Exploring the large voltage range of carbon/carbon supercapacitors in aqueous lithium sulfate electrolyte
被引:299
作者:
Gao, Qiang
论文数: 0引用数: 0
h-index: 0
机构:
CNRS Univ, Ctr Rech Mat Div, F-45071 Orleans, FranceCNRS Univ, Ctr Rech Mat Div, F-45071 Orleans, France
Gao, Qiang
[1
]
Demarconnay, Laurent
论文数: 0引用数: 0
h-index: 0
机构:
CNRS Univ, Ctr Rech Mat Div, F-45071 Orleans, FranceCNRS Univ, Ctr Rech Mat Div, F-45071 Orleans, France
Demarconnay, Laurent
[1
]
Raymundo-Pinero, Encarnacion
论文数: 0引用数: 0
h-index: 0
机构:
CNRS Univ, Ctr Rech Mat Div, F-45071 Orleans, FranceCNRS Univ, Ctr Rech Mat Div, F-45071 Orleans, France
Raymundo-Pinero, Encarnacion
[1
]
Beguin, Francois
论文数: 0引用数: 0
h-index: 0
机构:
CNRS Univ, Ctr Rech Mat Div, F-45071 Orleans, France
Poznan Univ Tech, Fac Chem Technol, PL-60965 Poznan, PolandCNRS Univ, Ctr Rech Mat Div, F-45071 Orleans, France
Beguin, Francois
[1
,2
]
机构:
[1] CNRS Univ, Ctr Rech Mat Div, F-45071 Orleans, France
[2] Poznan Univ Tech, Fac Chem Technol, PL-60965 Poznan, Poland
This study investigates the large voltage range of symmetric carbon/carbon capacitors in environmentally friendly aqueous lithium sulfate electrolyte. A high over-potential related to the hydrogen sorption mechanism at the negative electrode contributes usefully to enhance the operating voltage up to 1.9 V with an excellent stability during 10 000 charge/discharge cycles. Such a voltage value is two times higher than the values generally demonstrated with symmetric carbon/carbon capacitors in conventional aqueous media, while avoiding the disadvantages of the corrosive properties of acidic and basic electrolytes. Temperature programmed desorption analysis of the electrodes after long-term cycling gives the evidence that the maximum voltage is essentially limited by an irreversible electro-oxidation process at the positive electrode. If the potential of the positive electrode goes beyond a given value during cell operation, a massive electro-oxidation of carbon leads to a further deleterious increase of the maximum potential of the electrode and an increase of electrode resistance resulting in a decrease of capacitance. Inconvenience can be sidestepped by performing a controlled chemical oxidation of the carbon surface using hydrogen peroxide. As a consequence, the maximum potential of the electrode remains stable during operation of the cell at 1.9 V, and the system can be charged/discharged during 10 000 cycles with very moderate loss of capacitance or increase of resistance.