Hyo Joong Lee

Regenerative PbS and CdS Quantum Dot Sensitized Solar Cells with a Cobalt Complex as Hole Mediator

Metal sulfide (PbS and CdS) quantum dots (QDs) were prepared over mesoporous TiO2 films by improved successive ionic layer adsorption and reaction (SILAR) processes. The as-prepared QD-sensitized electrodes were combined with a cobalt complex redox couple [Co(o-phen)3]2+/3+ to make a regenerative liquid-type photovoltaic cell. The optimized PbS QD-sensitized solar cells exhibited promising incident photon-to-current conversion efficiency (IPCE) of over 50% and an overall conversion efficiency of 2% at 0.1 sun in a regenerative mode. The overall photovoltaic performance of the PbS QD-sensitized cells was observed to be dependent on the final turn of the SILAR process, giving a better result when the final deposition was Pb2+, not S2-. However, in the case of CdS QD-sensitized cells, S2- termination was better than that of Cd2+. The cobalt complex herein used as a regenerative redox couple was found to be more efficient in generating photocurrents from PbS QD cells than the typical hole scavenger Na2S in a three-electrode configuration. The CdS-sensitized cell with this redox mediator also showed better defined current-voltage curves and an IPCE reaching 40%.

Novel Quinoxaline-Based Organic Sensitizers for Dye-Sensitized Solar Cells

Novel quinoxaline-based organic sensitizers using vertical (RC-21) and horizontal (RC-22) conjugation between an electron-donating triphenylamine unit and electron-accepting quinoxaline unit have been synthesized and used for dye-sensitized solar cells (DSSCs), leading to the relatively high power conversion efficiencies of 3.30 and 5.56% for RC-21 and RC-22, respectively. This result indicates that the quinoxaline electron-accepting unit is quite a promising candidate in organic sensitizers.

Electrochemistry of conductive polymers. 45. Nanoscale conductivity of PEDOT and PEDOT:PSS composite films studied by current-sensing AFM.

[Poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate)] (PEDOT:PSS, Baytron P) composite films were prepared under various conditions and their conductivities were studied by the current-sensing atomic force microscopy (CS-AFM) technique. Topographic and current images of pristine and additive-treated PEDOT:PSS as well as electrochemically synthesized PEDOT films were obtained in nanoscale using the CS-AFM. The as-prepared pristine PEDOT:PSS films showed a low population of conductive spots isolated by large insulating regions; both their population and the conductivities increased upon addition of a few additives to the PEDOT:PSS solution before spin-coating. From the current-voltage (I-V) traces recorded at a few representative spots of different electronic states, much improved pathways for charge percolation appeared to have been established in the additive-treated films. Electrochemically prepared PEDOT films showed much better electrical properties compared with spin-casted films of chemically prepared polymers. The conductivity of all these films was shown to be significantly enhanced by the electrochemical doping process.

Reduced Graphene Oxide (rGO)-Wrapped Fullerene (C60) Wires

The assembly of reduced graphene oxide (rGO) and fullerene (C(60)) into hybrid (rGO/C(60)) wires was successfully performed by employing the liquid-liquid interfacial precipitation method. The rGO sheets spontaneously wrapped C(60) wires through the π-π interaction between rGO and C(60). Structural characterization of the rGO/C(60) wires was carried out by using UV/visible spectroscopy, scanning electron microscopy, and transmission electron microscopy. FET devices with rGO/C(60) wires were fabricated to investigate their electrical properties. The I(ds)-V(g) curves of the hybrid wires exhibited p-type semiconducting behavior both in vacuum and in air, indicating hole transport through rGO as a shell layer, whereas pure C(60) wires and rGO sheets showed n-type and ambipolar behaviors, respectively, under vacuum. Possible application of the fabricated wires, such as photovoltaic devices, was also demonstrated.

Preparation of multilayered CdSe quantum dot sensitizers by electrostatic layer-by-layer assembly and a series of post-treatments toward efficient quantum dot-sensitized mesoporous TiO2 solar cells.

A multilayer of CdSe quantum dots (QDs) was prepared on the mesoporous surface of a nanoparticulate TiO(2) film by a layer-by-layer (LBL) assembly using the electrostatic interaction of the oppositely charged QD surface for application as a sensitizer in QD-sensitized TiO(2) solar cells. To maximize the absorption of incident light and the generation of excitons by CdSe QDs within a fixed thickness of TiO(2) film, the experimental conditions of QD deposition were optimized by controlling the concentration of salt added into the QD-dissolved solutions and repeating the LBL deposition a few times. A proper concentration of salt was found to be critical in providing a deep penetration of QDs into the mesopore, thus leading to a dense and uniform distribution throughout the whole TiO(2) matrix while anchoring the oppositely charged QDs alternately in a controllable way. A series of post-treatments with (1) CdCl(2), (2) thermal annealing, and (3) ZnS-coating was found to be very critical in improving the overall photovoltaic properties, presumably through a better connection between QDs, effective passivation of QDs surface, and a high impedance of recombination, which were proved by transmission electron microscopy (TEM) and electrochemical impedance spectroscopy (EIS) experiments. With a proper post-treatment of multilayered QDs as a sensitizer, the overall power conversion efficiency in the CdSe QD-sensitized TiO(2) solar cells could reach 1.9% under standard illumination condition of simulated AM 1.5G (100 mW/cm(2)).

CdSe quantum dot (QD) and molecular dye hybrid sensitizers for TiO2 mesoporous solar cells: working together with a common hole carrier of cobalt complexes

Redox couples based on cobalt complexes were found to be effective in regenerating both inorganic CdSe quantum dot- and organic dye-sensitizers. The hybrid sensitizer composed of CdSe QD and ruthenium sensitizer (Z907Na) dye showed a maximum power conversion efficiency of 4.76% on using cobalt(o-phen)(3)(2+/3+) as a common redox mediator.

CuS/CdS Quantum Dot Composite Sensitizer and Its Applications to Various TiO2 Mesoporous Film-Based Solar Cell Devices

A nanoscale composite sensitizer composed of CuS and CdS quantum dots (QDs) was prepared by a simple but effective layer-by-layer reaction between a metal cation (Cu(2+) or Cd(2+)) and a sulfide anion (S(2-)). The as-prepared composite CuS/CdS QD sensitizer displayed an enhanced photon-to-current conversion over the sensitizing range of the visible spectrum compared to the counterpart of the pure CdS sensitizer. At the optimized ratio of the deposited amounts of CuS and CdS, the best CuS/CdS-sensitized mesoporous TiO2 cell with a polysulfide electrolyte showed an overall power conversion efficiency of 3.60% with a short circuit current (Jsc) of 11.77 mA/cm(2), an open circuit voltage (Voc) of 0.65 V, and a fill factor (FF) of 0.47. From the transmission electron microscopy images, the initially deposited CuS seemed to take a nucleation site to accumulate more CdS in the later deposition. The kinetic studies by impedance and Voc decay measurements also revealed that the CuS/CdS and CdS QD sensitizers made a similar interface between TiO2 and the electrolyte, but the former had a larger resistance of charge transfer with a longer lifetime of excitons after light absorption than the latter. To enhance the sensitizing power further, a multilayer QD sensitizer of CuS/CdS/CdSe was prepared by successive ionic layer adsorption and reaction (SILAR). This led to the best performance of 4.32% overall power conversion efficiency. Finally, a hybrid sensitizing system of inorganic QD (CuS/CdS) and organic dye (coded MK-2) was tested with a [Co(bpy)3](2+/3+) redox mediator. The CuS/CdS/MK-2 dye-sensitized cell showed over 3.0% efficiency under the standard illumination condition (1 sun).

Multifunctional conjugated polymers with main-chain donors and side-chain acceptors for dye sensitized solar cells (DSSCs) and organic photovoltaic cells (OPVs).

A novel multifunctional conjugated polymer (RCP-1) composed of an electron-donating backbone (carbazole) and an electron-accepting side chain (cyanoacetic acid) connected through conjugated vinylene and terthiophene has been synthesized and tested as a photosensitizer in two major molecule-based solar cells, namely dye sensitized solar cells (DSSCs) and organic photovoltaic cells (OPVs). Promising initial results on overall power conversion efficiencies of 4.11% and 1.04% are obtained from the basic structure of DSSCs and OPVs based on RCP-1, respectively. The well-defined donor (D)-acceptor (A) structure of RCP-1 has made it possible, for the first time, to reach over 4% of power conversion efficiency in DSSCs with an organic polymer sensitizer and good operation stability.

Layer-by-Layer-Assembled Quantum Dot Multilayer Sensitizers: How the Number of Layers Affects the Photovoltaic Properties of One-Dimensional ZnO Nanowire Electrodes

Layer cake: Multilayered CdSe quantum dot (QD) sensitizers are layer-by-layer assembled onto ZnO nanowires by making use of electrostatic interactions to study the effect of the layer number on the photovoltaic properties. The photovoltaic performance of QD-sensitized solar cells critically depends on this number as a result of the balance between light-harvesting efficiency and carrier-recombination probability.

Efficient Planar Perovskite Solar Cells Using Passivated Tin Oxide as an Electron Transport Layer

Abstract Planar perovskite solar cells using low‐temperature atomic layer deposition (ALD) of the SnO2 electron transporting layer (ETL), with excellent electron extraction and hole‐blocking ability, offer significant advantages compared with high‐temperature deposition methods. The optical, chemical, and electrical properties of the ALD SnO2 layer and its influence on the device performance are investigated. It is found that surface passivation of SnO2 is essential to reduce charge recombination at the perovskite and ETL interface and show that the fabricated planar perovskite solar cells exhibit high reproducibility, stability, and power conversion efficiency of 20%.