电容去离子
材料科学
海水淡化
化学工程
储能
铋
碳纤维
氯化物
纳米颗粒
纳米技术
复合数
复合材料
膜
冶金
化学
物理
工程类
功率(物理)
量子力学
生物化学
作者
Wenhui Shi,Xin Qian,Meiting Xue,Wenbin Que,Xinlong Gao,Dong Zheng,Wenxian Liu,Fangfang Wu,Jiangnan Shen,Xiehong Cao,Congjie Gao
标识
DOI:10.1021/acsami.1c00089
摘要
Capacitive deionization (CDI) is a promising cost-effective and low energy consumption technology for water desalination. However, most of the previous works focus on only one side of the CDI system, i.e., Na+ ion capture, while the other side that stores chloride ions, which is equally important, receives very little attention. This is attributed to the limited Cl- storage materials as well as their sluggish kinetics and poor stability. In this article, we demonstrate that a N-doped porous carbon framework is capable of suppressing the phase-transformation-induced performance decay of bismuth, affording an excellent Cl- storage and showing potential for water desalination. The obtained Bi-carbon composite (Bi/N-PC) shows a capacity of up to 410.4 mAh g-1 at 250 mA g-1 and a high rate performance. As a demonstration for water desalination, a superior desalination capacity of 113.4 mg g-1 is achieved at 100 mA g-1 with excellent durability. Impressively, the CDI system exhibits fast ion capturing with a desalination rate as high as 0.392 mg g-1 s-1, outperforming most of the recently reported Cl- capturing electrodes. This strategy is applicable to other Cl- storage materials for next-generation capacitive deionization.
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