Yuqing He, Yuqing Liu, Jianding Zhang, Dong Zheng, Xuzhuo Fan, Gang Zhang, Di Wang, Wenping Wang, Shikui Han
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引用次数: 0
摘要
光电化学(PEC)水分解为清洁和可再生能源的发展提供了一个理想的策略。然而,它的实际实施往往受到光生载流子的高复合率和光阳极的不稳定性的抑制。引入缺陷工程(如氧空位)和构建内部电场调制z型异质纳米结构(HNs)可以被认为是克服这些障碍的有效途径。本文开发了一种灵活的方法来合成具有氧空位的Z-scheme BiOI-CdS HNs,该方法在超薄BiOI纳米片和CdS半导体之间产生内部电场。这种Z-scheme机制显著促进了光生电子-空穴对的分离,从而提高了PEC性能。在1.5G AM照明(100 mW cm-2)下,biio -CdS光阳极在1.6 V vs RHE下的光电流密度为4.22 mA cm-2,优于裸biio和CdS。此外,光阳极表现出优异的稳定性,经过严格的4小时测试后,其初始光电流仅略有下降,在耐久性方面超过了其他同类产品。这项工作为更好地理解氧空位和构建高效稳定的Z-scheme光阳极提供了可能的PEC应用。
Colloidal Design and Preparation of an Internal Electric Modulated Z-Scheme BiOI-CdS Heteronanostructure with Oxygen-Rich Vacancies
Photoelectrochemical (PEC) water splitting offers an ideal strategy for the development of clean and renewable energy. However, its practical implementation is often inhibited by the high recombination rate of photogenerated charge carriers and the instability of photoanodes. Introducing defect engineering (such as oxygen vacancies) and constructing internal electric field-modulated Z-scheme heteronanostructures (HNs) can be considered as effective approaches to overcome these obstacles. Herein, a flexible method is developed for synthesizing Z-scheme BiOI-CdS HNs with oxygen vacancies, which induce an internal electric field between ultrathin BiOI nanosheets and a CdS semiconductor. This Z-scheme mechanism significantly promotes the separation of photogenerated electron–hole pairs, thereby enhancing the PEC performance. The BiOI-CdS photoanode achieves a photocurrent density of 4.22 mA cm–2 at 1.6 V vs RHE under AM 1.5G illumination (100 mW cm–2), outperforming bare BiOI and CdS. Moreover, the photoanode exhibits exceptional stability with only a slight decrease of approximately in its initial photocurrent after a rigorous 4 h test, surpassing other counterparts in terms of durability. This work affords a better understanding of oxygen vacancies and the construction of highly efficient and stable Z-scheme photoanodes for feasible PEC application.
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.