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酸诱导的还原多钒氧烷-烷氧基簇中氧原子缺陷的形成。

Acid-Induced, Oxygen-Atom Defect Formation in Reduced Polyoxovanadate-Alkoxide Clusters.

机构信息

Department of Chemistry, University of Rochester, Rochester, New York 14627, United States.

出版信息

J Am Chem Soc. 2020 Jun 3;142(22):9915-9919. doi: 10.1021/jacs.0c03864. Epub 2020 May 22.

Abstract

Here, we present the first example of acid-induced, oxygen-atom abstraction from the surface of a polyoxometalate cluster. Generation of the oxygen-deficient vanadium oxide, [VO(OCH)], was confirmed via independent synthesis. Spectroscopic analysis using infrared and electronic absorption spectroscopies affords resolution of the electronic structure of the oxygen-deficient cluster (oxidation state distribution = [VV]). This work has direct implications toward the elucidation of possible mechanisms of acid-assisted vacancy formation in bulk transition metal oxides, in particular electron-proton codoping that has recently been described for vanadium oxide (VO). Ultimately, these molecular models deepen our understanding of proton-dependent redox chemistry of transition metal oxide surfaces.

摘要

在这里,我们展示了首例从多金属氧酸盐簇表面进行酸诱导的氧原子提取的实例。通过独立合成证实了氧缺陷型氧化钒[VO(OCH)]的生成。使用红外和电子吸收光谱进行的光谱分析提供了氧缺陷型簇的电子结构分辨率(氧化态分布= [VV])。这项工作对于阐明在体过渡金属氧化物中酸辅助空位形成的可能机制具有直接意义,特别是对于最近描述的钒氧化物(VO)的电子-质子共掺杂。最终,这些分子模型加深了我们对过渡金属氧化物表面质子依赖的氧化还原化学的理解。

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