材料科学
自行车
表面改性
阴极
化学工程
涂层
对偶(语法数字)
钇
复合材料
纳米技术
兴奋剂
氧化物
光电子学
冶金
历史
考古
文学类
艺术
工程类
物理化学
化学
作者
Yan Huang,Shuang Cao,Xin Xie,Chao Wu,Sidra Jamil,Qinglan Zhao,Baobao Chang,Ying Wang,Xianyou Wang
标识
DOI:10.1021/acsami.0c01558
摘要
A crucial challenge for the commercialization of Ni-rich layered cathodes (LiNi0.88Co0.09Al0.03O2) is capacity decay during the cycling process, which originates from their interfacial instability and structural degradation. Herein, a one-step, dual-modified strategy is put forward to in situ synthesize the yttrium (Y)-doped and yttrium orthophosphate (YPO4)-modified LiNi0.88Co0.09Al0.03O2 cathode material. It is confirmed that the YPO4 coating layer as a good ion conductor can stabilize the solid-electrolyte interface, while the formative strong Y-O bond can bridle TM-O slabs to intensify the lattice structure in the state of deep delithium (>4.3 V). In particular, both the combined advantages effectively withstand the anisotropic strain generated upon the H2-H3 phase transition and further alleviate the crack generation in unit-cell dimensions, assuring a high-capacity delivery and fast Li+ diffusion kinetics. This dual-modified cathode shows advanced cycling stability (94.1% at 1C after 100 cycles in 2.7-4.3 V), even at a high cutoff voltage and high rate, and advanced rate capability (159.7 mAh g-1 at 10C). Therefore, it provides a novel solution to achieve both high capacity and highly stable cyclability in Ni-rich cathode materials.
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