Boosting CO2 Hydrogenation to Formate over Edge‐Sulfur Vacancies of Molybdenum Disulfide

Author:

Wang Zifeng12,Kang Yiran23,Hu Jingting12,Ji Qinqin23,Lu Zhixuan1,Xu Guilan12,Qi Yutai12,Zhang Mo12,Zhang Wangwang12,Huang Rui2,Yu Liang23,Tian Zhong‐qun1,Deng Dehui123ORCID

Affiliation:

1. State Key Laboratory of Physical Chemistry of Solid Surfaces, Collaborative Innovation Center of Chemistry for Energy Materials (iChEM), College of Chemistry and Chemical Engineering Xiamen University Xiamen 361005 China

2. State Key Laboratory of Catalysis, Collaborative Innovation Center of Chemistry for Energy Materials (iChEM), Dalian Institute of Chemical Physics Chinese Academy of Science Dalian 116023 China

3. University of Chinese Academy of Sciences Beijing 100039 China

Abstract

AbstractSynthesis of formate from hydrogenation of carbon dioxide (CO2) is an atom‐economic reaction but is confronted with challenges in developing high‐performance non‐precious metal catalysts for application of the process. Herein, we report a highly durable edge‐rich molybdenum disulfide (MoS2) catalyst for CO2 hydrogenation to formate at 200 °C, which delivers a high selectivity of over 99 % with a superior turnover frequency of 780.7 h−1 surpassing those of previously reported non‐precious metal catalysts. Multiple experimental characterization techniques combined with theoretical calculations reveal that sulfur vacancies at MoS2 edges are the active sites and the selective production of formate is enabled via a completely new water‐mediated hydrogenation mechanism, in which surface OH* and H* species in dynamic equilibrium with water serve as moderate hydrogenating agents for CO2 with residual O* reduced by hydrogen. This study provides a new route for developing low‐cost high‐performance catalysts for CO2 hydrogenation to formate.

Publisher

Wiley

Subject

General Chemistry,Catalysis

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