Enhanced Alkaline Hydrogen Evolution Reaction via Electronic Structure Regulation: Activating PtRh with Rare Earth Tm Alloying

Author:

Li Qingqing1,Zhang Botao2,Sun Chang1,Sun Xiaolei1,Li Zhenxing2,Du Yaping1,Liu Jin‐Cheng1ORCID,Luo Feng1

Affiliation:

1. Nankai University Tianjin Key Laboratory of Rare‐earth Materials and Applications School of Materials Science and Engineering Centre of Rare Earth and Inorganic Functional Materials Tianjin 300350 P. R. China

2. State Key Laboratory of Heavy Oil Processing College of New Energy and Materials China University of Petroleum (Beijing) Beijing 102249 P. R. China

Abstract

AbstractDeveloping high‐performance electrocatalysts for alkaline hydrogen evolution reaction (HER) is crucial for producing green hydrogen, yet it remains challenging due to the sluggish kinetics in alkaline environments. Pt is located near the peak of HER volcano plot, owing to its exceptional performance in hydrogen adsorption and desorption, and Rh plays an important role in H2O dissociation. Lanthanides (Ln) are commonly used to modulate the electronic structure of materials and further influence the adsorption/desorption of reactants, intermediates, and products, and noble metal‐Ln alloys are recognized as effective platforms where Ln elements regulate the catalytic properties of noble metals. Here Pt1.5Rh1.5Tm alloy is synthesized using the sodium vapor reduction method. This alloy demonstrates superior catalytic activity, being 4.4 and 6.6 times more effective than Pt/C and Rh/C, respectively. Density Functional Theory (DFT) calculations reveal that the upshift of d‐band center and the charge transfer induced by alloying promote adsorption and dissociation of H2O, making Pt1.5Rh1.5Tm alloy more favorable for the alkaline HER reaction, both kinetically and thermodynamically.

Funder

National Key Research and Development Program of China

Publisher

Wiley

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