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High‐Rate, Tunable Syngas Production with Artificial Photosynthetic Cells
Author(s) -
Zhang Hongwen,
Ming Jintao,
Zhao Jiwu,
Gu Quan,
Xu Chao,
Ding Zhengxin,
Yuan Rusheng,
Zhang Zizhong,
Lin Huaxiang,
Wang Xuxu,
Long Jinlin
Publication year - 2019
Publication title -
angewandte chemie
Language(s) - English
Resource type - Journals
eISSN - 1521-3757
pISSN - 0044-8249
DOI - 10.1002/ange.201902361
Subject(s) - syngas , artificial photosynthesis , catalysis , electrochemistry , chemistry , energy conversion efficiency , materials science , photochemistry , chemical engineering , optoelectronics , photocatalysis , electrode , organic chemistry , engineering
An artificial photosynthetic (APS) system consisting of a photoanodic semiconductor that harvests solar photons to split H 2 O, a Ni‐SNG cathodic catalyst for the dark reaction of CO 2 reduction in a CO 2 ‐saturated NaHCO 3 solution, and a proton‐conducting membrane enabled syngas production from CO 2 and H 2 O with solar‐to‐syngas energy‐conversion efficiency of up to 13.6 %. The syngas CO/H 2 ratio was tunable between 1:2 and 5:1. Integration of the APS system with photovoltaic cells led to an impressive overall quantum efficiency of 6.29 % for syngas production. The largest turnover frequency of 529.5 h −1 was recorded with a photoanodic N‐TiO 2 nanorod array for highly stable CO production. The CO‐evolution rate reached a maximum of 154.9 mmol g −1 h −1 in the dark compartment of the APS cell. Scanning electrochemical–atomic force microscopy showed the localization of electrons on the single‐nickel‐atom sites of the Ni‐SNG catalyst, thus confirming that the multielectron reduction of CO 2 to CO was kinetically favored.