Colloidal CdSe Nanoplatelets, A Model for Surface Chemistry/Optoelectronic Property Relations in Semiconductor Nanocrystals.

While the surface termination of quasi-spherical metal chalcogenide nanocrystals or quantum dots has been widely investigated, it remains unclear whether the ensuing surface chemistry models apply to similar nanocrystals with anisotropic shapes. In this work, we report on the surface-chemistry of 2D CdSe nanoplatelets, where we make use of an improved synthesis strategy that yields stable and aggregation free nanoplatelet suspensions with a photoluminescence quantum yield as high as 55%. We confirm that such nanoplatelets are enriched in Cd and, by means of 1H nuclear magnetic resonance spectroscopy, we show that the Cd-rich surface is terminated by X-type carboxylate ligands. Not unlike CdSe quantum dots (QDs), entire cadmium carboxylate entities can be displaced by the addition of amines, and the desorption isotherm points toward a considerable binding site heterogeneity. Moreover, we find that even the slightest displacement of cadmium carboxylate ligands quenches the nanoplatelet photoluminescence. These experimental findings are further confirmed by density functional theory (DFT) calculations on a 5 monolayer model CdSe nanoplatelet. These simulations show that the most labile ligands are located in the vicinity of facet edges, and that the displacement of ligands from such edge sites creates midgap states that can account for the observed photoluminescence quenching. Next to extending surface chemistry insights from colloidal QDs to nanoplatelets, this work indicates that CdSe nanoplatelets constitute a unique nanocrystal model system to establish a comprehensive description of midgap trap states, which includes their structural, chemical, and electronic properties.

Thermodynamic Equilibrium between Excitons and Excitonic Molecules Dictates Optical Gain in Colloidal CdSe Quantum Wells.

We show that optical gain in 2D CdSe colloidal quantum wells (CQWs) shows little saturation and coexists with exciton absorption over a broad range of excitation densities, in stark contrast with 0D CdSe colloidal quantum dots (CQDs). In addition, we demonstrate that photoexcited CQWs can absorb or emit light through the thermodynamically driven formation or radiative recombination of singlet excitonic molecules. Invoking stimulated emission through the molecule-exciton transition, we can quantify all of the remarkable gain characteristics of CQWs using only experimentally determined parameters, an advance that highlights a fundamental difference between multiexcitons in CQWs and CQDs. While strong confinement prohibits the dissociation of multiexcitons into separate excitons in 0D CQDs, excitons and excitonic molecules coexist in a 2D CQW at room temperature, with densities governed by an association/dissociation equilibrium, not by state-filling. Our finding points out future directions to optimize stimulated emission by excitonic 2D materials in general.

Study of surface and bulk electronic structure of II-VI semiconductor nanocrystals using Cu as a nanosensor.

Efficiency of the quantum dots based solar cells relies on charge transfer at the interface and hence on the relative alignment of the energy levels between materials. Despite a high demand to obtain size specific band offsets, very few studies exist where meticulous methods like photoelectron spectroscopy are used. However, semiconductor charging during measurements could result in indirect and possibly inaccurate measurements due to shift in valence and conduction band position. Here, in this report, we devise a novel method to study the band offsets by associating an atomic like state with the conduction band and hence obtaining an internal standard. This is achieved by doping copper in semiconductor nanocrystals, leading to the development of a characteristic intragap Cu-related emission feature assigned to the transition from the conduction band to the atomic-like Cu d state. Using this transition we determine the relative band alignment of II-VI semiconductor nanocrystals as a function of size in the below 10 nm size regime. The results are in excellent agreement with the available photoelectron spectroscopy data as well as the theoretical data. We further use this technique to study the excitonic band edge variation as a function of temperature in CdSe nanocrystals. Additionally, surface electronic structure of CdSe nanocrystals have been studied using quantitative measurements of absolute quantum yield and PL decay studies of the Cu related emission and the excitonic emission. The role of TOP and oleic acid as surface passivating ligand molecules has been studied for the first time.