Oxygen activation on Ba-containing perovskite materials

Author:

Zhu Yue12ORCID,Liu Dongdong34ORCID,Jing Huijuan12ORCID,Zhang Fei123,Zhang Xiaoben23ORCID,Hu Shiqing12ORCID,Zhang Liming12ORCID,Wang Jingyi12,Zhang Lixiao12,Zhang Wenhao12ORCID,Pang Bingjie14,Zhang Peng1,Fan Fengtao123,Xiao Jianping12ORCID,Liu Wei23ORCID,Zhu Xuefeng12ORCID,Yang Weishen12ORCID

Affiliation:

1. State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 457 Zhongshan Road, Dalian 116023, China.

2. University of Chinese Academy of Sciences, Beijing 100039, China.

3. Dalian National Laboratory for Clean Energy, Dalian 116023, China.

4. Dalian University of Technology, 2 Linggong Road, Dalian 116024, China.

Abstract

Oxygen activation, including oxygen reduction reaction (ORR) and oxygen evolution reaction (OER), is at the heart of many important energy conversion processes. However, the activation mechanism of Ba-containing perovskite materials is still ambiguous, because of the complex four-electron transfer process on the gas-solid interfaces. Here, we directly observe that BaO and BaO 2 segregated on Ba-containing material surface participate in the oxygen activation process via the formation and decomposition of BaO 2 . Tens of times of increase in catalytic activities was achieved by introducing barium oxides in the traditional perovskite and inert Au electrodes, indicating that barium oxides are critical for oxygen activation. We find that BaO and BaO 2 are more active than the B-site of perovskite for ORR and OER, respectively, and closely related to the high activity of Ba-containing perovskite.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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