Suppr超能文献

基于石墨炔(CH)的 GDY/CuI/MIL-53(Al) S 型异质结用于高效析氢。

Graphdiyne (CH)-Based GDY/CuI/MIL-53(Al) S-Scheme Heterojunction for Efficient Hydrogen Evolution.

机构信息

School of Chemistry and Chemical Engineering, Ningxia Key Laboratory of Solar Chemical Conversion Technology, Key Laboratory for Chemical Engineering and Technology, State Ethnic Affairs Commission, North Minzu University, Yinchuan750021, People's Republic of China.

College of Chemistry and Chemical Engineering, Jishou University, Jishou, Hunan416000, People's Republic of China.

出版信息

Langmuir. 2022 Dec 20;38(50):15632-15641. doi: 10.1021/acs.langmuir.2c02334. Epub 2022 Dec 12.

Abstract

Graphdiyne (g-CH) is a new carbon material composed of sp and sp hybrid carbon atoms. Since the synthesis by Li's team, graphdiyne has been widely studied in other fields because of its excellent properties. In this paper, graphdiyne was synthesized from copper-containing materials and the composite GDY/CuI/MIL-53(Al) S-scheme heterojunction is prepared for photocatalytic cracking of water to produce hydrogen. First, GDY/CuI was prepared by organic synthesis, and then GDY/CuI was anchored on the surface of MIL-53(Al) by ultrasonic stirring. After the continuous optimization of experimental conditions, the final hydrogen evolution rate is much higher than that of MIL-53(Al). This efficient photocatalytic performance can be attributed to the S-scheme heterojunction formed by the unique energy band arrangement. At the same time, the mechanism of charge transfer was demonstrated by irradiation X-ray photoelectron spectroscopy. The strong interaction among the three strongly promotes the separation and transfer of photogenerated electron-hole pairs.

摘要

石墨炔(g-CH)是一种由 sp 和 sp2 杂化碳原子组成的新型碳材料。自从 Li 的团队合成以来,由于其优异的性能,石墨炔在其他领域得到了广泛的研究。在本文中,通过含铜材料合成了石墨炔,并制备了 GDY/CuI/MIL-53(Al) S 型异质结用于光催化水裂解制氢。首先,通过有机合成制备 GDY/CuI,然后通过超声搅拌将 GDY/CuI 锚定在 MIL-53(Al)的表面。通过对实验条件的不断优化,最终的产氢速率远高于 MIL-53(Al)。这种高效的光催化性能可归因于独特能带排列形成的 S 型异质结。同时,通过 X 射线光电子能谱证明了电荷转移的机制。三种物质之间的强相互作用促进了光生电子空穴对的分离和转移。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验