Carbon-coated MoS 1.5 Te 0.5 nanocables for efficient sodium-ion storage in non-aqueous dual-ion batteries.
Yangjie LiuXiang HuJunwei LiGuobao ZhongJun YuanHongbing ZhanYongbing TangZhenhai WenPublished in: Nature communications (2022)
Sodium-based dual-ion batteries have received increased attention owing to their appealing cell voltage (i.e., >3 V) and cost-effective features. However, the development of high-performance anode materials is one of the key elements for exploiting this electrochemical energy storage system at practical levels. Here, we report a source-template synthetic strategy for fabricating a variety of nanowire-in-nanotube MS x Te y @C (M = Mo, W, Re) structures with an in situ-grown carbon film coating, termed as nanocables. Among the various materials prepared, the MoS 1.5 Te 0.5 @C nanocables are investigated as negative electrode active material in combination with expanded graphite at the positive electrode and NaPF 6 -based non-aqueous electrolyte solutions for dual-ion storage in coin cell configuration. As a result, the dual-ion lab-scale cells demonstrate a prolonged cycling lifespan with 97% capacity retention over 1500 cycles and a reversible capacity of about 101 mAh g -1 at specific capacities (based on the mass of the anode) of 1.0 A g -1 and 5.0 A g -1 , respectively.
Keyphrases
- ion batteries
- room temperature
- ionic liquid
- single cell
- reduced graphene oxide
- mass spectrometry
- cell therapy
- induced apoptosis
- quantum dots
- multiple sclerosis
- high resolution
- molecularly imprinted
- cell cycle arrest
- high intensity
- ms ms
- endoplasmic reticulum stress
- mesenchymal stem cells
- bone marrow
- oxidative stress
- cell death
- single molecule
- solid phase extraction
- visible light