Phase‐Dependent Reverse Electronic Metal‐Support Interaction to Boost Alkaline Hydrogen Evolution

B Binjie Li K Kunkun Nie (State Key Laboratory of Flexible Electronics (LoFE) & Institute of Flexible Electronics (IFE) Northwestern Polytechnical University Xi'an 710129 P. R. China) K Kangning Wang (Key Laboratory of Green and Precise Synthetic Chemistry and Applications Ministry of Education Huaibei Key Laboratory of Low‐Carbon Conversion of Small‐Molecule Resources School of Chemistry and Chemical Engineering Huaibei Normal University Huaibei P. R. China) X Xinpeng Tang (State Key Laboratory of Flexible Electronics (LoFE) & Institute of Flexible Electronics (IFE) Northwestern Polytechnical University Xi'an 710129 P. R. China) R Ruijia Wang L Lixin Yi Y Yujia Zhang Z Ziyi Wang J Jingtian Wang X Xiaorong Hao (State Key Laboratory of Flexible Electronics (LoFE) & Institute of Flexible Electronics (IFE) Northwestern Polytechnical University Xi'an 710129 P. R. China) C Chen Hu (Division of Quantitative Sciences Sidney Kimmel Comprehensive Cancer Center Johns Hopkins University School of Medicine Baltimore Maryland USA) W Wenlin Zhang (School of Physics, Hefei University of Technology , Hefei 230009,) Z Zhengqing Liu W Wei Huang

Abstract

Abstract Electronic metal‐support interaction (EMSI) represents a pivotal strategy for modulating the electronic structure of supported metals and enhancing their catalytic performance. However, limited reports have been conducted on the impact of the support crystal phase on EMSI. Here, a charge transfer inversion phenomenon associated with support crystal phase regulation is systematically revealed. Specifically, subnano‐sized noble metals (e.g., Pt, Rh, Ru) donate electrons to 2H‐MoS 2 support, whereas a reverse electron transfer direction is observed when these noble metals are supported on 1T‐MoS 2 . Electron‐enriched noble metals demonstrate significantly higher activity for alkaline hydrogen evolution compared to their electron‐deficient counterparts, with 1T‐MoS 2 @Pt achieving an exceptionally low overpotential of 18 mV at 10 mA cm −2 . Furthermore, an anion exchange membrane water electrolyzer (AEMWE) incorporating 1T‐MoS 2 @Pt as the cathode exhibits superior catalytic activity and sustained stability at ampere‐level current density. This work provides novel insights into developing efficient catalysts by regulating charge transfer dependent on the support crystal phase.

Article Details

Volume / Issue Vol. 38, Issue 7
Published February 01, 2026
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (14)

B

Binjie Li

K

Kunkun Nie

State Key Laboratory of Flexible Electronics (LoFE) & Institute of Flexible Electronics (IFE) Northwestern Polytechnical University Xi'an 710129 P. R. China

K

Kangning Wang

Key Laboratory of Green and Precise Synthetic Chemistry and Applications Ministry of Education Huaibei Key Laboratory of Low‐Carbon Conversion of Small‐Molecule Resources School of Chemistry and Chemical Engineering Huaibei Normal University Huaibei P. R. China

X

Xinpeng Tang

State Key Laboratory of Flexible Electronics (LoFE) & Institute of Flexible Electronics (IFE) Northwestern Polytechnical University Xi'an 710129 P. R. China

R

Ruijia Wang

L

Lixin Yi

Y

Yujia Zhang

Z

Ziyi Wang

J

Jingtian Wang

X

Xiaorong Hao

State Key Laboratory of Flexible Electronics (LoFE) & Institute of Flexible Electronics (IFE) Northwestern Polytechnical University Xi'an 710129 P. R. China

C

Chen Hu

Division of Quantitative Sciences Sidney Kimmel Comprehensive Cancer Center Johns Hopkins University School of Medicine Baltimore Maryland USA

W

Wenlin Zhang

School of Physics, Hefei University of Technology , Hefei 230009,

Z

Zhengqing Liu

W

Wei Huang