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用于电化学氧还原反应的非晶态氧化钛催化剂。

Noncrystalline Titanium Oxide Catalysts for Electrochemical Oxygen Reduction Reactions.

作者信息

Tominaka Satoshi, Ishihara Akimitsu, Nagai Takaaki, Ota Ken-Ichiro

机构信息

International Center for Materials Nanoarchitectonics (MANA), National Institute for Materials Science (NIMS), 1-1 Namiki, Tsukuba, Ibaraki 305-0044, Japan.

Institute of Advanced Sciences and Green Hydrogen Research Center, Yokohama National University, 79-5 Tokiwadai, Hodogaya-ku, Yokohama, Kanagawa 240-8501, Japan.

出版信息

ACS Omega. 2017 Aug 30;2(8):5209-5214. doi: 10.1021/acsomega.7b00811. eCollection 2017 Aug 31.

Abstract

Titanium oxides crystals are widely used in a variety of fields, but little has been reported on the functionalities of noncrystalline intermediates formed in their structural transformation. We measured the oxygen reduction reaction activity of titanium oxide nanoparticles heat-treated for a different time and found that the activity abruptly increased at a certain time of the treatment. We analyzed their structures by using X-ray pair distribution functions with the help of high-resolution transmission electron microscopy and X-ray photoelectron spectroscopy and ascertained that the abrupt increase in the activity corresponded to a structural transformation from a reduced lepidocrocite-type layered titanate to a disordered structure consisting of domains of brookite-like TiO octahedral linkages. The further treatment transformed these brookite-like domains into another phase having more edge-sharing sites like the TiO-type cubic structure. This finding would position noncrystalline, disordered structure as a possible origin of the catalytic activity, though nanocrystalline rutile particles might be also considered as the origin.

摘要

二氧化钛晶体在各种领域有着广泛应用,但关于其结构转变过程中形成的非晶态中间体的功能,此前报道甚少。我们测定了经过不同时长热处理的二氧化钛纳米颗粒的氧还原反应活性,发现活性在热处理的某一时刻会突然增加。借助高分辨率透射电子显微镜和X射线光电子能谱,我们利用X射线对分布函数分析了它们的结构,并确定活性的突然增加对应于从还原型纤铁矿型层状钛酸盐到由板钛矿型TiO八面体键合域组成的无序结构的结构转变。进一步处理将这些板钛矿型域转变为另一个具有更多类似TiO型立方结构边缘共享位点的相。这一发现将非晶态无序结构定位为催化活性的可能来源,尽管纳米晶金红石颗粒也可能被视为活性来源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aeb0/6641928/11cb0d6aa7f8/ao-2017-00811k_0005.jpg

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