Molten-salt synthesis of porous La0.6Sr0.4Co0.2Fe0.8O2.9 perovskite as an efficient electrocatalyst for oxygen evolution
Molten-salt synthesis of porous La0.6Sr0.4Co0.2Fe0.8O2.9 perovskite as an efficient electrocatalyst for oxygen evolution
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熔盐合成多孔La0.6Sr0.4Co0.2Fe0.8O2.9钙钛矿作为高效析氧电催化剂
DOI:
10.1007/s12274-018-2065-1
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发表时间:
2018-04
期刊:
影响因子:
9.9
通讯作者:
Wang Jian-Qiang
中科院分区:
文献类型:
--
作者:
Song Sanzhao;Zhou Jing;Zhang Shuo;Zhang Linjuan;Li Jiong;Wang Yu;Han Ling;Long Youwen;Hu Zhiwei;Wang Jian-Qiang
The development of an efficient and low-cost electrocatalyst for the oxygen evolution reaction (OER) via an eco-efficient route is a desirable, although challenging, outcome for overall water splitting. Herein, an iron-rich La0.6Sr0.4Co0.2Fe0.8O2.9 (LSCF28) perovskite with an open porous topographic structure was developed as an electrocatalyst by a straightforward molten-salt synthesis approach. It was found that porosity correlates with both the iron content and the molten-salt approach. Benefiting from the large surface area, high activity of the porous internal surface, and the optimal electronic configuration of redox sites, this inexpensive material exhibits high performance with a large mass activity of 40.8 A·g–1 at a low overpotential of 0.345 V in 0.1 M KOH, surpassing the state-of-the-art precious metal IrO2 catalyst and other well-known perovskites, such as Ba0.5Sr0.5Co0.8Fe0.2O3 and SrCoO2.7. Our work illustrates that the molten-salt method is an effective route to generate porous structures in perovskite oxides, which is important for energy conversion and storage devices.
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影响因子:
9.5
作者:
Hui Zhang;Jinyin Liu;Guanqi Zhao;Yongjun Gao;T. Tyliszczak;P. Glans;Jinghua Guo;Ding Ma;
通讯作者:
Hui Zhang;Jinyin Liu;Guanqi Zhao;Yongjun Gao;T. Tyliszczak;P. Glans;Jinghua Guo;Ding Ma;
影响因子:
16.6
作者:
Bao, Jian;Zhang, Xiaodong;Xie, Yi
通讯作者:
Xie, Yi
影响因子:
8.6
作者:
Kruk, M;Jaroniec, M;Ryoo, R
通讯作者:
Ryoo, R
影响因子:
16.6
作者:
Zhou S;Miao X;Zhao X;Ma C;Qiu Y;Hu Z;Zhao J;Shi L;Zeng J
通讯作者:
Zeng J
影响因子:
3.2
作者:
S. Hashimoto;Yasuhiro Fukuda;M. Kuhn;Kazuhisa Sato;K. Yashiro;J. Mizusaki
通讯作者:
S. Hashimoto;Yasuhiro Fukuda;M. Kuhn;Kazuhisa Sato;K. Yashiro;J. Mizusaki