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用于亚甲基蓝降解的蛋黄壳结构CuSe(CuSe)/g-CN异质结的高效光辅助类芬顿反应

Efficient photo-assisted Fenton-like reaction of yolk-shell CuSe(CuSe)/g-CN heterojunctions for methylene blue degradation.

作者信息

Liu ChangSheng, Xue ShaoLin

机构信息

College of Science, Donghua University Shanghai China

出版信息

RSC Adv. 2023 Mar 14;13(13):8464-8475. doi: 10.1039/d2ra08309d.

Abstract

Herein, a CuSe(CuSe) yolk-shell structure (CC) was synthesized when room temperature was 25 degree Celsius using CuO as a soft template, and the g-CN/CuSe(CuSe) heterojunction (CC-G) was formed by coupling appropriate amounts of g-CN in the selenization process to provide a novel, green, economical, and efficient photo-Fenton catalytic material. Photo-Fenton degradation experiments proved that in the presence of hydrogen peroxide (HO), a small amount of g-CN hybridization on Cu-based Fenton catalysts significantly improved methylene blue (MB) degradation. The suitable amount of g-CN hybridization was selected according to the degradation efficiency. The mass of g-CN constituted 20% of the mass of the CuO soft template. The composite material prepared using this combination (CC-G-20) exhibited the best MB degradation performance. The MB degradation efficiency in the CC-G-20/HO/visible light system was almost 98.3% after 60 min, which is higher than those of the parent materials (g-CN, 12.7%; CC, 58.6%) and had cyclic stability. The catalytic system can also stably degrade MB under dark conditions, where the MB degradation was almost 82% after 60 min. The heterojunction prevented excessive electrons and holes (e and h) recombination, stabilizing the reactive active substance of hydroxyl in the photo-Fenton-like catalytic system. Electron paramagnetic resonance and photoluminescence experiments confirmed this inference.

摘要

在此,以CuO为软模板,在室温为25摄氏度时合成了CuSe(CuSe)核壳结构(CC),并通过在硒化过程中耦合适量的g-CN形成g-CN/CuSe(CuSe)异质结(CC-G),以提供一种新型、绿色、经济且高效的光芬顿催化材料。光芬顿降解实验证明,在过氧化氢(HO)存在下,铜基芬顿催化剂上少量的g-CN杂化显著提高了亚甲基蓝(MB)的降解率。根据降解效率选择合适的g-CN杂化量。g-CN的质量占CuO软模板质量的20%。使用这种组合制备的复合材料(CC-G-20)表现出最佳的MB降解性能。在CC-G-20/HO/可见光体系中,60分钟后MB降解效率几乎达到98.3%,高于母体材料(g-CN为12.7%;CC为58.6%),且具有循环稳定性。该催化体系在黑暗条件下也能稳定降解MB,60分钟后MB降解率几乎达到82%。异质结阻止了过多的电子和空穴(e和h)复合,稳定了类光芬顿催化体系中羟基的活性反应物质。电子顺磁共振和光致发光实验证实了这一推断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7bd/10012337/3e5d17189cf6/d2ra08309d-f1.jpg

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