Effect of Intrinsic Ferroelectric Phase Transition on Hydrogen Evolution Electrocatalysis

Author:

Wang Fengmei12ORCID,Ju Lin3,Wu Binglan2,Li Shuhui2,Peng Jian4,Chen Yetao5,Getaye Sendeku Marshet2,Wang Kairui1,Cai Yuchen2,Yi Jun5,Yang Ying6,Wang Zhenxing2,Sun Xiaoming1

Affiliation:

1. State Key Laboratory of Chemical Resource Engineering College of Chemistry Beijing University of Chemical Technology Beijing 100029 P. R. China

2. CAS Key Laboratory of Nanosystem and Hierarchical Fabrication National Center for Nanoscience and Technology Beijing 100029 P. R. China

3. School of Physics and Electric Engineering Anyang Normal University Anyang 455000 P. R. China

4. Institute for Superconducting and Electronic Materials Australian Institute for Innovative Materials University of Wollongong, Innovation Campus Squires Way North Wollongong NSW 2522 Australia

5. School of Electronic Science and Engineering Fujian Key Laboratory of Ultrafast Laser Technology and Applications Xiamen University Xiamen 361005 P. R. China

6. Shaanxi Provincial Key Laboratory of Electroanalytical Chemistry Key Laboratory of Synthetic and Natural Functional Molecule of the Ministry of Education College of Chemistry & Materials Science Northwest University Xi'an 710127 P.R. China

Abstract

AbstractHeterogeneous electrocatalysis closely relies on the electronic structure of the catalytic materials. The ferroelectric‐to‐paraelectric phase transition of the materials also involves a change in the state of electrons that could impact the electrocatalytic activity, but such correlation remains unexplored. Here, we demonstrate experimentally and theoretically that the intrinsic electrocatalytic activity could be regulated as exampled by hydrogen evolution reaction catalysis over two‐dimensional ferroelectric CuInP2S6. The obvious discontinuity in the overpotential and apparent activation energy values for CuInP2S6 electrode are illustrated during the ferroelectric‐to‐paraelectric phase transition caused by copper displacement around Tc point (318 K), revealing the ferroelectro‐catalytic effect on thermodynamics and kinetics of electrocatalysis. When loading Pt single atom on the CuInP2S6, the paraelectric phase one showed an improved hydrogen evolution activity with smaller apparent activation energy over the ferroelectric phase counterpart. This is attributed to the copper hopping between two sulfur planes, which alternate between strong and weak H adsorption at the Pt sites to simultaneously promote H+ reactant adsorption and H2 product desorption.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Henan Province

Key Technologies Research and Development Program

Publisher

Wiley

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