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Synthesis of Hybrid Layered Electrode Materials via Chemical Pre-Intercalation of Linear Organic Molecules
Conference proceeding

Synthesis of Hybrid Layered Electrode Materials via Chemical Pre-Intercalation of Linear Organic Molecules

Mallory Clites and Ekaterina Pomerantseva
LOW-DIMENSIONAL MATERIALS AND DEVICES, v 10725, pp 107250S-107250S-9
01 Jan 2018

Abstract

Materials Science Materials Science, Multidisciplinary Optics Physical Sciences Physics Physics, Applied Science & Technology Technology
Chemical pre-intercalation is a low-temperature, scalable synthesis method that utilizes a sol-gel process to form layered oxides with positively-charged species inserted between the layers. We have shown that this approach can be used to successfully intercalate Li+, Na+, K+, Mg2+, and Ca2+ ions into the crystal structure of bilayered vanadium oxide (delta-V2O5). 1 Through this ion-intercalation, the interlayer spacing of the delta-MgxV2O5 (M=Li, Na, K, Mg, and Ca) structure can be controlled between 9.6 angstrom (delta-KxV2O5) and 13.4 angstrom (delta-MgxV2O5). 1 Moreover, the expanded spacing achieved for the delta-MgxV2O5 phase corresponded to increased electrochemical stability in both Li- and Na-ion cells.[1] While this study identified a correlation between expanded interlayer spacing and improved electrochemical stability over cycling, chemical pre-intercalation of ions does not allow for expansion beyond that exhibited by the delta-MgxV2O5 structure. In this work, we show that further expansion of the interlayer spacing can be achieved via pre-intercalation of positively-charged linear, organic cations. We report synthesis of hybrid inorganic/organic materials with a 1D nanobelt morphology. The layered structure of the hybrids is confirmed by both XRD and TEM analysis. delta-V2O5 preintercalated with cetyltrimethylammonia ions, CTA(+), demonstrated the interlayer spacings of all samples (31 angstrom), more than twice larger than the largest interlayer spacing achieved via pre-intercalation of inorganic ions. The effects of carbon chain-length and positively charged nitrogen termini on the interlayer spacing and electrochemical stability is investigated, with two N-termini on the cation (DMO+) resulting in increased electrochemical stability of the preintercalated phase.

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Web of Science research areas
Materials Science, Multidisciplinary
Optics
Physics, Applied
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