Nitrogen‐Doped Graphene Quantum Dots Enhance the Activity of Bi 2 O 3  Nanosheets for Electrochemical Reduction of CO 2  in a Wide Negative Potential Region | Zendy

Chen Zhipeng | Zendy; Mou Kaiwen | Zendy; Wang Xiaohan | Zendy; Liu Licheng | Zendy

Premium

Nitrogen‐Doped Graphene Quantum Dots Enhance the Activity of Bi 2 O 3 Nanosheets for Electrochemical Reduction of CO 2 in a Wide Negative Potential Region

Author(s) -

Chen Zhipeng,

Mou Kaiwen,

Wang Xiaohan,

Liu Licheng

Publication year - 2018

Publication title -

angewandte chemie international edition

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 5.831

H-Index - 550

eISSN - 1521-3773

pISSN - 1433-7851

DOI - 10.1002/anie.201807643

Subject(s) - overpotential , formate , graphene , materials science , electrochemistry , catalysis , quantum dot , oxide , electrocatalyst , bismuth , nanotechnology , inorganic chemistry , chemistry , electrode , organic chemistry , metallurgy

Large numbers of catalysts have been developed for the electrochemical reduction of CO 2 to value‐added liquid fuels. However, it remains a challenge to maintain a high current efficiency in a wide negative potential range for achieving a high production rate of the target products. Herein, we report a 2D/0D composite catalyst composed of bismuth oxide nanosheets and nitrogen‐doped graphene quantum dots (Bi 2 O 3 ‐NGQDs) for highly efficient electrochemical reduction of CO 2 to formate. Bi 2 O 3 ‐NGQDs demonstrates a nearly 100 % formate Faraday efficiency (FE) at a moderate overpotential of 0.7 V with a good stability. Strikingly, Bi 2 O 3 ‐NGQDs exhibit a high activity (average formate FE of 95.6 %) from −0.9 V to −1.2 V vs. RHE. Additionally, DFT calculations reveal that the origin of enhanced activity in this wide negative potential range can be attributed to the increased adsorption energy of CO 2 (ads) and OCHO* intermediate after combination with NGQDs.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research