scholarly journals Ternary nitride semiconductors in the rocksalt crystal structure

2019 ◽  
Vol 116 (30) ◽  
pp. 14829-14834 ◽  
Author(s):  
Sage R. Bauers ◽  
Aaron Holder ◽  
Wenhao Sun ◽  
Celeste L. Melamed ◽  
Rachel Woods-Robinson ◽  
...  

Inorganic nitrides with wurtzite crystal structures are well-known semiconductors used in optical and electronic devices. In contrast, rocksalt-structured nitrides are known for their superconducting and refractory properties. Breaking this dichotomy, here we report ternary nitride semiconductors with rocksalt crystal structures, remarkable electronic properties, and the general chemical formula MgxTM1−xN (TM = Ti, Zr, Hf, Nb). Our experiments show that these materials form over a broad metal composition range, and that Mg-rich compositions are nondegenerate semiconductors with visible-range optical absorption onsets (1.8 to 2.1 eV) and up to 100 cm2 V−1⋅s−1 electron mobility for MgZrN2 grown on MgO substrates. Complementary ab initio calculations reveal that these materials have disorder-tunable optical absorption, large dielectric constants, and electronic bandgaps that are relatively insensitive to disorder. These ternary MgxTM1−xN semiconductors are also structurally compatible both with binary TMN superconductors and main-group nitride semiconductors along certain crystallographic orientations. Overall, these results highlight MgxTM1−xN as a class of materials combining the semiconducting properties of main-group wurtzite nitrides and rocksalt structure of superconducting transition-metal nitrides.

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Simon D. Kloß ◽  
Arthur Haffner ◽  
Pascal Manuel ◽  
Masato Goto ◽  
Yuichi Shimakawa ◽  
...  

AbstractTransition metal nitrides are an important class of materials with applications as abrasives, semiconductors, superconductors, Li-ion conductors, and thermoelectrics. However, high oxidation states are difficult to attain as the oxidative potential of dinitrogen is limited by its high thermodynamic stability and chemical inertness. Here we present a versatile synthesis route using azide-mediated oxidation under pressure that is used to prepare the highly oxidised ternary nitride Ca4FeN4 containing Fe4+ ions. This nitridometallate features trigonal-planar [FeN3]5− anions with low-spin Fe4+ and antiferromagnetic ordering below a Neel temperature of 25 K, which are characterised by neutron diffraction, 57Fe-Mössbauer and magnetisation measurements. Azide-mediated high-pressure synthesis opens a way to the discovery of highly oxidised nitrides.


Metals ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 424
Author(s):  
Cuihua Zhao ◽  
Baishi Li ◽  
Xi Zhou ◽  
Jianhua Chen ◽  
Hongqun Tang

The electronic structures and optical properties of pure, Ag-doped and S-doped α-Fe2O3 were studied using density functional theory (DFT). The calculation results show that the structure of α-Fe2O3 crystal changes after Ag and S doping, which leads to the different points of the high symmetry of Ag-doped and S-doped α-Fe2O3 with that of pure α-Fe2O3 in the energy band, as well as different Brillouin paths. In addition, the band gap of α-Fe2O3 becomes smaller after Ag and S doping, and the optical absorption peak shifts slightly toward the short wavelength, with the increased peak strength of S/α-Fe2O3 and the decreased peak strength of Ag/α-Fe2O3. However, the optical absorption in the visible range is enhanced after Ag and S doping compared with that of pure α-Fe2O3 when the wavelength is greater than 380 nm, and the optical absorption of S-doped α-Fe2O3 is stronger than that of Ag-doped α-Fe2O3.


2015 ◽  
Vol 68 (4) ◽  
pp. 641 ◽  
Author(s):  
Struan J. W. Cummins ◽  
H. Putri Fraser ◽  
J. Robin Fulton ◽  
Martyn P. Coles ◽  
Christopher M. Fitchett

The β-ketoimine HC[MeC(O)][MeC(NHt-Bu)] (1H) (Me = methyl) was used as a ligand in the synthesis of organo-aluminium and gallium compounds. With Al, the NH functionality was deprotonated to form the N,O-chelating β-ketoiminate ligand in Al{HC[MeC(O)][MeC(Nt-Bu)]}Me2 (3) (t-Bu = tertiary butyl), whereas the neutral form coordinated to trimethylgallium via the oxygen atom to form the adduct GaMe3·{HC[MeC(O)][MeC(NHt-Bu)]} (4). Reaction of 1H with Ar†NH2 (Ar† = 2-t-BuC6H4) afforded the new N-aryl β-ketoimine HC[MeC(O)][MeC(NHAr†)] (2H), which reacted with Pd(OAc)2 (OAc = acetate = CH3CO2–) to afford the heteroleptic dimer {Pd[HC(MeC(O))(MeC(NAr†))](μ-OAc)}2 ([5]2). The homoleptic bis(β-ketoiminate) Pd{HC[MeC(O)][MeC(NAr†)]}2 (6) was isolated as a minor product of this reaction. The crystal structures of compounds 3, 4, [5]2, and 6 are reported.


1992 ◽  
Vol 11 (1) ◽  
pp. 192-195 ◽  
Author(s):  
Sally Brooker ◽  
Norbert Bertel ◽  
Dietmar Stalke ◽  
Mathias Noltemeyer ◽  
Herbert W. Roesky ◽  
...  

CrystEngComm ◽  
2018 ◽  
Vol 20 (3) ◽  
pp. 356-361 ◽  
Author(s):  
Xin Chen ◽  
Zhi-Yuan Yao ◽  
Chen Xue ◽  
Zhu-Xi Yang ◽  
Jian-Lan Liu ◽  
...  

For the first time, a main-group metal complex is used as a template for the formation of hybrid crystal structures and isomorphic hybrid crystals are obtained using transition and main-group metal complexes.


ChemInform ◽  
1988 ◽  
Vol 19 (45) ◽  
Author(s):  
H. W. ROESKY ◽  
B. MELLER ◽  
M. NOLTEMEYER ◽  
H.-G. SCHMIDT ◽  
U. SCHOLZ ◽  
...  

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