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双等离子体 Au 和 TiN 共催化剂促进光催化析氢。

Dual plasmonic Au and TiN cocatalysts to boost photocatalytic hydrogen evolution.

机构信息

School of Materials Science and Engineering, Jiangsu University, Zhenjiang, Jiangsu, 212013, PR China.

School of Materials Science and Engineering, Jiangsu University, Zhenjiang, Jiangsu, 212013, PR China; Hunan Key Laboratory of Applied Environmental Photocatalysis, Changsha University, Changsha, Hunan, 410022, PR China.

出版信息

Chemosphere. 2022 Mar;291(Pt 3):132987. doi: 10.1016/j.chemosphere.2021.132987. Epub 2021 Nov 25.

Abstract

Employing a suitable cocatalyst is very important to improve photocatalytic H evolution activity. Herein, two plasmonic cocatalysts, Au nanoparticles and TiN nanoparticles were in-situ coupled over the g-CN nanotube to form a ternary 0D/0D/1D Au/TiN/g-CN composite via a successive thermal polycondensation and chemical reduction method. The g-CN nanotube acted as a support for the growth of Au and TiN nanoparticles, leading to intimate contact between g-CN nanotube with Au nanoparticles and TiN nanoparticles. As a result, multiple interfaces and dual-junctions of Au/g-CN Schottky-junction and TiN/g-CN ohmic-junction were constructed, which helped to promote the charged carriers' separation and enhanced the photocatalytic performance. Furthermore, loading plasmonic cocatalysts of Au nanoparticles and TiN nanoparticles can enhance the light absorption capacity. Consequently, the Au/TiN/g-CN composite exhibited significantly enhanced photocatalytic H evolution activity (596 μmol g h) compared to g-CN or binary composites of Au/g-CN and TiN/g-CN. This work highlights the significant role of cocatalysts in photocatalysis.

摘要

采用合适的助催化剂对于提高光催化析氢活性非常重要。在此,通过连续的热缩聚和化学还原法,将两种等离子体助催化剂(金纳米粒子和氮化钛纳米粒子)原位耦合到 g-CN 纳米管上,形成了三元 0D/0D/1D Au/TiN/g-CN 复合材料。g-CN 纳米管作为 Au 和 TiN 纳米粒子生长的载体,导致 g-CN 纳米管与 Au 纳米粒子和 TiN 纳米粒子之间紧密接触。结果,构建了多个界面和 Au/g-CN 肖特基结和 TiN/g-CN 欧姆结的双重结,有助于促进载流子的分离并提高光催化性能。此外,负载等离子体助催化剂 Au 纳米粒子和 TiN 纳米粒子可以增强光吸收能力。因此,与 g-CN 或 Au/g-CN 和 TiN/g-CN 二元复合材料相比,Au/TiN/g-CN 复合材料表现出显著增强的光催化析氢活性(596 μmol g h)。这项工作强调了助催化剂在光催化中的重要作用。

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