Issue 7, 2021

H4,4,4-graphyne with double Dirac points as high-efficiency bifunctional electrocatalysts for water splitting

Abstract

In the light of ultrahigh atom utilization, high catalytic activity and low cost, single-atom catalysts (SACs) have been garnering extensive attention in the field of electrochemistry. In recent studies, however, bifunctional SACs for water splitting are rare, and face the challenge of high overpotential. In this work, a series of transition metal (TM) atoms supported on two-dimensional (2D) H4,4,4-graphyne monolayer were verified to be bifunctional SACs for HER/OER and OER/ORR by first-principles calculations. It is interesting that Co@H4,4,4-GY and Pt@H4,4,4-GY could be applied as high-efficiency catalysts for water splitting with low overpotentials of 0.04/0.45 and 0.17/0.69 V for HER/OER, respectively. In addition, Ni@H4,4,4-GY as bifunctional SACs also exhibits desirable catalytic activity for OER/ORR with low overpotentials of 0.34/0.29 V, even superior to commercial IrO2 and RuO2. Our results reveal that TM–substrate coordination and local electronic property show significant effects on the catalytic properties for HER/OER/ORR, and the d band center as an effective descriptor could be adopted to optimize the catalytic performance of the catalysts.

Graphical abstract: H4,4,4-graphyne with double Dirac points as high-efficiency bifunctional electrocatalysts for water splitting

Supplementary files

Article information

Article type
Paper
Submitted
04 Nov 2020
Accepted
04 Jan 2021
First published
06 Jan 2021

J. Mater. Chem. A, 2021,9, 4082-4090

H4,4,4-graphyne with double Dirac points as high-efficiency bifunctional electrocatalysts for water splitting

H. Zhang, W. Wei, S. Wang, H. Wang, B. Huang and Y. Dai, J. Mater. Chem. A, 2021, 9, 4082 DOI: 10.1039/D0TA10767K

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements