| Literature DB >> 33905227 |
Wenhui Shi1, Xin Qian1, Meiting Xue1, Wenbin Que2, Xinlong Gao2, Dong Zheng2, Wenxian Liu2, Fangfang Wu2, Jiangnan Shen1, Xiehong Cao2, Congjie Gao1.
Abstract
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.Entities:
Keywords: bismuth; capacitive deionization; chloride storage electrode; faradaic electrode; water desalination
Year: 2021 PMID: 33905227 DOI: 10.1021/acsami.1c00089
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229