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用于提升可见光驱动光催化和光电化学活性的分层 N 掺杂 TiO@BiWMoO 核壳纳米纤维。

Hierarchical N-doped TiO@BiWMoO core-shell nanofibers for boosting visible-light-driven photocatalytic and photoelectrochemical activities.

机构信息

Department of Biological Engineering, Biohybrid Systems Research Center (BSRC) Inha University, Incheon, 22212, Republic of Korea.

Department of Energy and Materials Engineering, Dongguk University-Seoul, Seoul, 04620, Republic of Korea.

出版信息

J Hazard Mater. 2020 Jun 5;391:122249. doi: 10.1016/j.jhazmat.2020.122249. Epub 2020 Feb 7.

Abstract

Heterogeneous photocatalysis has been proven to be a promising approach to overcome the great challenges encountered with conventional technologies for environmental remediation. Herein, for the first time, a novel hierarchical architecture of nitrogen-doped TiO@BiWMoO (N-T@BWMO-x, x = 0-1.0) was rationally designed and fabricated through an electrospinning route followed by a solvothermal process. The photocatalytic activity of the as-prepared samples was evaluated based on the degradation of tetracycline hydrochloride (TC) under visible-light irradiation. The results indicated that the molar fraction of W/Mo has a strong impact on the photocatalytic efficiency and photoelectrochemical performance of the N-T@BWMO composites. Compared to N-TiO and the binary composites, N-T@BWMO-0.25 exhibited outstanding photocatalytic activity and significant cycling stability. The enhanced photocatalytic activity can be synergistically linked to the excellent native adsorption, extended light-harvesting region, hierarchical structure, and strong interfacial interaction between N-TiO and BWMO, which can effectively prolong the lifetime of charge-carriers. Moreover, active species-trapping and electron paramagnetic resonance results confirmed that holes and superoxide radicals were the dominant active species responsible for TC removal. A possible photocatalytic mechanism underlying the degradation of TC by N-T@BWMO-0.25 is also proposed. We expect that our findings will provide new insights into the use of highly efficient core-shell heterostructure photocatalysts, with potential applications in environmental decontamination.

摘要

杂化光催化已被证明是克服传统环境修复技术所面临的巨大挑战的一种很有前途的方法。在此,首次通过静电纺丝和溶剂热工艺,合理设计并制备了一种新型的氮掺杂 TiO@BiWMoO(N-T@BWMO-x,x=0-1.0)分层结构。通过可见光照射下盐酸四环素(TC)的降解,评估了所制备样品的光催化活性。结果表明,W/Mo 的摩尔分数对 N-T@BWMO 复合材料的光催化效率和光电化学性能有很大的影响。与 N-TiO 和二元复合材料相比,N-T@BWMO-0.25 表现出了优异的光催化活性和显著的循环稳定性。增强的光催化活性可以协同归因于 N-TiO 和 BWMO 之间的优异本征吸附、扩展的光捕获区域、分层结构和强界面相互作用,这可以有效延长载流子的寿命。此外,活性物质捕获和电子顺磁共振结果证实,空穴和超氧自由基是去除 TC 的主要活性物质。还提出了 N-T@BWMO-0.25 降解 TC 的可能光催化机制。我们希望我们的研究结果将为高效核壳异质结构光催化剂的应用提供新的思路,在环境净化方面具有潜在的应用前景。

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