Affiliation:
1. Department of Chemical Engineering and Centre for Processable Electronics Imperial College London London SW7 2AZ UK
2. Chu Kochen Honors College Zhejiang University Hangzhou 310058 China
3. Department of Chemistry Molecular Sciences Research Hub Imperial College London London W12 0BZ UK
4. Department of Chemistry University of Manchester Manchester M13 9PL UK
5. Department of Chemistry University of Bath Bath BA2 7AY UK
Abstract
AbstractAchieving highly performant photoanodes for oxygen evolution is key to developing photoelectrochemical devices for solar water splitting. In this work, BiVO4 photoanodes are enhanced with a series of core–shell structured bimetallic nickel‐cobalt phosphides (MPs), and key insights into the role of co‐catalysts are provided. The best BiVO4/Ni1.5Co0.5P and BiVO4/Ni0.5Co1.5P photoanodes achieve a 3.5‐fold increase in photocurrent compared with bare BiVO4. It is discovered that this enhanced performance arises from a synergy between work function, catalytic activity, and capacitive ability of the MPs. Distribution of relaxation times analysis reveals that the contact between the MPs, BiVO4, and the electrolyte gives rise to three routes for hole injection into the electrolyte, all of which are significantly improved by the presence of a second metal cation in the co‐catalyst. Kinetic studies demonstrate that the significantly improved interfacial charge injection is due to a lower charge‐transfer resistance, enhanced oxygen‐evolution reaction kinetics, and larger surface hole concentrations, providing deeper insights into the carrier dynamics in these photoanode/co‐catalyst systems for their rational design.
Funder
UK Research and Innovation
Engineering and Physical Sciences Research Council
Subject
Biomaterials,Biotechnology,General Materials Science,General Chemistry
Cited by
4 articles.
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