http://scholar.google.com/citations?hl=en&user=95SvbM8AAAAJ
1.
Lagos, Maureen J; Sato, Fernando; Galvao, Douglas S; Ugarte, Daniel
Mechanical deformation of nanoscale metal rods: when size and shape matter Journal Article
Em: Physical Review Letters, vol. 106, não 5, pp. 055501, 2011.
@article{lagos2011mechanical,
title = {Mechanical deformation of nanoscale metal rods: when size and shape matter},
author = {Lagos, Maureen J and Sato, Fernando and Galvao, Douglas S and Ugarte, Daniel},
url = {http://journals.aps.org/prl/abstract/10.1103/PhysRevLett.106.055501},
year = {2011},
date = {2011-01-01},
journal = {Physical Review Letters},
volume = {106},
number = {5},
pages = {055501},
publisher = {American Physical Society},
abstract = {Face centered cubic metals deform mainly by propagating partial dislocations generating planar fault ribbons. How do metals deform if the size is smaller than the fault ribbons? We studied the elongation of Au and Pt nanorods by in situ electron microscopy and ab initio calculations. Planar fault activation barriers are so low that, for each temperature, a minimal rod size is required to become active for releasing elastic energy. Surface effects dominate deformation energetics; system size and shape determine the preferred fault gliding directions which induce different tensile and compressive behavior.
},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Face centered cubic metals deform mainly by propagating partial dislocations generating planar fault ribbons. How do metals deform if the size is smaller than the fault ribbons? We studied the elongation of Au and Pt nanorods by in situ electron microscopy and ab initio calculations. Planar fault activation barriers are so low that, for each temperature, a minimal rod size is required to become active for releasing elastic energy. Surface effects dominate deformation energetics; system size and shape determine the preferred fault gliding directions which induce different tensile and compressive behavior.
2.
Caetano, Ewerton WS; Freire, Valder N; dos Santos, Sergio G; Albuquerque, EL; Galvao, Douglas S; Sato, Fernando
Defects in Graphene-Based Twisted Nanoribbons: Structural, Electronic, and Optical Properties Journal Article
Em: Langmuir, vol. 25, não 8, pp. 4751–4759, 2009.
@article{caetano2009defects,
title = {Defects in Graphene-Based Twisted Nanoribbons: Structural, Electronic, and Optical Properties},
author = {Caetano, Ewerton WS and Freire, Valder N and dos Santos, Sergio G and Albuquerque, EL and Galvao, Douglas S and Sato, Fernando},
url = {http://pubs.acs.org/doi/abs/10.1021/la803929f},
year = {2009},
date = {2009-01-01},
journal = {Langmuir},
volume = {25},
number = {8},
pages = {4751--4759},
publisher = {ACS Publications},
abstract = {We present some computational simulations of graphene-based nanoribbons with a number of half-twists varying from 0 to 4 and two types of defects obtained by removing a single carbon atom from two different sites. Optimized geometries are found by using a mix of classical quantum semiempirical computations. According with the simulations results, the local curvature of the nanoribbons increases at the defect sites, especially for a higher number of half-twists. The HOMO−LUMO energy gap of the nanostructures has significant variation when the number of half-twists increases for the defective nanoribbons. At the quantum semiempirical level, the first optically active transitions and oscillator strengths are calculated using the full configuration interaction (CI) framework, and the optical absorption in the UV/vis range (electronic transitions) and in the infrared (vibrational transitions) are achieved. Distinct nanoribbons show unique spectral signatures in the UV/vis range, with the first absorption peaks in wavelengths ranging from the orange to the violet. Strong absorption is observed in the ultraviolet region, although differences in their infrared spectra are hardly discernible.},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
We present some computational simulations of graphene-based nanoribbons with a number of half-twists varying from 0 to 4 and two types of defects obtained by removing a single carbon atom from two different sites. Optimized geometries are found by using a mix of classical quantum semiempirical computations. According with the simulations results, the local curvature of the nanoribbons increases at the defect sites, especially for a higher number of half-twists. The HOMO−LUMO energy gap of the nanostructures has significant variation when the number of half-twists increases for the defective nanoribbons. At the quantum semiempirical level, the first optically active transitions and oscillator strengths are calculated using the full configuration interaction (CI) framework, and the optical absorption in the UV/vis range (electronic transitions) and in the infrared (vibrational transitions) are achieved. Distinct nanoribbons show unique spectral signatures in the UV/vis range, with the first absorption peaks in wavelengths ranging from the orange to the violet. Strong absorption is observed in the ultraviolet region, although differences in their infrared spectra are hardly discernible.
3.
Rodrigues, Varlei; Sato, Fernando; Galvao, Douglas S; Ugarte, Daniel
Is Small Perfect? Size Limit to Defect Formation in Pyramidal Pt Nanocontacts Journal Article
Em: arXiv preprint arXiv:0707.4187, 2007.
@article{rodrigues2007small,
title = {Is Small Perfect? Size Limit to Defect Formation in Pyramidal Pt Nanocontacts},
author = {Rodrigues, Varlei and Sato, Fernando and Galvao, Douglas S and Ugarte, Daniel},
url = {http://xxx.tau.ac.il/abs/0707.4187},
year = {2007},
date = {2007-01-01},
journal = {arXiv preprint arXiv:0707.4187},
abstract = {We report high resolution transmission electron microscopy and ab initio calculation results for the defect formation in Pt nanocontacts (NCs). Our results show that there is a size limit to the existence of twins (extended structural defects). Defects are always present but blocked away from the tip axes. The twins may act as scattering plane, influencing contact electron transmission for Pt NC at room temperature and Ag/Au NC at low temperature.},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
We report high resolution transmission electron microscopy and ab initio calculation results for the defect formation in Pt nanocontacts (NCs). Our results show that there is a size limit to the existence of twins (extended structural defects). Defects are always present but blocked away from the tip axes. The twins may act as scattering plane, influencing contact electron transmission for Pt NC at room temperature and Ag/Au NC at low temperature.
2011
3.
Lagos, Maureen J; Sato, Fernando; Galvao, Douglas S; Ugarte, Daniel
Mechanical deformation of nanoscale metal rods: when size and shape matter Journal Article
Em: Physical Review Letters, vol. 106, não 5, pp. 055501, 2011.
Resumo | Links | BibTeX | Tags: Defects, DFT, Mechanical Properties, Metallic Nanowires
@article{lagos2011mechanical,
title = {Mechanical deformation of nanoscale metal rods: when size and shape matter},
author = {Lagos, Maureen J and Sato, Fernando and Galvao, Douglas S and Ugarte, Daniel},
url = {http://journals.aps.org/prl/abstract/10.1103/PhysRevLett.106.055501},
year = {2011},
date = {2011-01-01},
journal = {Physical Review Letters},
volume = {106},
number = {5},
pages = {055501},
publisher = {American Physical Society},
abstract = {Face centered cubic metals deform mainly by propagating partial dislocations generating planar fault ribbons. How do metals deform if the size is smaller than the fault ribbons? We studied the elongation of Au and Pt nanorods by in situ electron microscopy and ab initio calculations. Planar fault activation barriers are so low that, for each temperature, a minimal rod size is required to become active for releasing elastic energy. Surface effects dominate deformation energetics; system size and shape determine the preferred fault gliding directions which induce different tensile and compressive behavior.
},
keywords = {Defects, DFT, Mechanical Properties, Metallic Nanowires},
pubstate = {published},
tppubtype = {article}
}
Face centered cubic metals deform mainly by propagating partial dislocations generating planar fault ribbons. How do metals deform if the size is smaller than the fault ribbons? We studied the elongation of Au and Pt nanorods by in situ electron microscopy and ab initio calculations. Planar fault activation barriers are so low that, for each temperature, a minimal rod size is required to become active for releasing elastic energy. Surface effects dominate deformation energetics; system size and shape determine the preferred fault gliding directions which induce different tensile and compressive behavior.
2009
2.
Caetano, Ewerton WS; Freire, Valder N; dos Santos, Sergio G; Albuquerque, EL; Galvao, Douglas S; Sato, Fernando
Defects in Graphene-Based Twisted Nanoribbons: Structural, Electronic, and Optical Properties Journal Article
Em: Langmuir, vol. 25, não 8, pp. 4751–4759, 2009.
Resumo | Links | BibTeX | Tags: Defects, Mobius, NanoRibbons, Twisting
@article{caetano2009defects,
title = {Defects in Graphene-Based Twisted Nanoribbons: Structural, Electronic, and Optical Properties},
author = {Caetano, Ewerton WS and Freire, Valder N and dos Santos, Sergio G and Albuquerque, EL and Galvao, Douglas S and Sato, Fernando},
url = {http://pubs.acs.org/doi/abs/10.1021/la803929f},
year = {2009},
date = {2009-01-01},
journal = {Langmuir},
volume = {25},
number = {8},
pages = {4751--4759},
publisher = {ACS Publications},
abstract = {We present some computational simulations of graphene-based nanoribbons with a number of half-twists varying from 0 to 4 and two types of defects obtained by removing a single carbon atom from two different sites. Optimized geometries are found by using a mix of classical quantum semiempirical computations. According with the simulations results, the local curvature of the nanoribbons increases at the defect sites, especially for a higher number of half-twists. The HOMO−LUMO energy gap of the nanostructures has significant variation when the number of half-twists increases for the defective nanoribbons. At the quantum semiempirical level, the first optically active transitions and oscillator strengths are calculated using the full configuration interaction (CI) framework, and the optical absorption in the UV/vis range (electronic transitions) and in the infrared (vibrational transitions) are achieved. Distinct nanoribbons show unique spectral signatures in the UV/vis range, with the first absorption peaks in wavelengths ranging from the orange to the violet. Strong absorption is observed in the ultraviolet region, although differences in their infrared spectra are hardly discernible.},
keywords = {Defects, Mobius, NanoRibbons, Twisting},
pubstate = {published},
tppubtype = {article}
}
We present some computational simulations of graphene-based nanoribbons with a number of half-twists varying from 0 to 4 and two types of defects obtained by removing a single carbon atom from two different sites. Optimized geometries are found by using a mix of classical quantum semiempirical computations. According with the simulations results, the local curvature of the nanoribbons increases at the defect sites, especially for a higher number of half-twists. The HOMO−LUMO energy gap of the nanostructures has significant variation when the number of half-twists increases for the defective nanoribbons. At the quantum semiempirical level, the first optically active transitions and oscillator strengths are calculated using the full configuration interaction (CI) framework, and the optical absorption in the UV/vis range (electronic transitions) and in the infrared (vibrational transitions) are achieved. Distinct nanoribbons show unique spectral signatures in the UV/vis range, with the first absorption peaks in wavelengths ranging from the orange to the violet. Strong absorption is observed in the ultraviolet region, although differences in their infrared spectra are hardly discernible.
2007
1.
Rodrigues, Varlei; Sato, Fernando; Galvao, Douglas S; Ugarte, Daniel
Is Small Perfect? Size Limit to Defect Formation in Pyramidal Pt Nanocontacts Journal Article
Em: arXiv preprint arXiv:0707.4187, 2007.
Resumo | Links | BibTeX | Tags: Defects, DFT, Metallic Nanowires, Structure, TEM
@article{rodrigues2007small,
title = {Is Small Perfect? Size Limit to Defect Formation in Pyramidal Pt Nanocontacts},
author = {Rodrigues, Varlei and Sato, Fernando and Galvao, Douglas S and Ugarte, Daniel},
url = {http://xxx.tau.ac.il/abs/0707.4187},
year = {2007},
date = {2007-01-01},
journal = {arXiv preprint arXiv:0707.4187},
abstract = {We report high resolution transmission electron microscopy and ab initio calculation results for the defect formation in Pt nanocontacts (NCs). Our results show that there is a size limit to the existence of twins (extended structural defects). Defects are always present but blocked away from the tip axes. The twins may act as scattering plane, influencing contact electron transmission for Pt NC at room temperature and Ag/Au NC at low temperature.},
keywords = {Defects, DFT, Metallic Nanowires, Structure, TEM},
pubstate = {published},
tppubtype = {article}
}
We report high resolution transmission electron microscopy and ab initio calculation results for the defect formation in Pt nanocontacts (NCs). Our results show that there is a size limit to the existence of twins (extended structural defects). Defects are always present but blocked away from the tip axes. The twins may act as scattering plane, influencing contact electron transmission for Pt NC at room temperature and Ag/Au NC at low temperature.
