TY - JOUR
T1 - Nanoscale Engineering of P-Block Metal-Based Catalysts Toward Industrial-Scale Electrochemical Reduction of CO2
AU - Li, Pengfei
AU - Yang, Fangqi
AU - Li, Jing
AU - Zhu, Qiang
AU - Xu, Jian Wei
AU - Loh, Xian Jun
AU - Huang, Kuo-wei
AU - Hu, Wenping
AU - Lu, Jiong
N1 - KAUST Repository Item: Exported on 2023-07-31
Acknowledgements: P.L. and F.Y. contributed equally to this work. J.Lu. acknowledges the support from MOE grants (MOE-T2EP50121-0008, MOE-T2EP10221-0005) and Agency for Science, Technology and Research (A*STAR) under its AME IRG Grants (Project No. M21K2c0113) and (Project No. M22K2c0082) and IMRE-NUS Chemistry joint collaboration project (A-8000301-00-00). W.H. acknowledges the support from the National Natural Science Foundation of China (52121002). J.Li. acknowledges the support from the National Natural Science Foundation of China (22272004) and the Fundamental Research Funds for the Central Universities (YWF-22-L-1256).
PY - 2023/7/27
Y1 - 2023/7/27
N2 - The efficient conversion of CO2 to value-added products represents one of the most attractive solutions to mitigate climate change and tackle the associated environmental issues. In particular, electrochemical CO2 reduction to fuels and chemicals has garnered tremendous interest over the last decades. Among all products from CO2 reduction, formic acid is considered one of the most economically vital CO2 reduction products. P-block metals (especially Bi, Sn, In, and Pb) have been extensively investigated and recognized as the most efficient catalytic materials for the CO2 electroreduction to formate. Despite remarkable progress, the future implementation of this technology at the industrial-scale hinges on the ability to solve remaining roadblocks. In this review, the current research status, challenges, and prospects of p-block metal-based catalysts primarily for CO2 electroreduction to formate are comprehensively reviewed. The rational design and nanostructure engineering of these p-block metal catalysts for the optimization of their electrochemical performances are discussed in detail. Subsequently, the recent progress in the development of state-of-the-art operando characterization techniques together with the design of advanced electrochemical cells to uncover the intrinsic catalysis mechanism is discussed. Lastly, a perspective on future directions including tackling critical challenges to realize its early industrial implementation is presented.
AB - The efficient conversion of CO2 to value-added products represents one of the most attractive solutions to mitigate climate change and tackle the associated environmental issues. In particular, electrochemical CO2 reduction to fuels and chemicals has garnered tremendous interest over the last decades. Among all products from CO2 reduction, formic acid is considered one of the most economically vital CO2 reduction products. P-block metals (especially Bi, Sn, In, and Pb) have been extensively investigated and recognized as the most efficient catalytic materials for the CO2 electroreduction to formate. Despite remarkable progress, the future implementation of this technology at the industrial-scale hinges on the ability to solve remaining roadblocks. In this review, the current research status, challenges, and prospects of p-block metal-based catalysts primarily for CO2 electroreduction to formate are comprehensively reviewed. The rational design and nanostructure engineering of these p-block metal catalysts for the optimization of their electrochemical performances are discussed in detail. Subsequently, the recent progress in the development of state-of-the-art operando characterization techniques together with the design of advanced electrochemical cells to uncover the intrinsic catalysis mechanism is discussed. Lastly, a perspective on future directions including tackling critical challenges to realize its early industrial implementation is presented.
UR - http://hdl.handle.net/10754/693301
UR - https://onlinelibrary.wiley.com/doi/10.1002/aenm.202301597
U2 - 10.1002/aenm.202301597
DO - 10.1002/aenm.202301597
M3 - Article
SN - 1614-6832
JO - Advanced Energy Materials
JF - Advanced Energy Materials
ER -