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Published June 10, 2020 | Supplemental Material
Journal Article Open

Fermi Level Engineering of Passivation and Electron Transport Materials for p-Type CuBi₂O₄ Employing a High‐Throughput Methodology

Abstract

Metal oxide semiconductors are promising for solar photochemistry if the issues of excessive charge carrier recombination and material degradation can be resolved, which are both influenced by surface quality and interface chemistry. Coating the semiconductor with an overlayer to passivate surface states is a common remedial strategy but is less desirable than application of a functional coating that can improve carrier extraction and reduce recombination while mitigating corrosion. In this work, a data‐driven materials science approach utilizing high‐throughput methodologies, including inkjet printing and scanning droplet electrochemical cell measurements, is used to create and evaluate multi‐element coating libraries to discover new classes of candidate passivation and electron‐selective contact materials for p‐type CuBi₂O₄. The optimized overlayer (Cu_(1.5)TiO₂) improves the onset potential by 110 mV, the photocurrent by 2.8×, and the absorbed photon‐to‐current efficiency by 15.5% compared to non‐coated photoelectrodes. It is shown that these enhancements are related to reduced surface recombination through passivation of surface defect states as well as improved carrier extraction efficiency through Fermi level engineering. This work presents a generalizable, high‐throughput method to design and optimize passivation materials for a variety of semiconductors, providing a powerful platform for development of high‐performance photoelectrodes for incorporation into solar‐fuel generation systems.

Additional Information

© 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim. Received: January 31, 2020; Revised: March 17, 2020; Published online: May 4, 2020. Z.Z. and S.A.L. contributed equally to this work. This material was based upon work performed by the Joint Center for Artificial Photosynthesis, a DOE Energy Innovation Hub, supported through the Office of Science of U.S. Department of Energy under Award Number DE‐SC0004993. EDX mapping was performed at the Molecular Foundry, supported by the Office of Science, Office of Basic Energy Science, of the U.S. Department of Energy under Contract No. DE‐AC02‐05CH11231. Z.Z. also acknowledges the Chinese scholarship council (CSC) for providing funding. The authors declare no conflict of interest.

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