Tin-Based Oxide, Alloy, and Selenide Li-Ion Battery Anodes Derived from a Bimetallic Metal-Organic Material

被引:6
作者
Foley, Sarah [1 ,2 ]
Geaney, Hugh [1 ,2 ]
Kennedy, Tadhg [1 ,2 ]
Aminu, Ibrahim [1 ,2 ]
Bree, Gerard [1 ,2 ]
McCarthy, Kieran [1 ,2 ]
Darwish, Shaza [1 ,2 ]
Connolly, Sinead [1 ,2 ]
Mukherjee, Soumya [1 ,2 ]
Lebedev, Vasily [1 ,2 ]
Zaworotko, Michael J. [1 ,2 ]
Ryan, Kevin M. [1 ,2 ]
机构
[1] Univ Limerick, Bernal Inst, Limerick V94 T9PX, Ireland
[2] Univ Limerick, Dept Chem Sci, Limerick V94 T9PX, Ireland
基金
爱尔兰科学基金会;
关键词
HIGH-PERFORMANCE ANODE; LITHIUM-ION; ELECTROCHEMICAL-BEHAVIOR; SOLVOTHERMAL SYNTHESIS; CARBON NANOTUBES; GRAPHENE SHEETS; X-RAY; SNS2; COMPOSITE; NANOSTRUCTURES;
D O I
10.1021/acs.jpcc.0c06395
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Here we report the formation of three distinct Sn-based active materials for Li-ion battery anodes, formed from the same metal-organic material (MOM) precursor sql-1-Cu-SNIFSIX. The materials were obtained under three different anneal conditions in air, Ar, and a Se-rich atmosphere, leading to the selective formation of SnO2/CuO/C (oxide), Cu6Sn5/C (stannide), and Cu2SnSe3/SnSe2/C (selenide) composites. The lithiation and delithiation mechanisms were investigated for each material in the potential range of 0-3 V. Over extended cycling periods, the reversible alloying of Li with Sn was the only process evident for the stannide, with minimal activity occurring at potentials greater than 1 V. In contrast to this, the oxide and selenide composites exhibit both conversion (1-3 V) and Li/Sn alloying (0-1 V) behavior in this potential range; however, the stability of the conversion reaction was found to be poor, inhibiting the capacity retention of both materials. Notably, when the reaction mechanisms were restricted to Li/Sn alloying only by limiting the potential range to 0-1 V, all three composite materials significantly outperformed a Sn nanopowder electrode, illustrating the benefits of utilizing composite electrodes to stabilize the Sn alloying reaction over extended cycling periods.
引用
收藏
页码:1180 / 1189
页数:10
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