材料科学
电极
曲折
石墨烯
离子
传质
纳米技术
锂(药物)
光电子学
复合材料
化学工程
热力学
物理
工程类
内分泌学
医学
物理化学
量子力学
化学
多孔性
作者
Zedong Zhao,Minqiang Sun,Wuji Chen,Yao Liu,Long Zhang,Nanchen Dongfang,Yingbo Ruan,Jiajia Zhang,Peng Wang,Lei Dong,Yongyao Xia,Hongbin Lu
标识
DOI:10.1002/adfm.201809196
摘要
Abstract 3D thick electrode design is a promising strategy to increase the energy density of lithium‐ion batteries but faces challenges such as poor rate and limited cycle life. Herein, a coassembly method is employed to construct low‐tortuosity, mechanically robust 3D thick electrodes. LiFe 0.7 Mn 0.3 PO 4 nanoplates (LFMP NPs) and graphene are aligned along the growth direction of ice crystals during freezing and assembled into sandwich frameworks with vertical channels, which prompts fast ion transfer within the entire electrode and reveals a 2.5‐fold increase in ion transfer performance as opposed to that of random structured electrodes. In the sandwich framework, LFMP NPs are entrapped in the graphene wall in a “plate‐on‐sheet” contact mode, which avoids the detachment of NPs during cycling and also constitutes electron transfer highways for the thick electrode. Such vertical‐channel sandwich electrodes with mass loading of 21.2 mg cm −2 exhibit a superior rate capability (0.2C–20C) and ultralong cycle life (1000 cycles). Even under an ultrahigh mass loading of 72 mg cm −2 , the electrode still delivers an areal capacity up to 9.4 mAh cm −2 , ≈2.4 times higher than that of conventional electrodes. This study provides a novel strategy for designing thick electrodes toward high performance batteries.
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