TY - JOUR
T1 - Covalent bond connectivity, medium range order, and physical properties in TeX and TeXAs glasses
AU - Ma, Hong li
AU - Zhang, Xiang Hua
AU - Lucas, Jacques
AU - Senapati, Hema
AU - Bohmer, Roland
AU - Angell, Charles
N1 - Funding Information:
The authors express appreciation for the financial support of this work from the D.R.E.T. (French Ministry of Defense) and from the U.S. Office of Naval Research under Agreement N00014-84-K-0289. We thank C. T. Moynihan for helpful discussions.
PY - 1992/1
Y1 - 1992/1
N2 - Data on the new As-Te-Se-I glasses are analyzed to determine whether the extended order determined by bond connectivity via the average coordination number, 〈r〉, controls the physical properties as it does in the case of the Ge-As-Se system. When appropriate allowance is made for partial 4-coordination of Te in Te- and I-rich glasses, the calorimetric glass transition temperature Tg is found to be a universal function of 〈r〉 as in Ge-As-Se (4-3-2) glasses. However, no special behavior is found at the Phillips-Thorpe rigidity percolation threshhold value, 〈r〉=2.4 as in the 4-3-2 case. The 〈r〉-dependences of both linear and non-linear aspects of relaxation appear smaller in the present system, and no extrema are in evidence. This is interpreted to indicate that the 2- vs 3-dimensional nature of crosslinking, by As vs. Ge, respectively, of the basic chain structures obtained at all 〈r〉=2 compositions, is an important property-controlling factor.
AB - Data on the new As-Te-Se-I glasses are analyzed to determine whether the extended order determined by bond connectivity via the average coordination number, 〈r〉, controls the physical properties as it does in the case of the Ge-As-Se system. When appropriate allowance is made for partial 4-coordination of Te in Te- and I-rich glasses, the calorimetric glass transition temperature Tg is found to be a universal function of 〈r〉 as in Ge-As-Se (4-3-2) glasses. However, no special behavior is found at the Phillips-Thorpe rigidity percolation threshhold value, 〈r〉=2.4 as in the 4-3-2 case. The 〈r〉-dependences of both linear and non-linear aspects of relaxation appear smaller in the present system, and no extrema are in evidence. This is interpreted to indicate that the 2- vs 3-dimensional nature of crosslinking, by As vs. Ge, respectively, of the basic chain structures obtained at all 〈r〉=2 compositions, is an important property-controlling factor.
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U2 - 10.1016/S0022-4596(05)80310-X
DO - 10.1016/S0022-4596(05)80310-X
M3 - Article
AN - SCOPUS:0040251470
SN - 0022-4596
VL - 96
SP - 181
EP - 191
JO - Journal of Solid State Chemistry
JF - Journal of Solid State Chemistry
IS - 1
ER -