Amorphous Double Cocatalyst Enhanced BiVO4 Photoanode for Efficient Solar-Driven Water Splitting

IF 8.2 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY
Guihong Li, Zetian He, Haiyang Li, Guofang Du, Wenfeng Li, Shiqing Ma, Tie Shi, Daimei Chen* and Yilei Li, 
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Abstract

Photoelectrochemical (PEC) water splitting has emerged as an effective method to address energy and environmental challenges. In this study, a novel BiVO4/FeOOH/CACo photoanode is developed by integrating FeOOH and cobalt cinnamate (CACo) cocatalysts onto the BiVO4 surface for enhanced PEC water splitting. Compared with the reversible hydrogen electrode (RHE), the photocurrent density of the fabricated photoanode reached 3.15 mA cm–2 at 1.23 VRHE, which is 3.15 times greater than that of pure BiVO4, demonstrating good stability. Furthermore, the photoelectrochemical water splitting of hydrogen and oxygen production rates of the photoanode in a seawater environment achieved rates of 4.71 μmol h–1 cm–2 and 2.87 μmol h–1 cm–2, respectively. Systematic characterizations combined with density functional theory (DFT) calculations elucidate the dual cocatalyst synergy: FeOOH serves as a hole transport layer to accelerate carrier migration toward the CACo layer, while their cooperative interaction suppresses electron–hole recombination and enhances photogenerated carrier mobility. This dual cocatalyst system effectively suppresses the recombination of electron–hole pairs, enhances the migration of photogenerated carriers, and improves the photochemical water splitting activity. This study presents a feasible strategy for the application of amorphous cocatalysts in PEC systems.

Abstract Image

非晶双助催化剂增强BiVO4光阳极用于高效太阳能驱动的水分解。
光电化学(PEC)水分解已成为解决能源和环境挑战的有效方法。在这项研究中,通过将FeOOH和肉桂酸钴(CACo)共催化剂整合到BiVO4表面,开发了一种新的BiVO4/FeOOH/CACo光阳极,以增强PEC水分解。与可逆氢电极(RHE)相比,制备的光阳极在1.23 VRHE下的光电流密度达到3.15 mA cm-2,是纯BiVO4的3.15倍,具有良好的稳定性。此外,在海水环境下,光电阳极的氢和氧的光电分解速率分别达到4.71 μmol h-1 cm-2和2.87 μmol h-1 cm-2。系统表征结合密度泛函理论(DFT)计算阐明了双助催化剂的协同作用:FeOOH作为空穴传输层加速载流子向CACo层的迁移,而它们的协同相互作用抑制电子-空穴复合并增强光生载流子迁移率。该双助催化剂体系有效抑制了电子-空穴对的复合,增强了光生载流子的迁移,提高了光化学水裂解活性。本研究为非晶态助催化剂在PEC体系中的应用提供了一种可行的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Materials & Interfaces
ACS Applied Materials & Interfaces 工程技术-材料科学:综合
CiteScore
16.00
自引率
6.30%
发文量
4978
审稿时长
1.8 months
期刊介绍: ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.
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