Structure of the Intermediate Phase Glasses GeSe3 and GeSe4: The Deployment of Neutron Diffraction With Isotope Substitution

被引:15
作者
Rowlands, Ruth F. [1 ]
Zeidler, Anita [1 ,2 ]
Fischer, Henry E. [3 ]
Salmon, Philip S. [1 ,2 ]
机构
[1] Univ Bath, Dept Phys, Bath, Avon, England
[2] Corning Inc, Sci & Technol Div, Corning, NY 14831 USA
[3] Inst Laue Langevin, Diffract Grp, Grenoble, France
基金
英国工程与自然科学研究理事会;
关键词
chalcogenide glass; glass structure; neutron diffraction; rigidity percolation; intermediate phase; CHALCOGENIDE GLASSES; SELF-ORGANIZATION; RAMAN-SCATTERING; NETWORK GLASSES; LIQUID GESE2; RANGE ORDER; AS-SE; GE; TOPOLOGY; NMR;
D O I
10.3389/fmats.2019.00133
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The method of neutron diffraction with isotope substitution was used to measure the full set of partial pair-correlation functions for each of the network-forming glasses GeSe3 and GeSe4, which lie at the boundaries of the so-called intermediate phase in the Ge-Se system. The results show the formation of chemically ordered networks, where selenium chains are cross-linked by Ge(Se-4)(1/2) tetrahedra, in contrast to glassy GeSe2 where the chemical order is broken. In all of these materials, the Ge-centered structural motifs are distributed unevenly on an intermediate length scale, as indicated by the appearance of a first sharp diffraction peak in the Bhatia-Thornton concentration-concentration partial structure factor. The new experimental work provides benchmark results for guiding in the development of realistic structural models, which can be used to explore the network rigidity and other structure-related properties of the glass. In this context, there are discrepancies between experiment and the predictions of first-principles molecular dynamics simulations that are particularly marked in respect of the Ge-Ge correlation functions, which are sensitive to the connectivity of the Ge-centered structural motifs.
引用
收藏
页数:15
相关论文
共 86 条
[1]   Angular rigidity in tetrahedral network glasses with changing composition [J].
Bauchy, M. ;
Micoulaut, M. ;
Celino, M. ;
Le Roux, S. ;
Boero, M. ;
Massobrio, C. .
PHYSICAL REVIEW B, 2011, 84 (05)
[2]   DENSITY-FUNCTIONAL EXCHANGE-ENERGY APPROXIMATION WITH CORRECT ASYMPTOTIC-BEHAVIOR [J].
BECKE, AD .
PHYSICAL REVIEW A, 1988, 38 (06) :3098-3100
[3]   NEUTRON-DIFFRACTION STUDY OF LIQUID ACETONITRILE .1. CD3C14N [J].
BERTAGNOLLI, H ;
CHIEUX, P ;
ZEIDLER, MD .
MOLECULAR PHYSICS, 1976, 32 (03) :759-773
[4]   Structural aspects of the electrical resistivity of binary alloys [J].
Bhatia, A. B. ;
Thornton, D. E. .
PHYSICAL REVIEW B-SOLID STATE, 1970, 2 (08) :3004-3012
[5]   Meeting experimental challenges to physics of network glasses: Assessing the role of sample homogeneity [J].
Bhosle, S. ;
Gunasekera, K. ;
Chen, Ping ;
Boolchand, P. ;
Micoulaut, M. ;
Massobrio, C. .
SOLID STATE COMMUNICATIONS, 2011, 151 (24) :1851-1855
[6]   Melt Homogenization and Self-Organization in Chalcogenides-Part II [J].
Bhosle, Siddhesh ;
Gunasekera, Kapila ;
Boolchand, Punit ;
Micoulaut, Matthieu .
INTERNATIONAL JOURNAL OF APPLIED GLASS SCIENCE, 2012, 3 (03) :205-220
[7]   Rigidity transitions in binary Ge-Se glasses and the intermediate phase [J].
Boolchand, P ;
Feng, X ;
Bresser, WJ .
JOURNAL OF NON-CRYSTALLINE SOLIDS, 2001, 293 :348-356
[8]  
Boolchand P, 2001, J OPTOELECTRON ADV M, V3, P703
[9]   Origin of structural analogies and differences between the atomic structures of GeSe4 and GeS4 glasses: A first principles study [J].
Bouzid, Assil ;
Le Roux, Sebastien ;
Ori, Guido ;
Boero, Mauro ;
Massobrio, Carlo .
JOURNAL OF CHEMICAL PHYSICS, 2015, 143 (03)
[10]   Note: Accounting for pressure effects on the calculated equilibrium structure of glassy GeSe2 [J].
Bouzid, Assil ;
Massobrio, Carlo .
JOURNAL OF CHEMICAL PHYSICS, 2012, 137 (04)