LiCa3As2H and Ca14As6X7 (X = C, H, N): Two New Arsenide Hydride Phases Grown from Ca/Li Metal Flux

被引:6
作者
Blankenship, Trevor V. [1 ]
Wang, Xiaoping [2 ]
Hoffmann, Christina [2 ]
Latturner, Susan E. [1 ]
机构
[1] Florida State Univ, Dept Chem & Biochem, Tallahassee, FL 32306 USA
[2] Oak Ridge Natl Lab, Chem & Engn Mat Div, Oak Ridge, TN 37831 USA
基金
美国国家科学基金会;
关键词
ZINTL PHASES; CRYSTAL-STRUCTURE; HYDROGEN; A=CA; SR; YB; STABILIZATION; DIFFRACTION; BINARY; BA;
D O I
10.1021/ic501722d
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The reaction of arsenic with sources of light elements in a Ca/Li melt leads to the formation of two new arsenide hydride phases. The predominant phase Ca14As6X7 (X = C4(-), N3(-), H-) exhibits a new tetragonal structure type in the space group P4/mbm (a = 15.749(1) angstrom, c = 9.1062(9) angstrom, z = 4, R1 = 0.0150). The minor phase LiCa3As2H also has a new structure type in the orthorhombic space group Puma (a = 11.4064(7) angstrom, b = 4.2702(3) angstrom, c = 11.8762(8)angstrom, z = 4, R1 = 0.0135). Both phases feature hydride and arsenide anions separated by calcium cations. The red color of these compounds indicates they should be charge-balanced. DOS calculations on LiCa3As2H confirm a band gap of 1.4 eV; UV vis spectroscopy on Ca14As6X7 shows a band gap of 1.6 eV. Single-crystal neutron diffraction studies were necessary to determine the mixed occupancy of carbon, nitrogen, and hydrogen anions on the six light-element sites in Ca14As6X7; these data indicated an overall stoichiometry of Ca(14)AS(6)C(0.445)N(1.135)H(4.915).
引用
收藏
页码:10620 / 10626
页数:7
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