阳极
材料科学
阴极
电容器
储能
功率密度
氧化还原
化学工程
纳米技术
电压
电极
化学
电气工程
功率(物理)
冶金
热力学
物理化学
工程类
物理
作者
Tae-Hyeong Kim,Sanghui Kang,Sanghyeon Park,Chan‐Woo Lee,Iyan Subiyanto,Bumjin Kim,Jeonghun Baek,Heon‐Jin Choi,Hyunuk Kim,Jungjoon Yoo
标识
DOI:10.1016/j.jpowsour.2024.234449
摘要
Developing of high-energy, high-power-density energy storage devices is challenging. Despite being promising electrode materials for these devices, metal–organic frameworks (MOFs) have poor electrical conductivity and weak ligand–metal coordination. Here, the highly conductive MOF, Ni3(HITP)2, which comprises radially oriented microspheres, is adopted as the anode for Li-ion capacitors (LICs). The half-cell demonstrates high reversible capacity (834 mAh g−1) at 50 mA g−1 with minimal capacity reduction, attributable to the participation of C and N functional groups of the ligand and Ni2+ in the redox reactions during charge/discharge. Especially, density functional theory calculations show that, apart from the inner rings, participation of the outer rings of Ni3(HITP)2 in the redox reactions is responsible for the high Li + storage capacity. An LIC with a Ni3(HITP)2 anode and commercial activated-carbon cathode demonstrates high specific energy (120.7 Wh kg−1) at 89.2 W kg−1, nearly twice as high as that of graphite-based LICs, and maintains specific energy of 25.8 Wh kg−1 even at high specific power (7.16 kW kg−1), over the range 1–4.4 V, along with high cycling stability (76% capacity retention over 10000 cycles). The proposed radially oriented Ni3(HITP)2 microspheres have potential for application as the anode in high-performance energy storage devices.
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