电容去离子
海水淡化
阴极
海水
阳极
电池(电)
电化学
插层(化学)
钠
无机化学
化学工程
化学
材料科学
电极
冶金
膜
地质学
海洋学
物理
工程类
物理化学
功率(物理)
量子力学
生物化学
作者
Moon Son,Jaegyu Shim,Sanghun Park,Nakyung Yoon,Kwanho Jeong,Kyung Hwa Cho
出处
期刊:Desalination
[Elsevier BV]
日期:2022-03-25
卷期号:531: 115713-115713
被引量:10
标识
DOI:10.1016/j.desal.2022.115713
摘要
The seawater battery desalination (SWB-D) system has a unique feature of storing energy while desalinating water. Contrary to other electrochemical processes, such as capacitive de-ionization or battery electrode deionization, SWB-D can be used to directly desalinate seawater owing to the high sodium uptake of the sodium metal composed anode. However, a relatively long time is required for desalination in this newly developed SWB-D because of the sluggish oxygen evolution reaction at the cathode, hindering the practical application of the SWB-D system for desalination. Hence, we propose using a sodium-intercalating cathode (nickel hexacyanoferrate; NiHCF) instead of a capacitive material (carbon felt) in the SWB-D system to overcome this limitation. The redox reaction of NiHCF doubled the applied current from 1 to 2 mA (from 6.5 to 13.0 A m −2 ) under an initial threshold voltage of 4.5 V, resulting in nearly twice the salt removal rate for the hypersaline water treatment (1.2 M NaCl). In addition, the energy efficiency of the system significantly increased from approximately 61% to 86%. Therefore, using an intercalation cathode in the SWB-D system can minimize the time required for hypersaline water treatment with a higher energy efficiency. • Hypersaline water treated by seawater battery desalination • Redox reaction of NiHCF doubled the applied current • NiHCF cathode exhibited nearly twice the salt removal rate. • Significant increase in system energy efficiency from 61% to 86%
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