Energetics at the Edge: Direct Optical Mapping of Bulk and Interfacial Electronic Structure in CdSe Quantum Dots using Broadband Electronic Sum Frequency Generation Microspectroscopy

2019 ◽  
Author(s):  
Brianna R. Watson ◽  
Benjamin Doughty ◽  
Tessa Calhoun

Understanding and controlling the electronic structure of nanomaterials is the key to tailoring their use in a wide range of practical applications. Despite this need, many important electronic states are invisible to conventional optical measurements and are typically identified indirectly based on their inferred impact on luminescence properties. This is especially common and important in the study of nanomaterial surfaces and their associated defects. Surface trap states play a crucial role in photophysical processes yet remain remarkably poorly understood. Here we demonstrate for the first time that broadband electronic sum frequency generation (eSFG) microspectroscopy can directly map the optically bright and dark states of nanoparticles, including the elusive below gap states. This new approach is applied to model cadmium selenide (CdSe) quantum dots (QDs), where the energies of interfacial trap states have eluded direct optical characterization for decades. Our eSFG measurements show clear signatures of electronic transitions both above the band gap, which we assign to previously reported one- and two-photon transitions associated with the CdSe core, as well as broad spectral signatures below the bandgap that are attributed to interfacial trap states. In addition to the core states, this analysis reveals two distinct distributions of below gap states providing the first direct optical measurement of both shallow and deep trapping sites on this system. Finally, chemical modification of the surfaces via oxidation results in the relative increase in the signals originating from the interfacial trap states. Overall, our eSFG experiments provide an avenue to directly map the entirety of QD bulk and interfacial electronic structure, which is expected to open up opportunities to study how these materials are grown <i>in situ</i> and how surface states can be controlled to tune functionality.

2019 ◽  
Author(s):  
Brianna R. Watson ◽  
Benjamin Doughty ◽  
Tessa Calhoun

Understanding and controlling the electronic structure of nanomaterials is the key to tailoring their use in a wide range of practical applications. Despite this need, many important electronic states are invisible to conventional optical measurements and are typically identified indirectly based on their inferred impact on luminescence properties. This is especially common and important in the study of nanomaterial surfaces and their associated defects. Surface trap states play a crucial role in photophysical processes yet remain remarkably poorly understood. Here we demonstrate for the first time that broadband electronic sum frequency generation (eSFG) microspectroscopy can directly map the optically bright and dark states of nanoparticles, including the elusive below gap states. This new approach is applied to model cadmium selenide (CdSe) quantum dots (QDs), where the energies of interfacial trap states have eluded direct optical characterization for decades. Our eSFG measurements show clear signatures of electronic transitions both above the band gap, which we assign to previously reported one- and two-photon transitions associated with the CdSe core, as well as broad spectral signatures below the bandgap that are attributed to interfacial trap states. In addition to the core states, this analysis reveals two distinct distributions of below gap states providing the first direct optical measurement of both shallow and deep trapping sites on this system. Finally, chemical modification of the surfaces via oxidation results in the relative increase in the signals originating from the interfacial trap states. Overall, our eSFG experiments provide an avenue to directly map the entirety of QD bulk and interfacial electronic structure, which is expected to open up opportunities to study how these materials are grown <i>in situ</i> and how surface states can be controlled to tune functionality.


Materials ◽  
2018 ◽  
Vol 11 (11) ◽  
pp. 2266
Author(s):  
Dismas Choge ◽  
Huaixi Chen ◽  
Lei Guo ◽  
Guangwei Li ◽  
Wanguo Liang

In this study, simultaneous second-harmonic generation (SHG), sum frequency generation (SFG), and Raman conversion based on MgO-doped periodically poled lithium niobate (MgO:PPLN) for multi-wavelength generation is demonstrated. The approach used is based on a single MgO:PPLN crystal poled with a uniform period of 10.2 µm that phase matches SHG and SFG, simultaneously. Using a simplified double-pass geometry, up to 0.8 W of blue light at 487 nm is achieved by a frequency-doubling 974 nm laser diode pump, and 0.5 W of orange light at 598 nm is generated by frequency mixing 974 nm pump with C-band (1527–1565 nm) tunable laser source. At high pump powers of the 974 nm laser source, other unexpected peaks at 437, 536, 756, 815 and 1038 nm were observed, of which the 1038 nm line is due to Stimulated Raman Scattering within the MgO:PPLN crystal. The resulting multi-wavelength light source may find a wide range of applications in biomedicine and basic research.


2016 ◽  
Vol 16 (7) ◽  
pp. 763-771
Author(s):  
M. Abdullah ◽  
Farah T. Mohammed Noori ◽  
Amin H. Al-Khursan

Symmetry ◽  
2021 ◽  
Vol 13 (2) ◽  
pp. 294
Author(s):  
Thomas Noblet ◽  
Laurent Dreesen ◽  
Abderrahmane Tadjeddine ◽  
Christophe Humbert

Given the tunability of their optical properties over the UV–Visible–Near IR spectral range, ligand-capped quantum dots (QDs) are employed for the design of optical biosensors with low detection threshold. Thanks to non-linear optical spectroscopies, the absorption properties of QDs are indeed used to selectively enhance the local vibrational response of molecules located in their vicinity. Previous studies led to assume the existence of a vibroelectronic QD–molecule coupling based on dipolar interaction. However, no systematic study on the strength of this coupling has been performed to date. In order to address this issue, we use non-linear optical Two-Color Sum-Frequency Generation (2C-SFG) spectroscopy to probe thick QD layers deposited on calcium fluoride (CaF2) prisms previously functionalized by a self-assembled monolayer of phenyltriethoxysilane (PhTES) molecules. Here, 2C-SFG is performed in Attenuated Total Reflection (ATR) configuration. By comparing the molecular vibrational enhancement measured for QD–ligand coupling and QD–PhTES coupling, we show that the spatial dependence of the QD–molecule interactions (∼1/r3, with r the QD–molecule distance) is in agreement with the hypothesis of a dipole–dipole interaction.


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