Two polyoxovanadates for visible light driven photocatalytic performance†

IF 2.6 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY CrystEngComm Pub Date : 2024-10-07 DOI:10.1039/D4CE00494A
Li Huang, Yufan Yang, Xiaoyang Yu, Xiaonan Li, Yuan Shen, Runhong Song and Hong Zhang
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Abstract

The synthesis of novel polyoxovanadates (POVs) has received considerable critical attention. Herein, two new POVs, {V12P8} (1) and {V16P8} (2), have been designed and synthesized based on phenylphosphonic acid (PhPO3H2) under solvothermal conditions. The structure of 2 is a 16-nuclearity POV composed of four rare zigzag {V4} secondary building units (SBUs). To the best of our knowledge, 2 is the first POV synthesized with PhPO3H2 including this zigzag SBU, which is also very rare among all POVs. Moreover, 2 is the highest-nuclearity isopolyoxovanadate (IPOV) synthesized using PhPO3H2 as the only organic ligand so far. The photocatalytic properties of 1 and 2 were studied under visible light. Both 1 and 2 demonstrate good performance in photocatalytic oxidation of 1,5-dihydroxynaphthalene (1,5-DHN). Compound 1 also has a photocatalytic effect on MB degradation, with 87% of MB degradation within 8 minutes.

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可见光驱动光催化性能的两种聚氧化钒酸盐†
新型聚氧乙烯钒酸盐(POVs)的合成受到了广泛关注。本文以苯基膦酸 (PhPO3H2) 为基础,在溶热条件下设计并合成了{V12P8} (1) 和 {V16P8} (2)两种新型 POV。2 的结构是由四个稀有的人字形{V4}二级构建单元(SBU)组成的 16 核 POV。据我们所知,2 是第一个用 PhPO3H2 合成的 POV,其中包括这种人字形 SBU,这在所有 POV 中也是非常罕见的。此外,2 是迄今为止使用 PhPO3H2 作为唯一有机配体合成的核度最高的异多氧钒酸盐(IPOV)。研究了 1 和 2 在可见光下的光催化特性。1 和 2 在光催化氧化 1,5-二羟基萘(1,5-DHN)方面都表现出良好的性能。化合物 1 对甲基溴降解也有光催化作用,8 分钟内甲基溴降解率达 87%。
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来源期刊
CrystEngComm
CrystEngComm 化学-化学综合
CiteScore
5.50
自引率
9.70%
发文量
747
审稿时长
1.7 months
期刊介绍: Design and understanding of solid-state and crystalline materials
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Back cover Back cover Back cover Synthesis of 3D composite materials based on ultrathin LDH nanowalls grown in situ on graphene surface and fast-response NO2 gas sensing performance at room temperature† Variations in crystals of flufenamic acid of its methyl and tert-butyl analogues as impurities as determined by partial dissolutions†
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