阴极
材料科学
氧化镍
镍
锂(药物)
氧化物
聚合物
离子
纳米技术
相间
无机化学
复合材料
化学
有机化学
冶金
物理化学
内分泌学
生物
医学
遗传学
作者
Jianyu Li,Chi‐Hao Chang,Arumugam Manthiram
标识
DOI:10.1021/acs.chemmater.9b04102
摘要
Boosting the Ni content in LiMO<sub>2</sub> (M = Ni, Co, Mn, etc.) layered oxides is a promising way to establish high-energydensity, low-cost cathodes, but the poor cathode surface stability is a daunting challenge for their practical viability. Herein, by constructing a dual-functional binder framework with a conductive polymer - polyaniline (PANI), the ultrahigh-Ni layered oxide cathode (LiNi<sub>0.94</sub>Co<sub>0.06</sub>O<sub>2</sub>) exhibits significantly improved cyclability, with a capacity retention greatly increased from 47% to 81% over 1,000 cycles in full cells. It is demonstrated that the acidic species (e.g. HF) in the electrolyte can be efficiently scavenged through a protonation process of PANI, hence the cathode surface reactivity is greatly suppressed and the rock-salt phase propagation into bulk structure is considerably alleviated. Furthermore, the PANI binder system effectively prevents both the cathode-electrolyte interphase (CEI) and anode-electrolyte interphase (AEI) from degrading to a thick “triple-layer” architecture upon extensive cycling, resulting in more robust, thinner CEI and AEI with regulated interphasial chemistry. Moreover, the delocalized π-conjugated electrons along the backbone of PANI facilitate fast electron transfer and promote rate capability even at low temperatures (-20 °C). Finally, this work sheds light on rational binder engineering for developing high-energy-density lithium-ion batteries with acceptable cycle life.
科研通智能强力驱动
Strongly Powered by AbleSci AI