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Dive into the research topics where Diego P. dos Santos is active.

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Featured researches published by Diego P. dos Santos.


Journal of the American Chemical Society | 2012

Mapping the Energy Distribution of SERRS Hot Spots from Anti- Stokes to Stokes Intensity Ratios

Diego P. dos Santos; Marcia L. A. Temperini; Alexandre G. Brolo

The anomalies in the anti-Stokes to Stokes intensity ratios in single-molecule surface-enhanced resonance Raman scattering were investigated. Brilliant green and crystal violet dyes were the molecular probes, and the experiments were carried out on an electrochemically activated Ag surface. The results allowed new insights into the origin of these anomalies and led to a new method to confirm the single-molecule regime in surface-enhanced Raman scattering. Moreover, a methodology to estimate the distribution of resonance energies that contributed to the imbalance in the anti-Stokes to Stokes intensity ratios at the electromagnetic hot spots was proposed. This method allowed the local plasmonic resonance energies on the metallic surface to be spatially mapped.


ChemPhysChem | 2016

Detection of Plasmon Coupling between Silver Nanowires Based on Hyperspectral Darkfield and SERS Imaging and Supported by DDA Theoretical Calculations.

Jonnatan J. Santos; Evandro Ivanov; Diego P. dos Santos; Henrique E. Toma; Paola Corio

We report the unprecedented observation of plasmon coupling between silver nanowires, showing how the surface-enhanced Raman scattering depends upon this interaction and how the spectrum can be shaped by the hot spot. Such observations were accomplished by Raman spectroscopy mapping of silver nanowires modified with rhodamine. The local spectra on the hot spots were measured by darkfield hyperspectral microscopy, a powerful but uncommonly used technique that is capable of determining the location, structure, and spectra of the hot spots. The result obtained by the simulation of two parallel nanowires based on the discrete dipole approximation (DDA) method was in excellent agreement with the results obtained experimentally.


Journal of the Brazilian Chemical Society | 2015

Ultrafast Dynamics of Au Nanopyramid Interfaces Prepared by Nanosphere Lithography: Effect of Substrate Chemical Composition

Guilherme F. Ferbonink; E.R. Spada; Diego P. dos Santos; Maria L. Sartorelli; Rene A. Nome

This work describes ultrafast spectroscopy studies of Au triangular pyramid particle arrays deposited over glass (termed Au/glass), and 190 nm indium tin oxide (ITO) film (termed Au/ITO/glass) prepared by nanosphere lithography. The linear absorption spectra of Au/glass and Au/ITO/glass exhibit surface plasmon resonances at 800 and 870 nm, respectively, in good agreement with discrete dipole approximation simulations. Ultrafast pump-probe measurements at wavelengths below resonance, at resonance, and above the surface plasmon resonance for each of these two systems are presented. The pump-probe measurements on both systems can be well fit with a model accounting for electron-electron scattering, electron-phonon coupling, and acoustic oscillations on top of cooling of the gold lattice. Numerical simulations employing a two-temperature model are consistent with the single-color pump-probe exponential decays. The wavelength-dependent pump-probe results are interpreted in terms of the complex wavelength-dependent refractive index of gold. We show that this interpretation is consistent with diffractive-optic four-wave mixing spectroscopy measurements of absorptive and dispersive parts of the third-order nonlinear polarization at 800 nm.


Journal of Applied Physics | 2018

Enhanced reproducibility of planar perovskite solar cells by fullerene doping with silver nanoparticles

Marissa Higgins; Fernando Ely; Renata Nome; Rene A. Nome; Diego P. dos Santos; Hyunjoo Choi; Seungjin Nam; M. A. Quevedo-Lopez

A small cross-section of silver nanoparticles (AgNPs) placed at the rear-part of the solar cell avoids the parasitic absorption of the nanoparticles which is the biggest barrier for plasmonic structures when acting as photocurrent enhancers. Herein, we demonstrate p-i-n planar perovskite solar cells with the structure ITO/PEDOT:PSS/MAPbI3/PCBM/Ni:Au, where the PCBM electron extraction layer (EEL) was intentionally modified with variable amounts of AgNPs. The addition of small amounts of AgNPs (e.g., 5 wt. %) into the PCBM improved the overall reproducibility and reliability of the solar cell fabrication process after optimization. Plasmonic simulations suggest that any plasmonic-optical effects are relatively small compared to sample absorbance due to perovskite alone. It has been concluded that plasmonic-electrical effects play a major role in averaged performance improvement. Therefore, the addition of small AgNPs in low concentration to the EEL layer accounts for higher Jsc, Voc and FF as a result of a better perovskite coverage by the EEL and an improved charge carrier collection as evidenced by morphological and electrical analysis.A small cross-section of silver nanoparticles (AgNPs) placed at the rear-part of the solar cell avoids the parasitic absorption of the nanoparticles which is the biggest barrier for plasmonic structures when acting as photocurrent enhancers. Herein, we demonstrate p-i-n planar perovskite solar cells with the structure ITO/PEDOT:PSS/MAPbI3/PCBM/Ni:Au, where the PCBM electron extraction layer (EEL) was intentionally modified with variable amounts of AgNPs. The addition of small amounts of AgNPs (e.g., 5 wt. %) into the PCBM improved the overall reproducibility and reliability of the solar cell fabrication process after optimization. Plasmonic simulations suggest that any plasmonic-optical effects are relatively small compared to sample absorbance due to perovskite alone. It has been concluded that plasmonic-electrical effects play a major role in averaged performance improvement. Therefore, the addition of small AgNPs in low concentration to the EEL layer accounts for higher Jsc, Voc and FF as a result of a...


Journal of Physical Chemistry C | 2009

Electrochemical Control of the Time-Dependent Intensity Fluctuations in Surface-Enhanced Raman Scattering (SERS)

Diego P. dos Santos; Gustavo F. S. Andrade; Marcia L. A. Temperini; Alexandre G. Brolo


Journal of Physical Chemistry C | 2012

Side-by-Side Assembly of Gold Nanorods Reduces Ensemble-Averaged SERS Intensity

Anna Lee; Aftab Ahmed; Diego P. dos Santos; Neil Coombs; Jai Il Park; Reuven Gordon; Alexandre G. Brolo; Eugenia Kumacheva


Journal of Nanoscience and Nanotechnology | 2009

Using polycarbonate membranes as templates for the preparation of Au nanostructures for surface-enhanced Raman scattering.

E.A. Batista; Diego P. dos Santos; Gustavo F. S. Andrade; Antonio C. Sant'Ana; Alexandre G. Brolo; Marcia L. A. Temperini


Physical Chemistry Chemical Physics | 2015

Critical assessment of enhancement factor measurements in surface-enhanced Raman scattering on different substrates

Daniel C. Rodrigues; Michele L. de Souza; Klester S. Souza; Diego P. dos Santos; Gustavo F. S. Andrade; Marcia L. A. Temperini


Mikrochimica Acta | 2016

Fabrication of gold nanoparticle-coated paper and its use as a sensitive substrate for quantitative SERS analysis

Javier E.L. Villa; Diego P. dos Santos; Ronei J. Poppi


Journal of Physical Chemistry C | 2016

Single-Molecule Surface-Enhanced (Resonance) Raman Scattering (SE(R)RS) as a Probe for Metal Colloid Aggregation State

Diego P. dos Santos; Marcia L. A. Temperini; Alexandre G. Brolo

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Gustavo F. S. Andrade

Universidade Federal de Juiz de Fora

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Rene A. Nome

State University of Campinas

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Evandro Ivanov

University of São Paulo

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Javier E.L. Villa

State University of Campinas

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