Abstract
Hypothesis: Controlling nanomaterial interfaces for emerging technologies has driven the need to understand the molecular species located there; however, challenges arise using traditional analytical techniques to directly characterize the molecular structure and local environments of these interfacial species due to their low relative populations. We hypothesized that vibrational sum frequency generation (vSFG) spectroscopy would be uniquely sensitive to the chemical modification of nanoparticle surfaces that is obscured using traditional bulk sensitive methods. Experiments: Octadecylamine ligands were removed from model CdSe quantum dot surfaces using a common precipitation-resuspension procedure with polar protic and aprotic nonsolvents. Vibrational spectra of the ligands at the surface were collected with vSFG to directly probe the ligand ordering and coverage. Photoluminescence (PL), optical absorption, NMR, and mass spectrometry measurements were conducted for comparison. Findings: vSFG was found to be sensitive to subtle changes in ligand disorder over multiple precipitation-resuspension washes, and a limit to the number of ligand molecules removed from the surface and subsequent amount of disorder introduced to their packing was clearly observed. We also find that nonsolvents do not remain associated with the surface after washing.
Original language | English |
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Pages (from-to) | 389-395 |
Number of pages | 7 |
Journal | Journal of Colloid and Interface Science |
Volume | 537 |
DOIs | |
State | Published - Mar 1 2019 |
Funding
T.R.C. and B.R.W.'s research was supported by the University of Tennessee, Knoxville. B.D. was sponsored by the Laboratory Directed Research and Development Program of Oak Ridge National Laboratory, managed by UT-Battelle, LLC, for the U.S. Department of Energy. Y.-Z. M. and J.F.C. were supported by the U.S. Department of Energy, Office of Science, Basic Energy Sciences, Chemical Sciences, Geosciences, and Biosciences Division. The QTRAP® 5500 mass spectrometer used in this work were provided on loan by SCIEX through a Cooperative Research and Development Agreement (CRADA NFE-10-02966). The authors also acknowledge Dr. Carlos A. Steren for his assistance collecting and interpreting the NMR data. T.R.C. and B.R.W.’s research was supported by the University of Tennessee, Knoxville. B.D. was sponsored by the Laboratory Directed Research and Development Program of Oak Ridge National Laboratory , managed by UT-Battelle, LLC, for the U.S. Department of Energy. Y.-Z. M. and J.F.C. were supported by the U.S. Department of Energy , Office of Science , Basic Energy Sciences , Chemical Sciences, Geosciences, and Biosciences Division . The QTRAP® 5500 mass spectrometer used in this work were provided on loan by SCIEX through a Cooperative Research and Development Agreement ( CRADA NFE-10-02966 ). The authors also acknowledge Dr. Carlos A. Steren for his assistance collecting and interpreting the NMR data.
Funders | Funder number |
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U.S. Department of Energy | |
Office of Science | |
Basic Energy Sciences | |
Oak Ridge National Laboratory | |
Laboratory Directed Research and Development | |
University of Tennessee | |
SCIEX | CRADA NFE-10-02966 |
Chemical Sciences, Geosciences, and Biosciences Division |
Keywords
- Molecular ordering
- Nonlinear spectroscopy
- Surface analysis
- Vibrational spectroscopy