John B. Asbury , Pennsylvania State University
The approach permits us to elucidate the interactions of molecular ligands with colloidal quantum dot surfaces through the vibrational spectra of the ligands and to simultaneously establish the corresponding charge trap energies and densities associated with the ligands. We obtain molecular information about ligand-nanocrystal interactions giving rise to trap states by observing transient vibrational spectra of ligands that are perturbed by the localization of charge in surface trap states. We observe transient bleach spectra corresponding to the spectra of ligands in their neutral states (negative-going narrow features) and simultaneously measure transient absorption spectra of the ligands that are perturbed by the change in charge distribution associated with the charge trapping event. These narrow vibrational features are superimposed onto a broad electronic transition that we have shown results from excitation of trapped charges back into delocalized core states of the nanocrystal. Thus, the spectrum of the electronic transition provides information about the charge trap depth. The combination of information about molecular interactions at quantum dot surfaces and the corresponding electronic properties arising from those interactions provides a new tool to understand how ligand-nanocrystal interactions determine the electronic properties of nanocrystalline materials.
Having developed the technique, we began collaborating with a leader in the colloidal quantum dot solar cell field, Edward H. Sargent, and together have made significant strides toward understanding how molecular interactions of ligands with quantum dot surfaces influence the electronic properties of devices. Our work has led to development of world-record power conversion efficiency colloidal quantum dot solar cells recently reported in Nature Materials (2011).