钝化
电解质
碳酸丙烯酯
电化学
材料科学
化学工程
无机化学
碳纤维
碳酸盐
化学
碳酸钠
电极
图层(电子)
钠
纳米技术
有机化学
复合材料
物理化学
工程类
复合数
作者
Mouad Dahbi,Takeshi Nakano,Naoaki Yabuuchi,Shun Fujimura,Kuniko Chihara,Kei Kubota,Jin‐Young Son,Yi‐Tao Cui,Hiroshi Oji,Shinichi Komaba
标识
DOI:10.1002/celc.201600365
摘要
Abstract Electrochemical sodium insertion for hard carbon is examined in a cyclic alkylene carbonate based solution containing a NaClO 4 or NaPF 6 salt with a fluoroethylene carbonate (FEC) additive to study electrolyte dependency for sodium‐ion batteries. NaPF 6 ‐based electrolytes provide superior reversibility and cyclability of sodium insertion into hard carbon compared with NaClO 4 ‐based ones. The FEC‐derived passivation film improves capacity retention because of better passivation with a thinner surface layer, as revealed by hard and soft X‐ray photoelectron spectroscopy (PES). The use of both the NaPF 6 salt and FEC additive results in a synergetic effect on passivation for the hard‐carbon electrode, leading to enhanced cycle performance. Hard‐carbon electrodes with polyvinylidene difluoride binder in propylene carbonate based electrolytes containing NaPF 6 and FEC demonstrate excellent capacity retention with a reversible capacity of about 250 mAh g −1 . The difference in capacity retention for the electrolytes is expected to originate as a consequence of the difference in the surface interphase layer formed on the hard‐carbon electrodes. Surface analyses with PES and time‐of‐flight secondary ion mass spectrometry reveal differences in surface and passivation chemistry which depend on the salts, solvents, and FEC additives used for the hard‐carbon negative electrodes.
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