Gang Haiyin, Deng Haoyu, Yan Lvji, Wu Bichao, Alhassan Sikpaam Issaka, Cao Yiyun, Wei Dun, Wang Haiying
School of Metallurgy and Environment, Central South University, Changsha 410083, China.
College of Engineering, Chemical and Environmental Engineering Department, University of Arizona, Tucson, USA.
J Colloid Interface Sci. 2023 May 15;638:252-262. doi: 10.1016/j.jcis.2023.01.093. Epub 2023 Jan 24.
The practical application of carbon anode in capacitive deionization (CDI) is greatly hindered by their poor adsorption capacity and co-ion effect. Herein, an N-doped graphene-like carbon (NC) decorated with Fe/FeC nanoparticles composite (Fe/FeC@NC) with large specific surface area and plentiful porosity is fabricated via a facile and scalable method, namely sol-gel method combined with Fe-catalyzed carbonization. As expected, it exhibits superior CDI performance as a Cl-storage electrode, with Cl adsorption capacity as high as 102.3 mg g at 1000 mg L Cl concentration and 1.4 V voltage, and a stable capacity of 68.5 mg g for 60 cycles in 500 mg L Cl concentration and 100 mA g current density. More importantly, on the basis of electrochemical tests, ex-situ X-ray diffraction, ex-situ X-ray photoelectron spectroscopy (XPS), and XPS analysis with argon ion depth etching, it is revealed that the chlorine storage mechanism of the Fe/FeC@NC electrode is dominated by the surface-related redox pseudocapacitance behavior of Fe/Fe couple occurring on or near the surface, enabling fast and reversible ion storage. This work proposes an economical and environmentally friendly general method for the design and development of high-performance Cl-storage electrodes for CDI, and offers an in-depth insight into the Cl storage mechanism of Fe decorated carbon electrodes, further promoting the development of CDI technology.
碳阳极在电容去离子化(CDI)中的实际应用因其较差的吸附容量和共离子效应而受到极大阻碍。在此,通过一种简便且可扩展的方法,即溶胶 - 凝胶法与铁催化碳化相结合,制备了一种具有大比表面积和丰富孔隙率的、由Fe/FeC纳米颗粒复合修饰的N掺杂类石墨烯碳(NC)(Fe/FeC@NC)。正如预期的那样,作为一种氯存储电极,它表现出优异的CDI性能,在1000 mg L Cl浓度和1.4 V电压下,氯吸附容量高达102.3 mg g,在500 mg L Cl浓度和100 mA g电流密度下,60个循环的稳定容量为68.5 mg g。更重要的是,基于电化学测试、非原位X射线衍射、非原位X射线光电子能谱(XPS)以及氩离子深度蚀刻的XPS分析,揭示了Fe/FeC@NC电极的氯存储机制主要由在表面或表面附近发生的Fe/Fe偶极的表面相关氧化还原赝电容行为主导,从而实现快速且可逆的离子存储。这项工作提出了一种经济且环保的通用方法,用于设计和开发用于CDI的高性能氯存储电极,并深入洞察了铁修饰碳电极的氯存储机制,进一步推动了CDI技术的发展。