Literature DB >> 32165994

Tracking the Progression of Anion Reorientational Behavior between α-Phase and β-Phase Alkali-Metal Silanides, MSiH3, by Quasielastic Neutron Scattering.

Mirjana Dimitrievska1,2, Jean-Noël Chotard3, Raphaël Janot3, Antonio Faraone1, Wan Si Tang1,4,5, Alexander V Skripov6, Terrence J Udovic1.   

Abstract

Quasielastic neutron scattering (QENS) measurements over a wide range of energy resolutions were used to probe the reorientational behavior of the pyramidal SiH3 - anions in the monoalkali silanides (MSiH3, where M = K, Rb, and Cs) within the low-temperature ordered β-phases, and for CsSiH3, the high-temperature disordered α-phase and intervening hysteretic transition region. Maximum jump frequencies of the β-phase anions near the β-α transitions range from around 109 s-1 for β-KSiH3 to 1010 s-1 and higher for β-RbSiH3 and β-CsSiH3. The β-phase anions undergo uniaxial 3-fold rotational jumps around the anion quasi-C 3 symmetry axis. CsSiH3 was the focus of further studies to map out the evolving anion dynamical behavior at temperatures above the β-phase region. As in α-KSiH3 and α-RbSiH3, the highly mobile anions (with reorientational jump frequencies approaching and exceeding 1012 s-1) in the disordered α-CsSiH3 are all adequately modeled by H jumps between 24 different locations distributed radially around the anion center of gravity, although even higher anion reorientational disorder cannot be ruled out. QENS data for CsSiH3 in the transition region between the α- and β-phases corroborated the presence of dynamically distinct intermediate (i-) phase. The SiH3 - anions within i-phase appear to undergo uniaxial small-angular-jump reorientations that are more akin to the lower-dimensional β-phase anion motions rather than to the multidimensional α-phase anion motions. Moreover, they possess orientational mobilities that are an order-of-magnitude lower than those for α-phase anions but also an order-of-magnitude higher than those for β-phase anions. Combined QENS and neutron powder diffraction results strongly suggest that this i-phase is associated chiefly with the more short-range-ordered, nanocrystalline portions (invisible to diffraction) that appear to dominate the CsSiH3.

Entities:  

Year:  2019        PMID: 32165994      PMCID: PMC7067043          DOI: 10.1021/acs.jpcc.8b08257

Source DB:  PubMed          Journal:  J Phys Chem C Nanomater Interfaces        ISSN: 1932-7447            Impact factor:   4.126


  5 in total

1.  Catalytic modification in dehydrogenation properties of KSiH3.

Authors:  Ankur Jain; Takayuki Ichikawa; Shotaro Yamaguchi; Hiroki Miyaoka; Yoshitsugu Kojima
Journal:  Phys Chem Chem Phys       Date:  2014-10-31       Impact factor: 3.676

2.  Potassium silanide (KSiH3): a reversible hydrogen storage material.

Authors:  Jean-Noël Chotard; Wan Si Tang; Pascal Raybaud; Raphaël Janot
Journal:  Chemistry       Date:  2011-09-27       Impact factor: 5.236

3.  Structural and vibrational properties of silyl (SiH3(-)) anions in KSiH3 and RbSiH3: new insight into Si-H interactions.

Authors:  Verina F Kranak; Yuan-Chih Lin; Maths Karlsson; Janos Mink; Stefan T Norberg; Ulrich Häussermann
Journal:  Inorg Chem       Date:  2015-02-10       Impact factor: 5.165

4.  DAVE: A Comprehensive Software Suite for the Reduction, Visualization, and Analysis of Low Energy Neutron Spectroscopic Data.

Authors:  Richard Tumanjong Azuah; Larry R Kneller; Yiming Qiu; Philip L W Tregenna-Piggott; Craig M Brown; John R D Copley; Robert M Dimeo
Journal:  J Res Natl Inst Stand Technol       Date:  2009-12-01

5.  Hydrogenation properties of KSi and NaSi Zintl phases.

Authors:  Wan Si Tang; Jean-Noël Chotard; Pascal Raybaud; Raphaël Janot
Journal:  Phys Chem Chem Phys       Date:  2012-10-14       Impact factor: 3.676

  5 in total

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