With the fast‐growing demand for green and safe energy sources, rechargeable ion batteries have gradually occupied the major current market of energy storage devices due to their advantages of high capacities, long cycling life, superior rate ability, and so on. Metallic Sn‐based anodes are perceived as one of the most promising alternatives to the conventional graphite anode and have attracted great attention due to the high theoretical capacities of Sn in both lithium‐ion batteries (LIBs) (994 mA h g−1) and sodium‐ion batteries (847 mA h g−1). Though Sony has used Sn–Co–C nanocomposites as its commercial LIB anodes, to develop even better batteries using metallic Sn‐based anodes there are still two main obstacles that must be overcome: poor cycling stability and low coulombic efficiency. In this review, the latest and most outstanding developments in metallic Sn‐based anodes for LIBs and SIBs are summarized. And it covers the modification strategies including size control, alloying, and structure design to effectually improve the electrochemical properties. The superiorities and limitations are analyzed and discussed, aiming to provide an in‐depth understanding of the theoretical works and practical developments of metallic Sn‐based anode materials.
Rechargeable lithium/iodine (Li/I) batteries have attracted much attention because of their high gravimetric/volumetric energy densities, natural abundance and low cost. However, problems of the system, such as highly unstable iodine species under high temperature, their subsequent dissolution in electrolyte and continually reacting with lithium anode prevent the practical use of rechargeable Li/I cells. A polymer-iodine composite (polyvinylpyrrolidone-iodine) with high thermostability is employed as cathode material in rechargeable Li/I battery with an organic electrolyte. Because of the chemical interaction between polyvinylpyrrolidone (PVP) and polyiodide, most of the polyiodide in the cathode could be effectively trapped during charging/discharging. In-situ Raman observation revealed the evolution of iodine species in this system could be controlled during the process of I ↔ I ↔ I. Herein, the Li/I battery delivered a high discharge capacity of 278 mAh g at 0.2 C and exhibited a very low capacity decay rate of 0.019% per cycle for prolonged 1100 charge/discharge cycles at 2 C. More importantly, a high areal capacity of 4.1 mAh cm was achieved for the electrode with high iodine loading of 21.2 mg cm. This work may inspire new approach to design the Li/I (or Li/polyiodide) system with long cycle life.
Sn/N-doped carbon microcage composites (Sn/NMCs) are synthesized through a simple spray drying process and these composites exhibit excellent electrochemical performance in both LIBs and SIBs.
MXenes
have been widely explored in energy storage because of their
extraordinary properties; however, the majority of research on their
application was staged at multilayered MXenes or assisted by carbon
materials. Scientifically speaking, the two most distinctive properties
of MXenes are usually neglected, composed of large interlayer spacing
and abundant surface chemistry, which distinguish MXenes from other
two-dimensional materials. Herein, few-layered MXene (f-MXene) nanosheet
powders can be easily prepared according to the modified solution-phase
flocculation method, completely avoiding the restacking phenomenon
of f-MXene nanosheets in preparation and oxidation issues during the
storage process. Via further employing the solvothermal
reaction and annealing treatment, we successfully constructed pillared
SnS/Ti3C2T
x
composites
decorated with in situ formed TiO2 nanoparticles.
In the composites, MXenes can play the role of a conductive network,
a buffer matrix for volume expansion of SnS, while the active SnS
nanoplates can fully deliver the advantage of high capacity and further
induce interlayer engineering of Ti3C2T
x
during cycling. As a result, the pillared
SnS/Ti3C2T
x
MXene
composites exhibit obvious improvement in electrochemical performance.
Interestingly, there is an apparent enhancement of capacity at succedent
cycling, which can be ascribed to the “pillar effect”
of Ti3C2T
x
MXenes.
The efforts and attempts made in this work can further broaden the
development of pillared MXene composites.
HIGHLIGHTS • A facile NH 4 + method was proposed to prepare Sn nanocomplex pillared few-layered Ti 3 C 2 T x MXene nanosheets. • The MXene nanosheets showed excellent lithium-ion storage performances among MXene-based materials, which can maintain 1016 mAh g −1 after 1200 cycles at 2000 mA g −1 and deliver a stable capacity of 680 mAh g −1 at 5 A g −1. ABSTRACT MXenes have attracted great interest in various fields, and pillared MXenes open a new path with larger interlayer spacing. However, the further study of pillared MXenes is blocked at multilayered state due to serious restacking phenomenon of few-layered MXene nanosheets. In this work, for the first time, we designed a facile NH 4+ method to fundamentally solve the restacking issues of MXene nanosheets and succeeded in achieving pillared few-layered MXene. Sn nanocomplex pillared few-layered Ti 3 C 2 T x (STCT) composites were synthesized by
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