Hydrogenated amorphous silicon thin film anode for proton conducting batteries

被引:25
|
作者
Meng, Tiejun [1 ]
Young, Kwo [1 ,2 ]
Beglau, David [1 ]
Yan, Shuli [2 ]
Zeng, Peng [3 ]
Cheng, Mark Ming-Cheng [3 ]
机构
[1] BASF Battery Mat Ovon, Rochester Hills, MI 48309 USA
[2] Wayne State Univ, Dept Chem Engn & Mat Sci, Detroit, MI 48202 USA
[3] Wayne State Univ, Dept Elect & Comp Engn, Detroit, MI 48202 USA
关键词
Amorphous silicon; Thin films; Ionic liquid; Non-aqueous electrolyte; Nickel/metal hydride battery; METAL HYDRIDE ELECTRODE; CHEMICAL-VAPOR-DEPOSITION; FUEL-CELL APPLICATIONS; LITHIUM-ION BATTERIES; HIGH-CAPACITY; RAMAN-SPECTRA; ELECTROCHEMICAL PROPERTIES; CYCLIC VOLTAMMETRY; STORAGE; LIQUIDS;
D O I
10.1016/j.jpowsour.2015.10.045
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
Hydrogenated amorphous Si (a-Si:H) thin films deposited by chemical vapor deposition were used as anode in a non-conventional nickel metal hydride battery using a proton-conducting ionic liquid based non-aqueous electrolyte instead of alkaline solution for the first time, which showed a high specific discharge capacity of 1418 mAh g(-1) for the 38th cycle and retained 707 mAh g(-1) after 500 cycles. A maximum discharge capacity of 3635 mAh g(-1) was obtained at a lower discharge rate, 510 mA g(-1). This electrochemical discharge capacity is equivalent to about 3.8 hydrogen atoms stored in each silicon atom. Cyclic voltammogram showed an improved stability 300 mV below the hydrogen evolution potential. Both Raman spectroscopy and Fourier transform infrared spectroscopy studies showed no difference to the pre-existing covalent Si-H bond after electrochemical cycling and charging, indicating a noncovalent nature of the Si-H bonding contributing to the reversible hydrogen storage of the current material. Another a-Si:H thin film was prepared by an rf-sputtering deposition followed by an ex-situ hydrogenation, which showed a discharge capacity of 2377 mAh g(-1). (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:31 / 38
页数:8
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