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一种含反式钴水合物的十六核钴掺杂钨锗酸盐:合成、结构与光催化性能

A Hexadecanuclear Cobalt-Added Tungstogermanate Containing Counter Cobalt Hydrates: Synthesis, Structure and Photocatalytic Properties.

作者信息

Zhao Qing, Li Xuyan, Wang Yu, Lv Hongjin, Yang Guoyu

机构信息

MOE Key Laboratory of Cluster Science, School of Chemistry and Chemical Engineering, Beijing Institute of Technology, Beijing 102488, China.

出版信息

Nanomaterials (Basel). 2023 Jul 5;13(13):2009. doi: 10.3390/nano13132009.

Abstract

The synthesis and exploration of the properties of structurally-new polyoxometalates (POMs) has been attracting considerable research interest. In this work, a hexadecanuclear cobalt-added tungstogermanate, H(NH)Na{Co(HO)}{Co(μ-OH)(PO)}·23-HO (), was synthesized under hydrothermal conditions and characterized by various techniques. Compound can effectively drive the heterogeneous photocatalytic hydrogen evolution reaction in the presence of [Ir(ppy)(dtbbpy)][PF] as the photosensitizer, with triethanolamine (TEOA) and N-Hydroxy succinimide (NHS) used as the dual sacrificial reagents. Control experiments revealed the important role of NHS in enhancing the hydrogen-evolution activities. Under optimal catalytic conditions, a hydrogen yield of 54.21 μmol was achieved after 10-h photocatalysis, corresponding to a hydrogen evolution rate of 1807.07 μmol·g·h. Stability studies demonstrated that catalyst can be isolated and reused for three successive photocatalytic cycles with negligible decline of the H yield, indicating the stability and recycling robustness of catalyst .

摘要

新型结构多金属氧酸盐(POMs)的合成及其性质探索一直吸引着大量的研究兴趣。在本工作中,一种添加十六核钴的钨锗酸盐H(NH)Na{Co(HO)}{Co(μ-OH)(PO)}·23-HO()在水热条件下被合成,并通过多种技术进行了表征。化合物在[Ir(ppy)(dtbbpy)][PF]作为光敏剂、三乙醇胺(TEOA)和N-羟基琥珀酰亚胺(NHS)作为双牺牲试剂的情况下,能够有效地驱动非均相光催化析氢反应。对照实验揭示了NHS在提高析氢活性方面的重要作用。在最佳催化条件下,经过10小时的光催化后,氢气产率达到54.21 μmol,对应析氢速率为1807.07 μmol·g·h。稳定性研究表明,催化剂可以被分离并重复用于三个连续的光催化循环,氢气产率的下降可忽略不计,这表明催化剂具有稳定性和循环耐用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e72/10343794/60af0f096437/nanomaterials-13-02009-g001.jpg

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