电容去离子
材料科学
海水淡化
尖晶石
法拉第效率
化学工程
吸附
金属有机骨架
电极
电容
介孔材料
冶金
纳米技术
电化学
膜
化学
物理化学
生物化学
有机化学
工程类
催化作用
作者
Biswajit Mishra,Swayamprakash Biswal,Bijay P. Tripathi
标识
DOI:10.1021/acs.estlett.4c00374
摘要
Water desalination by capacitive deionization techniques has often suffered from the relegating performance of carbon-based non-Faradaic electrode materials. To overcome the rate-limiting charge transfer kinetics and weak ion adsorption tendency, a metal–organic framework (MOF)-derived hybrid electrode with an exceptional flow capacitive deionization performance is reported here. Using MIL-88(FeNi) as a sacrificial template, we synthesized a porous graphitic framework decorated with nanosized spinel NiFe2O4 (NiFe2O4@PC-500) electrodes, maintaining a parent rod-shaped morphology with a large surface area of 1227 m2/g. The synergistic interaction of NiFe2O4 nanoparticles with the mesoporous graphitic framework exhibited remarkable desalination performance with a salt adsorption capacity of ∼34 mg/g and ∼89% salt removal at 1.2 V, surpassing those of traditional carbon-based electrodes. Moreover, NiFe2O4@PC-500 maintained its desalination capacity and structural integrity over prolonged desalination cycles with a specific capacitance of ∼206 F/g and capacitive retention over 500 cycles. This study presents a universal approach for strategically implementing MOF-derived heterostructures as potent flow electrode materials.
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