纳米笼
材料科学
法拉第效率
阴极
层状双氢氧化物
电流密度
电极
电化学
电导率
化学工程
光电子学
锂(药物)
纳米技术
异质结
氢氧化物
催化作用
工程类
物理
医学
内分泌学
物理化学
化学
量子力学
生物化学
作者
Shixia Chen,Junhui Luo,Nuoyan Li,Xinxin Han,Jun Wang,Qiang Deng,Zheling Zeng,Shuguang Deng
标识
DOI:10.1016/j.ensm.2020.05.002
摘要
Layered double hydroxides (LDHs) are promising lithium polysulfides (LiPSs) mediators, but the implementation of LDHs-based cathodes as high-performance lithium-sulfur batteries (LSBs) is hindered by their poor electrical conductivity and limited active sites. Herein, we report a hollow NiCo-LDH/Co9S8 (H-LDH/Co9S8) heterostructure with ordered nanocage morphology by in situ transformations of ZIF-67. The H-LDH/Co9S8 heterostructure could physically inhibit the LiPSs diffusion and accommodate sufficient sulfur. The abundant exposed O- and Co-adsorption sites could firmly entrap LiPSs and electrocatalytically boosted their conversion kinetics. Moreover, the intimated interfaces of NiCo-LDH and Co9S8 domains endow a significantly improved electron conductivity and Li+ ion diffusivity. As a result, H-LDH/Co9S8 delivers a high discharge capacity of 1339.1 mAh g−1 at the current density of 0.1C and shows an ultrastable lifespan over 1500 cycles with a small capacity decay of 0.047% per cycle and stable coulombic efficiency above 98% at the current density of 1.0C. This work paves a new way to fabricate and utilize LDH materials as high-performance LSB cathodes and provides new insights into the multifunctional heterostructure as ultralong life span electrodes.
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