Phytic acid-induced self-assembled chitosan gel-derived N, P–co-doped porous carbon for high-performance CO2 capture and supercapacitor

超级电容器 杂原子 热解 吸附 化学工程 壳聚糖 材料科学 气凝胶 多孔性 兴奋剂 碳纤维 电容 化学 无机化学 纳米技术 有机化学 电极 复合材料 复合数 工程类 物理化学 光电子学 戒指(化学)
作者
Jianfei Xiao,Yuan Wang,Tian C. Zhang,Like Ouyang,Shaojun Yuan
出处
期刊:Journal of Power Sources [Elsevier]
卷期号:517: 230727-230727 被引量:41
标识
DOI:10.1016/j.jpowsour.2021.230727
摘要

Heteroatom-doped porous carbon materials (HPCMs) have attracted great attention due to their excellent physical and chemical properties and the enhanced performance of multiple heteroatom co-doping. Herein, N, P-co-doped porous carbon materials (NPPCs) are developed via a novel synthesis of the phytic acid-induced self-assembled chitosan aerogel followed by pyrolysis and activation. Phytic acid serves as a P source, acid regulator and structure-directing agent for improved activation efficiency to create more pores. A little of NaNO3 is used both as a template and activator simultaneously. The porosity and N content of such NPPCs are controlled by rationally tuning the pyrolysis temperature and the mount of NaNO3. The NPPC-0.75-600 delivers a good CO2 adsorption capability of 3.02 and 5.31 mmol g−1 at 100 and 500 kPa, respectively, and has an excellent stability with almost no adsorption capacity decay even after successive 20 cycles. For supercapacitors (SCs), the NPPC-0.75-700 also displays a high capacitance of 231.2 F g−1 at 1 A g−1 and an outstanding stability at circa 96.7% initial capacity after 10000 cycles. These results highlight the great potential of such NPPCs in CO2 capture and SCs, and the novel synthetical route offers new insights for the readily scalable production of HPCMs.
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