Energy storage performance of hybrid aqueous supercapacitor based on nano-Li2MnSiO4 and activated carbon

被引:10
作者
Chaturvedi, Prerna [1 ]
Sil, Anjan [2 ,3 ]
Sharma, Yogesh [1 ,3 ,4 ]
机构
[1] IIT Roorkee, Dept Appl Sci & Engn, Energy Storage Lab, Saharanpur Campus, Saharanpur 247001, India
[2] IIT Roorkee, Dept Met & Mat Engn, Roorkee 247667, Uttar Pradesh, India
[3] IIT Roorkee, Ctr Nanotechnol, Roorkee 247667, Uttar Pradesh, India
[4] IIT Roorkee, Dept Phys, Roorkee 247667, Uttar Pradesh, India
关键词
Li2MnSiO4; Asymmetric supercapacitor; Aqueous electrolyte; Nanocrystalline; POSITIVE ELECTRODE MATERIAL; ELECTROCHEMICAL PERFORMANCES; ASYMMETRIC SUPERCAPACITOR; HIGH-CAPACITY; OXIDE; NANOCOMPOSITE; NANOPARTICLES; COST; MNO2;
D O I
10.1007/s11581-016-1683-4
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
Novel asymmetric supercapacitor (ASC) composed of nanocrystalline Li2MnSiO4 (LMS) and activated carbon (AC) in aqueous electrolyte is investigated. ASC is tested in three different electrolytes, viz. 2 M KOH, 2 M LiOH, and 2MLi(2)SO(4). The aqueous solution of 2 M KOH is found to be an appropriate electrolyte in terms of better capacitance, cyclability, and rate capability probably due to a smaller hydration sphere radius and larger ionic conductivity of K+ ions. The electrochemical performance of ASC is examined using cyclic voltammetry (CV) and galvanostatic charge-discharge (GCD) cycling, and results are complimented with electrochemical impedance spectroscopy (EIS). Novel ASC exhibits the specific capacitance of 60 (similar to 5) F g(-1) at 3 mV s(-1) in 2 M KOH. The excellent cyclability (till 5000 cycles) is also observed. The improved supercapacitive properties are mainly ascribed to the unique morphology of LMS (surface area similar to 30 m(2) g(-1) and homogenous meso-pore distribution) which provides easy percolation of electrolytic ions to provide better formation of electric double layer with minor redox behavior. The ex situ X-ray diffraction (XRD) measurement was carried out on a cycled electrode to support the plausible reaction mechanism.
引用
收藏
页码:1719 / 1728
页数:10
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