电容去离子
生物炭
杂原子
海水淡化
吸附
活性炭
电化学
材料科学
化学工程
兴奋剂
碳纤维
盐(化学)
比表面积
化学
纳米技术
电极
复合材料
膜
光电子学
有机化学
戒指(化学)
生物化学
热解
复合数
工程类
催化作用
物理化学
作者
Changlin Wang,Yuqi Li,Yixuan Qiao,Nyan Lynn Tut,Dingfei Deng,Qianfeng Pan,Guangyuan Yao,Yang Wang
标识
DOI:10.1016/j.jece.2023.111560
摘要
Capacitive deionization (CDI) is a promising desalination technology. In the design and fabrication of high-performance CDI electrodes, the modification of activated carbon is widely adopted to improve the desalination capacity. In this work, aiming at the regulation of surface potential, activated carbon was doped with N and S, showing improved conductivity, wettability, and optimized pore structure. The difference in the potential of zero charge (Epzc) generated by the heteroatom doping was employed to enlarge the actual adsorption voltage window, and to improve the salt adsorption capacity (SAC) and total salt adsorption capacity at long periods. SAC of 14.4 mg g-1 was achieved with a high average salt absorption rate (ASAR) of 8.2 mg g-1 min-1 under 1.2 V in a 500 mg L-1 NaCl solution. Moreover, the total SAC of asymmetric configuration of N, S-doped biochar of 50 cycles achieved 545.8 mg g-1, 19.7% more than that of the symmetric configuration of unmodified biochar. The doping of N and S atoms on biochar brings excellent electrochemical performance and desalination capacity, and the rational utilization of Epzc after heteroatom doping provides a reasonable method for the design of CDI configuration.
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