化学
异质结
光催化
石墨氮化碳
纳米颗粒
碳纤维
氮化物
化学工程
氮化碳
纳米技术
光电子学
催化作用
复合数
图层(电子)
有机化学
复合材料
物理
材料科学
工程类
作者
Miao Xuan,Xiao Bai,Peng Zhang,Bolong Wang,Shuyan Wang,Yuzhu Yang,Zenggang Lin,Sixia Li,Binbin Wang,Weisheng Liu
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2025-02-06
卷期号:64 (6): 2637-2648
被引量:6
标识
DOI:10.1021/acs.inorgchem.4c03685
摘要
Incorporating two-phase heterojunctions with matching band structures represents a promising strategy for developing photocatalysts with enhanced efficiency. This work prefers a novel approach that employs a template-assisted strategy based on a porous structured UCCN@CeO2 0D/2D S-scheme heterojunction. The proposed method aims to improve photocatalytic activity by harnessing the synergistic effects of monodispersed CeO2 nanoparticles and ultrathin N-defect CN nanosheets. The catalyst demonstrates a remarkable photocatalytic hydrogen evolution rate, reaching an impressive value of 5.59 mmol h–1 g–1 when subjected to simulated sunlight irradiation. Furthermore, the photocatalyst maintains a substantial activity level, yielding 2.35 mmol h–1 g–1 under visible light (≥400 nm). The significant improvement in the photocatalytic performance of the UCCN@CeO2 catalyst is attributed to the unique structural design and effective charge separation facilitated by the S-scheme mechanism. Kelvin probe force microscopy, theoretical calculations, and femtosecond transient absorption spectroscopy affirm the efficient charge transportation across the catalyst interface. Additionally, electron spin resonance spectroscopy measurements further support the charge transfer pathway in the S-scheme. This research presents an innovative approach for designing and developing CN-based catalysts featuring S-scheme heterojunctions, aiming to improve their efficiency and practical use in photocatalytic applications.
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