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Hybrid capacitive deionization (HCDI), which consists of one Faradaic and one carbon electrode, has recently developed as a high-efficiency and environmentally friendly water desalination technique. The advancement of HCDI, however, is hampered by a scarcity of high quality Faradaic materials. Here we demonstrated that conducting poly-p-phenylene (PPP) with a coplanar molecular structure of the extended Π-conjugated skeleton can be used as a reversible electrode material to capture either cations (Na+, K+, Ca2+) or anions (Cl−, F−, NO3−, and SO42−) from various salt solutions. This is benefited from its broad potential window and n−/p-doping characteristics. The desalination performance of PPP was evaluated systematically with the constructed HCDI cells in different electrolytes, which can deliver excellent salt adsorption capacity, charge efficiency, and long-term cycling stability. Further, based on complex capacitance analysis, the kinetic features and mechanism for the ion insertion-adsorption processes were further elucidated, which offers both a new perspective for understanding the salt removal performance of PPP and a practical method for investigating other pseudocapacitive intercalation materials.
Kong et al. (Fri,) studied this question.