Conductive Zeolite Supported Indium–Tin Alloy Nanoclusters for Selective and Scalable Formic Acid Electrosynthesis

Author:

Zhang Zhen12ORCID,Li Minzhe3,Yang Shuwen45,Ma Qianyi1,Dang Jianan45,Feng Renfei6,Bai Zhengyu5,Liu Dianhua3,Feng Ming7,Chen Zhongwei14ORCID

Affiliation:

1. Department of Chemical Engineering University of Waterloo Waterloo ON N2L 3G1 Canada

2. State Key Laboratory of Solidification Processing Center for Nano Energy Materials School of Materials Science and Engineering Northwestern Polytechnical University Xi'an 710072 China

3. State Key Laboratory of Chemical Engineering East China University of Science and Technology Shanghai 200237 China

4. State Key Laboratory of Catalysis Power Battery & Systems Research Center Dalian Institute of Chemical Physics Chinese Academy of Sciences Dalian 116023 China

5. School of Chemistry and Chemical Engineering Key Laboratory of Green Chemical Media and Reactions Ministry of Education Henan Normal University Xinxiang Henan 453007 China

6. Canadian Light Source Saskatoon SK S7N 2V3 Canada

7. Key Laboratory of Functional Materials Physics and Chemistry of the Ministry of Education Jilin Normal University Changchun 130103 China

Abstract

AbstractUpgrading excess CO2 toward the electrosynthesis of formic acid is of significant research and commercial interest. However, simultaneously achieving high selectivity and industrially relevant current densities of CO2‐to‐formate conversion remains a grand challenge for practical implementations. Here, an electrically conductive zeolite support is strategically designed by implanting Sn ions into the skeleton structure of a zeolite Y, which impregnates ultrasmall In0.2Sn0.8 alloy nanoclusters into the supercages of the tailored 12‐ring framework. The prominent electronic and geometric interactions between In0.2Sn0.8 nanoalloy and zeolite support lead to the delocalization of electron density that enhances orbital hybridizations between In active site and *OCHO intermediate. Thus, the energy barrier for the rate‐limiting *OCHO formation step is reduced, facilitating the electrocatalytic hydrogenation of CO2 to formic acid. Accordingly, the developed zeolite electrocatalyst achieves an industrial‐level partial current density of 322 mA cm−2 and remarkable Faradaic efficiency of 98.2% for formate production and stably maintains Faradaic efficiency above 93% at an industrially relevant current density for over 102 h. This work opens up new opportunities of conductive zeolite‐based electrocatalysts for industrial‐level formic acid electrosynthesis from CO2 electrolysis and toward practically accessible electrocatalysis and energy conversion.

Funder

University of Waterloo

Natural Sciences and Engineering Research Council of Canada

National Natural Science Foundation of China

Publisher

Wiley

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