利用优越的光电催化水净化技术制备α-MnO2@NiMoO4异质结构

EcoEnergy Pub Date : 2025-04-08 DOI:10.1002/ece2.70003
Hongchao Ma, Yan Chen, Huijun Li, Yinghuan Fu, Dedong Sun, Guowen Wang, Xiang Guo, Shixue Dou, Vadivel Subramaniam, Ashish Kumar, Krishnamoorthy Ramachandran, Xinghui Liu
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引用次数: 0

摘要

异质结构催化剂是光解废水高效修复的催化剂,但合理构建具有高质量界面的光电催化剂仍是一个挑战。本文采用简单的水热法制备了具有NiMoO4纳米片与α-MnO2纳米线界面均匀的异质结构NiMoO4@α-MnO2。NiMoO4@α-MnO2表现出如下显著优势:(1)α-MnO2纳米线像输送营养物质的动脉一样充当电荷输送通道,促进诱导电荷的迁移和分离;(2)污染物可以静电富集到NiMoO4@α-MnO2表面。具体来说,附着在α-MnO2表面的蛛丝状NiMoO4纳米片具有较大的表面积,有利于电解质的渗透和活性位点的利用。(3)展开后的蛛丝状NiMoO4,就像人造卫星上一个巨大的扩展太阳能电池板,可以收集更多的太阳能,产生大量的电子(e−)/空穴(h+)对和活性物质,提供了多种传递途径,加快了降解反应的速度。优化后的异质结构NiMoO4@α-MnO2-3.5催化剂具有优异的PEC活性和降解活性艳蓝KN-R的稳定性。根据α-MnO2和NiMoO4的能带结构和自由基猝灭实验,提出了α-MnO2和NiMoO4之间的z型异质结。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Fabricating α-MnO2@NiMoO4 Heterostructure Architecture With Superior Photoelectrocatalytic Water Purification

Fabricating α-MnO2@NiMoO4 Heterostructure Architecture With Superior Photoelectrocatalytic Water Purification

Heterostructure catalyst is highly efficient for photoelectrolytic (PEC) wastewater remediation, while rationally constructing the photoelectrocatalyst with a high-quality interface is still challenging. Herein, a simple hydrothermal process prepares a heterostructure NiMoO4@α-MnO2 with a uniform interface between NiMoO4 nanosheets and α-MnO2 nanowires. NiMoO4@α-MnO2 exhibited significant advantages as follows: (1) α-MnO2 nanowires act as charge transport channels like the arteries that transport nutrients, promoting the migration and separation of induced charges; (2) the pollutants can be electrostatically concentrated to the surface of the NiMoO4@α-MnO2. Specifically, the gossamer-like NiMoO4 nanosheets adhering on the surface of the α-MnO2 have a large surface area, beneficial for electrolyte penetration and utilization of active sites. (3) Unfolded gossamer-like NiMoO4, like a vast extended solar panel of an artificial satellite, can harvest more solar energy, generating lots of electron (e)/hole (h+) pairs and active species, offering multiple transfer pathways and speeding up the rate of the degradation reaction. The optimized heterostructured NiMoO4@α-MnO2-3.5 catalysts showed superior PEC activity and remarkable stability for degrading reactive brilliant blue KN-R. Z-scheme heterojunction between α-MnO2 and NiMoO4 is proposed based on their energy band structure and free radical quenching experiment.

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