AVS 65th International Symposium & Exhibition
    Electronic Materials and Photonics Division Tuesday Sessions
       Session EM+2D+AN+MI+MP+NS-TuA

Paper EM+2D+AN+MI+MP+NS-TuA12
Investigation of Localized Electronic structures of PbSe Quantum Dot Superlattice on a Highly Oriented Pyrolytic Graphite (HOPG)

Tuesday, October 23, 2018, 6:00 pm, Room 101A

Session: Solar/Energy Harvesting and Quantum Materials and Applications
Presenter: Il Jo Kwak, University of California at San Diego
Authors: I.J. Kwak, University of California at San Diego
S. Ueda, University of California at San Diego
A. Abelson, University of California, Irvine
C. Qian, University of California, Irvine
M. Law, University of California, Irvine
A.C. Kummel, University of California at San Diego
Correspondent: Click to Email

Lead-Chalcogenide quantum dots are of interest due to the facility of adjustment of their electrical and optical properties. Using a colloidal self-assembly technique, extended arrays of nanocrystal QDs superlattices can be generated. The quantum confinement within individual QDs in the superlattice is relaxed and delocalization of wave functions occurs due to coupling of the QDs. In the QD solids, bulk-like electronic bands with a bandwidth of 100~200 meV are expected to form which yield much higher carrier mobility and diffusion length compared to weakly-coupled QDs; however, the electronic properties of such highly ordered QD arrays are not fully understood. The local density of state of a highly ordered monolayer PdSe superlattice was investigated by low temperature scanning tunneling microscopy.

A monolayer of PbSe QDs was prepared using the Langmuir Schaefer deposition technique. First, oleate-capped PbSe QDs dispersed in hexane were drop casted onto diethylene glycol surface. After the hexane was evaporated, a (111) in-plane oriented polycrystalline FCC superlattice was formed on the diethylene glycol surface. NH4SCN solution was applied onto the oleate-capped PbSe superlattice film. The injection of NH4SCN initiates the ligand exchange and phase transformation from an FCC to a simple cubic structure superlattice. A monolayer QD superlattice was prepared on a HOPG substrate. Afterward, the HOPG sample was loaded into a commercial UHV scanning tunneling microscopy chamber with a base pressure of 1x10-10torr. The sample was annealed to remove hydrocarbons and ligands from the surface. The topography of the QDs was observed with a tungsten tip. The STM images were acquired in constant current mode.

STM imaging showed the PbSe QD monolayer had 4-fold symmetry with an average inter QD spacing of 7nm. It is also found the height fluctuation of the QDs was 1nm indicating size variation of the QDs and imperfect crystal structure of the superlattice. Scanning tunneling spectroscopy was performed to investigate the electronic structure of the PdSe QDs using a variable z-mode with an external lock-in amplifier in the bias range of -2 to 2V. Single site STS showed resonant peaks from molecular orbitals of QDs before the ligand exchange process; however, the peaks were not observed after the ligand exchange due to necking between the QDs in the superlattice. In addition, the size of band gap was decreased as increasing the number of nearest neighboring QDs due to necking between QDs. Layer 2 QDs showed more p-type behavior than layer 1 QDs possibly due to the band bending effect at the interface of HOPG and QD superlattice.