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用于增强光催化降解甲基橙的二维异质结构工程

Engineering of Two-Dimensional Heterostructures for Enhanced Photocatalytic Decontamination of Methyl Orange.

作者信息

Chen Junli, Jin Xinyi, Zhang Pengcheng, Song Nan, Gao Pan, Fischer Roland A, Mukherjee Soumya

机构信息

College of Materials and Chemical Engineering, Collaborative Innovation Center of Environmental Pollution Control and Ecological Restoration, Zhengzhou University of Light Industry, Zhengzhou 450002, P. R. China.

Chair of Inorganic and Metal-Organic Chemistry, Department of Chemistry, School of Natural Sciences and Catalysis Research Center, Technische Universität München, Lichtenbergstraße 4, Garching b. München 85748, Germany.

出版信息

ACS Appl Eng Mater. 2025 May 14;3(5):1292-1301. doi: 10.1021/acsaenm.5c00134. eCollection 2025 May 23.

DOI:10.1021/acsaenm.5c00134
PMID:40433148
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12104971/
Abstract

Two-dimensional (2D)/2D heterostructured catalysts have garnered significant attention in photocatalytic environmental remediation due to their relevance in optoelectronic, as well as solar energy conversion systems. However, fast photocarrier separation of 2D/2D heterojunctions, made from the stacking of different layered materials through strong chemical bonds rather than weak van der Waals interactions, remains an unmet challenge. To address this, herein, a generation of 2D/2D p-n heterojunction photocatalysts, composed of BiOCl and HMo Nb O nanosheets, was fabricated via chemical absorption and hydrolysis strategies. This close heterojunction interface enhanced the separation and migration of photoinduced electron-hole (e-h) pairs. As a result, the prepared ultrathin BiOCl/HMo Nb O heterostructure catalysts demonstrated superior photocatalytic degradation of methyl orange (MO) under UV-visible light, with the optimized photocatalysts (BiOCl/NbMo) achieving MO removal efficiencies 2.94 and 2.22 times greater than those of pristine BiOCl and NbMo materials, respectively. Further, hydroxyl radicals (·OH), positive holes (h), and superoxide anions (·O ) were also confirmed to play key roles in MO removal within the photocatalytic system. This work offers insights into the rational design and construction of high-performance 2D/2D heterojunction photocatalysts for environmental remediation.

摘要

二维(2D)/2D异质结构催化剂因其在光电子以及太阳能转换系统中的相关性,在光催化环境修复方面受到了广泛关注。然而,通过强化学键而非弱范德华相互作用堆叠不同层状材料制成的2D/2D异质结的快速光载流子分离,仍然是一个尚未解决的挑战。为了解决这一问题,本文通过化学吸附和水解策略制备了由BiOCl和HMoNbO纳米片组成的2D/2D p-n异质结光催化剂。这种紧密的异质结界面增强了光生电子-空穴(e-h)对的分离和迁移。结果,制备的超薄BiOCl/HMoNbO异质结构催化剂在紫外-可见光下表现出优异的光催化降解甲基橙(MO)性能,优化后的光催化剂(BiOCl/NbMo)对MO的去除效率分别比原始BiOCl和NbMo材料高2.94倍和2.22倍。此外,羟基自由基(·OH)、正空穴(h)和超氧阴离子(·O)也被证实在光催化体系中MO的去除过程中起关键作用。这项工作为合理设计和构建用于环境修复的高性能2D/2D异质结光催化剂提供了见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cf8/12104971/4252ccd43fdc/em5c00134_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cf8/12104971/18aaeae16250/em5c00134_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cf8/12104971/56fe2e9948a3/em5c00134_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cf8/12104971/e7d3ae9deb5f/em5c00134_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cf8/12104971/60fda0c9fe8b/em5c00134_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cf8/12104971/4252ccd43fdc/em5c00134_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cf8/12104971/18aaeae16250/em5c00134_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cf8/12104971/56fe2e9948a3/em5c00134_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cf8/12104971/e7d3ae9deb5f/em5c00134_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cf8/12104971/60fda0c9fe8b/em5c00134_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cf8/12104971/4252ccd43fdc/em5c00134_0004.jpg

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Highly efficient visible-light driven dye degradation via 0D BiVO nanoparticles/2D BiOCl nanosheets p-n heterojunctions.通过 0D BiVO 纳米粒子/2D BiOCl 纳米片 p-n 异质结实现高效可见光驱动的染料降解。
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