材料科学
吸附
热解
化学工程
电解质
电容
碳纤维
电流密度
水溶液
氮气
纳米技术
兴奋剂
多孔性
比表面积
电极
光电子学
复合材料
有机化学
复合数
催化作用
物理化学
化学
物理
工程类
量子力学
作者
Yuan Wang,Jianfei Xiao,Hanzhi Wang,Tian C. Zhang,Shaojun Yuan
标识
DOI:10.1016/j.jmst.2021.05.035
摘要
Abstract Designing of hetero-atomic doped carbon-based systems through pyrolysis of abundant element organic precursors is a novel approach to construct rational porous carbon materials. Herein, a highly-cross-linked triazine polymer is employed to fabricate N, P co-doped porous carbon (A-TDP-12) with tunable active nitrogen in the carbon framework for simultaneous enhancement of CO2 capture capability and Supercapacitance (SC). The synthesized A-TDP-12 possesses a typical hierarchically porous framework (micro-pores and meso-pores) with a large surface area (1332 m2 g−1) and a rich content of N (7.89 atomic %) and P (0.74 atomic %). It delivers a CO2 adsorption capacity of 1.52 and 5.68 mmol g−1 at 1 and 5 bar, respectively, with almost no decay after successive 8 recycles. In 6 M KOH aqueous electrolyte, A-TDP-12 exhibits a superior specific capacitance of 172.7 F g−1 at a current density of 1 A g−1. Even at a high current density of 10 A g−1, 80% of its initial capacity still remains. This work not only offers a novel strategy for fabricating promising adsorbents and electrodes for CO2 uptake and SCs, but also provides new insights into design of porous carbon material for related applications.
科研通智能强力驱动
Strongly Powered by AbleSci AI