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Effect of Intrinsic Ferroelectric Phase Transition on Hydrogen Evolution Electrocatalysis.
Wang, Fengmei; Ju, Lin; Wu, Binglan; Li, Shuhui; Peng, Jian; Chen, Yetao; Getaye Sendeku, Marshet; Wang, Kairui; Cai, Yuchen; Yi, Jun; Yang, Ying; Wang, Zhenxing; Sun, Xiaoming.
Afiliação
  • Wang F; State Key Laboratory of Chemical Resource Engineering, College of Chemistry, Beijing University of Chemical Technology, Beijing, 100029, P. R. China.
  • Ju L; CAS Key Laboratory of Nanosystem and Hierarchical Fabrication, National Center for Nanoscience and Technology, Beijing, 100029, P. R. China.
  • Wu B; School of Physics and Electric Engineering, Anyang Normal University, Anyang, 455000, P. R. China.
  • Li S; CAS Key Laboratory of Nanosystem and Hierarchical Fabrication, National Center for Nanoscience and Technology, Beijing, 100029, P. R. China.
  • Peng J; CAS Key Laboratory of Nanosystem and Hierarchical Fabrication, National Center for Nanoscience and Technology, Beijing, 100029, P. R. China.
  • Chen Y; Institute for Superconducting and Electronic Materials, Australian Institute for Innovative Materials, University of Wollongong, Innovation Campus, Squires Way, North Wollongong, NSW 2522, Australia.
  • Getaye Sendeku M; School of Electronic Science and Engineering, Fujian Key Laboratory of Ultrafast Laser Technology and Applications, Xiamen University, Xiamen, 361005, P. R. China.
  • Wang K; CAS Key Laboratory of Nanosystem and Hierarchical Fabrication, National Center for Nanoscience and Technology, Beijing, 100029, P. R. China.
  • Cai Y; State Key Laboratory of Chemical Resource Engineering, College of Chemistry, Beijing University of Chemical Technology, Beijing, 100029, P. R. China.
  • Yi J; CAS Key Laboratory of Nanosystem and Hierarchical Fabrication, National Center for Nanoscience and Technology, Beijing, 100029, P. R. China.
  • Yang Y; School of Electronic Science and Engineering, Fujian Key Laboratory of Ultrafast Laser Technology and Applications, Xiamen University, Xiamen, 361005, P. R. China.
  • Wang Z; 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.
  • Sun X; CAS Key Laboratory of Nanosystem and Hierarchical Fabrication, National Center for Nanoscience and Technology, Beijing, 100029, P. R. China.
Angew Chem Int Ed Engl ; 63(18): e202402033, 2024 Apr 24.
Article em En | MEDLINE | ID: mdl-38407516
ABSTRACT
Heterogeneous 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.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article