Abstract: Capacitive deionization (CDI) is a promising technology for Cd2+ removal owing to the advantages such as simple and convenient operation, low energy consumption, and free of secondary pollution. The key challenge limiting its development is the low adsorption capacity of electrode materials for Cd2+. In this work, we used glucose as carbon source, thiourea and sulfur as the dopant to prepare porous carbon materials co-doped with S and N through high-temperature carbonization, and explored its electrochemical adsorption performance for Cd2+, by using the prepared carbon material as the electrode. The symmetrical CDI system assembled with identical material for both electrodes achieved a removal capacity of 53 mg·g-1 for Cd2+ at 1.2 V. Furthermore, it was found that with the increase of S and N doping, the surface of carbon materials carries negative charges. Therefore, the asymmetric CDI system assembled by using it as the anode and commercial activated carbon YP-50F as the cathode, and Cd2+ removal capacity reached 88.37 mg·g-1, which was 66.73% higher than symmetrical CDI system. After seven cycles of adsorption-desorption, the capacity retention rate also increased from 62.2% to 81.5%. The removal mechanism of Cd2+ was explored by XPS, and the results showed that it was the synergism of double electric layer and surface functional groups. The matching strategy of high-perfor-mance porous carbon electrodes and asymmetric electrodes developed in this work would pave the way for practical application of CDI technology in the treatment of Cd2+ and other heavy metal wastewater.
覃玲霜, 刘醒, 邓立波. 葡萄糖衍生多孔碳的表面电荷调控与电吸附Cd2+性能[J]. 材料导报, 2024, 38(6): 23040284-8.
QIN Lingshuang, LIU Xing, DENG Libo. Tailoring of the Surface Charge of Glucose-derived Porous Carbons and Their Performance for Electrosorption of Cd2+. Materials Reports, 2024, 38(6): 23040284-8.
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