石墨烯
超级电容器
水溶液
氧化物
纳米金刚石
共价键
材料科学
化学工程
纳米技术
化学
有机化学
电化学
电极
复合材料
物理化学
冶金
工程类
钻石
作者
Zhenjie Lu,Lianjin Wei,Xiangjie Guo,Wenhao Ding,Tianning Xie,Ying Zhang,Shugang Pan,Lixin Xie,Xin Wang,Junwu Zhu,Yongsheng Fu
标识
DOI:10.1021/acs.iecr.5c01153
摘要
Conventional aqueous symmetric carbon-based supercapacitors face intrinsic voltage limitations (typically ≤ 1.0 V), fundamentally constraining their energy density potential. In this work, oxygen-functionalized detonation nanodiamonds (ONDs) and graphene oxide (GO) are self-assembled into three-dimensional (3D) rGO-OND ultraelastic aerogels through sp3–sp2 carbon hybridization. This hierarchical 3D architecture establishes dual-conductive pathways for electrons and phonons while maintaining exceptional mechanical resilience. The optimized rGO-10%OND composite demonstrates groundbreaking electrochemical performance in symmetric supercapacitor configurations. The optimized rGO-10%OND, as electrode materials in the aqueous symmetric supercapacitor device, can stably operate for charging and discharging within an unprecedented voltage window of 0–2.0 V, surpassing conventional limits by 100%. Meanwhile, the Coulombic efficiency and capacitance retention are both close to 100% after 10000 cycles. It achieved an energy density of 23.1 Wh kg–1 at a power density of 1000 W kg–1. In situ scanning electrochemical microscopy (SECM) and in situ Raman spectroscopy demonstrate that the excellent electrochemical performance is mainly attributed to exceptional redox reactivity, accelerated ion diffusion kinetics, and remarkable structural integrity of rGO-10%OND.
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