School of Chemical Engineering, North China University of Science and Technology, Tangshan 063009, China.
Ministry of Education Key Laboratory of Testing Technology for Manufacturing Process, Southwest University of Science and Technology, Mianyang 621010, China.
J Colloid Interface Sci. 2020 Jul 15;572:216-226. doi: 10.1016/j.jcis.2020.03.069. Epub 2020 Mar 25.
In this paper, we reported a one-step activation strategy to prepare highly graphitized N-doped porous carbon materials (KDC-FAC) derived from biomass, and adopted ferric ammonium citrate (FAC) as active agent. At high temperature, FAC was decomposed into Fe- and NH-based materials, further increasing graphitization degree, introducing N-containing functional groups and forming porous structure. KDC-FAC has superior electrocatalytic activity and stability towards V/V and VO/VO redox reactions. High graphitization degree can enhance the conductivity of carbon material, and porous structure is conducive to increase reaction area of vanadium redox couples. Moreover, N-containing functional groups are beneficial to improve the electrode wettability and serve as active sites. The single cell tests demonstrate that KDC-FAC modified cell exhibits good adaptability under high current density and superb stability in cycling test. Compared with pristine cell, the energy efficiency of KDC-FAC modified cell is increased by 9% at 150 mA cm. This biomass-derived carbon-based material proposed in our work is expected to be an excellent catalyst for vanadium redox flow battery.
在本文中,我们报道了一种一步激活策略,用于制备源自生物质的高石墨化 N 掺杂多孔碳材料 (KDC-FAC),并采用柠檬酸铁铵 (FAC) 作为活性剂。在高温下,FAC 分解为 Fe 和 NH 基材料,进一步提高石墨化程度,引入含 N 官能团并形成多孔结构。KDC-FAC 对 V/V 和 VO/VO 氧化还原反应具有优异的电催化活性和稳定性。高石墨化程度可以提高碳材料的导电性,而多孔结构有利于增加钒氧化还原对的反应面积。此外,含 N 官能团有利于提高电极润湿性并作为活性位点。单电池测试表明,KDC-FAC 改性电池在高电流密度下具有良好的适应性和循环测试中的出色稳定性。与原始电池相比,KDC-FAC 改性电池的能量效率在 150 mA cm 时提高了 9%。本工作中提出的这种源自生物质的碳基材料有望成为钒氧化还原流电池的优秀催化剂。