Abstract

AbstractPotassium ion batteries (PIBs) have attracted enormous attention due to their low cost and high abundance of potassium resources. Here, self‐hybridized BiOBr0.5I0.5 with a flower‐like structure composed of 2D nanosheets is assembled and used as PIBs anode. According to the systematic theoretical calculations, the unbalanced charge distribution between Br and I atoms induces an intensified internal electric field and a wide van der Waals gap; while the decreasing of electron polarons caused by the hybridized structure improves the stability and electronic conductivity of the system. Moreover, the K+ ion uptake induces an energetic evolution in polaronic states in the BiOBr0.5I0.5 crystal skeleton, whereby the dynamic K+ ion‐halogen atoms correlation in situ forms hole‐like polarons, which substantially promotes K+ ion diffusion kinetics and the corresponding reaction kinetics during charge/discharge processes, imparting significant implications for the design of high‐performance energy storage electrode materials by engineering the interface interaction and electronic structure. Therefore, with this atomic orbital self‐hybridized structure, the K+ ion diffusion kinetics and the corresponding reaction kinetics during the charge/discharge process are both enhanced remarkably, thus enabling a high electrochemical performance of 155 mAh g−1 at 1000 mA g−1 over 4000 cycles in PIBs with the BiOBr0.5I0.5 as the anode.

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