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Spindle-like FeySs/N-doped carbon nanohybrids for high-performance sodium ion battery anodes

作     者:Aihua Jin Mi-Ju Kim Kug-Seung Lee Seung-Ho Yu Yung-Eun Sung 

作者机构:Center for Nanoparticle Research Institute for Basic Science (IBS) Seoul 08826 Republic of Korea School cf Chemical and Biological Engineering Seoul National University Seoul 08826 Republic cf Korea Beamline Department Pohang Accelerator Laboratory (PAL) Pohang 790-784 Republic of Korea Department of Chemistry and Chemical Biology Cornell University Ithaca New York 14853 USA 

出 版 物:《Nano Research》 (纳米研究(英文版))

年 卷 期:2019年第12卷第3期

页      面:695-700页

核心收录:

学科分类:07[理学] 0702[理学-物理学] 

主  题:sodium ion batteries iron sulfides metal organic frameworks X-ray absorption spectroscopy X-ray photoelectron spectroscopy 

摘      要:Iron sulfides have bee n con sidered as one of the most promising can didates for sodium ion battery anode materials due to their high theoretical capacity and low cost. I n this work, spin dle-like Fe7S8 with n itroge rvdoped carb on (FeiS/N-C) nano hybrids are successfully syn thesized via a solvothermal method by sulfidation iron-based metal organic framework (FeMOF). As sodium ion battery an odes, FeySs/N-C nano hybrids exhibit high reversible capacity of 450.8 mAh g-1 at 200 mA·g^-1, and 406.7 mAh·g^-1 at 500 mA·g^-1 even after 500 cycles. They also show excellent rate properties and delivering the capacity of 327.8 mAh·g^-1 at a very high current density of 3.2 A·g^-1. These outstanding electrochemical performa nces can be attributed to the unique structure of Fe7S8/ N-C nan ohybrids. The nano scale dime nsion in their size can be ben eficial for facile ion and electro n tran sports. Furthermore, the stable n itroge n doped carb on frameworks can also improve electrical conductivity and relieve the problems related to volume expansion. X-ray absorption spectroscopy and X-ray photoelectron spectroscopy analyses have been performed to study reactions occurred in spindle-like FeySs/N-C nanohybrid electrode at both bulk and surface.

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