电场
异质结
材料科学
纳米纤维
动力学
兴奋剂
多孔性
催化作用
转化(遗传学)
碳纳米纤维
化学工程
纳米技术
光电子学
复合材料
化学
碳纳米管
物理
有机化学
工程类
生物化学
量子力学
基因
作者
Hao Wang,Nanping Deng,Yayi Lu,Yongbing Jin,Geng Li,Bowen Cheng,Weimin Kang
标识
DOI:10.1016/j.apcatb.2024.124289
摘要
In this study, the CoP-Co2P heterojunction nanoparticles embedded in N-doping porous carbon nanofibers (CoP-Co2P/NPCNFs) are designed and prepared. The highly conductive grid of NPCNFs can physically confining lithium polysulfide (LiPS) and provide facilitated channels for Li+ transport. Furthermore, due to the spontaneous built-in electric field (BIEF) based on at the formed heterogeneous interfaces of CoP-Co2P, the heterojunction can significantly catalyze bi-directional conversion of LiPS and chemically adsorb LiPS which confirmed by the DFT calculations, suppressing the "shuttle effect" of LiPS. Thus, the Li-S batteries with the CoP-Co2P/NPCNFs modified separators exhibit a high initial specific capacity of 1322.86 mAh g−1 at 1 mA cm−2 and stable 695 cycles with a low decay rate (0.069 %). More importantly, the assembled pouch cell also can run with ultra-low specific capacity decay rate. Additionally, the pouch battery can also be applied to the operation of fans, temperature and humidity meters, mobile phone charging, etc.
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