Co3+-Rich Na1.95CoP2O7 Phosphates as Efficient Bifunctional Catalysts for Oxygen Evolution and Reduction Reactions in Alkaline Solution

被引:13
作者
Gui, Liangqi [1 ]
Miao, Xiaoyun [1 ]
Lei, Chengjun [1 ]
Wang, Kailin [1 ]
Zhou, Wei [1 ,2 ,3 ]
He, Beibei [1 ,2 ,3 ]
Wang, Qing [1 ,4 ]
Zhao, Ling [1 ,2 ,3 ]
机构
[1] China Univ Geosci, Fac Mat Sci & Chem, Wuhan 430074, Hubei, Peoples R China
[2] China Univ Geosci Wuhan, Zhejiang Inst, Hangzhou 311305, Zhejiang, Peoples R China
[3] China Univ Geosci, Engn Res Ctr Nanogeo Mat, Minist Educ, Wuhan 430074, Hubei, Peoples R China
[4] Penn State Univ, Dept Mat Sci & Engn, University Pk, PA 16802 USA
基金
中国国家自然科学基金;
关键词
bifunctional catalysts; defect engineering; highly efficient; sodium cobalt phosphate; WATER OXIDATION CATALYST; PEROVSKITE; COBALT; ELECTROCATALYSTS; ELECTRODE; OXIDES; CARBON; FE; PYROPHOSPHATE; NANOPARTICLES;
D O I
10.1002/chem.201901848
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Implementing sustainable energy conversion and storage technologies is highly reliant on crucial oxygen electrocatalysis, such as the oxygen evolution reaction (OER) and oxygen reduction reaction (ORR). However, the pursuit of low cost, energetic efficient and robust bifunctional catalysts for OER and ORR remains a great challenge. Herein, the novel Na-ion-deficient Na2-xCoP2O7 catalysts are proposed to efficiently electrocatalyze OER and ORR in alkaline solution. The engineering of Na-ion deficiency can tune the electronic structure of Co, and thus tailor the intrinsically electrocatalytic performance. Among the sodium cobalt phosphate catalysts, the Na1.95CoP2O7 (NCPO5) catalyst exhibits the lowest Delta E (E-J10,E-OER-E-J-1,E-ORR) of only 0.86 V, which favorably outperforms most of the reported non-noble metal catalysts. Moreover, the Na-ion deficiency can stabilize the phase structure and morphology of NCPO5 during the OER and ORR processes. This study highlights the Na-ion deficient Na2-xCoP2O7 as a promising class of low-cost, highly active and robust bifunctional catalysts for OER and ORR.
引用
收藏
页码:11007 / 11014
页数:8
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