided by the Au-loaded and N-doped TiO2 plate nanoarray photoanode plays an equally important role by initiating multi-electron CO2 reduction.This work provides fresh insights into the PEC system design to reach the multi-electron reduction reaction and facilitate the C-C coupling reaction toward high-value multicarbon(C2+)chemical production via CO2 conversion.
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