Urupalli Bharagav, Kim Dong-Seog, Shin Gi-Seung, Oh Geun-Jae, Van Tran Tuong, Yoon Ji-Wook, Yu Yeon-Tae
Division of Advanced Materials Engineering, Research centre for Advanced Materials Development, eonbuk National University, Jeonju, 54896, South Korea.
Small. 2025 Aug;21(34):e2501833. doi: 10.1002/smll.202501833. Epub 2025 Jun 26.
The spatial inhomogeneity of interfacial modifications, despite conventional approaches like co-catalyst deposition and dopant incorporation, presents a critical bottleneck in achieving optimal charge carrier dynamics and sustained photocatalytic performance at semiconductor heterojunctions. To address this challenge, this study introduces a novel approach by encapsulating the wide-bandgap semiconductor AgWO (AWO) in a particulate shell of plasmonic hot spots (metallic Ag), forming a well-defined interface that facilitates consistent charge transfer and enhances photocatalytic efficiency. The engineered AgWO@Ag (AWO@Ag) is strategically integrated with ZnInS (ZIS) nanosheets to design core-shell integrated Z-scheme heterojunction. The optimized integration of AWO@Ag (12.5%) over ZIS nanosheets demonstrates a remarkable hydrogen generation performance, achieving 3142 µmol hg, surpassing the performance of pure ZnInS (1311 µmol hg). Through rational interface design with strong redox abilities, the system achieves an impressive methyl orange photodegradation efficiency of 97.16% within 60 min. Additionally, it exhibits photoanodic currents of 3.98 mA cm at 2.2 V versus RHE in a neutral electrolytic medium, demonstrating enhanced water oxidation capability facilitated by AWO@Ag integration. The system's exceptional performance across hydrogen generation, dye degradation, and water oxidation, validates that this advanced structural design enables stable and sustained photocatalytic performance through its multifunctional properties.
尽管有共催化剂沉积和掺杂剂掺入等传统方法,但界面修饰的空间不均匀性仍是在半导体异质结处实现最佳载流子动力学和持续光催化性能的关键瓶颈。为应对这一挑战,本研究引入了一种新方法,即将宽带隙半导体AgWO(AWO)封装在等离子体热点(金属Ag)的颗粒壳中,形成一个明确的界面,促进一致的电荷转移并提高光催化效率。经过工程设计的AgWO@Ag(AWO@Ag)与ZnInS(ZIS)纳米片进行策略性整合,以设计核壳集成Z型异质结。在ZIS纳米片上优化整合12.5%的AWO@Ag表现出卓越的产氢性能,达到3142 μmol hg,超过了纯ZnInS(1311 μmol hg)的性能。通过具有强氧化还原能力的合理界面设计,该系统在60分钟内实现了令人印象深刻的97.16%的甲基橙光降解效率。此外,在中性电解介质中,相对于可逆氢电极(RHE)在2.2 V时,它表现出3.98 mA cm的光阳极电流,表明AWO@Ag的整合促进了水氧化能力的增强。该系统在产氢、染料降解和水氧化方面的卓越性能验证了这种先进的结构设计通过其多功能特性能够实现稳定和持续的光催化性能。