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α-MnO催化剂在析氧反应中的活性影响因素:隐钾锰矿的电导率与暴露表面积

Factors Governing the Activity of α-MnO Catalysts in the Oxygen Evolution Reaction: Conductivity versus Exposed Surface Area of Cryptomelane.

作者信息

Heese-Gärtlein Justus, Morales Dulce M, Rabe Anna, Bredow Thomas, Schuhmann Wolfgang, Behrens Malte

机构信息

Faculty of Chemistry and, Center for Nanointegration Duisburg-Essen (CENIDE), University of Duisburg-Essen, Universitätsstr. 7, 45114, Essen, Germany.

Analytical Chemistry-Center for Electrochemical Sciences (CES), Faculty of Chemistry and Biochemistry, Ruhr University Bochum, Universitätsstr. 150, 44780, Bochum, Germany.

出版信息

Chemistry. 2020 Sep 21;26(53):12256-12267. doi: 10.1002/chem.201905090. Epub 2020 Sep 4.

Abstract

Cryptomelane (α-(K)MnO ) powders were synthesized by different methods leading to only slight differences in their bulk crystal structure and chemical composition, while the BET surface area and the crystallite size differed significantly. Their performance in the oxygen evolution reaction (OER) covered a wide range and their sequence of increasing activity differed when electrocatalysis in alkaline electrolyte and chemical water oxidation using Ce were compared. The decisive factors that explain this difference were identified in the catalysts' microstructure. Chemical water oxidation activity is substantially governed by the exposed surface area, while the electrocatalytic activity is determined largely by the electric conductivity, which was found to correlate with the particle morphology in terms of needle length and aspect ratio in this sample series. This correlation is rather explained by an improved conductivity due to longer needles than by structure sensitivity as was supported by reference experiments using H O decomposition and carbon black as additive. The most active catalyst R-cryptomelane reached a current density of 10 mA cm at a potential 1.73 V without, and at 1.71 V in the presence of carbon black. The improvement was significantly higher for the catalyst with lower initial activity. However, the materials showed a disappointing catalytic stability during alkaline electrochemical OER, whereas the crystal structure was found to be stable at working conditions.

摘要

通过不同方法合成了锰钾矿(α-(K)MnO )粉末,其体相晶体结构和化学成分仅有细微差异,而BET表面积和微晶尺寸差异显著。它们在析氧反应(OER)中的性能范围很广,当比较碱性电解质中的电催化和使用Ce的化学水氧化时,其活性增加顺序有所不同。在催化剂的微观结构中确定了解释这种差异的决定性因素。化学水氧化活性主要由暴露的表面积决定,而电催化活性很大程度上由电导率决定,在该样品系列中发现电导率与针状长度和长径比方面的颗粒形态相关。这种相关性更多地是由于针状更长导致电导率提高,而不是结构敏感性,使用H O分解和炭黑作为添加剂的参考实验支持了这一点。最具活性的催化剂R-锰钾矿在无炭黑时电位为1.73 V、有炭黑时电位为1.71 V时达到10 mA cm 的电流密度。对于初始活性较低的催化剂,这种改善更为显著。然而,这些材料在碱性电化学OER过程中表现出令人失望的催化稳定性,而晶体结构在工作条件下是稳定的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0ba/7540518/03d69e455118/CHEM-26-12256-g001.jpg

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