References cited

Li, Q. Y.; Yang S.; Tang, Y.; et al.; Asymmetric Hybridization Orbitals at the Charged Interface Initiates New Surface Reactions: A Quantum Mechanics Exploration. J. Phys. Chem. C 2019, 123, 25278−25285.

期刊名:The journal of physical chemistry, C. Nanomaterials and interfaces

题目:Asymmetric Hybridization Orbitals at the Charged Interface Initiates New Surface Reactions: A Quantum Mechanics Exploration

作者:Li, Qnyi;Yang, Sen;Tang, Ying;Yang, Gang;Li, Hang

摘要:Although the first report of Hofmeister effects is more than 130 years old, the origins of the Hofmeister series remain debated. In this study, quantum mechanics (QM) analyses, dispersion-corrected p-DFT calculations, and dynamic light scattering (DLS) determinations are combined with the aim to unravel such a scientific basis. QM analyses show that asymmetric hybridization occurs for the outer-shell nsnp(z) orbitals at charged interfaces, and the asymmetric spz hybridization further initiates two unique processes for the interfacial ions: unusual polarization with a greatly enlarged polarizability and a new type covalent bonding of surface reactions with the asymmetric spz hybridization. The asymmetric hybridization theory is then applied and verified by surface reactions of K+ and Na+ with the charged montmorillonite surface. As predicted by QM analyses, p-DFT calculations show that, under no or low electric fields, the covalent bonding does not exist for both Na+ and K+, while under strong electric fields, covalent bonding is produced for K+ with surface-O atoms but remains absent for Na+. Also, as predicted by QM analyses, the DLS results confirm that the interfacial Na+ reactions are governed by two forces, as Coulomb interaction and unusual polarization, while in addition to these two forces (unusual polarization of K+ is 2.067 times as that of Na+), covalent bonding emerges for the interfacial and plays a dominant role. This study provides new scientific bases of Hofmeister effects at the subatomic level, which is of critical importance in both physical and biological systems.

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