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可见光照射下生物质衍生活性炭负载硫化镉纳米材料对罗丹明B的光降解作用

Photodegradation of Rhodamine B over Biomass-Derived Activated Carbon Supported CdS Nanomaterials under Visible Irradiation.

作者信息

Huang Hai-Bo, Wang Yu, Cai Feng-Ying, Jiao Wen-Bin, Zhang Ning, Liu Cheng, Cao Hai-Lei, Lü Jian

机构信息

Fujian Provincial Key Laboratory of Soil Environmental Health and Regulation, College of Resources and Environment, Fujian Agriculture and Forestry University, Fuzhou, China.

State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, China.

出版信息

Front Chem. 2017 Dec 20;5:123. doi: 10.3389/fchem.2017.00123. eCollection 2017.

DOI:10.3389/fchem.2017.00123
PMID:29326925
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5742335/
Abstract

A family of new composite materials was successfully prepared through the deposition of as-synthesized CdS nanomaterials on lotus-seedpod-derived activated carbon (SAC). The SAC supports derived at different activation temperatures exhibited considerably large surface areas and various microstructures that were of great importance in enhancing photocatalytic performance of CdS@SAC composite materials toward the photodegradation of rhodamine B (RhB) under visible irradiation. The best-performing CdS@SAC-800 showed excellent photocatalytic activity with a rate constant of ca. 2.40 × 10 min, which was approximately 13 times higher than that of the CdS nanomaterials. Moreover, the estimated band gap energy of CdS@SAC-800 was significantly lowered down to 1.99 eV compared to that of the CdS precursor (2.22 eV), which suggested considerable strength of interface contact between the CdS and SAC support, as well as efficient light harvesting capacity of the composite material. Further photocatalytic study indicated that the SAC supports enhanced the separation of photogenerated electrons and holes in this system. Improved photocatalytic activity of the composite materials was largely due to the increased generation of catalytically active species such as , OH•, [Formula: see text] etc. This work provided a facile and low-cost pathway to fabricate photocatalysts for viable degradation of organic dye molecules.

摘要

通过将合成的硫化镉(CdS)纳米材料沉积在莲子壳衍生的活性炭(SAC)上,成功制备了一系列新型复合材料。在不同活化温度下得到的SAC载体具有相当大的表面积和各种微观结构,这对于提高CdS@SAC复合材料在可见光照射下对罗丹明B(RhB)光降解的光催化性能非常重要。性能最佳的CdS@SAC - 800表现出优异的光催化活性,速率常数约为2.40×10⁻³ min⁻¹,约为CdS纳米材料的13倍。此外,与CdS前驱体(2.22 eV)相比,CdS@SAC - 800的估计带隙能量显著降低至1.99 eV,这表明CdS与SAC载体之间的界面接触强度相当大,以及复合材料具有高效的光捕获能力。进一步的光催化研究表明,SAC载体增强了该体系中光生电子和空穴的分离。复合材料光催化活性的提高在很大程度上归因于催化活性物种如·OH、[公式:见原文]等的生成增加。这项工作为制备用于有效降解有机染料分子的光催化剂提供了一种简便且低成本的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fbc/5742335/f62f2583a7ad/fchem-05-00123-g0010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fbc/5742335/3048b242a25a/fchem-05-00123-g0009.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fbc/5742335/3ab51a72efbe/fchem-05-00123-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fbc/5742335/149d107a93bf/fchem-05-00123-g0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fbc/5742335/f62f2583a7ad/fchem-05-00123-g0010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fbc/5742335/3048b242a25a/fchem-05-00123-g0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fbc/5742335/b0733d502d0a/fchem-05-00123-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fbc/5742335/dd9d26827819/fchem-05-00123-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fbc/5742335/0fec27969b8f/fchem-05-00123-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fbc/5742335/6e9222e7c7fc/fchem-05-00123-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fbc/5742335/cce1d3962ff7/fchem-05-00123-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fbc/5742335/7dc9e3be71d1/fchem-05-00123-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fbc/5742335/3ab51a72efbe/fchem-05-00123-g0007.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fbc/5742335/f62f2583a7ad/fchem-05-00123-g0010.jpg

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