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Dehydration‐Triggered Ionic Channel Engineering in Potassium Niobate for Li/K‐Ion Storage
Author(s) -
Zhang Shilin,
Fan Qining,
Liu Ye,
Xi Shibo,
Liu Xiufan,
Wu Zhibin,
Hao Junnan,
Pang Wei Kong,
Zhou Tengfei,
Guo Zaiping
Publication year - 2020
Publication title -
advanced materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 10.707
H-Index - 527
eISSN - 1521-4095
pISSN - 0935-9648
DOI - 10.1002/adma.202000380
Subject(s) - materials science , ionic bonding , ion , ionic conductivity , electrochemistry , potassium , energy storage , lithium niobate , chemical physics , diffusion , electrolyte , nanotechnology , chemical engineering , electrode , optoelectronics , chemistry , thermodynamics , power (physics) , physics , organic chemistry , engineering , metallurgy
Boosting charge transfer in materials is critical for applications involving charge carriers. Engineering ionic channels in electrode materials can create a skeleton to manipulate their ion and electron behaviors with favorable parameters to promote their capacity and stability. Here, tailoring of the atomic structure in layered potassium niobate (K 4 Nb 6 O 17 ) nanosheets and facilitating their application in lithium and potassium storage by dehydration‐triggered lattice rearrangement is reported. The spectroscopy results reveal that the interatomic distances of the NbO coordination in the engineered K 4 Nb 6 O 17 are slightly elongated with increased degrees of disorder. Specifically, the engineered K 4 Nb 6 O 17 shows enhanced electrical and ionic conductivity, which can be attributed to the enlarged interlamellar spacing and subtle distortions in the fine atomic arrangements. Moreover, subsequent experimental results and calculations demonstrate that the energy barrier for Li + /K + diffusion is significantly lower than that in pristine K 4 Nb 6 O 17 . Interestingly, the diffusion coefficient of K + is one order of magnitude higher than that of Li + , and the engineered K 4 Nb 6 O 17 presents superior electrochemical performance for K + to Li + . This work offers an ionic engineering strategy to enable fast and durable charge transfer in materials, holding great promise for providing guidance for the material design of related energy storage systems.