Vanadium- and manganese-based metal-organic frameworks for potential environmental and catalysis applications

IF 20.3 1区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR Coordination Chemistry Reviews Pub Date : 2024-09-25 DOI:10.1016/j.ccr.2024.216231
Yangdan Pan , Soheila Sanati , Reza Abazari , Agata Jankowska , Joanna Goscianska , Varsha Srivastava , Ulla Lassi , Junkuo Gao
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Abstract

Industrialization has significantly compromised air quality, environmental health, and human well-being. Therefore, it is highly necessary to develop efficient and cost-effective strategies to resolve the issue of environmental pollution while promoting sustainable energy production. Catalysts play a crucial role in the synthesis and conversion of valuable chemicals by providing more active sites that accelerate catalytic reactions, leading to proper activity and selectivity. However, challenges such as catalyst stability, cost-effectiveness, high surface area, reusability, and low loading amount need to be addressed. In this regard, metal organic frameworks (MOFs) could be an intelligent choice due to their tunable structure through altering metal centers and organic ligands along with their structural flexibility, high specific surface area, and diversity. These porous materials have found extensive application in heterogeneous catalysis and environmental remediation thanks to their low cost, abundance in nature and feasible preparation routes. Among first-row transition metal-based MOFs like vanadium (V)- and manganese (Mn)-containing structures have gained popularity in environmental remediation and catalysis due to their different redox states, stability, cost-effectiveness. As limited number of review articles have addressed V and Mn-containing MOFs compared to other first-row transition metals like Ni, Co, Cu and Fe, this review aims at exploring recent advancements in the V- and Mn-based MOFs, their composites, and derivatives within heterogeneous catalysis, highlighting applications in oxidative fuel desulfurization, CO2 reduction, epoxidation, hydroxylation, oxidation of organic compounds, and environmental remediation, including the adsorption and elimination of organic dyes and CO2 capture and conversion. Also, the review emphasizes the structure-performance relationship, offering new insights for overcoming existing challenges and advancing the field.

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基于钒和锰的金属有机框架在环境和催化方面的潜在应用
工业化严重损害了空气质量、环境健康和人类福祉。因此,在促进可持续能源生产的同时,极有必要制定高效且具有成本效益的战略来解决环境污染问题。催化剂通过提供更多的活性位点来加速催化反应,从而获得适当的活性和选择性,在有价值化学品的合成和转化过程中发挥着至关重要的作用。然而,催化剂的稳定性、成本效益、高表面积、可重复使用性和低负载量等挑战亟待解决。在这方面,金属有机框架(MOFs)可能是一个明智的选择,因为它们可以通过改变金属中心和有机配体来调整结构,同时还具有结构灵活、比表面积高和多样性等特点。这些多孔材料成本低廉,在自然界中含量丰富,制备方法可行,因此在异相催化和环境修复领域得到了广泛应用。在第一排过渡金属基 MOFs 中,含钒(V)和锰(Mn)结构的 MOFs 因其不同的氧化还原状态、稳定性和成本效益而在环境修复和催化领域广受欢迎。与镍、钴、铜和铁等其他第一排过渡金属相比,研究含钒和锰 MOFs 的综述文章数量有限,因此本综述旨在探讨钒基和锰基 MOFs 及其复合材料和衍生物在异相催化领域的最新进展,重点介绍其在氧化燃料脱硫、二氧化碳还原、环氧化、羟基化、有机化合物氧化和环境修复(包括吸附和消除有机染料以及二氧化碳捕获和转化)中的应用。此外,该综述还强调了结构与性能之间的关系,为克服现有挑战和推动该领域的发展提供了新的见解。
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来源期刊
Coordination Chemistry Reviews
Coordination Chemistry Reviews 化学-无机化学与核化学
CiteScore
34.30
自引率
5.30%
发文量
457
审稿时长
54 days
期刊介绍: Coordination Chemistry Reviews offers rapid publication of review articles on current and significant topics in coordination chemistry, encompassing organometallic, supramolecular, theoretical, and bioinorganic chemistry. It also covers catalysis, materials chemistry, and metal-organic frameworks from a coordination chemistry perspective. Reviews summarize recent developments or discuss specific techniques, welcoming contributions from both established and emerging researchers. The journal releases special issues on timely subjects, including those featuring contributions from specific regions or conferences. Occasional full-length book articles are also featured. Additionally, special volumes cover annual reviews of main group chemistry, transition metal group chemistry, and organometallic chemistry. These comprehensive reviews are vital resources for those engaged in coordination chemistry, further establishing Coordination Chemistry Reviews as a hub for insightful surveys in inorganic and physical inorganic chemistry.
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