磷化物
锗
阳极
材料科学
电化学
插层(化学)
钠
电极
无机化学
光电子学
化学
冶金
硅
金属
物理化学
作者
Hailin Shen,Zhongtao Ma,Bingchao Yang,Bingkun Guo,Yingchun Lyu,Peng Wang,Hangsheng Yang,Qianqian Li,Hongtao Wang,Zhongyuan Liu,Anmin Nie
标识
DOI:10.1016/j.jpowsour.2019.05.088
摘要
Layered germanium phosphide, which combines the advantages of both germanium and phosphorus, is believed to be a potential anode for sodium ion battery. Here, the sodium storage mechanism and electrochemical performance of layered germanium phosphide have been deeply investigated by advanced in-situ transmission electron microscopy technique combining half-cell testing. Dynamic reaction process reveals that individual layered germanium phosphide nanoflake undergoes total area expansion of 248% without any detectable fracture or cracking in sodiation. In contrast, germanium phosphide experiences multi-step reactions, i.e. intercalation and alloying, accompanied by sequentially forming NaxGeP (0 < x < 1/3), layered NaGe3P3, and amorphous NaGe and NayP (0 < y ≤ 3). Moreover, the germanium phosphide electrode delivers a high first discharge/charge capacity of 1124/996 mA h g−1 within voltage window of 0.005–2.5 V. By narrowing voltage window in 0.15–1.5 V, the electrode displays good cycle stability with the capacity retention of 330 mA h g−1 after 100 cycles. Our study provides useful fundamental understanding and practical strategy for the application of germanium phosphide as anode in sodium ion batteries.
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