锐钛矿
阴极
化学工程
锂(药物)
材料科学
金属
相(物质)
储能
吸附
金红石
纳米技术
无机化学
化学
催化作用
冶金
有机化学
量子力学
物理
光催化
医学
功率(物理)
物理化学
内分泌学
工程类
作者
Kaiquan He,Hong Tan,Shizhen Li,Pu Hu,Chaoqun Shang
标识
DOI:10.1016/j.jallcom.2023.173169
摘要
The Li-S batteries possessing high theoretical energy density are promising for next-generation energy storage. However, the shuttle effect and slow conversion of lithium polysulfides seriously hinder the practical application. In this contribution, introducing metallic Cu to modify dual-phase TiO2 (rutile/anatase) grown on N-doped carbon nanosheets (denoted as Cu/mTiO2-NC) can act as a buffer layer to confine the active S species in the cathode region effectively. The corresponding systematic experiments show that the Cu/mTiO2-NC provides sufficient surface affinity to adsorb and capture polysulfides and has a highly conductive C/N skeleton to achieve rapid electron migration. Moreover, the metallic Cu can react with polysulfides to further immobilize polysulfides. Thus, the Li-S batteries, with the aid of optimal Cu/mTiO2-NC, exhibit a desirable discharge capacity of 811 mAh g–1 after 100 cycles at 0.2 C, which is 50% higher than that without Cu/mTiO2-NC. Moreover, the optimum Li-S batteries deliver a discharge capacity of 435.45 mAh g–1 after 600 cycles at 0.5 C, corresponding to attenuation per cycle of only 0.09%.
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