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超临界CHOH触发的g-CN中的同型异质结和基团用于增强光催化析氢

Supercritical CHOH-Triggered Isotype Heterojunction and Groups in g-CN for Enhanced Photocatalytic H Evolution.

作者信息

Mao Liuhao, Zhai Binjiang, Shi Jinwen, Kang Xing, Lu Bingru, Liu Yanbing, Cheng Cheng, Jin Hui, Lichtfouse Eric, Guo Liejin

机构信息

State Key Laboratory of Multiphase Flow in Power Engineering (MFPE), International Research Center for Renewable Energy (IRCRE), Xi'an Jiaotong University (XJTU), 28 West Xianning Road, Xi'an 710049, China.

出版信息

ACS Nano. 2024 May 28;18(21):13939-13949. doi: 10.1021/acsnano.4c03922. Epub 2024 May 15.

Abstract

The structure tuning of bulk graphitic carbon nitride (g-CN) is a critical way to promote the charge carriers dynamics for enhancing photocatalytic H-evolution activity. Exploring feasible post-treatment strategies can lead to effective structure tuning, but it still remains a great challenge. Herein, a supercritical CHOH (ScMeOH) post-treatment strategy (250-300 °C, 8.1-11.8 MPa) is developed for the structure tuning of bulk g-CN. This strategy presented advantages of time-saving (less than 10 min), high yield (over 80%), and scalability due to the enhanced mass transfer and high reactivity of ScMeOH. During the ScMeOH post-treatment process, CHOH molecules diffused into the interlayers of g-CN and subsequently participated in -methylation and hydroxylation reactions with the intralayers, resulting in a partial phase transformation from g-CN into carbon nitride with a poly(heptazine imide)-like structure (Q-PHI) as well as abundant methyl and hydroxyl groups. The modified g-CN showed enhanced photocatalytic activity with an H-evolution rate 7.2 times that of pristine g-CN, which was attributed to the synergistic effects of the g-CN/Q-PHI isotype heterojunction construction, group modulation, and surface area increase. This work presents a post-treatment strategy for structure tuning of bulk g-CN and serves as a case for the application of supercritical fluid technology in photocatalyst synthesis.

摘要

块状石墨相氮化碳(g-CN)的结构调控是促进电荷载流子动力学以提高光催化析氢活性的关键途径。探索可行的后处理策略可实现有效的结构调控,但这仍然是一个巨大的挑战。在此,开发了一种超临界CHOH(ScMeOH)后处理策略(250-300°C,8.1-11.8 MPa)用于块状g-CN的结构调控。由于ScMeOH增强的传质和高反应活性,该策略具有省时(少于10分钟)、高产率(超过80%)和可扩展性的优点。在ScMeOH后处理过程中,CHOH分子扩散到g-CN的层间,随后与层内发生甲基化和羟基化反应,导致g-CN部分相转变为具有聚(七嗪酰亚胺)样结构(Q-PHI)以及大量甲基和羟基的氮化碳。改性后的g-CN表现出增强的光催化活性,析氢速率是原始g-CN的7.2倍,这归因于g-CN/Q-PHI同型异质结构建、基团调控和表面积增加的协同效应。这项工作提出了一种块状g-CN结构调控的后处理策略,并作为超临界流体技术在光催化剂合成中应用的一个实例。

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