Lifen Xiao; Haiyan Lu; Yongjin Fang; Maria L. Sushko; Yuliang Cao; Xinping Ai; Hanxi Yang; Jun Liu
文献索引:10.1002/aenm.201703238
全文:HTML全文
Hard carbon is regarded as the most promising anode material for commercialization of Na ion batteries because of its high capacity and low cost. At present, the practical utilization of hard carbon anodes is largely limited by the low initial Coulombic efficiency (ICE). Na ions have been found to adopt an adsorption–insertion storage mechanism. In this paper a systematic way to control the defect concentration and porosity of hard carbon with similar overall architectures is shown. This study elucidates that the defects in the graphite layers are directly related to the ICE as they would trap Na ions and create a repulsive electric field for other Na ions so as to shorten the low‐voltage intercalation capacity. The obtained low defect and porosity hard carbon electrode has achieved the highest ICE of 86.1% (94.5% for pure hard carbon material by subtracting that of the conductive carbon black), reversible capacity of 361 mA h g−1, and excellent cycle stability (93.4% of capacity retention over 100 cycles). This result sheds light on feasible design principles for high performance Na storage hard carbon: suitable carbon layer distance and defect free graphitic layers.
Eco‐Friendly Higher Manganese Silicide Thermoelectric Materi...
2018-04-06 [10.1002/aenm.201800056] |
Carrier Transport and Recombination in Efficient “All‐Small‐...
2018-04-03 [10.1002/aenm.201800264] |
High Voltage Operation of Ni‐Rich NMC Cathodes Enabled by St...
2018-03-30 [10.1002/aenm.201800297] |
Lewis Acid Doping Induced Synergistic Effects on Electronic ...
2018-03-29 [10.1002/aenm.201703672] |
Electrochemical CO2 Reduction with Atomic Iron‐Dispersed on ...
2018-03-25 [10.1002/aenm.201703487] |
首页 |
期刊大全 |
MSDS查询 |
化工产品分类 |
生物活性化合物 |
关于我们 |
免责声明:知识产权问题请联系 service1@chemsrc.com
Copyright © 2024 ChemSrc All Rights Reserved