Bidirectional activation technology towards foam-like carbon nanosheets and its coupling with oxygen-deficient α‐MnO2 for ammonium-ion hybrid supercapacitors

超级电容器 联轴节(管道) 氧气 材料科学 碳纳米泡沫 离子 碳纤维 化学工程 纳米技术 化学 电极 电化学 复合材料 多孔性 复合数 有机化学 工程类 物理化学
作者
Dewei Wang,Zhaorui Sun,Xinliang Han
出处
期刊:Journal of The Taiwan Institute of Chemical Engineers [Elsevier BV]
卷期号:145: 104845-104845 被引量:12
标识
DOI:10.1016/j.jtice.2023.104845
摘要

Aqueous non-metallic ammonium ions (NH4+) have newly been developed as a promising charge carrier for electrochemical energy storage owing to their high safety, abundance, and tiny hydrated ionic size. Producing reliable electrode materials with excellent electrochemical performance, however, remains a significant issue. we proposed a bidirectional chemical activation strategy, which effective coupling “in to out” and “out to in” etching manner, to synthesize foam-like porous carbon nanosheets (FCNSs) with the surface area much larger than that samples obtained from the unidirectional mode. Meanwhile, oxygen-deficient α‐MnO2 nanorods can be rationally obtained through mild redox reaction, both of which display excellent capacitive performance in dilute (NH4)2SO4 electrolyte (0.5 M). the as-synthesized FCNSs and oxygen-deficient α‐MnO2 nanorods can deliver a specific capacitance of 257.5 F g−1 and 525.1 F g−1, respectively, demonstrating their huge potential to assemble ammonium-ion hybrid supercapacitor (A-HSC). Benefitting from the feasible electrochemical performance for both anode and cathode, the resulting A-HSC displays a specific capacitance of 180.8 F g−1 (calculated based on both anode and cathode) within 0–1.6 V, and a low self-discharge rate, which outperforms the state-of-the-art A-HSC devices. Importantly, the energy storage mechanism has been elucidated from several ex-situ characterizations.
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