Issue 15, 2022

N-doping induced lattice-strained porous PdIr bimetallene for pH-universal hydrogen evolution electrocatalysis

Abstract

Porous Pd-based metallene with highly curved, ultrathin and porous architectural features is a promising candidate for the hydrogen evolution reaction (HER), and structural design and component modification can effectively enhance its performance. Herein, we present a powerful approach to boost the HER performance of porous PdIr bimetallene through N-doping, which can effectively modulate the electronic structure and induce the strain effect of the designed N-doped porous PdIr bimetallene (N-PdIr bimetallene). The porous N-PdIr bimetallene exhibits superior all-pH HER activity and stability. To generate a cathodic current density of 10 mA cm−2, the required overpotential for the porous N-PdIr bimetallene is 26, 34 and 59 mV in 0.5 M H2SO4, 1 M KOH and 1 M phosphate buffer solution (PBS), respectively, which outperform those of commercial Pt/C. The proposed N-doping approach is a very powerful strategy for boosting metallene electrocatalytic performance, beyond the HER.

Graphical abstract: N-doping induced lattice-strained porous PdIr bimetallene for pH-universal hydrogen evolution electrocatalysis

Supplementary files

Article information

Article type
Paper
Submitted
21 Jan 2022
Accepted
03 Mar 2022
First published
03 Mar 2022

J. Mater. Chem. A, 2022,10, 8364-8370

N-doping induced lattice-strained porous PdIr bimetallene for pH-universal hydrogen evolution electrocatalysis

Q. Mao, K. Deng, W. Wang, P. Wang, Y. Xu, Z. Wang, X. Li, L. Wang and H. Wang, J. Mater. Chem. A, 2022, 10, 8364 DOI: 10.1039/D2TA00590E

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