TY - JOUR
T1 - Efficient wettability-controlled electroreduction of CO2 to CO at Au/C interfaces
AU - Shi, Run
AU - Guo, Jiahao
AU - Zhang, Xuerui
AU - Waterhouse, Geoffrey I.N.
AU - Han, Zhaojun
AU - Zhao, Yunxuan
AU - Shang, Lu
AU - Zhou, Chao
AU - Jiang, Lei
AU - Zhang, Tierui
N1 - Funding Information:
The authors are grateful for financial support from the National Key Projects for Fundamental Research and Development of China (2017YFA0206904, 2017YFA0206900, 2016YFB0600901, 2018YFB1502002), the National Natural Science Foundation of China (51825205, U1662118, 51772305, 51572270, 21871279, 21802154, 21902168), the Beijing Natural Science Foundation (2191002, 2194089, 2182078), the Strategic Priority Research Program of the Chinese Academy of Sciences (XDB17000000), the Beijing Municipal Science and Technology Project (Z181100005118007), the Royal Society-Newton Advanced Fellowship (NA170422), the International Partnership Program of Chinese Academy of Sciences (GJHZ1819, GJHZ201974), the K. C. Wong Education Foundation and the Youth Innovation Promotion Association of the CAS. G.I.N.W. acknowledges funding support from the University of Auckland Faculty Research Development Fund, the Energy Education Trust of New Zealand, and the MacDiarmid Institute for Advanced Materials and Nanotechnology. The XAFS experiments were conducted in 1W1B beamline of Beijing Synchrotron Radiation Facility (BSRF).
Publisher Copyright:
© 2020, The Author(s).
PY - 2020/6/15
Y1 - 2020/6/15
N2 - The electrochemical CO2 reduction reaction (CO2RR) represents a very promising future strategy for synthesizing carbon-containing chemicals in a more sustainable way. In spite of great progress in electrocatalyst design over the last decade, the critical role of wettability-controlled interfacial structures for CO2RR remains largely unexplored. Here, we systematically modify the structure of gas-liquid-solid interfaces over a typical Au/C gas diffusion electrode through wettability modification to reveal its contribution to interfacial CO2 transportation and electroreduction. Based on confocal laser scanning microscopy measurements, the Cassie-Wenzel coexistence state is demonstrated to be the ideal three phase structure for continuous CO2 supply from gas phase to Au active sites at high current densities. The pivotal role of interfacial structure for the stabilization of the interfacial CO2 concentration during CO2RR is quantitatively analysed through a newly-developed in-situ fluorescence electrochemical spectroscopic method, pinpointing the necessary CO2 mass transfer conditions for CO2RR operation at high current densities.
AB - The electrochemical CO2 reduction reaction (CO2RR) represents a very promising future strategy for synthesizing carbon-containing chemicals in a more sustainable way. In spite of great progress in electrocatalyst design over the last decade, the critical role of wettability-controlled interfacial structures for CO2RR remains largely unexplored. Here, we systematically modify the structure of gas-liquid-solid interfaces over a typical Au/C gas diffusion electrode through wettability modification to reveal its contribution to interfacial CO2 transportation and electroreduction. Based on confocal laser scanning microscopy measurements, the Cassie-Wenzel coexistence state is demonstrated to be the ideal three phase structure for continuous CO2 supply from gas phase to Au active sites at high current densities. The pivotal role of interfacial structure for the stabilization of the interfacial CO2 concentration during CO2RR is quantitatively analysed through a newly-developed in-situ fluorescence electrochemical spectroscopic method, pinpointing the necessary CO2 mass transfer conditions for CO2RR operation at high current densities.
UR - http://www.scopus.com/inward/record.url?scp=85086445711&partnerID=8YFLogxK
U2 - 10.1038/s41467-020-16847-9
DO - 10.1038/s41467-020-16847-9
M3 - Article
C2 - 32541875
AN - SCOPUS:85086445711
VL - 11
JO - Nature Communications
JF - Nature Communications
SN - 2041-1723
IS - 1
M1 - 3028
ER -