Understanding the mechanism of carbonization and KOH activation of polyaniline leading to enhanced electrosorption performance
Capacitive deionization (CDI) emerged as a new water desalination technology in which ions are removed from brackish water by being attracted and stored in two polarized electrodes. The electrode material plays a very important role affecting other fundamental parameters such as the salt adsorption...
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Veröffentlicht in: | Carbon (New York) 2020-01, Vol.156, p.346-358 |
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Sprache: | eng |
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Zusammenfassung: | Capacitive deionization (CDI) emerged as a new water desalination technology in which ions are removed from brackish water by being attracted and stored in two polarized electrodes. The electrode material plays a very important role affecting other fundamental parameters such as the salt adsorption capacity (SAC), conductivity, desalination kinetics, and energy consumption. Typically, the CDI electrodes are carbon-based materials, fulfilling requirements such as high specific surface area (SSA), chemical stability, and conductivity. Here, we make a comprehensive study of the variables involved in the polyaniline activated carbons (PAC) preparation. A new mechanism is proposed to explain how the carbonization/activation conditions have influence on textural properties (SSA and pore volume) of PAC. We found that carbonization at temperatures ≤600 °C are mandatory to provide more KOH-reactive carbon intermediates due to their turbostratic structure. After activation at 850 °C, remarkable pore volume (2.30 cm³/g) and SSA (∼3600 m2/g) were achieved, which has direct influence on promoting high electrode capacitance (213 F/g), SAC (22.2 mg/g), and charge efficiency (81%). This SAC is among the highest values reported for CDI desalination using carbon electrodes. This work enlightens the mechanism to achieve high performance activated carbons providing a promising electrode material for CDI desalination.
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ISSN: | 0008-6223 1873-3891 |
DOI: | 10.1016/j.carbon.2019.09.058 |