Coupling High‐Entropy Core with Rh Shell for Efficient pH‐Universal Hydrogen Evolution

Author:

Wei Min1,Sun Yuyan1,Zhang Junyu1,Zeng Jianrong23,Wang Jike1ORCID

Affiliation:

1. The Institute for Advanced Studies Wuhan University Wuhan 430072 P. R. China

2. Shanghai Synchrotron Radiation Facility Shanghai Advanced Research Institute Chinese Academy of Sciences Shanghai 201204 P. R. China

3. Shanghai Institute of Applied Physics Chinese Academy of Sciences Shanghai 201800 P. R. China

Abstract

AbstractConstructing high‐entropy alloys (HEAs) with core–shell (CS) nanostructure is efficient for enhancing catalytic activity. However, it is extremely challenging to incorporate the CS structure with HEAs. Herein, PtCoNiMoRh@Rh CS nanoparticles (PtCoNiMoRh@Rh) with ∼5.7 nm for pH‐universal hydrogen evolution reaction (HER) are reported for the first time. The PtCoNiMoRh@Rh just require 9.1, 24.9, and 17.1 mV to achieve −10 mA cm−2 in acid, neutral, and alkaline electrolyte, and the corresponding mass activity are 5.8, 2.79, and 91.8 times higher than that of Rh/C. Comparing to PtCoNiMoRh nanoparticles, the PtCoNiMoRh@Rh exhibit excellent HER activity attributed to the decrease of Rh 4d especially 4d5/2 unoccupied state induced by the multi‐active sites in HEA, as well as the synergistic effect in Rh shell and HEA core. Theorical calculation exhibits that Rh‐dyz, dx2, and dxz orbitals experience a negative shift with shell thickness increasing. The HEAs with CS structure would facilitate the rational design of high‐performance HEAs catalysts.

Publisher

Wiley

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