Issue 35, 2021

Pt modified Ni–Mo-based hydrates as bifunctional electrocatalysts for overall water splitting

Abstract

Pt-Modified Ni–Mo-based nanomaterials were prepared by a simple and effective method. The modified Ni–Mo-based materials exhibited excellent catalytic performance in KOH solution by adjusting the amount of Pt introduced. Due to the introduction of platinum, a large number of defects are formed, thereby improving the performance of the catalyst. At a current density of 100 mA cm−2, overpotentials of 242 and 448 mV are required for the hydrogen evolution reaction and the oxygen evolution reaction, respectively. The system needs a cell voltage of 1.58 V to reach a current density of 10 mA cm−2. In addition, the material exhibits good stability for up to 45 hours, which is considered high for bifunctional electrocatalysts. In addition, the effects of hydrothermal and immersion methods on the catalytic performance of platinum were explored. The immersion method shows a strong potential.

Graphical abstract: Pt modified Ni–Mo-based hydrates as bifunctional electrocatalysts for overall water splitting

Supplementary files

Article information

Article type
Paper
Submitted
27 Apr 2021
Accepted
28 Jul 2021
First published
28 Jul 2021

New J. Chem., 2021,45, 16313-16318

Pt modified Ni–Mo-based hydrates as bifunctional electrocatalysts for overall water splitting

Y. Guan and Y. Liu, New J. Chem., 2021, 45, 16313 DOI: 10.1039/D1NJ02046C

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