Huidong Zang

Magneto-Optical Investigations on the Formation and Dissociation of Intermolecular Charge-Transfer Complexes at Donor-Acceptor Interfaces in Bulk-Heterojunction Organic Solar Cells

The electron-hole pairs can be formed in intermolecular charge-transfer (CT) states between two adjacent molecules due to Coulomb interaction in organic semiconducting materials. In general, the exciton dissociation can experience the intermediate states: intermolecular CT states at the donor-acceptor interfaces to generate a photocurrent in organic solar cells. This article reports the magneto-optical studies on intermolecular CT states in the generation of photocurrent by using magnetic field effects of photocurrent (MFE(PC)) and light-assisted dielectric response (LADR). The MFE(PC) and LADR studies reveal that internal electrical drifting and local Coulomb interaction can largely change the formation and dissociation of CT states by changing internal charge-transport channels and local Coulomb interaction through morphological development upon thermal annealing. Therefore, the MFE(PC) and LADR can be used as effective magneto-optical tools to investigate charge recombination, separation, and transport in organic solar cells.

Nonradiative Energy Transfer from Individual CdSe/ZnS Quantum Dots to Single-Layer and Few-Layer Tin Disulfide

The combination of zero-dimensional (0D) colloidal CdSe/ZnS quantum dots with tin disulfide (SnS2), a two-dimensional (2D)-layered metal dichalcogenide, results in 0D-2D hybrids with enhanced light absorption properties. These 0D-2D hybrids, when exposed to light, exhibit intrahybrid nonradiative energy transfer from photoexcited CdSe/ZnS quantum dots to SnS2. Using single nanocrystal spectroscopy, we find that the rate for energy transfer in 0D-2D hybrids increases with added number of SnS2 layers, a positive manifestation toward the potential functionality of such 2D-based hybrids in applications such as photovoltaics and photon sensing.

Using Perovskite Nanoparticles as Halide Reservoirs in Catalysis and as Spectrochemical Probes of Ions in Solution

The ability of cesium lead halide (CsPbX3; X = Cl(-), Br(-), I(-)) perovskite nanoparticles (P-NPs) to participate in halide exchange reactions, to catalyze Finkelstein organohalide substitution reactions, and to colorimetrically monitor chemical reactions and detect anions in real time is described. With the use of tetraoctylammonium halide salts as a starting point, halide exchange with the P-NPs was performed to calibrate reactivity, stability, and extent of ion exchange. The exchange of CsPbI3 with Cl(-) or Br(-) causes a significant blue-shift in absorption and photoluminescence, whereas reacting I(-) with CsPbBr3 causes a red-shift of similar magnitudes. With the high local halide concentrations and the facile nature of halide exchange in mind, we then explored the ability of P-NPs to catalyze organohalide exchange in Finkelstein like reactions. Results indicate that the P-NPs serve as excellent halide reservoirs for substitution of organohalides in nonpolar media, leading to not only different organohalide products, but also a complementary color change over the course of the reaction, which can be used to monitor kinetics in a precise manner. The merits of using P-NP as spectrochemical probes for real time assaying is then expanded to other anions which can react with, or result in unique, classes of perovskites.

Hybrid quantum dot-tin disulfide field-effect transistors with improved photocurrent and spectral responsivity

We report an improved photosensitivity in few-layer tin disulfide (SnS2) field-effect transistors (FETs) following doping with CdSe/ZnS core/shell quantum dots (QDs). The hybrid QD-SnS2 FET devices achieve more than 500% increase in the photocurrent response compared with the starting SnS2-only FET device and a spectral responsivity reaching over 650 A/W at 400 nm wavelength. The negligible electrical conductance in a control QD-only FET device suggests that the energy transfer between QDs and SnS2 is the main mechanism responsible for the sensitization effect, which is consistent with the strong spectral overlap between QD photoluminescence and SnS2 optical absorption as well as the large nominal donor-acceptor interspacing between QD core and SnS2. We also find enhanced charge carrier mobility in hybrid QD-SnS2 FETs which we attribute to a reduced contact Schottky barrier width due to an elevated background charge carrier density.

Core-size dependent photoluminescence blinking of isolated quantum dot-fullerene hybrids

We demonstrate the possibility to bias the photoluminescence blinking of isolated colloidal quantum dots coupled to fullerenes by varying the quantum dot core size. Changing the core size affects the energy offset between the donor and acceptor and directly affects the driving force for electron transfer between the two moieties. Single particle photoluminescence measurements reveal dramatic reduction in the on-time associated with the photoluminescence blinking in quantum dot-fullerene hybrids when the quantum dot core size decreases, a manifestation associated with enhanced electron transfer. Special Issue Comment: This project is about the blink properties of QDs in the presence of electron acceptor moieties and it connects with two articles from this Special Issue involving treatments when solving single molecules.1,2