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对A位缺钡的BaCoFeZrYO氧化物作为高效析氢反应电催化剂的评估。

Evaluation of A-Site Ba-Deficient Ba CoFeZrYO Oxides as Electrocatalysts for Efficient Hydrogen Evolution Reaction.

作者信息

Li Xiangnan, He Liqing, Zhong Xiongwei, Zhang Jie, Luo Shijing, Yi Wendi, Zhang Luozheng, Hu Manman, Tang Jun, Zhou Xianyong, Zhao Xingzhong, Xu Baomin

机构信息

Department of Materials Science and Engineering, Southern University of Science and Technology, Shenzhen, Guangdong 518055, China.

Department of Physics, Wuhan University, Wuhan, Hubei 430072, China.

出版信息

Scanning. 2018 Sep 12;2018:1341608. doi: 10.1155/2018/1341608. eCollection 2018.

DOI:10.1155/2018/1341608
PMID:30298097
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6157210/
Abstract

Exploring earth-abundant and cost-effective catalysts with high activity and stability for a hydrogen evolution reaction (HER) is of great importance to practical applications of alkaline water electrolysis. Here, we report on A-site Ba-deficiency doping as an effective strategy to enhance the electrochemical activity of BaCoFeZrYO for HER, which is related to the formation of oxygen vacancies around active Co/Fe ions. By comparison with the benchmarking BaSrCoFeO , one of the most spotlighted perovskite oxides, the BaCoFeZrYO oxide has lower overpotential and smaller Tafel slope. Furthermore, the BaCoFeZrYO catalyst is ultrastable in an alkaline solution. The enhanced HER performance originated from the increased active atoms adjacent to oxygen vacancies on the surface of the BaCoFeZrYO catalyst induced by Ba-deficiency doping. The low-coordinated active atoms and adjacent oxygen ions may play the role of heterojunctions that synergistically facilitate the Volmer process and thus render stimulated HER catalytic activity. The preliminary results suggest that Ba-deficiency doping is a feasible method to tailor the physical and electrochemical properties of perovskite, and that BaCoFeZrYO is a potential catalyst for HER.

摘要

探索具有高活性和稳定性的、地球上储量丰富且成本效益高的析氢反应(HER)催化剂对于碱性水电解的实际应用至关重要。在此,我们报道A位Ba缺陷掺杂作为一种有效策略来增强BaCoFeZrYO用于HER的电化学活性,这与活性Co/Fe离子周围氧空位的形成有关。与最受关注的钙钛矿氧化物之一的基准材料BaSrCoFeO相比,BaCoFeZrYO氧化物具有更低的过电位和更小的塔菲尔斜率。此外,BaCoFeZrYO催化剂在碱性溶液中具有超高稳定性。HER性能的增强源于Ba缺陷掺杂诱导的BaCoFeZrYO催化剂表面与氧空位相邻的活性原子增加。低配位的活性原子和相邻的氧离子可能起到异质结的作用,协同促进Volmer过程,从而产生增强的HER催化活性。初步结果表明,Ba缺陷掺杂是一种调整钙钛矿物理和电化学性质的可行方法,并且BaCoFeZrYO是一种潜在的HER催化剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6dd8/6157210/68ae23fc459a/SCANNING2018-1341608.008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6dd8/6157210/bb0b9e13d04e/SCANNING2018-1341608.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6dd8/6157210/3d95671fa8e9/SCANNING2018-1341608.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6dd8/6157210/f9933cbc659a/SCANNING2018-1341608.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6dd8/6157210/542fc9e864e2/SCANNING2018-1341608.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6dd8/6157210/37172e957400/SCANNING2018-1341608.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6dd8/6157210/c4e397e7ef04/SCANNING2018-1341608.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6dd8/6157210/8ab2e3c36539/SCANNING2018-1341608.007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6dd8/6157210/68ae23fc459a/SCANNING2018-1341608.008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6dd8/6157210/bb0b9e13d04e/SCANNING2018-1341608.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6dd8/6157210/3d95671fa8e9/SCANNING2018-1341608.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6dd8/6157210/f9933cbc659a/SCANNING2018-1341608.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6dd8/6157210/542fc9e864e2/SCANNING2018-1341608.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6dd8/6157210/37172e957400/SCANNING2018-1341608.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6dd8/6157210/c4e397e7ef04/SCANNING2018-1341608.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6dd8/6157210/8ab2e3c36539/SCANNING2018-1341608.007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6dd8/6157210/68ae23fc459a/SCANNING2018-1341608.008.jpg

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