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电荷传输通道和非金属等离子体协同增强CdS/TiN敏化的FeVO光阳极表面反应动力学和电荷分离,以实现高效的光电化学析氢。

Charge transport channel and nonmetallic plasmon synergistically augment surface reaction kinetics and charge separation for efficient photoelectrochemical hydrogen evolution of CdS/TiN-sensitized FeVO photoanode.

作者信息

Zheng Zhiyuan, Sun Canqun, Ma Mengjie, Wang Tianqi, Wang Lijuan, Fu Junli, Zhou Qing, Liang Yujie, Wang Wenzhong

机构信息

School of Science, Minzu University of China, Beijing 100081, China.

School of Science, Minzu University of China, Beijing 100081, China.

出版信息

J Colloid Interface Sci. 2025 Apr;683(Pt 1):585-599. doi: 10.1016/j.jcis.2024.12.090. Epub 2024 Dec 15.

DOI:10.1016/j.jcis.2024.12.090
PMID:39700567
Abstract

Achieving simultaneous enhancement in the light energy utilization efficiency, bulk charge carrier separation and surface charge carrier injection efficiency as well as the surface reaction kinetics of water oxidation is a formidable challenge for photoanodes in photoelectrochemical (PEC) water splitting hydrogen generation. Herein, nanoparticle-assembled flower-like CdS spheres and nonmetallic plasmonic TiN nanoparticles are exploited to successively sensitize FeVO nanoporous film (NPF) photoanode for achieving efficient PEC hydrogen evolution. The sensitization of TiN and CdS simultaneously integrates type-II band structure, surface plasmon resonance and Schottky junction into FeVO NPF photoanode, synergistically achieving simultaneous enhancement in the light energy utilization efficiency, bulk charge carrier separation efficiency, surface reaction kinetics of water oxidation and surface charge carrier injection efficiency. As a result, the highest charge separation and injection efficiencies of CdS/TiN-sensitized FeVO NPF photoanode are respectively increased by 25.5 and 1.96 times to those of bare FeVO NPF photoanode. Furthermore, the designed and constructed CdS/TiN-sensitized FeVO NPF photoanode exhibits substantially boosted unbiased solar-light-driven PEC hydrogen evolution ability with a photocurrent density of 2.12 mA/cm, which is two orders of magnitude (662 times) higher than that of the unsensitized FeVO NPF photoanode. The findings in this work provide a novel and promising strategy to design and construct high-performance FeVO-based nonmetallic plasmonic photoanodes for potential application in PEC hydrogen evolution.

摘要

在光电化学(PEC)水分解制氢中,要同时提高光阳极的光能利用效率、体电荷载流子分离效率、表面电荷载流子注入效率以及水氧化的表面反应动力学,是一项艰巨的挑战。在此,利用纳米颗粒组装的花状CdS球和非金属等离子体TiN纳米颗粒依次敏化FeVO纳米多孔膜(NPF)光阳极,以实现高效的PEC析氢。TiN和CdS的敏化将II型能带结构、表面等离子体共振和肖特基结同时整合到FeVO NPF光阳极中,协同实现了光能利用效率、体电荷载流子分离效率、水氧化的表面反应动力学和表面电荷载流子注入效率的同时提高。结果,CdS/TiN敏化的FeVO NPF光阳极的最高电荷分离和注入效率分别比裸FeVO NPF光阳极提高了25.5倍和1.96倍。此外,设计并构建的CdS/TiN敏化的FeVO NPF光阳极表现出显著增强的无偏压太阳光驱动的PEC析氢能力,光电流密度为2.12 mA/cm²,比未敏化的FeVO NPF光阳极高两个数量级(662倍)。这项工作中的发现为设计和构建高性能的基于FeVO的非金属等离子体光阳极提供了一种新颖且有前景的策略,用于PEC析氢的潜在应用。

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