材料科学
阳极
电极
二硫化钼
储能
阴极
金红石
电化学
电解质
化学工程
异质结
纳米技术
锐钛矿
多孔性
光电子学
复合材料
光催化
催化作用
功率(物理)
电气工程
化学
物理
生物化学
物理化学
量子力学
工程类
作者
Hongwei Zhang,Jianjun Song,Jiayi Li,Junan Feng,Yanyan Ma,Linlin Ma,Hao Liu,Yuanbin Qin,Xiaoxian Zhao,Fengyun Wang
标识
DOI:10.1021/acsami.2c02080
摘要
As a promising energy-storage and conversion anode material for high-power sodium-ion batteries operated at room temperature, the practical application of layered molybdenum disulfide (MoS2) is hindered by volumetric expansion during cycling. To address this issue, a rational design of MoS2 with enlarged lattice spacing aligned vertically on hierarchically porous Ti3C2Tx MXene nanosheets with partially oxidized rutile and anatase dual-phased TiO2 (MoS2@MXene@D-TiO2) composites via one-step hydrothermal method without following anneal process is reported. This unique "plane-to-surface" structure accomplishes hindering MoS2 from aggregating and restacking, enabling sufficient electrode/electrolyte interaction simultaneously. Meanwhile, the heterogeneous structure among dual-phased TiO2, MoS2, and MXene could constitute a built-in electric field, promoting high Na+ transportation. As a result, the as-constructed 3D MoS2@MXene@D-TiO2 heterostructure delivers admirable high-rate reversible capacity (359.6 mAh g-1 up to 5 A g-1) at room temperature, excellent cycling stability (about 200 mAh g-1) at a low temperature of -30 °C, and superior electrochemical performance in Na+ full batteries by coupling with a Na3V2(PO4)3 cathode. This ingenious design is clean and facile to inspire the potential of advanced low-dimensional heterogeneous structure electrode materials in the application of high-performance sodium-ion batteries.
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