The requirement of energy-storage equipment needs to develop the lithium ion battery (LIB) with high electrochemical performance. The surface modification of commercial LiFePO4 (LFP) by utilizing zeolitic imidazolate frameworks-8 (ZIF-8) offers new possibilities for commercial LFP with high electrochemical performances. In this work, the carbonized ZIF-8 (CZIF-8) was coated on the surface of LFP particles by the in situ growth and carbonization of ZIF-8. Transmission electron microscopy indicates that there is an approximate 10 nm coating layer with metal zinc and graphite-like carbon on the surface of LFP/CZIF-8 sample. The N2 adsorption and desorption isotherm suggests that the coating layer has uniform and simple connecting mesopores. As cathode material, LFP/CZIF-8 cathode-active material delivers a discharge specific capacity of 159.3 mAh g−1 at 0.1C and a discharge specific energy of 141.7 mWh g−1 after 200 cycles at 5.0C (the retention rate is approximate 99%). These results are attributed to the synergy improvement of the conductivity, the lithium ion diffusion coefficient, and the degree of freedom for volume change of LFP/CZIF-8 cathode. This work will contribute to the improvement of the cathode materials of commercial LIB. Electronic supplementary materialThe online version of this article (doi:10.1007/s40820-017-0154-4) contains supplementary material, which is available to authorized users.

Sulfur reactivity in lithium−sulfur batteries highly depends on its distribution and morphology during cycling, which is of great significance to suppress the shuttle effect and promote conversion reaction. Herein, cobalt phosphide nanoflakes are prepared and used as a sulfur host. An improved redox kinetics from sulfur to lithium sulfide and the corresponding fast lithium-ion diffusion are observed to greatly promote the electrochemical performance of lithium−sulfur batteries. Meanwhile, for the first time, we propose "effective triple phase contact" and "insulated dead sulfur" to account for cycling performance differences of CoP@S and rGO@S batteries. The flower-like sulfur induced by CoP nanoflakes during cycling provides extra lithium-ion diffusion and electron transfer ways compared with agglomerated sulfur in the rGO@S cathode. The CoP@S battery shows good rate performance and delivers 520 mA h g −1 after 1000 cycles with an excellent Coulombic efficiency of 99%. In contrast, no conversion reaction happens after 600 cycles in the rGO@S battery, implying no existence of reactive sulfur. This research reveals the effect of morphological evolution of sulfur on the cycling performance and affords an insight for developing high-performance lithium−sulfur batteries.

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