Metallic-like WN as electron harvester decorated on sulfur vacancy rich CdS single crystal for boosting photocatalytic hydrogen production

IF 9 1区 工程技术 Q1 ENERGY & FUELS
Wei Deng , Yifan Shao , Xuqiang Hao , Ping Li , Zhiliang Jin
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Abstract

Developing efficient, stable, low-cost, and earth-rich cocatalysts has been proven to be an effective strategy for achieving highly active semiconductor-based photocatalytic hydrogen evolution from water splitting. Herein, a Schottky junction was rationally fabricated by noble-metal-free metallic tungsten nitride (WN) and sulfur vacancies-rich CdS single crystals (WN/CdS) for competent photocatalytic H2 evolution. The density functional theory (DFT) calculation results indicated that metallic properties of WN. Systematic investigations reveal that metallic-like WN can be acted as a novel superior electron harvester to rapid capture and transfer photogenerated charges, which can be confirmed by the fluorescence, time-resolved fluorescence spectra (TRPL) and photoelectrochemical characterization and in-situ XPS. And the sulfur vacancies also can act as electron trappers to enhance carrier separation and electron transfer. Thus, the synergistic effect of sulfur vacancies and Schottky junction greatly enhance the photocatalytic H2 production activity. In addition, the more negative zeta potential of 10 %WN/CdS means the stronger protons adsorption well as promoted hydrogen evolution activity. The maximum photocatalytic H2 evolution activity of 15.02 mmol g−1 is achieved over 10 % WN/CdS composite, which is about 2.34 folds of pristine CdS, respectively. Meanwhile, a super photostability over ten consecutive cycles of light irradiation of 100 h is also achieved for photocatalytic hydrogen generation. This work certifies the metallic WN is a promising candidate to construct higher-performance heterostructured photocatalyst for efficient energy conversion.
金属状WN作为电子收集器装饰在富含硫空位的CdS单晶上,促进光催化制氢
开发高效、稳定、低成本和富土的助催化剂已被证明是实现高活性半导体光催化水裂解析氢的有效策略。本文利用无贵金属的金属氮化钨(WN)和富含硫空位的CdS单晶(WN/CdS)合理地制备了一个肖特基结,用于光催化析氢。密度泛函理论(DFT)计算结果表明了WN的金属性能。系统的研究表明,类金属WN可以作为一种新型的优越的电子收集器,快速捕获和转移光生电荷,这可以通过荧光、时间分辨荧光光谱(TRPL)、光电化学表征和原位XPS得到证实。硫空位还可以作为电子诱捕剂,促进载流子分离和电子转移。因此,硫空位和肖特基结的协同作用大大提高了光催化制氢活性。此外,10% WN/CdS的负zeta电位越大,表明其对质子的吸附能力越强,析氢活性越强。10% WN/CdS复合材料的最大光催化析氢活性为15.02 mmol g−1,分别为原始CdS的2.34倍左右。同时,光催化制氢在连续10个100 h的光照射周期内也实现了超光稳定性。这一工作证明了金属WN是一种很有前途的构建高性能异质结构光催化剂的候选材料,用于高效的能量转换。
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
Renewable Energy
Renewable Energy 工程技术-能源与燃料
CiteScore
18.40
自引率
9.20%
发文量
1955
审稿时长
6.6 months
期刊介绍: Renewable Energy journal is dedicated to advancing knowledge and disseminating insights on various topics and technologies within renewable energy systems and components. Our mission is to support researchers, engineers, economists, manufacturers, NGOs, associations, and societies in staying updated on new developments in their respective fields and applying alternative energy solutions to current practices. As an international, multidisciplinary journal in renewable energy engineering and research, we strive to be a premier peer-reviewed platform and a trusted source of original research and reviews in the field of renewable energy. Join us in our endeavor to drive innovation and progress in sustainable energy solutions.
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