TY - JOUR
T1 - Neutron diffraction study of liquid As-Se and As-Te systems
AU - Usuki, Takeshi
AU - Itoh, Keiji
AU - Kameda, Yasuo
AU - Uemura, Osamu
N1 - Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 1998/11
Y1 - 1998/11
N2 - The neutron diffraction measurement in liquid AsxSe1-x and AsxTe1-x alloys with x=0.20∼0.571 has been carried out to analyze the local atomic arrangement in these liquid alloys. The first sharp diffraction peak (FSDP) of the structure factor, S(Q), in the liquid As-Se alloys was observed at all x, indicating that existing structural units are partially connected as in the amorphous state, while, the FSDP in the liquid As-Te alloys almost disappears, particularly, in the Te rich composition range. The first peak of atomic pair distribution function, g(r), in the liquid As-Se alloys is well-resolved, reflecting the strong As-Se covalent bondings. On the other hand, the first peak of g(r) in the liquid As-Te alloys is broadened and its position largely shifts with x. Results by the least square analysis for diffraction intensities have been summarized as follows: The connecting AsSe3/2 pyramidal unit, which is the basic structural element at As2Se3, is formed over a wide composition range in the As-Se alloys but bondings between like atoms such as Se-Se and As-As are present only in the limited composition range. On the other hand, in the liquid As-Te alloys both As-As and Te-Te bondings, in addition to the As-Te one, can be observed at all x containing As2Te3. The results have also pointed out that the metallic property of the liquid As-Te alloys is attributable to the change of the bonding nature relating to Te on melting.
AB - The neutron diffraction measurement in liquid AsxSe1-x and AsxTe1-x alloys with x=0.20∼0.571 has been carried out to analyze the local atomic arrangement in these liquid alloys. The first sharp diffraction peak (FSDP) of the structure factor, S(Q), in the liquid As-Se alloys was observed at all x, indicating that existing structural units are partially connected as in the amorphous state, while, the FSDP in the liquid As-Te alloys almost disappears, particularly, in the Te rich composition range. The first peak of atomic pair distribution function, g(r), in the liquid As-Se alloys is well-resolved, reflecting the strong As-Se covalent bondings. On the other hand, the first peak of g(r) in the liquid As-Te alloys is broadened and its position largely shifts with x. Results by the least square analysis for diffraction intensities have been summarized as follows: The connecting AsSe3/2 pyramidal unit, which is the basic structural element at As2Se3, is formed over a wide composition range in the As-Se alloys but bondings between like atoms such as Se-Se and As-As are present only in the limited composition range. On the other hand, in the liquid As-Te alloys both As-As and Te-Te bondings, in addition to the As-Te one, can be observed at all x containing As2Te3. The results have also pointed out that the metallic property of the liquid As-Te alloys is attributable to the change of the bonding nature relating to Te on melting.
KW - Liquid As-chalcogen alloys
KW - Local atomic arrangement
KW - Neutron diffraction
KW - Pair distribution function
KW - Structure factor
UR - http://www.scopus.com/inward/record.url?scp=0032204894&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0032204894&partnerID=8YFLogxK
U2 - 10.2320/matertrans1989.39.1135
DO - 10.2320/matertrans1989.39.1135
M3 - Article
AN - SCOPUS:0032204894
SN - 1345-9678
VL - 39
SP - 1135
EP - 1139
JO - Materials Transactions
JF - Materials Transactions
IS - 11
ER -