Magnesium/Lithium Hybrid Batteries Based on SnS2-MoS2 with Reversible Conversion Reactions

被引:13
作者
Fan, Xin [1 ,2 ]
Tebyetekerwa, Mike [1 ,3 ]
Wu, Yilan [1 ]
Gaddam, Rohit Ranganathan [4 ]
Zhao, Xiu Song [1 ]
机构
[1] Univ Queensland, Sch Chem Engn, Brisbane, Qld 4072, Australia
[2] North Univ China, Sch Mat Sci & Technol, Taiyuan 030051, Shanxi, Peoples R China
[3] Univ Queensland, Dow Ctr Sustainable Engn Innovat, Sch Chem Engn, Brisbane, Qld 4072, Australia
[4] Indian Inst Sci Educ & Res, Dept Chem Engn, Bhopal, India
来源
ENERGY MATERIAL ADVANCES | 2022年 / 2022卷
基金
澳大利亚研究理事会;
关键词
MG2+/LI+; CATHODES; SULFUR; INTERCALATION; GRAPHENE; NANOCOMPOSITES; COMPOSITES; NANOFLAKES; NANOSHEETS; CHEMISTRY;
D O I
10.34133/2022/9846797
中图分类号
O59 [应用物理学];
学科分类号
摘要
The magnesium/lithium hybrid batteries (MLHBs) featuring dendrite-less deposition with Mg anode and Li-storage cathode are a promising alternative to Li-ion batteries for large-scale energy storage. However, their limited energy density limits their practical implementation. To improve this, beyond the commonly proposed intercalation compounds, high-capacity conversion-type cathodes based on heterostructures of tin sulphide-molybdenum disulphide (SnS2-MoS2) are proposed in this work. Individual SnS2 is already a promising high-capacity electrode material for multivalent batteries and undergoes conversion reactions during the ion storage process. The introduction of S-deficient MoS2 enhances the reversibility of SnS2 in the conversion reaction via strong polysulfide anchoring and catalytic effect. Our results show that the SnS2-MoS2 electrode achieves a high charge capacity of similar to 600 mAhg(-1) at 50mAg(-1) and an excellent rate capability of 240mAhg(-1) at 1000mAhg(-1) with a negligible capacity fading rate of 0.063% per cycle across 1000 cycles. The results highlight a new direction toward designing 2D heterostructures as high-capacity cathodes beyond intercalation-type cathodes for multivalent-ion batteries.
引用
收藏
页数:14
相关论文
共 68 条
[1]  
Acerce M, 2015, NAT NANOTECHNOL, V10, P313, DOI [10.1038/NNANO.2015.40, 10.1038/nnano.2015.40]
[2]   Deterministic Two-Dimensional Polymorphism Growth of Hexagonal n-Type SnS2 and Orthorhombic p-Type SnS Crystals [J].
Ahn, Ji-Hoon ;
Lee, Myoung-Jae ;
Heo, Hoseok ;
Sung, Ji Ho ;
Kim, Kyungwook ;
Hwang, Hyein ;
Jo, Moon-Ho .
NANO LETTERS, 2015, 15 (06) :3703-3708
[3]  
[Anonymous], 2020, NRELTP540078461, P1
[4]   Prototype systems for rechargeable magnesium batteries [J].
Aurbach, D ;
Lu, Z ;
Schechter, A ;
Gofer, Y ;
Gizbar, H ;
Turgeman, R ;
Cohen, Y ;
Moshkovich, M ;
Levi, E .
NATURE, 2000, 407 (6805) :724-727
[5]   A Trip to Oz and a Peak Behind the Curtain of Magnesium Batteries [J].
Bonnick, Patrick ;
Muldoon, John .
ADVANCED FUNCTIONAL MATERIALS, 2020, 30 (21)
[6]   Two-Dimensional Titanium Carbide MXene As a Cathode Material for Hybrid Magnesium/Lithium-Ion Batteries [J].
Byeon, Ayeong ;
Zhao, Meng-Qiang ;
Ren, Chang E. ;
Halim, Joseph ;
Kota, Sankalp ;
Urbankowski, Patrick ;
Anasori, Babak ;
Barsoum, Michel W. ;
Gogotsi, Yury .
ACS APPLIED MATERIALS & INTERFACES, 2017, 9 (05) :4296-4300
[7]   Ultrathin MoS2/Nitrogen-Doped Graphene Nanosheets with Highly Reversible Lithium Storage [J].
Chang, Kun ;
Geng, Dongsheng ;
Li, Xifei ;
Yang, Jinli ;
Tang, Yongji ;
Cai, Mei ;
Li, Ruying ;
Sun, Xueliang .
ADVANCED ENERGY MATERIALS, 2013, 3 (07) :839-844
[8]   High performance hybrid Mg-Li ion batteries with conversion cathodes for low cost energy storage [J].
Chen, Xinzhi ;
Wang, Suqing ;
Wang, Haihui .
ELECTROCHIMICA ACTA, 2018, 265 :175-183
[9]   Interface Promoted Reversible Mg Insertion in Nanostructured Tin-Antimony Alloys [J].
Cheng, Yingwen ;
Shao, Yuyan ;
Parent, Lucas R. ;
Sushko, Maria L. ;
Li, Guosheng ;
Sushko, Peter V. ;
Browning, Nigel D. ;
Wang, Chongmin ;
Liu, Jun .
ADVANCED MATERIALS, 2015, 27 (42) :6598-+
[10]   High performance batteries based on hybrid magnesium and lithium chemistry [J].
Cheng, Yingwen ;
Shao, Yuyan ;
Ji-Guang Zhang ;
Sprenkle, Vincent L. ;
Liu, Jun ;
Li, Guosheng .
CHEMICAL COMMUNICATIONS, 2014, 50 (68) :9644-9646