RuO2 nanoparticles supported on MnO2 nanorods as high efficient bifunctional electrocatalyst of lithium-oxygen battery

被引:90
|
作者
Xu, Yue-Feng [1 ]
Chen, Yuan [1 ]
Xu, Gui-Liang [3 ]
Zhang, Xiao-Ru [1 ]
Chen, Zonghai [3 ]
Li, Jun-Tao [2 ]
Huang, Ling [1 ]
Amine, Khalil [3 ]
Sun, Shi-Gang [1 ,2 ]
机构
[1] Xiamen Univ, Dept Chem, State Key Lab Phys Chem Solid Surfaces, Coll Chem & Chem Engn, Xiamen 361005, Peoples R China
[2] Xiamen Univ, Coll Energy, Xiamen 361005, Peoples R China
[3] Argonne Natl Lab, Chem Sci & Engn Div, 9700 South Cass Ave, Lemont, IL 60439 USA
关键词
RuO2 nanoparticles on MnO2 nanorods; Bifunctional electrocatalysts; ORR; OER; Lithium-oxygen battery; LI-O-2; BATTERIES; CATHODE CATALYST; POROUS GRAPHENE; LONG-LIFE; CAPACITY; RECHARGEABILITY; ELECTROLYTE; CAPABILITY; SOLVENTS; OXIDES;
D O I
10.1016/j.nanoen.2016.08.009
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
RuO2 nanoparticles supported on MnO2 nanorods (denoted as np-RuO2/nr-MnO2) were synthesized via a two-step hydrothermal reaction. SEM and TEM images both illustrated that RuO2 nanoparticles are well dispersed on the surface of MnO2 nanorods in the as-prepared np-RuO2/nr-MnO2 material. Electrochemical results demonstrated that the np-RuO2/nr-MnO2 as oxygen cathode of Li-O-2 batteries could maintain a reversible capacity of 500 mA h g(-1) within 75 cycles at a rate of 50 mA g(-1), and a higher capacity of 4000 mA h g(-1) within 20 cycles at a rate as high as 200 mA g(-1). Moreover, the cell with the np-RuO2/nr-MnO2 catalyst presented much lower voltage polarization (about 0.58 V at a rate of 50 mA g(-1)) than that measured with only MnO2 nanorods during charge/discharge processes. The catalytic property of the np-RuO2/nr-MnO2 and MnO2 nanorods were further compared by conducting studies of using rotating disk electrode (RDE), chronoamperommetry and linear sweep voltammetry. The results illustrated that the np-RuO2/nr-MnO2 exhibited excellent bifunctional electrocatalytic activities towards both oxygen reduction reaction (ORR) and oxygen evolution reaction (OER). Furthermore, in-situ high-energy X-ray diffraction was employed to trace evolution of species on the np-RuO2/nr-MnO2 cathode during the discharge processes. In-situ XRD patterns demonstrated the formation process of the discharge products that consisted of mainly Li2O2. Ex-situ SEM images were recorded to investigate the morphology and decomposition of the sphere-like Li2O2, which could be observed clearly after discharge process, while are decomposed almost after charge process. The excellent electrochemical performances of the np-RuO2/nr-MnO2 as cathode of Li-O-2 battery could be contributed to the excellent bifunctional electrocatalytic activities for both the ORR and OER, and to the one-dimensional structure which would benefit the diffusion of oxygen and the storage of Li2O2 in the discharge process of Li-O-2 battery. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:63 / 70
页数:8
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