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与水氧化电催化相关的SrCaFeO钙钛矿中氧缺陷及其有序化如何控制电导率

How Oxygen Deficiency and Its Ordering Control Electrical Conductivity in Sr Ca FeO Perovskites as Related to Water Oxidation Electrocatalysis.

作者信息

Vuong Jiam, Derakhshan Shahab, Tavassol Hadi

机构信息

Department of Chemistry and Biochemistry, California State University, Long Beach, 1250 Bellflower Boulevard, Long Beach, California 90840, United States.

出版信息

ACS Mater Au. 2024 Sep 27;4(6):654-663. doi: 10.1021/acsmaterialsau.4c00098. eCollection 2024 Nov 13.

Abstract

We report on the analysis of oxygen vacancies (OVs) content and ordering of Sr Ca FeO perovskites and explain how OVs change the electrical conductivity and oxygen evolution catalytic activity of these compounds. The structure and OV content are tuned by controlling the -site composition and the reaction atmosphere. X-ray diffraction (XRD) and thermogravimetric analysis (TGA) are used to identify the crystal structures and to quantify bulk oxygen vacancy contents. Our analysis shows that OV content and crystal structure govern the electronic transport properties of the Sr Ca FeO system. The electrical conductivity of oxygen-deficient perovskites (ODPs) is significantly higher than those in brownmillerites (by at least 2 orders of magnitude). Seebeck coefficient measurements identified that the Sr-rich ODPs and brownmillerites are -type semiconductors, while Ca-rich brownmillerites are either insulators (within the experimental temperature range) or p-type semiconductors at lower temperatures (<750 K). Electrical conductivity of -type semiconductors (Sr-rich compounds) reduces with higher OV content, and in brownmillerites with ≥ 1.25, a transition to -type semiconductor is observed at temperatures above 750 K. Our analysis shows that the hole and electron concentrations are similar in these brownmillerites, indicating major contributions from ionic transport. Finally, we show how oxygen deficiency alters the electrical conductivity and catalytic activity of the Sr Ca FeO system in noncomplementary ways.

摘要

我们报道了对SrCaFeO钙钛矿中氧空位(OVs)含量和有序性的分析,并解释了氧空位如何改变这些化合物的电导率和析氧催化活性。通过控制位点组成和反应气氛来调节结构和氧空位含量。利用X射线衍射(XRD)和热重分析(TGA)来确定晶体结构并量化体相氧空位含量。我们的分析表明,氧空位含量和晶体结构决定了SrCaFeO体系的电子传输性质。缺氧钙钛矿(ODPs)的电导率明显高于褐锰矿(至少高出2个数量级)。塞贝克系数测量表明,富Sr的ODPs和褐锰矿是n型半导体,而富Ca的褐锰矿在实验温度范围内是绝缘体,或在较低温度(<750K)下是p型半导体。n型半导体(富Sr化合物)的电导率随着氧空位含量的增加而降低,对于氧含量≥1.25的褐锰矿,在750K以上的温度下观察到向p型半导体的转变。我们的分析表明,这些褐锰矿中的空穴和电子浓度相似,表明离子传输起主要作用。最后,我们展示了氧缺陷如何以非互补的方式改变SrCaFeO体系的电导率和催化活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a629/11565281/d639b14a1338/mg4c00098_0001.jpg

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