Degradation Responses of Activated-Carbon-Based EDLCs for Higher Voltage Operation and Their Factors

被引:157
作者
Ishimoto, Shuichi [1 ,2 ]
Asakawa, Yuichiro [1 ]
Shinya, Masanori [1 ]
Naoi, Katsuhiko [1 ]
机构
[1] Tokyo Univ Agr & Technol, Inst Symbiot Sci & Technol, Tokyo 1848558, Japan
[2] Nippon Chemi Con Corp, Ibaraki 3188505, Japan
关键词
COMPLEX CAPACITANCE ANALYSIS; IONIC LIQUID; ELECTRODES; ELECTROLYTES; SPECTROSCOPY;
D O I
10.1149/1.3126423
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
To investigate the degradation mechanisms of electric double-layer capacitor (EDLC) components using 1.0 M triethylmethylammonium (TEMA) tetrafluoroborate (BF4) in propylene carbonate (PC), the failure-mode processes of positive and negative electrodes were characterized as a function of the applied voltage (2.5-4.0 V). When the cell voltage ranges below 3.0 V, no impedance spectra or surface morphology changes were observed, indicating that no side reactions occur in this case. In the voltage range from 3.0 to 3.7 V, the exfoliation of graphene layers in activated carbon (AC) and the formation of cracks were observed in the positive electrode over 4.9 V vs Li/Li+ possibly due to the gasification of surface functional groups with adsorbed water. On the negative electrode, the adsorbed water is electrochemically reduced to H-2 gas and OH-. The generated OH-induces the Hoffman elimination of TEMA(+) and activates the hydrolysis of PC. These water-induced side reactions could be the most critical factors for higher voltage operation. In the higher voltage range (over 3.7 V), the accumulation of solid electrolyte interface films by electrochemical oxidation and the reduction of PC were observed for both electrodes, indicating that the electrochemical oxidation and the reduction of PC on the AC surfaces occur above 5.2 V and below 1.5 V vs Li/Li+, respectively. (C) 2009 The Electrochemical Society. [DOI: 10.1149/1.3126423] All rights reserved.
引用
收藏
页码:A563 / A571
页数:9
相关论文
共 30 条
[1]   An asymmetric hybrid nonaqueous energy storage cell [J].
Amatucci, GG ;
Badway, F ;
Du Pasquier, A ;
Zheng, T .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2001, 148 (08) :A930-A939
[2]   High temperature carbon-carbon supercapacitor using ionic liquid as electrolyte [J].
Balducci, A. ;
Dugas, R. ;
Taberna, P. L. ;
Simon, P. ;
Plee, D. ;
Mastragostino, M. ;
Passerini, S. .
JOURNAL OF POWER SOURCES, 2007, 165 (02) :922-927
[3]   Ageing behaviour of electrochemical double layer capacitors Part I. Experimental study and ageing model [J].
Bohlen, Oliver ;
Kowal, Julia ;
Sauer, Dirk Uwe .
JOURNAL OF POWER SOURCES, 2007, 172 (01) :468-475
[4]   A CONFORMATIONAL-ANALYSIS OF PROPYLENE CARBONATE MOLECULES ADSORBED AT THE MERCURY-ELECTRODE [J].
BRASSEUR, R ;
HURWITZ, HD .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1983, 148 (02) :249-270
[5]   Ultracapacitors: why, how, and where is the technology [J].
Burke, A .
JOURNAL OF POWER SOURCES, 2000, 91 (01) :37-50
[6]   Intercalation into and film formation on pyrolytic graphite in a supercapacitor-type electrolyte (C2H5)4NBF4/propylene carbonate [J].
Campana, F. P. ;
Hahn, M. ;
Foelske, A. ;
Ruch, P. ;
Koetz, R. ;
Siegenthaler, H. .
ELECTROCHEMISTRY COMMUNICATIONS, 2006, 8 (08) :1363-1368
[7]   Comparison of commercial supercapacitors and high-power lithium-ion batteries for power-assist applications in hybrid electric vehicles I. Initial characterization [J].
Chu, A ;
Braatz, P .
JOURNAL OF POWER SOURCES, 2002, 112 (01) :236-246
[8]  
Conway B.E., 1999, Electrochemical Supercapacitors: Scientific Fundamentals and Technological Applications, P138
[9]  
de Levie R., 1964, Electrochim. Acta., V9, P1231, DOI DOI 10.1016/0013-4686(64)85015-5
[10]   Incorporation of homogeneous, nanoscale MnO2 within ultraporous carbon structures via self-limiting electroless deposition:: Implications for electrochemical capacitors [J].
Fischer, Anne E. ;
Pettigrew, Katherine A. ;
Rolison, Debra R. ;
Stroud, Rhonda M. ;
Long, Jeffrey W. .
NANO LETTERS, 2007, 7 (02) :281-286