Enhanced Room-Temperature catalytic oxidation of formaldehyde via A novel Na-Doped MnO2/Co3O4 Catalyst: Oxygen vacancy engineering and application in Aqueous-Gas hybrid purification system

IF 7.5 1区 工程技术 Q2 ENERGY & FUELS
Fuel Pub Date : 2025-10-03 DOI:10.1016/j.fuel.2025.137053
Wenjie Zhai , Jiaqi Zang , Liming Chai, Xiyue Ma, Yuting Wang, Zhaoyang Tan, Jianbin Zhang
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引用次数: 0

Abstract

The degradation of indoor formaldehyde (HCHO) is crucial for safeguarding human health, yet the rational design and controlled synthesis of highly efficient non-noble metal catalysts remain challenging. In particular, strategies that enhance oxygen vacancy concentration through targeted dopant modification have emerged as promising approaches to boost catalytic oxidation activity. Herein, a novel Na-doped MnO2/Co3O4 ternary composite, (MnO2/Na0.7MnO2.05)/Co3O4, was successfully synthesized via a one-step hydrothermal treatment followed by high-temperature calcination, yielding uniform spherical architectures with high specific surface area (129.59 m2·g−1) and mesoporous texture. Subsequent Na incorporation effectively increased the proportion of Mn3+ species and oxygen vacancies, thereby enhancing the mobility of surface-adsorbed oxygen (Oads) and lattice oxygen (Olatt), which collectively facilitated the catalytic oxidation of HCHO. The as-prepared catalyst demonstrated excellent degradation performance: at 30 °C, a 62.42 % removal efficiency of 10 mL 100 mg L-1 aqueous HCHO was achieved within 1 h, reaching 96.39 % after 8 h. Mechanistic insights obtained from EPR spectroscopy, reactive oxygen species (ROS) detection, and density functional theory (DFT) calculations further elucidated the adsorption and degradation pathways of HCHO in solution. Notably, beyond conventional aqueous-phase studies, the catalyst was further integrated into a hybrid aqueous-gas purification system employing a commercial air-conditioning fan. Under this practical configuration, a 56.36 % degradation efficiency was achieved for 4000 mL 10 mg·L-1 aqueous HCHO within 5 h at room temperature. This study not only demonstrates a new material design strategy by coupling alkali-metal doping with a MnO2/Co3O4 binary composite, but also pioneers a hybrid degradation concept that bridges aqueous-phase and gas-phase purification. The results highlight both the structural–electronic regulation of the catalyst and its engineering feasibility, providing new insights into catalyst development and offering a promising pathway toward the practical implementation of room-temperature VOCs removal.
新型na掺杂MnO2/Co3O4催化剂增强甲醛室温催化氧化:氧空位工程及其在水-气混合净化系统中的应用
室内甲醛(HCHO)的降解对保障人体健康至关重要,但高效非贵金属催化剂的合理设计和可控合成仍然是一个挑战。特别是,通过靶向掺杂剂修饰提高氧空位浓度的策略已经成为提高催化氧化活性的有希望的方法。本文通过一步水热处理和高温煅烧,成功合成了一种新型的na掺杂MnO2/Co3O4三元复合材料(MnO2/Na0.7MnO2.05)/Co3O4,得到了具有高比表面积(129.59 m2·g−1)和介孔结构的均匀球形结构。随后的Na掺入有效地增加了Mn3+的比例和氧空位,从而增强了表面吸附氧(Oads)和晶格氧(Olatt)的迁移率,共同促进了HCHO的催化氧化。制备的催化剂表现出优异的降解性能:在30°C条件下,10 mL 100 mg L-1水溶液HCHO的去除率在1 h内达到62.42%,8 h后达到96.39%。通过EPR光谱、活性氧(ROS)检测和密度泛函理论(DFT)计算进一步阐明了HCHO在溶液中的吸附和降解途径。值得注意的是,除了传统的水相研究之外,该催化剂还被进一步集成到采用商用空调风扇的水-气混合净化系统中。在此实际配置下,在室温下,4000 mL 10 mg·L-1水溶液HCHO在5 h内的降解效率为56.36%。这项研究不仅展示了一种通过将碱金属掺杂与MnO2/Co3O4二元复合材料耦合的新材料设计策略,而且开创了一种桥接水相和气相净化的混合降解概念。研究结果强调了催化剂的结构-电子调控及其工程可行性,为催化剂的开发提供了新的见解,并为实际实施室温VOCs去除提供了一条有希望的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Fuel
Fuel 工程技术-工程:化工
CiteScore
12.80
自引率
20.30%
发文量
3506
审稿时长
64 days
期刊介绍: The exploration of energy sources remains a critical matter of study. For the past nine decades, fuel has consistently held the forefront in primary research efforts within the field of energy science. This area of investigation encompasses a wide range of subjects, with a particular emphasis on emerging concerns like environmental factors and pollution.
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