Promises of Main-Group Metal Chalcogenide-Based Broken-Gap van der Waals Heterojunctions for Tunneling Field Effect Transistors

2021 ◽  
Vol 3 (2) ◽  
pp. 898-904
Author(s):  
Shengying Xie ◽  
Hao Jin ◽  
Jianwei Li ◽  
Yadong Wei
Keyword(s):  
Field Effect ◽  
Field Effect Transistors ◽  
Van Der Waals ◽  
Main Group ◽  
Metal Chalcogenide ◽  
Group Metal ◽  
Main Group Metal ◽  
Tunneling Field Effect Transistors ◽  
Broken Gap

Cationic Main-Group Metal Chalcogenide with a 1-D Polymeric Structure, [{In(dien)}2(InTe4)]·Cl

2008 ◽  
Vol 47 (19) ◽  
pp. 8586-8588 ◽  
Author(s):  
Chun-Ying Li ◽  
Xiao-Xia Chen ◽  
Jian Zhou ◽  
Qin-Yu Zhu ◽  
Zhi-Xin Lei ◽  
...  
Keyword(s):  
Main Group ◽  
Metal Chalcogenide ◽  
Polymeric Structure ◽  
Group Metal ◽  
Main Group Metal

ChemInform Abstract: Cationic Main-Group Metal Chalcogenide with a 1-D Polymeric Structure, [{In(dien)}2(InTe4)]×Cl.

ChemInform ◽  
2008 ◽  
Vol 39 (51) ◽  
Author(s):  
Chun-Ying Li ◽  
Xiao-Xia Chen ◽  
Jian Zhou ◽  
Qin-Yu Zhu ◽  
Zhi-Xin Lei ◽  
...  
Keyword(s):  
Main Group ◽  
Metal Chalcogenide ◽  
Polymeric Structure ◽  
Group Metal ◽  
Main Group Metal

Reversible Addition of Carbon Dioxide to Main Group Metal Complexes at Temperatures about 0 °C

2021 ◽  
Author(s):  
Tatyana S. Koptseva ◽  
Vladimir G. Sokolov ◽  
Sergey Yu. Ketkov ◽  
Elena A. Rychagova ◽  
Anton V. Cherkasov ◽  
...  
Keyword(s):  
Carbon Dioxide ◽  
Metal Complexes ◽  
Main Group ◽  
Group Metal ◽  
Reversible Addition ◽  
Main Group Metal

Effect of delocalization of nonbonding electron density on the stability of the M–Ccarbene bond in main group metal-imidazol-2-ylidene complexes: a computational and structural database study

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Samuel Tetteh ◽  
Albert Ofori
Keyword(s):  
Electron Density ◽  
Lone Pair ◽  
Main Group ◽  
Binding Energies ◽  
Electrostatic Model ◽  
Group Metal ◽  
Main Group Metal ◽  
Structural Database ◽  
The Stability ◽  
Lone Pair Electrons

Abstract The M–Ccarbene bond in metal (M) complexes involving the imidazol-2-ylidene (Im) ligand has largely been described using the σ-donor only model with donation of σ electrons from the sp-hybridized orbital of the carbene carbon into vacant orbitals on the metal centre. Analyses of the M–Ccarbene bond in a series of group IA, IIA and IIIA main group metal complexes show that the M-Im interactions are mostly electrostatic with the M–Ccarbene bond distances greater than the sum of the respective covalent radii. Estimation of the binding energies of a series of metal hydride/fluoride/chloride imidazol-2-ylidene complexes revealed that the stability of the M–Ccarbene bond in these complexes is not always commensurate with the σ-only electrostatic model. Further natural bond orbital (NBO) analyses at the DFT/B3LYP level of theory revealed substantial covalency in the M–Ccarbene bond with minor delocalization of electron density from the lone pair electrons on the halide ligands into antibonding molecular orbitals on the Im ligand. Calculation of the thermodynamic stability of the M–Ccarbene bond showed that these interactions are mostly endothermic in the gas phase with reduced entropies giving an overall ΔG > 0.

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