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Rational design of pyrrolic-N dominated carbon material derived from aminated lignin for Zn-ion supercapacitors

吸附 胺化 碳纤维 木质素 超级电容器 化学 化学工程 石墨烯 阴极 材料科学 有机化学 纳米技术 电化学 复合数 催化作用 物理化学 电极 复合材料 工程类
作者
Jiajia Guo,Syed Comail Abbas,Haitao Huang,Zifeng Hua,Md Manik Mian,Shilin Cao,Xiaojuan Ma,Yonghao Ni
出处
期刊:Journal of Colloid and Interface Science [Elsevier]
卷期号:641: 155-165 被引量:24
标识
DOI:10.1016/j.jcis.2023.03.056
摘要

Developing highly efficient, sustainable carbon cathodes is essential for emerging Zn-ion hybrid supercapacitors (ZICs). Herein, lignin's novel chemical modification (amination) has been developed to produce high quantity pyrrolic-N moieties as active sites. Furthermore, chemically modified amine moieties in lignin are vital as a natural self-activating template to generate hierarchical porosity in the 2D (graphene-like) architecture with exceedingly high surface area (2926.4 m2g−1). The rationally introduced dominated pyrrolic-N moieties boost the Zn-ion storage capacity and reaction kinetics due to the dual energy storage mechanism and efficient charge transfer between pyrrolic-N and Zn+2 ions. Furthermore, the pyrrolic-N species are energetically favorable for the adsorption of Zn+2 ions by the formation of N-Zn+2 chemical bonds. Besides, the nitrogen oxides reduce the intrinsic resistance and induce a more polarized surface, resulting in high wettability and efficient transfer of electrolytes into the pores of hydrophobic carbon materials. Subsequently, the chemically modified lignin-derived activated carbon material (Chem-ACM) as a cathode in ZICs delivers a high capacity of 161.2 mA h g−1 at 1 A g−1 with the admirable energy density of 106.7 W h kg−1 at 897 W kg−1 and excellent retention capacity (94%) after 10,000 cycles. Mainly, the assembled quasi solid-state ZICs using Chem-ACM retains the remarkable storage capacity (202 mA h g−1 at 0.2 Ag−1) even at a high bending angle. Notably, the Chem-ACM has been further employed in symmetric supercapacitors as an electrode, and it displays exceptional specific capacitance of 354 Fg−1 at 0.5 Ag−1 with tremendous energy (43.5 W h kg−1) and the power density (0.53 kW kg−1). Additionally, the charge storage capability of Chem-ACM is positively dependent on high nitrogen contents, and it is extrapolated that pyrrolic-N moieties are dominant active sites. Hence, the designed amination-assisted biocarbon synthesis provides a new way to prepare high nitrogen-containing biocarbon for ZICs and further understand pyrrolic-N species' impact on Zn-ion storage.
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