硅片级InGaN/GaN纳米线上的高耦合动态调制电催化剂用于连续酸性光电化学水氧化

IF 27.4 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Wengang Gu, Wei Chen, Weiyi Wang, Xin Liu, Zhixiang Gao, Yang Kang, Yuanmin Luo, Yang Li, Wei Hu, Ran Long, Haiding Sun
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引用次数: 0

摘要

光电化学水分解被认为是最有前途的可持续制氢途径之一。然而,由于水氧化反应的动力学迟缓和光阳极的稳定性差,严重限制了光电化学器件的整体性能,特别是在酸性条件下,这给实际应用带来了很大的挑战。本文提出了具有动态电子调制效应的独特CoRuOx纳米团簇与晶圆级InGaN纳米线的耦合,显示出优异的光电化学活性和酸性水氧化的稳定性。与负载典型的RuO₂助催化剂的InGaN纳米线相比,CoRuOx/InGaN光阳极的应用偏压光子电流效率从0.77%提高到2.25%,在强酸性条件下稳定运行500 min以上。这种提升的性能主要归因于Co诱导的动态电子调制,该调制在保持CoRuOx/InGaN光阳极稳定运行的同时增强了氧的析出。最初,Co位增加了Ru的氧化态,增强了析氧活性。此外,在PEC操作过程中,Co位点稳定了Ru位点,防止了助催化剂的溶解。这种独特的自适应工艺显著提高了光阳极的稳定性和活性,为实现高效耐用的光电阳极在PEC中的应用开辟了一条有效的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Highly Coupled Dynamically Modulated Electrocatalysts on Wafer-Scale InGaN/GaN Nanowires on Silicon for Successive Acidic Photoelectrochemical Water Oxidation

Highly Coupled Dynamically Modulated Electrocatalysts on Wafer-Scale InGaN/GaN Nanowires on Silicon for Successive Acidic Photoelectrochemical Water Oxidation
Photoelectrochemical water splitting is considered one of the most promising paths for sustainable hydrogen production. However, the sluggish kinetics of the water oxidation reaction and poor stability of the photoanode significantly limit the overall performance of the photoelectrochemical device, particularly under acidic conditions, which poses great challenges for practical applications. Herein, the coupling of unique CoRuOx nanoclusters with dynamic electronic modulation effects to wafer-scale InGaN nanowires is proposed, demonstrating superior photoelectrochemical activity and stability for acidic water oxidation. Compared with InGaN nanowires loaded with typical RuO₂ cocatalysts, CoRuOx/InGaN photoanodes achieve a remarkable improvement in applied bias photon-to-current efficiency from 0.77% to 2.25%, with stable operation for over 500 min under strongly acidic conditions. Such boosted performance is attributed mainly to Co induced dynamic electronic modulation, which enhances oxygen evolution while maintaining the stable operation of CoRuOx/InGaN photoanodes. Initially, the Co sites increased the oxidation state of Ru, enhancing the activity of oxygen evolution. Moreover, during PEC operation, the Co sites stabilized the Ru sites, preventing dissolution of cocatalyst. This unique self-adaptive process significantly enhances the stability and activity of the photoanode, opening an effective avenue to achieve efficient and durable photoanodes for PEC applications.
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来源期刊
Advanced Materials
Advanced Materials 工程技术-材料科学:综合
CiteScore
43.00
自引率
4.10%
发文量
2182
审稿时长
2 months
期刊介绍: Advanced Materials, one of the world's most prestigious journals and the foundation of the Advanced portfolio, is the home of choice for best-in-class materials science for more than 30 years. Following this fast-growing and interdisciplinary field, we are considering and publishing the most important discoveries on any and all materials from materials scientists, chemists, physicists, engineers as well as health and life scientists and bringing you the latest results and trends in modern materials-related research every week.
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