Comparative study of electrosorption performance of solar reduced graphene oxide in flow-between and flow-through capacitive deionization architectures

被引:21
作者
Datar, Shreerang D. [1 ]
Mohanapriya, K. [1 ]
Ahirrao, Dinesh J. [1 ]
Jha, Neetu [1 ]
机构
[1] Inst Chem Technol, Dept Phys, Mumbai 400019, Maharashtra, India
关键词
Capacitive deionization; Electrochemistry; Electrosorption capacity; Electrosorption rate; Graphene; CARBON AEROGEL; CHARGE EFFICIENCY; AQUEOUS-SOLUTIONS; ENERGY RECOVERY; ELECTRODES; REMOVAL; IONS; NACL; SUPERCAPACITOR; SELECTIVITY;
D O I
10.1016/j.seppur.2020.117972
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
There are a large number of capacitive deionization (CDI) cell architectures developed with different levels of complexities associated. Here, we compare flow-between (FB-CDI) and flow-through (FTE-CDI) capacitive deionization setups with respect to electrosorption performances by using solar reduced graphene oxide (SRGO) as an electrode material. SRGO is synthesised using solar irradiation and characterized for crystallinity, structure and morphology using x-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy and scanning electron microscopy (SEM). The electrode material is studied for charge storage using cyclic voltammetry and galvanostatic charge-discharge in aqueous sodium chloride and potassium chloride solutions. To compare the two capacitive deionization architectures with respect to electrosorption performance, we use two different cations, i.e sodium and potassium to study its effect on hydrated radius and hydration ratio of these cations. The electrosorption performance is estimated by varying the voltage between two electrodes and concentrations of salt solutions. The electrosorption capacity obtained is high 46.1 mg/g for FTE-CDI, whereas electrosorption rate is high i.e 0.026 mg/g/s for FB-CDI for potassium chloride solution. Further the obtained values of electrosorption capacities are validated by Langmuir and Freundlich adsorption isotherms. We confirm that the data fits well with Langmuir adsorption isotherm for both the cations. We further validate the electrosorption data by modified Donnan (mD) model.
引用
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页数:10
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[1]   Sweet-Lime-Peels-Derived Activated-Carbon-Based Electrode for Highly Efficient Supercapacitor and Flow-Through Water Desalination [J].
Ahirrao, Dinesh J. ;
Tambat, Sneha ;
Pandit, A. B. ;
Jha, Neetu .
CHEMISTRYSELECT, 2019, 4 (09) :2610-2625
[2]  
Ahirrao Dinesh J., 2019, CARBON
[3]  
Alfredy T., 2019, J WATER REUSE DESALI
[4]   The feasibility of boron removal from water by capacitive deionization [J].
Avraham, Eran ;
Noked, Malachi ;
Soffer, Abraham ;
Aurbach, Doron .
ELECTROCHIMICA ACTA, 2011, 56 (18) :6312-6317
[5]   Membrane capacitive deionization [J].
Biesheuvel, P. M. ;
van der Wal, A. .
JOURNAL OF MEMBRANE SCIENCE, 2010, 346 (02) :256-262
[6]   A dual-ion electrochemistry deionization system based on AgCl-Na0.44MnO2 electrodes [J].
Chen, Fuming ;
Huang, Yinxi ;
Guo, Lu ;
Ding, Meng ;
Yang, Hui Ying .
NANOSCALE, 2017, 9 (28) :10101-10108
[7]   Kinetic and isotherm studies on the electrosorption of NaCl from aqueous solutions by activated carbon electrodes [J].
Chen, Zhaolin ;
Song, Cunyi ;
Sun, Xiaowei ;
Guo, Hongfei ;
Zhu, Guangdong .
DESALINATION, 2011, 267 (2-3) :239-243
[8]   Flow-electrode capacitive deionization with highly enhanced salt removal performance utilizing high-aspect ratio functionalized carbon nanotubes [J].
Cho, Younghyun ;
Yoo, Chung-Yul ;
Lee, Seung Woo ;
Yoon, Hana ;
Lee, Ki Sook ;
Yang, SeungCheol ;
Kim, Dong Kook .
WATER RESEARCH, 2019, 151 :252-259
[9]   The effect of the flow-regime, reversal of polarization, and oxygen on the long term stability in capacitive de-ionization processes [J].
Cohen, Izaak ;
Avraham, Eran ;
Bouhadana, Yaniv ;
Soffer, Abraham ;
Aurbach, Doron .
ELECTROCHIMICA ACTA, 2015, 153 :106-114
[10]   Enhanced Charge Efficiency in Capacitive Deionization Achieved by Surface-Treated Electrodes and by Means of a Third Electrode [J].
Cohen, Izaak ;
Avraham, Eran ;
Noked, Malachi ;
Soffer, Abraham ;
Aurbach, Doron .
JOURNAL OF PHYSICAL CHEMISTRY C, 2011, 115 (40) :19856-19863