电化学
氧化还原
储能
材料科学
离域电子
氢气储存
法拉第效率
电极
电容感应
电化学储能
电化学能量转换
化学工程
纳米技术
超级电容器
氢
光化学
化学
功率(物理)
有机化学
电气工程
物理
工程类
物理化学
冶金
量子力学
作者
Tianyang Chen,Harish Banda,Luming Yang,Jian Li,Yugang Zhang,Riccardo Parenti,Mircea Dincă
标识
DOI:10.26434/chemrxiv-2022-brq5c
摘要
Designing materials for electrochemical energy storage with short charging times and high charge capacities is a longstanding challenge. The fundamental difficulty lies in installing a high density of redox couples into a stable material that can efficiently conduct both ions and electrons. Here, we report all-organic, fused aromatic materials that store up to 310 mAh g–1 and charge in as little as 33 seconds. This performance stems from abundant quinone/imine functionalities that act as redox-active sites, engage in hydrogen bonding for outstanding stability upon cycling, and enable bulk electronic delocalization for high-rate energy storage. The hydrogen bonding-assisted bulk charge storage here contrasts with the surface-confined or hydration-dependent behavior of traditional inorganic electrodes. These materials outperform state-of-the-art faradaic and capacitive electrodes in both capacity and power capability.
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