材料科学
碳化
阳极
锂(药物)
纳米棒
钼
金属有机骨架
碳纤维
纳米技术
电化学
纳米结构
涂层
多孔性
化学工程
电极
复合材料
复合数
吸附
冶金
化学
有机化学
扫描电子显微镜
医学
物理化学
工程类
内分泌学
作者
Wei Tian,Han Hu,Yixian Wang,Peng Li,Jingyan Liu,Jialiang Liu,Xiaobo Wang,Xiangdong Xu,Zhongtao Li,Qingshan Zhao,Hui Ning,Wenting Wu,Mingbo Wu
出处
期刊:ACS Nano
[American Chemical Society]
日期:2018-02-09
卷期号:12 (2): 1990-2000
被引量:231
标识
DOI:10.1021/acsnano.7b09175
摘要
Molybdenum (Mo)-based compounds with properly engineered nanostructures usually possess improved reversible lithium storage capabilities, which offer great promise to boost the performance of lithium-ion batteries (LIBs). Nevertheless, a lack of efficient and high-yield methods for constructing rational nanostructures has largely restricted the application of these potentially important materials. Herein we demonstrate a metal–organic frameworks (MOFs) mediated strategy to successfully synthesize a series of one-dimensional Mo-based/carbon composites with distinct nanostructures. In this process, starting from well-designed MoO3 nanorods, the crystal control growth is first proposed that a layer of MOFs is achieved to be controllably grown on surfaces of MoO3, forming an obvious core–shell structure, and then the adopted precursor can be in situ transformed into MoO2 or Mo2C which are both well confined in conductive porous carbons through direct carbonization at different temperatures, where the MOFs shell serve as both carbon sources and the reactant to react with MoO3 simultaneously. Benefiting from this design, all optimized products exhibit enhanced electrochemical performances when evaluated as anode materials for LIBs, especially the hollow MoO2/C and core–shell Mo2C/C electrodes, show best reversible capacities up to 810 and 530 mAh g–1 even after 600 cycles at a current density of 1 A g–1, respectively. So this work may broaden the application of MOFs as a kind of coating materials and elucidates the attractive lithium storage performances of molybdenum-based compounds.
科研通智能强力驱动
Strongly Powered by AbleSci AI