Hydrothermal preparation, crystal chemistry, and redox properties of iron muscovite clay

Shiliang Zhou, Erica S. Howard, Jue Liu, Nicholas H. Bashian, Kyle Nolan, Sankarganesh Krishnamoorthy, Geovanni M. Rangel, Moulay Tahar Sougrati, G. K.Surya Prakash, Katharine Page, Brent C. Melot

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

The development of functional materials based on Earthabundant, environmentally benign compositions is critical for ensuring their commercial viability and sustainable production. Here we present an investigation into the crystal chemistry and electrochemical properties of the muscovite clay KFe2.75Si3.25O10(OH)2. We first report a low-temperature hydrothermal reaction that allows for a significant degree of control over sample crystallinity, particle morphology, and cation distribution through the lattice. A complex sequence of stacking faults is identified and characterized using a combination of Mossbauer spectroscopy and total scattering neutron experiments. We then show the existence of a reversible electrochemical process using galvanostatic cycling with complementary cyclic voltammetry suggesting that the redox activity occurs primarily on the surface of the particles. We conclude by determining that the ability to (de)intercalate Li ions from the material is hindered by the strong negative charge on the transition metal silicate layers, which prevents the displacement of the interlayer K ions. This work calls attention to a hugely Earth-abundant family of minerals that possesses useful electrochemical properties that warrant further exploration.

Original languageEnglish
Pages (from-to)34024-34032
Number of pages9
JournalACS Applied Materials and Interfaces
Volume9
Issue number39
DOIs
StatePublished - Oct 4 2017

Funding

B.C.M., S.Z., E.S.H., and K.N. gratefully acknowledge financial support through a CAREER award from the National Science Foundation under Grant No. DMR-1554204 as well as from the Research Corporation for Science Advancement in the form of a Cottrell Scholar award. Use of the Advanced Photon Source at Argonne National Laboratory was supported by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, under Contract No. DE-AC02-06CH11357. A portion of this work was completed with the NOMAD instrument at the Spallation Neutron Source, a US Department of Energy Office of Science User Facility operated by Oak Ridge National Laboratory. Prof. Lorenzo Stievano is acknowledged for fruitful discussions of Mössbauer data. Prof. Travis Williams is acknowledged and thanked for his help in the collection and analysis NMR data. S.K. and G.K.S.P. thank the Loker Hydrocarbon Research Institute for the financial support. J.L. and K.P. gratefully acknowledge financial support for modeling and analysis of neutron and X-ray data through the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, Early Career Research Program, Award No. KC040602, under contract no. DE-AC05-00OR22725.

FundersFunder number
Office of Basic Energy Sciences
National Science Foundation1554204
U.S. Department of Energy
Office of Science
Loker Hydrocarbon Research Institute, University of Southern CaliforniaKC040602

    Keywords

    • Crystal chemistry
    • Electrochemistry
    • Neutron diffraction
    • Phyllosilicates
    • Stacking faults

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