In‐Situ‐Grown Cu Dendrites Plasmonically Enhance Electrocatalytic Hydrogen Evolution on Facet‐Engineered Cu2O

Author:

Zhang Hao12ORCID,Diao Jiefeng3,Liu Yonghui4,Zhao Han5,Ng Bryan K. Y.6,Ding Zhiyuan7,Guo Zhenyu8,Li Huanxin9,Jia Jun4,Yu Chang10,Xie Fang1,Henkelman Graeme3,Titirici Maria‐Magdalena8,Robertson John49,Nellist Peter7,Duan Chunying11,Guo Yuzheng4,Riley D. Jason1,Qiu Jieshan10

Affiliation:

1. Department of Materials and London Center for Nanotechnology Imperial College London London SW7 2AZ UK

2. Chemistry Research Laboratory Department of Chemistry University of Oxford Oxford OX1 3TA UK

3. Department of Chemistry and the Oden Institute for Computational Engineering and Sciences The University of Texas at Austin Austin TX 78712 USA

4. School of Electrical Engineering and Automation Wuhan University Wuhan 430072 P. R. China

5. Department of Chemistry University of Zurich Winterthurerstrasse 190 Zurich CH‐8057 Switzerland

6. Wolfson Catalysis Centre Department of Chemistry University of Oxford Oxford OX1 3QR UK

7. Department of Materials University of Oxford Oxford OX1 3PH UK

8. Department of Chemical Engineering Imperial College London London SW7 2AZ UK

9. Department of Engineering University of Cambridge Cambridge CB2 1PZ UK

10. State Key Lab of Fine Chemicals School of Chemical Engineering Liaoning Key Lab for Energy Materials and Chemical Engineering Dalian University of Technology Dalian 116024 P. R. China

11. School of Chemistry Dalian University of Technology Dalian Liaoning 116024 P. R. China

Abstract

AbstractHerein, facet‐engineered Cu2O nanostructures are synthesized by wet chemical methods for electrocatalytic HER, and it is found that the octahedral Cu2O nanostructures with exposed crystal planes of (111) (O‐Cu2O) has the best hydrogen evolution performance. Operando Raman spectroscopy and ex‐situ characterization techniques showed that Cu2O is reduced during HER, in which Cu dendrites are grown on the surface of the Cu2O nanostructures, resulting in the better HER performance of O‐Cu2O after HER (O‐Cu2O‐A) compared with that of the as‐prepared O‐Cu2O. Under illumination, the onset potential of O‐Cu2O‐A is ca. 52 mV positive than that of O‐Cu2O, which is induced by the plasmon‐activated electrochemical system consisting of Cu2O and the in‐situ generated Cu dendrites. Incident photon‐to‐current efficiency (IPCE) measurements and the simulated UV–Vis spectrum demonstrate the hot electron injection (HEI) from Cu dendrites to Cu2O. Ab initio nonadiabatic molecular dynamics (NAMD) simulations revealed the transfer of photogenerated electrons (27 fs) from Cu dendrites to Cu2O nanostructures is faster than electron relaxation (170 fs), enhancing its surface plasmons activity, and the HEI of Cu dendrites increases the charge density of Cu2O. These make the energy level of the catalyst be closer to that of H+/H2, evidenced by the plasmon‐enhanced HER electrocatalytic activity.

Funder

Imperial College London

China Scholarship Council

Engineering and Physical Sciences Research Council

National Energy Research Scientific Computing Center

Welch Foundation

Publisher

Wiley

Subject

Mechanical Engineering,Mechanics of Materials,General Materials Science

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