Temperature-controlled synthesis of heterostructured Ru-Ru2P nanoparticles embedded in carbon nanofibers for highly efficient hydrogen production

29Citations
Citations of this article
5Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Developing highly efficient, cost-effective, and stable electrocatalysts for hydrogen evolution reaction (HER) is of considerable importance but remains challenging. Herein, we report the fabrication of a robust Ru-based electrocatalyst, which comprises heterostructured Ru-Ru2P nanoparticles that are embedded in the N,P-codoped carbon nanofibers (CNFs), through a synthetic strategy involving electrospinning and temperature-controlled pyrolysis treatment. The as-prepared Ru-Ru2P catalyst (Ru-Ru2P@CNFs) shows excellent HER catalytic activities with low overpotentials of 11 and 14 mV in acidic and alkaline media, respectively, to achieve a current density of 10 mA cm−2, which are superior to the individual components of pure Ru and Ru2P catalysts. Density functional theory calculations demonstrate the existence of electronic coupling effect between Ru and Ru2P at the heterointerfaces, leading to a well-modulated electronic structure with optimized hydrogen adsorption strength and enhanced electrical conductivity for efficient HER electrocatalysis. In addition, the overall synthetic strategy can be generalized for the synthesis of a series of transitional metal phosphide-based nanofibers, thereby holding a remarkable capacity for various potential applications. [Figure not available: see fulltext.]

Cite

CITATION STYLE

APA

Wei, Y., Xu, G., Wei, Y., Ji, L., Wang, T., Liu, Z., & Wang, S. (2022). Temperature-controlled synthesis of heterostructured Ru-Ru2P nanoparticles embedded in carbon nanofibers for highly efficient hydrogen production. Science China Materials, 65(10), 2675–2684. https://doi.org/10.1007/s40843-022-2001-7

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free