Molten salt activation combined with in-situ surface graphitization towards wood-derived self-supporting carbon electrodes with high volumetric specific capacity for zinc-ion hybrid supercapacitors

被引:0
|
作者
Wei, Junjie [1 ]
Wang, Fan [1 ]
Zheng, Xinyue [1 ]
Wang, Yuxin [1 ]
Wang, Jinpeng [1 ]
Liu, Yu [1 ]
Du, Junjie [2 ]
Zheng, Xin [1 ]
Wu, Sai [1 ]
Pang, Yajun [1 ]
Shen, Zhehong [1 ]
Chen, Hao [1 ]
机构
[1] Zhejiang A&F Univ, Natl Engn & Technol Res Ctr Wood Based Resources C, Zhejiang Prov Collaborat Innovat Ctr Bamboo Resour, Coll Chem & Mat Engn,Key Lab Wood Sci & Technol Zh, Hangzhou 311300, Peoples R China
[2] Northwestern Polytech Univ, Key Lab Flexible Elect Zhejiang Prov, Ningbo Inst, 218 Qingyi Rd, Ningbo 315103, Peoples R China
关键词
Wood; Carbon; Self-supporting; Supercapacitor; Electrode; RECENT PROGRESS; GRAPHENE;
D O I
10.1016/j.indcrop.2024.120047
中图分类号
S2 [农业工程];
学科分类号
0828 ;
摘要
Despite significant advancements in enhancing the gravimetric and areal specific capacities of carbon electrodes for zinc-ion hybrid supercapacitors (ZHSCs), the attainment of a high volumetric specific capacity remains a pivotal challenge. This research suggests an innovative method to boost the volumetric specific capacity of carbon electrodes by constructing self-supporting carbon electrodes derived from wood. The process involves a synergistic application of molten salt activation and in-situ surface graphitization. Specifically, pine wood (Pinus sylvestris var. mongolica Litv.) undergoes initial carbonization, followed by treatment with a molten salt electrolyte, generating a carbon material distinguished by a penetrating channel structure, a rich micro-mesoporous network, and distinct characteristics such as self-support and surface graphitization. These qualities contribute to a significant increase in the volumetric specific capacity of the resultant carbon electrode, achieving up to 26.3 mAh cm-3 at 2 mA cm-2, surpassing commercial activated carbon and analogous materials in ZHSC applications. Additionally, a coin-cell ZHSC utilizing this innovative carbon electrode demonstrates exceptional performance, reaching up to 5.6 mAh or 12.6 F per individual ZHSC, equivalent to 12.5 F cm-3 by volume. This performance not only outperforms commercial coin-cell supercapacitors but also aligns closely with the performance metrics of certain commercial coin-cell aqueous batteries. This approach provides a viable solution for augmenting the volumetric specific capacity of carbon electrodes in ZHSCs.
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页数:9
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