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锰钴混合氧化物还原的研究:锰含量的作用。

Study of Reduction of MnCoO Mixed Oxides: The Role of Manganese Content.

作者信息

Bulavchenko Olga A, Afonasenko Tatyana N, Ivanchikova Anastasya V, Murzin Vadim Yu, Kremneva Anna M, Saraev Andrey A, Kaichev Vasily V, Tsybulya Sergey V

机构信息

Boreskov Institute of Catalysis, Ak. Lavrentiev Avenue, 5, Novosibirsk 630090, Russia.

Novosibirsk State University, Pirogov Street, 2, Novosibirsk 630090, Russia.

出版信息

Inorg Chem. 2021 Nov 1;60(21):16518-16528. doi: 10.1021/acs.inorgchem.1c02379. Epub 2021 Oct 14.

Abstract

A series of Mn-Co mixed oxides with a gradual variation of the Mn/Co molar ratio were prepared by coprecipitation of cobalt and manganese nitrates. The structure, chemistry, and reducibility of the oxides were studied by X-ray diffraction (XRD), X-ray absorption spectroscopy, X-ray photoelectron spectroscopy (XPS), and temperature-programmed reduction (TPR). It was found that at concentrations of Mn below 37 atom %, a solid solution with a cubic spinel structure is formed. At concentrations above 63 atom %, a solid solution is formed on the basis of a tetragonal spinel, while at concentrations in a range of 37-63 atom %, a two-phase system, which contains tetragonal and cubic oxides, is formed. To elucidate the reduction route of mixed oxides, two approaches were used. The first was based on a gradual change in the chemical composition of Mn-Co oxides, illustrating slow changes in the TPR profiles. The second approach consisted in a combination of XRD and pseudo- XPS techniques, which made it possible to directly determine the structure and chemistry of the oxides under reductive conditions. It was shown that the reduction of Mn-Co mixed oxides proceeds via two stages. During the first stage, (Mn, Co)O is reduced to (Mn, Co)O. During the second stage, the solid solution (Mn, Co)O is transformed into metallic cobalt and MnO. The introduction of manganese cations into the structure of cobalt oxide leads to a decrease in the rate of both reduction stages. However, the influence of additional cations on the second reduction stage is more noticeable. This is due to crystallographic peculiarities of the compounds: the conversion from the initial oxide (Mn, Co)O into the intermediate oxide (Mn, Co)O requires only a small displacement of cations, whereas the formation of metallic cobalt from (Mn, Co)O requires a rearrangement of the entire structure.

摘要

通过硝酸钴和硝酸锰的共沉淀法制备了一系列锰钴摩尔比逐渐变化的混合氧化物。采用X射线衍射(XRD)、X射线吸收光谱、X射线光电子能谱(XPS)和程序升温还原(TPR)对氧化物的结构、化学性质和还原性进行了研究。结果发现,当锰的浓度低于37原子%时,形成具有立方尖晶石结构的固溶体。当浓度高于63原子%时,基于四方尖晶石形成固溶体,而当浓度在37 - 63原子%范围内时,形成包含四方和立方氧化物的两相体系。为了阐明混合氧化物的还原途径,采用了两种方法。第一种方法基于锰钴氧化物化学成分的逐渐变化,说明了TPR曲线的缓慢变化。第二种方法是将XRD和伪XPS技术相结合,这使得直接确定还原条件下氧化物的结构和化学性质成为可能。结果表明,锰钴混合氧化物的还原过程分两个阶段进行。在第一阶段,(Mn, Co)O被还原为(Mn, Co)O。在第二阶段,固溶体(Mn, Co)O转变为金属钴和MnO。将锰阳离子引入氧化钴结构中会导致两个还原阶段的速率降低。然而,额外阳离子对第二还原阶段的影响更为明显。这是由于化合物的晶体学特性:从初始氧化物(Mn, Co)O转变为中间氧化物(Mn, Co)O只需要阳离子的小位移,而从(Mn, Co)O形成金属钴则需要整个结构的重排。

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