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氮空位诱导原位形成g-CN p-n同质结以促进可见光驱动析氢

Nitrogen vacancy induced in situ g-CN p-n homojunction for boosting visible light-driven hydrogen evolution.

作者信息

Liao Yuwei, Wang Guohong, Wang Juan, Wang Kai, Yan Suding, Su Yaorong

机构信息

Hubei Key Laboratory of Pollutant Analysis and Reuse Technology, College of Chemistry and Chemical Engineering, Institute for Advanced Materials, Hubei Normal University, Huangshi 435002, PR China.

Hubei Key Laboratory of Pollutant Analysis and Reuse Technology, College of Chemistry and Chemical Engineering, Institute for Advanced Materials, Hubei Normal University, Huangshi 435002, PR China.

出版信息

J Colloid Interface Sci. 2021 Apr;587:110-120. doi: 10.1016/j.jcis.2020.12.009. Epub 2020 Dec 7.

Abstract

Graphitic carbon nitride (g-CN) as a novel photocatalyst with great potentials has been extensively employed in solar-driven energy conversion. Herein, the novel in situ g-CN p-n homojunction photocatalyst with nitrogen vacancies (NV-g-CN) is successfully fabricated via hydrothermal synthesis followed by two-step calcination. The in situ NV-g-CN homojunction can be employed as an effective photocatalyst for hydrogen generation through water splitting under visible light, and the optimum rate constant of 3259.1 μmolgh is achieved, which is 8.7 times as high as that of pristine g-CN. Moreover, the markedly increased photocatalytic performance is ascribed to the enhanced light utilization, large specific surface area and unique nitrogen-vacated p-n homojunction structure, which provides more active sites and improves the separation of photo-excited electron-hole pairs. Besides, the underlying mechanism for efficient charge transportation and separation is also proposed. This work demonstrates that the remodeling of g-CN p-n homojunction with nitrogen vacancies is a feasible way as highly efficient photocatalysts and might inspire some new strategies for energy and environmental applications.

摘要

石墨相氮化碳(g-CN)作为一种具有巨大潜力的新型光催化剂,已被广泛应用于太阳能驱动的能量转换。在此,通过水热合成并经过两步煅烧,成功制备了具有氮空位的新型原位g-CN p-n同质结光催化剂(NV-g-CN)。原位NV-g-CN同质结可作为一种有效的光催化剂,用于在可见光下通过水分解产生氢气,实现了3259.1 μmolgh的最佳速率常数,是原始g-CN的8.7倍。此外,光催化性能的显著提高归因于光利用率的提高、大比表面积和独特的氮空位p-n同质结结构,这提供了更多的活性位点并改善了光激发电子-空穴对的分离。此外,还提出了高效电荷传输和分离的潜在机制。这项工作表明,用氮空位重塑g-CN p-n同质结是作为高效光催化剂的一种可行方法,并可能激发一些用于能源和环境应用的新策略。

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