Wrapping Tin Sulfide Nanocatalysts with Graphene Oxide Nanosheets for Improved Electroreduction of Carbon Dioxide to Formic Acid

H Haonan Chen (School of Flexible Electronics (Future Technologies), Key Laboratory of Flexible Electronics, and Institute of Advanced Materials, Nanjing Tech University, 30 South Puzhu Road, Nanjing 211816, P. R. China) X Xinya Chen (School of Flexible Electronics (Future Technologies), Key Laboratory of Flexible Electronics, and Institute of Advanced Materials, Nanjing Tech University, 30 South Puzhu Road, Nanjing 211816, P. R. China) Q Qinghua Liu (National Synchrotron Radiation Laboratory) Z Zhiwei Yang (Key Laboratory of Colloid and Interface Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering) Y Yaning Liu (Department of Chemistry and Biochemistry) L Lu Jiang (School of Flexible Electronics (Future Technologies), Key Laboratory of Flexible Electronics, and Institute of Advanced Materials, Nanjing Tech University, 30 South Puzhu Road, Nanjing 211816, P. R. China) M Miao Ji (State Key Laboratory of Flexible Electronics (LoFE) & Institute ofadvanced Materials (IAM) School of Flexible Electronics (FutureTechnologies) Nanjing Tech University (NanjingTech) Nanjing Jiangsu China) X Xiao Huang (Department of Chemistry) G Gongqiang Li G Gang Lu

Abstract

ABSTRACT Electroreduction of carbon dioxide (CO 2 ) to formic acid is an important piece of puzzle in carbon neutralization and modern chemical industry. However, the catalytic activity and selectivity of this reaction still need to be improved for practical applications. Herein, we reveal that a highly active, selective, and stable electroreduction of CO 2 to formic acid could be realized by wrapping tin sulfide (SnS x ) nanoparticles with graphene oxide (GO) nanosheets. The GO wrapping helps to preserve the crystal size of SnS x (2∼4 nm) and confine the sulfur atoms in SnS x , obtaining a promising catalyst. As a result, a high current density of 126.25 ± 0.78 mA cm −2 and high Faradaic efficiency (FE) of 99.9 ± 1.1% toward formic acid is achieved in a flow cell. The current density could be further improved to 554.41 ± 2.32 mA cm −2 in a membrane electrolyzer. Additionally, our catalytic system demonstrates a high stability exceeding 50 h at ampere‐level current. This finding provides a valuable insight for further development of highly efficient and selective catalysts for electroreduction of CO 2 to high‐value carbon‐containing products. Our strategy may also be applied to preserve the structures of many other amorphous or nanocrystal catalysts for efficient and stable electrocatalysis.

Article Details

Volume / Issue Vol. 65, Issue 17
Published April 20, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (10)

H

Haonan Chen

School of Flexible Electronics (Future Technologies), Key Laboratory of Flexible Electronics, and Institute of Advanced Materials, Nanjing Tech University, 30 South Puzhu Road, Nanjing 211816, P. R. China

X

Xinya Chen

School of Flexible Electronics (Future Technologies), Key Laboratory of Flexible Electronics, and Institute of Advanced Materials, Nanjing Tech University, 30 South Puzhu Road, Nanjing 211816, P. R. China

Q

Qinghua Liu

National Synchrotron Radiation Laboratory

Z

Zhiwei Yang

Key Laboratory of Colloid and Interface Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering

Y

Yaning Liu

Department of Chemistry and Biochemistry

L

Lu Jiang

School of Flexible Electronics (Future Technologies), Key Laboratory of Flexible Electronics, and Institute of Advanced Materials, Nanjing Tech University, 30 South Puzhu Road, Nanjing 211816, P. R. China

M

Miao Ji

State Key Laboratory of Flexible Electronics (LoFE) & Institute ofadvanced Materials (IAM) School of Flexible Electronics (FutureTechnologies) Nanjing Tech University (NanjingTech) Nanjing Jiangsu China

X

Xiao Huang

Department of Chemistry

G

Gongqiang Li

G

Gang Lu