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Silicon phosphide (SiP) has attracted a great deal of attention in the field of energy storage because of its unique properties of stable semiconducting two-dimensional structure and promising theo...

With the growing demand for high specific volume energy-density, surface modifications are devoted to increasing the electrochemical performances of LiCoO2 at high operating voltage. In this work, LiCoO2 materials with a phosphate-rich coating layer are developed using a facile spray-drying method. The stable phosphate-rich coating layer acts as protection and effectively suppresses the impedance growth in LiCoO2 cells. The phosphate-rich layer coated LiCoO2 samples show long cycle-life and good rate performance when cycled with a high cut-off voltage of 4.5 V at room temperature and 45 °C.

Layered germanium phosphide (GeP), a recently developed two-dimensional material, promises highly attractive theoretical capacity for use as a lithium-ion battery anode. Here, we comprehensively investigate its electrochemical performance and the modification mechanism. GeP flakes demonstrate large initial discharge/charge capacity and high initial Coulombic efficiency. However, the cycling performance is disappointing in the potential window of 0.001-3 V in which capacity retention is only ∼18% after 100 cycles. In situ transmission electron microscopy reveals that the poor cycling behavior results in the unexpected large volume change induced by complex reaction processes in cycles. Serious cracking and fracture appear clearly on the electrode surface after cycling. Narrowing the working voltage window to 0.001-0.85 V, cycling stability will be greatly enhanced, with 75% capacity retaining after 100 cycles and ∼50% left after 350 cycles due to the absence of the dealloying of Li

Binders play a significant role in the electrochemical performance of electrodes in batteries, especially for high-capacity conversion/alloying-type electrodes. However, the effects of binders on the electrochemical performance of the conversion/alloying-type anodes in sodium ion batteries are not widely investigated. In this work, we use SnS 2 as a model anode and comparatively investigate the performance of six different types of binders in SnS 2 electrodes of sodium ion batteries by half-cell testing. The binders are sodium carboxymethyl cellulose (CMC-Na), sodium polyacrylate (PAA-Na), CMC-Na-PAA-Na (1:1, wt%, denoted as PAA-CMC), sodium alginate (ALG-Na), PVDF, PTFE. The PAA-CMC binder electrodes exhibit outstanding cycling and rate performance, delivering a reversible capacity of 400 mAh g −1 at the current density of 100 mA g −1 within 70 cycles. Our results indicate that the binder with a large fraction of carboxylate and hydroxyl groups, which lead to stronger hydrogen bonds and/or covalent chemical bonds with the carbon black and active materials, is advantageous for the electrochemical performances of SnS 2 electrodes. The synergistic interactions among the binder and the surface of both the active materials of SnS 2 and the conductive additive of ketjen black have been also schematically proposed in this study.

Although various cathode materials have been explored to improve the energy density of lithium-ion batteries, LiCoO2 is still the first choice for 3C consumer electronics due to the high tap density and high volumetric energy density. However, only 0.5 mol of lithium ions can be extracted from LiCoO2 to avoid side reactions and irreversible structure change, which typically occur at high voltage (>4.2 V). To improve the electrochemical performances of the LiCoO2 cathode material at high cut-off voltage and elevated temperature for higher energy density, an in situ formed spinel interfacial coating layer of LiCoxMn2–xO4 is achieved by the reaction of the surface region of the LiCoO2 host. The capacity retention of the modified LiCoO2 cycled at a high voltage of 4.5 V is significantly increased from 15.5 to 82.0% after 300 cycles at room temperature, due to the stable spinel interfacial inhibiting interfacial reactions between LiCoO2 and the electrolyte as confirmed by impedance spectroscopy. We further dem...

The lithium-rich Li[Li0.2Ni0.13Mn0.54Co0.13]O2 nanoplates were synthesized using a molten-salt method. The nanoplates showed an initial reversible discharge capacity of 233 mA&middot, h&middot, g&minus, 1, with a fast capacity decay. The morphology and micro-structural change, after different cycles, were studied by a scanning electron microscope (SEM) and transmission electron microscopy (TEM) to understand the mechanism of the capacity decay. Our results showed that the cracks generated from both the particle surface and the inner, and increased with long-term cycling at 0.1 C rate (C = 250 mA&middot, 1), together with the layered to spinel and rock-salt phase transitions. These results show that the cracks and phase transitions could be responsible for the capacity decay. The results will help us to understand capacity decay mechanisms, and to guide our future work to improve the electrochemical performance of lithium-rich cathode materials.

Layered germanium phosphide, which combines the advantages of both germanium and phosphorus, is believed to be a potential anode for sodium ion battery. Here, the sodium storage mechanism and electrochemical performance of layered germanium phosphide have been deeply investigated by advanced in-situ transmission electron microscopy technique combining half-cell testing. Dynamic reaction process reveals that individual layered germanium phosphide nanoflake undergoes total area expansion of 248% without any detectable fracture or cracking in sodiation. In contrast, germanium phosphide experiences multi-step reactions, i.e. intercalation and alloying, accompanied by sequentially forming NaxGeP (0