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磷掺杂共价三嗪框架的高效可见光驱动光催化产氢。

Efficient Visible-Light-Driven Photocatalytic Hydrogen Evolution on Phosphorus-Doped Covalent Triazine-Based Frameworks.

出版信息

ACS Appl Mater Interfaces. 2018 Dec 5;10(48):41415-41421. doi: 10.1021/acsami.8b16013. Epub 2018 Nov 21.

Abstract

Seeking efficient visible-light-driven photocatalysts for water splitting to produce H has attracted much attention. Chemical doping is an effective strategy to enhance photocatalytic performance. Herein, we reported phosphorus-doped covalent triazine-based frameworks (CTFs) for photocatalytic H evolution. Phosphorus-doped CTFs were fabricated by a facile thermal treatment using easily available red phosphorus as the external phosphorus species. The introduction of phosphorus atoms into the frameworks modified the optical and electronic property of CTFs, thus promoting the generation, separation, and migration of photoinduced electron-hole pairs. Consequently, the photocatalytic H-production efficiency of phosphorus-doped CTFs was greatly improved, which was 4.5, 3.9, and 1.8 times as high as that of undoped CTFs and phosphorus-doped g-CN calcined from melamine and urea, respectively.

摘要

寻找高效的可见光驱动光催化剂用于水分解以产生 H 已引起了广泛关注。化学掺杂是增强光催化性能的有效策略。在此,我们报道了用于光催化 H 演化的磷掺杂共价三嗪基框架(CTFs)。磷掺杂 CTFs 通过使用易得的红磷作为外部磷物种的简便热处理来制备。磷原子的引入修饰了 CTFs 的光学和电子性质,从而促进了光生电子-空穴对的产生、分离和迁移。因此,磷掺杂 CTFs 的光催化 H 产生效率大大提高,分别是未掺杂 CTFs 和由三聚氰胺和尿素煅烧得到的磷掺杂 g-CN 的 4.5、3.9 和 1.8 倍。

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