4.8 Article

Bi-Sb Nanocrystals Embedded in Phosphorus as High-Performance Potassium Ion Battery Electrodes

期刊

ACS NANO
卷 14, 期 9, 页码 11648-11661

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.0c04203

关键词

potassium; battery; phosphorus; nanotechnology; nanocrystals

资金

  1. Young Scholar Fellowship Program by the Ministry of Science and Technology in Taiwan [MOST 108-2636-E-007-013, MOST 108-2622-8-007-016, MOST 109-2636-E-007-011]
  2. National Tsing Hua University [107Q2708E1]

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The development of high-performance potassium ion battery (KIB) electrodes requires a nanoengineering design aimed at optimizing the construction of active material/buffer material nanocomposites. These nanocomposites will alleviate the stress resulting from large volume changes induced by K+ ion insertion/extraction and enhance the electrical and ion conductivity. We report the synthesis of phosphorus-embedded ultrasmall bismuth-antimony nanocrystals (BixSb1-x@P, (0 <= x <= 1)) for KIB anodes via a facile solution precipitation at room temperature. BixSb1-x@P nanocomposites can enhance potassiation-depotassiation reactions with K(+ )ions, owing to several attributes. First, by adjusting the feed ratios of the Bi/Sb reactants, the composition of BixSb1-x nanocrystals can be systematically tuned for the best KIB anode performance. Second, extremely small (diameter approximate to 3 nm) BixSb1-x nanocrystals were obtained after cycling and were fixed firmly inside the P matrix. These nanocrystals were effective in buffering the large volume change and preventing the collapse of the electrode. Third, the P matrix served as a good medium for both electron and K+ ion transport to enable rapid charge and discharge processes. Fourth, thin and stable solid electrolyte interface (SEI) layers that formed on the surface of the cycled BixSb1-x@P electrodes resulted in low resistance of the overall battery electrode. Lastly, in situ X-ray diffraction analysis of K+ ion insertion/extraction into/from the BxSb1-x@P electrodes revealed that the potassium storage mechanism involves a simple, direct, and reversible reaction pathway: (Bi, Sb) <-> K(Bi, Sb) <-> K-3(Bi, Sb). Therefore, electrodes with the optimized composition, i.e., Bi0.5Sb0.5@P, exhibited excellent electrochemical performance (in terms of specific capacity, rate capacities, and cycling stability) as KIB anodes. Bi0.5Sb0.5@P anodes retained specific capacities of 295.4 mA h g(-1) at 500 mA g(-1) and 339.1 mA h g(-1) at 1 A g(-1) after 800 and 550 cycles, respectively. Furthermore, a capacity of 258.5 mA h g(-1) even at 6.5 A g(-1) revealed the outstanding rate capability of the Sb-based KIB anodes. Proof-of-concept KIBs utilizing Bi0.5Sb0.5@P as an anode and PTCDA (perylenetetracarboxylic dianhydride) as a cathode were used to demonstrate the applicability of Bi0.5Sb0.5@P electrodes to full cells. This study shows that BixSb1-x@P nanocomposites are promising carbon-free anode materials for KIB anodes and are readily compatible with the commercial slurry-coating process applied in the battery manufacturing industry.

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