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二维 SnS/g-CN 异质结的制备及其在光催化水分解析氢中的增强作用。

Fabrication of 2D SnS/g-CN heterojunction with enhanced H evolution during photocatalytic water splitting.

机构信息

School of Chemical Engineering, Northwest University, No. 229 Taibai North Road, Xi'an 710069, China; School of Physics, Northwest University, No. 229 Taibai North Road, Xi'an 710069, China; Institute of Modern Physics, Northwest University, Xi'an 710069, China.

School of Chemical Engineering, Northwest University, No. 229 Taibai North Road, Xi'an 710069, China.

出版信息

J Colloid Interface Sci. 2018 Aug 15;524:313-324. doi: 10.1016/j.jcis.2018.04.038. Epub 2018 Apr 10.

Abstract

In this work, the 2D SnS/g-CN heterojunctions were successfully prepared by heating the homogeneous dispersion of SnS nanosheets and g-CN nanosheets using a microwave muffle. SEM, TEM and HRTEM images indicated that the SnS nanosheets were loaded on the surface of the g-CN nanosheets. The UV-vis spectra show that the absorption intensity of the as-prepared samples was increased and the absorption range was also extended from 420 nm to approximately 600 nm. The H production rate over 5 wt% SnS/g-CN can reach 972.6 μmol·h·g under visible light irradiation (λ > 420 nm) using TEOA as the sacrifice agent and Pt as the electron trap, which is 2.9 and 25.6 times higher than those of the pristine g-CN and SnS, respectively. According to the obtained PL spectra, photocurrent and EIS spectra, the enhanced performance for H generation over the heterojunctions is primarily ascribed to the rapid charge transfer arising from the suitable band gap positions leading to an improved photocatalytic performance. The recycling experiments indicated that the as-prepared composites exhibit good stability in H production. Additionally, a possible enhanced mechanism for H evolution was deduced based on the results obtained by various characterization techniques.

摘要

在这项工作中,通过使用微波马弗炉加热 SnS 纳米片和 g-CN 纳米片的均匀分散体,成功制备了 2D SnS/g-CN 异质结。SEM、TEM 和 HRTEM 图像表明,SnS 纳米片负载在 g-CN 纳米片的表面上。紫外-可见光谱表明,所制备样品的吸收强度增加,吸收范围也从 420nm 扩展到约 600nm。以 TEOA 为牺牲剂,Pt 为电子捕获剂,在可见光照射下(λ>420nm),5wt%SnS/g-CN 的 H 产率可达 972.6μmol·h·g-1,分别是原始 g-CN 和 SnS 的 2.9 倍和 25.6 倍。根据获得的 PL 光谱、光电流和 EIS 光谱,异质结在 H 生成方面的增强性能主要归因于快速的电荷转移,这是由于合适的能带位置导致光催化性能的提高。回收实验表明,所制备的复合材料在 H 生产中表现出良好的稳定性。此外,根据各种表征技术的结果,推断出了一种可能的 H 演化增强机制。

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