Bond and electronic relaxation dynamics of graphene, gold clusters, and water ice

Undercoordinated atoms and nonbonding electrons exist widely in nanomaterials and in network-structural materials with their impact under-estimated. Bonds around under-coordinated sites and nonbond lone pairs follow irregular relaxation dynamic rules with the rules remaining unclear. A quantum theor...

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Main Author: Zhang, Xi
Other Authors: Sun Changqing
Format: Theses and Dissertations
Language:English
Published: 2013
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Online Access:http://hdl.handle.net/10356/52459
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-524592023-07-04T16:49:45Z Bond and electronic relaxation dynamics of graphene, gold clusters, and water ice Zhang, Xi Sun Changqing School of Electrical and Electronic Engineering DRNTU::Science::Physics::Electricity and magnetism Undercoordinated atoms and nonbonding electrons exist widely in nanomaterials and in network-structural materials with their impact under-estimated. Bonds around under-coordinated sites and nonbond lone pairs follow irregular relaxation dynamic rules with the rules remaining unclear. A quantum theory was proposed to calculate the under-coordinated effects on the electronic structure of materials by incorporating bond order-length-strength (BOLS) correlation theory to tight-binding Hamiltonian (BOLS-TB), adopting mean-field Hubbard term to calculate the electron-electron interactions. Consistency between the BOLS-TB calculation and density functional theory (DFT) calculation on graphene nanoribbons (GNRs) verified that i) the physical origin of the band gap expansion lays in the enhancement of edge potentials and hopping integrals due to the shorter and stronger bonds between undercoordinated atoms; and ii) nonbond electrons at the edge of zigzag-edged GNRs and atomic vacancies accompanied with the broken bond contribute to the Dirac-Fermi polaron (DFP) with a local magnetic momentum; iii) the formation of triple bond at the edge of armchair-edged and reconstruct-edged GNRs annihilates the nonbond electron and prevent formation of DFPs. Size-dependent surface bond contraction, potential well depression, electron and energy entrapment and valence band polarization of Au nanoclusters and nanocages were also verified by DFT calculations and BOLS-TB analysis. Results of transition state calculations of the carbon monoxide oxidization confirmed that smaller clusters (Au13 and cage Au12) reduced the activation energy much more than larger clusters (Au55 and cage Au42), since the significantly red shift of the valence band of ultra-lowly coordinated clusters makes the valence 5d electrons ultra-highly catalytic. The hidden force opposing H2O compression behind the repulsion between nonbonding lone pair and bonding pair of hydrogen bond was revealed by theoretical analysis and molecular dynamics (MD) and ab initio MD calculations: i) the compression shortens and strengthens the intermolecular ‘‘O2- : H+/p’’ lone-pair and stretching phonons (<400 cm-1) are thus stiffened; ii) the repulsion pushes the bonding electron pair away from the H+/p and hence elongates and weakens the ‘‘H+/p–O2-” bond, making stretching phonons (>3000 cm-1) softened upon compression. Three springs model was proposed to build up the fundamental physical model of ‘‘O2- : H+/p–O2-” bond, in order to explain the complicated and anomalous behavior of water and ice. Current progress in bond relaxation dynamics around the under-coordinated sites and nonbond lone pairs paves a path to the mysteries of nanomaterials and net-work structural materials. Doctor of Philosophy (EEE) 2013-05-09T03:40:53Z 2013-05-09T03:40:53Z 2013 2013 Thesis http://hdl.handle.net/10356/52459 en 185 p. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic DRNTU::Science::Physics::Electricity and magnetism
spellingShingle DRNTU::Science::Physics::Electricity and magnetism
Zhang, Xi
Bond and electronic relaxation dynamics of graphene, gold clusters, and water ice
description Undercoordinated atoms and nonbonding electrons exist widely in nanomaterials and in network-structural materials with their impact under-estimated. Bonds around under-coordinated sites and nonbond lone pairs follow irregular relaxation dynamic rules with the rules remaining unclear. A quantum theory was proposed to calculate the under-coordinated effects on the electronic structure of materials by incorporating bond order-length-strength (BOLS) correlation theory to tight-binding Hamiltonian (BOLS-TB), adopting mean-field Hubbard term to calculate the electron-electron interactions. Consistency between the BOLS-TB calculation and density functional theory (DFT) calculation on graphene nanoribbons (GNRs) verified that i) the physical origin of the band gap expansion lays in the enhancement of edge potentials and hopping integrals due to the shorter and stronger bonds between undercoordinated atoms; and ii) nonbond electrons at the edge of zigzag-edged GNRs and atomic vacancies accompanied with the broken bond contribute to the Dirac-Fermi polaron (DFP) with a local magnetic momentum; iii) the formation of triple bond at the edge of armchair-edged and reconstruct-edged GNRs annihilates the nonbond electron and prevent formation of DFPs. Size-dependent surface bond contraction, potential well depression, electron and energy entrapment and valence band polarization of Au nanoclusters and nanocages were also verified by DFT calculations and BOLS-TB analysis. Results of transition state calculations of the carbon monoxide oxidization confirmed that smaller clusters (Au13 and cage Au12) reduced the activation energy much more than larger clusters (Au55 and cage Au42), since the significantly red shift of the valence band of ultra-lowly coordinated clusters makes the valence 5d electrons ultra-highly catalytic. The hidden force opposing H2O compression behind the repulsion between nonbonding lone pair and bonding pair of hydrogen bond was revealed by theoretical analysis and molecular dynamics (MD) and ab initio MD calculations: i) the compression shortens and strengthens the intermolecular ‘‘O2- : H+/p’’ lone-pair and stretching phonons (<400 cm-1) are thus stiffened; ii) the repulsion pushes the bonding electron pair away from the H+/p and hence elongates and weakens the ‘‘H+/p–O2-” bond, making stretching phonons (>3000 cm-1) softened upon compression. Three springs model was proposed to build up the fundamental physical model of ‘‘O2- : H+/p–O2-” bond, in order to explain the complicated and anomalous behavior of water and ice. Current progress in bond relaxation dynamics around the under-coordinated sites and nonbond lone pairs paves a path to the mysteries of nanomaterials and net-work structural materials.
author2 Sun Changqing
author_facet Sun Changqing
Zhang, Xi
format Theses and Dissertations
author Zhang, Xi
author_sort Zhang, Xi
title Bond and electronic relaxation dynamics of graphene, gold clusters, and water ice
title_short Bond and electronic relaxation dynamics of graphene, gold clusters, and water ice
title_full Bond and electronic relaxation dynamics of graphene, gold clusters, and water ice
title_fullStr Bond and electronic relaxation dynamics of graphene, gold clusters, and water ice
title_full_unstemmed Bond and electronic relaxation dynamics of graphene, gold clusters, and water ice
title_sort bond and electronic relaxation dynamics of graphene, gold clusters, and water ice
publishDate 2013
url http://hdl.handle.net/10356/52459
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