TY - GEN
T1 - Investigation of HNO3-treated carbon xerogel electrodes for capacitive deionization applications
AU - Gao, X.
AU - Landon, J.
AU - Neathery, J. K.
AU - Liu, K.
PY - 2013
Y1 - 2013
N2 - Carbon xerogel (CX) materials were synthesized via polycondensation reactions on a carbon cloth sheet, and the resulting sheets were used as electrodes in a capacitive deionization (CDI) cell. To study the effect of oxidation degree for the CX on the electrosorption performance, the electrodes were activated in concentrated HNO3 at various temperatures. Electrosorption examined in a flow cell shows that the electrosorption capacity significantly increases from 3.27 mg (NaCl) g-1 (Carbon) (corresponding to the untreated sample) to 5.46 mg (NaCl) g-1 (Carbon) (for the sample treated at 20°C). However, this value cannot be further improved by adding additional functional groups to the carbon surface by treating the sample at higher temperatures. These additional functional groups may interfere with the double layer used for ion adsorption. Finally, we conclude that the CX materials mildly treated in HNO3 could be a way of greatly improving the deionization capacity of CX for CDI applications.
AB - Carbon xerogel (CX) materials were synthesized via polycondensation reactions on a carbon cloth sheet, and the resulting sheets were used as electrodes in a capacitive deionization (CDI) cell. To study the effect of oxidation degree for the CX on the electrosorption performance, the electrodes were activated in concentrated HNO3 at various temperatures. Electrosorption examined in a flow cell shows that the electrosorption capacity significantly increases from 3.27 mg (NaCl) g-1 (Carbon) (corresponding to the untreated sample) to 5.46 mg (NaCl) g-1 (Carbon) (for the sample treated at 20°C). However, this value cannot be further improved by adding additional functional groups to the carbon surface by treating the sample at higher temperatures. These additional functional groups may interfere with the double layer used for ion adsorption. Finally, we conclude that the CX materials mildly treated in HNO3 could be a way of greatly improving the deionization capacity of CX for CDI applications.
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U2 - 10.1149/05330.0219ecst
DO - 10.1149/05330.0219ecst
M3 - Conference contribution
AN - SCOPUS:84906821874
SN - 9781607684824
T3 - ECS Transactions
SP - 219
EP - 233
BT - Energy Technology/Battery (General) - 223rd ECS Meeting
T2 - Symposium on Energy Technology/Battery - Joint General Session - 223rd Meeting of the Electrochemical Society
Y2 - 12 May 2013 through 16 May 2013
ER -