Zhou Fengkai, Wang Shasha, Wang Zeyu, Wang Fujun, Wang Lu, Mao Jifu
Shanghai Frontiers Science Center of Advanced Textiles, College of Textiles, Donghua University, Shanghai 201620, China; Key Laboratory of Textile Science & Technology, Ministry of Education, College of Textiles, Donghua University, Shanghai 201620, China.
Shanghai Frontiers Science Center of Advanced Textiles, College of Textiles, Donghua University, Shanghai 201620, China; Key Laboratory of Textile Science & Technology, Ministry of Education, College of Textiles, Donghua University, Shanghai 201620, China; Key Laboratory of Textile Industry for Biomedical Textile Materials and Technology, Donghua University, Shanghai 201620, China.
J Colloid Interface Sci. 2025 Dec 15;700(Pt 2):138502. doi: 10.1016/j.jcis.2025.138502. Epub 2025 Jul 20.
Desalination of abundant seawater into usable freshwater is an effective strategy to alleviate the crisis of freshwater resources. However, relying solely on Na/Cl trapping electrode materials proves inefficient, and residual high concentrations of Cl/Na corrode the electrodes, compromising desalination performance and thus not constituting true desalination. To overcome these challenges, sucrose-derived porous activated carbon (SBC) is developed via rapid dehydration, pre‑carbonization, and high-temperature annealing for Na and Cl capture electrodes in hybrid capacitive deionization (HCDI) for seawater desalination. The Na capturing electrode was fabricated through in situ polymerization of MnO on SBC (SBC@MnO), and the Cl capturing electrode was prepared by coating SBC with sodium-pre-intercalated MnO combined with in situ polymerization of polypyrrole (SBC@NaMnO@PPy). Both electric double-layer capacitance and Faradaic pseudocapacitance primarily govern the ion adsorption and storage. Functionalized SBC exhibited enhanced specific capacitance, a notable desalination capacity (57.22 mg g), and a remarkably high desalination rate (1.06 mg g s). X-ray photoelectron spectroscopy analysis revealed that the primary adsorption mechanisms involved ion insertion associated with the redox reactions of the electrode materials and surface adsorption. Furthermore, this approach exhibited effective purification capabilities for seawater, river water, and rainwater, thereby expanding the potential application scope of the HCDI.
将丰富的海水淡化成可用的淡水是缓解淡水资源危机的有效策略。然而,仅依靠钠/氯捕获电极材料效率低下,且残留的高浓度氯/钠会腐蚀电极,损害脱盐性能,因此不能构成真正的脱盐。为了克服这些挑战,通过快速脱水、预碳化和高温退火开发了蔗糖衍生的多孔活性炭(SBC),用于混合电容去离子化(HCDI)海水淡化中的钠和氯捕获电极。通过在SBC上原位聚合MnO制备钠捕获电极(SBC@MnO),通过用钠预插层的MnO涂覆SBC并结合聚吡咯的原位聚合制备氯捕获电极(SBC@NaMnO@PPy)。双电层电容和法拉第赝电容主要控制离子的吸附和存储。功能化的SBC表现出增强的比电容、显著的脱盐容量(57.22 mg g)和极高的脱盐速率(1.06 mg g s)。X射线光电子能谱分析表明,主要吸附机制包括与电极材料的氧化还原反应相关的离子插入和表面吸附。此外,该方法对海水、河水和雨水具有有效的净化能力,从而扩大了HCDI的潜在应用范围。