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具有超高锂存储容量的二氧化锡量子点嵌入碳纳米笼网络

A SnO Quantum Dots Embedded Carbon Nanocage Network with Ultrahigh Li Storage Capacity.

作者信息

Zhang Yanan, Yan Dong, Liu Zefei, Ye Youwen, Cheng Fei, Li Huanrong, Lu An-Hui

机构信息

National-Local Joint Engineering Laboratory for Energy Conservation in Chemical Process Integration and Resources Utilization, Tianjin Key Laboratory of Chemical Process Safety, School of Chemical Engineering and Technology, Hebei University of Technology, Guangrong Road 8, Hongqiao District, Tianjin 300130, P. R. China.

State Key Laboratory of Fine Chemicals, School of Chemical Engineering, Dalian University of Technology, Linggong Road 2, Ganjingzi District, Dalian 116024, P. R. China.

出版信息

ACS Nano. 2021 Apr 27;15(4):7021-7031. doi: 10.1021/acsnano.1c00088. Epub 2021 Apr 14.

Abstract

Tin-based materials with high specific capacity have been studied as high-performance anodes for energy storage devices. Herein, a SnO ( = 0, 1, 2) quantum dots@carbon hybrid is designed and prepared by a binary oxide-induced surface-targeted coating of ZIF-8 followed by pyrolysis approach, in which SnO quantum dots (under 5 nm) are dispersed uniformly throughout the nitrogen-containing carbon nanocage. Each nanocage is cross-linked to form a highly conductive framework. The resulting SnO@C hybrid exhibits a large BET surface area of 598 m g, high electrical conductivity, and excellent ion diffusion rate. When applied to LIBs, the SnO@C reveals an ultrahigh reversible capacity of 1824 mAh g at a current density of 0.2 A g, and superior capacities of 1408 and 850 mAh g even at high rates of 2 and 5 A g, respectively. The full cell assembled using LiFePO as cathode exhibits the high energy density and power density of 335 Wh kg and 575 W kg at 1 C based on the total active mass of cathode and anode. Combined with XRD analysis, the superior electrochemical performance can be attributed to the SnO-ZnO-C asynchronous and united lithium storage mechanism, which is formed by the well-designed multifeatured construction composed of SnO quantum dots, interconnected carbon network, and uniformly dispersed ZnO nanoparticles. Importantly, this designed synthesis can be extended for the fabrication of other electrode materials by simply changing the binary oxide precursor to obtain the desired active component or modulating the type of MOFs coating to achieve high-performance LIBs.

摘要

具有高比容量的锡基材料已被研究用作储能设备的高性能阳极。在此,通过二元氧化物诱导的ZIF-8表面靶向涂层随后热解的方法,设计并制备了一种SnO ( = 0, 1, 2)量子点@碳杂化物,其中SnO量子点(小于5纳米)均匀分散在含氮碳纳米笼中。每个纳米笼相互交联形成一个高导电框架。所得的SnO@C杂化物具有598 m g的大比表面积、高电导率和优异的离子扩散速率。当应用于锂离子电池时,SnO@C在0.2 A g的电流密度下显示出1824 mAh g的超高可逆容量,即使在2 A g和5 A g的高倍率下,分别具有1408和850 mAh g的优异容量。使用LiFePO作为阴极组装的全电池基于阴极和阳极的总活性质量,在1 C时表现出335 Wh kg和575 W kg的高能量密度和功率密度。结合XRD分析,优异的电化学性能可归因于由精心设计的由SnO量子点、相互连接的碳网络和均匀分散的ZnO纳米颗粒组成的多特征结构形成的SnO-ZnO-C异步联合锂存储机制。重要的是,这种设计合成可以通过简单地改变二元氧化物前驱体以获得所需的活性成分或调节MOFs涂层的类型来扩展用于制造其他电极材料,以实现高性能锂离子电池。

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