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Density Functional Theory Study of Ligand Binding on CdSe (0001), (0001̄), and (112̄0) Single Crystal Relaxed and Reconstructed Surfaces: Implications for Nanocrystalline Growth
Abstract
To gain a better understanding of the influence of ligand-surface interactions on nanocrystalline growth, periodic density functional theory calculations were employed in the study of the binding of organic ligands on the relaxed nonpolar (1120) and polar Se terminated (0001) surfaces and the relaxed and vacancy and adatom reconstructed Cd terminated (0001) surface. We examined chemisorption properties of phosphine, amine, phosphine oxide, carboxylic acid, and phosphinic acid model ligands, including preferred binding sites and geometries, vibrational frequencies, and binding energetics, and compared findings to intrinsic growth via addition of CdSe molecules or Cd and Se atoms. Our results indicate that binding of the ligands is preferred in the electron-poor 1-fold sites on all surfaces, with secondary coordination of the acidic ligands through the hydroxyl hydrogen to the electron-rich surface sites. In general ligand adsorption directly obstructs binding sites for growth species on the (1120) surface and only indirectly on the two polar surfaces. The order of binding affinities on the (1120) and (0001) surfaces is PH(3) < OPH(3) approximately HCOOH < NH(3) < OPH(2)OH and that on the (0001) surface is OPH(3) approximately HCOOH < OPH(2)OH < NH(3) < PH(3). Our findings corroborate the experimental observation that incorporation of the nonbulky phosphinic acid-type ligands with high affinity and high selectivity for both the (1120) and (0001) surfaces strongly enhances unidirectional growth on the (0001) surface, while incorporation of either bulky ligands or ligands with moderate affinity does not. Higher affinity of all traditionally used ligands for the (1120) surface compared to the (0001) surface also suggests that new ligands should be engineered to achieve the synthesis of novel shapes that require preferential growth on the (1120) surface.
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Cites
Shape control of CdSe nanocrystals
Peng, X., Manna, L., Yang, W., Wickham, J., Scher, E., Kadavanich, A., & Alivisatos, A. P. (2000) · Nature · doi:10.1038/35003535 · Cited by 4,487
Dabbousi, B. O., Rodriguez-Viejo, J., Mikulec, F. V., Heine, J. R., Mattoussi, H., Ober, R., Jensen, K. F., & Bawendi, M. G. (1997) · The Journal of Physical Chemistry B · doi:10.1021/jp971091y · Cited by 4,229
Self-citationPerspectives on the Physical Chemistry of Semiconductor Nanocrystals
Alivisatos, A. P. (1996) · The Journal of Physical Chemistry · doi:10.1021/jp9535506 · Cited by 3,595
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Utilizing Self-Exchange To Address the Binding of Carboxylic Acid Ligands to CdSe Quantum Dots
Fritzinger, B., Capek, R. K., Lambert, K., Martins, J. C., & Hens, Z. (2010) · Journal of the American Chemical Society · doi:10.1021/ja104351q · Cited by 377
Binding of Phosphonic Acids to CdSe Quantum Dots: A Solution NMR Study
Gomes, R., Hassinen, A., Szczygiel, A., Zhao, Q., Vantomme, A., Martins, J. C., & Hens, Z. (2011) · The Journal of Physical Chemistry Letters · doi:10.1021/jz1016729 · Cited by 306
Effect of Surface Ligands on Optical and Electronic Spectra of Semiconductor Nanoclusters
Kilina, S., Ivanov, S., & Tretiak, S. (2009) · Journal of the American Chemical Society · doi:10.1021/ja9005749 · Cited by 277
Metadata
- Authors
- Rempel, J. Y., Trout, B. L., Bawendi, M. G., & Jensen, K. F.
- Venue
- The Journal of Physical Chemistry B
- Publisher
- American Chemical Society (ACS)
- Published
- 2006-08-23
- Volume
- 110
- Issue
- 36
- Pages
- 18007-18016
- ISSN
- 1520-5207 (ISSN-L)
- 1520-6106
- OpenAlex
- W2037013877
- Cited by
- 167
- References
- 3
- FWCI
- 4.77
- Type
- journal article
- Language
- en
- Open access
- closed
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