Cheng Hon Alfred Huan

Surface plasmon enhanced band edge luminescence of ZnO nanorods by capping Au nanoparticles

The author observe sixfold enhancement in the near band gap emission of ZnO nanorods by employing surface plasmon of Au nanoparticles, while the defect-related emission is completely suppressed. Time-resolved photoluminescence indicates that the decay process becomes much faster by Au capping. The remarkable enhancement of the ultraviolet emission intensities and transition rates is ascribed to the charge transfer and efficient coupling between ZnO nanorods and Au surface plasmons. The suppression of the green emission might be due to a combined effect of Au surface plasmon and passivation of the ZnO nanorod surface traps.

The Physics of ultrafast saturable absorption in graphene

The ultrafast saturable absorption in graphene is experimentally and theoretically investigated in the femtosecond (fs) time regime. This phenomenon is well-modeled with valence band depletion, conduction band filling and ultrafast intraband carrier thermalization. The latter is dominated by intraband carrier-carrier scattering with a scattering time of 8 ( +/- 3) fs, which is far beyond the time resolution of other ultrafast techniques with hundred fs laser pulses. Our results strongly suggest that graphene is an excellent atomic layer saturable absorber.

Dynamics of bound exciton complexes in CdS nanobelts.

Intrinsic defects such as vacancies, interstitials, and anti-sites often introduce rich luminescent properties in II-VI semiconductor nanomaterials. A clear understanding of the dynamics of the defect-related excitons is particularly important for the design and optimization of nanoscale optoelectronic devices. In this paper, low-temperature steady-state and time-resolved photoluminescence (PL) spectroscopies have been carried out to investigate the emission of cadmium sulfide (CdS) nanobelts that originates from the radiative recombination of excitons bound to neutral donors (I(2)) and the spatially localized donor-acceptor pairs (DAP), in which the assignment is supported by first principle calculations. Our results verify that the shallow donors in CdS are contributed by sulfur vacancies while the acceptors are contributed by cadmium vacancies. At high excitation intensities, the DAP emission saturates and the PL is dominated by I(2) emission. Beyond a threshold power of approximately 5 μW, amplified spontaneous emission (ASE) of I(2) occurs. Further analysis shows that these intrinsic defects created long-lived (spin triplet) DAP trap states due to spin-polarized Cd vacancies which become saturated at intense carrier excitations.

Iron Pyrite Thin Film Counter Electrodes for Dye-Sensitized Solar Cells: High Efficiency for Iodine and Cobalt Redox Electrolyte Cells

Iron pyrite has been the material of interest in the solar community due to its optical properties and abundance. However, the progress is marred due to the lack of control on the surface and intrinsic chemistry of pyrite. In this report, we show iron pyrite as an efficient counter electrode (CE) material alternative to the conventional Pt and poly(3,4-ethylenedioxythiophene (PEDOT) CEs in dye-sensitized solar cells (DSSCs). Pyrite film CEs prepared by spray pyrolysis are utilized in I3(-)/I(-) and Co(III)/Co(II) electrolyte-mediated DSSCs. From cyclic voltammetry and impedance spectroscopy studies, the catalytic activity is found to be comparable with that of Pt and PEDOT in I3(-)/I(-) and Co(III)/Co(II) electrolyte, respectively. With the I3(-)/I(-) electrolyte, photoconversion efficiency is found to be 8.0% for the pyrite CE and 7.5% for Pt, whereas with Co(III)/Co(II) redox DSSCs, efficiency is found to be the same for both pyrite and PEDOT (6.3%). The excellent performance of the pyrite CE in both the systems makes it a distinctive choice among the various CE materials studied.

Fluorophore-Doped Core–Multishell Spherical Plasmonic Nanocavities: Resonant Energy Transfer toward a Loss Compensation

Plasmonics exhibits the potential to break the diffraction limit and bridge the gap between electronics and photonics by routing and manipulating light at the nanoscale. However, the inherent and strong energy dissipation present in metals, especially in the near-infrared and visible wavelength ranges, significantly hampers the applications in nanophotonics. Therefore, it is a major challenge to mitigate the losses. One way to compensate the losses is to incorporate gain media into plasmonics. Here, we experimentally show that the incorporation of gain material into a local surface plasmonic system (Au/silica/silica dye core-multishell nanoparticles) leads to a resonant energy transfer from the gain media to the plasmon. The optimized conditions for the largest loss compensation are reported. Both the coupling distance and the spectral overlap are the key factors to determine the resulting energy transfer. The interplay of these factors leads to a non-monotonous photoluminescence dependence as a function of the silica spacer shell thickness. Nonradiative transfer rate is increased by more than 3 orders of magnitude at the resonant condition, which is key evidence of the strongest coupling occurring between the plasmon and the gain material.

Effect of nitrogen doping on optical properties and electronic structures of SrTiO3 films

The nitrogen-doping induced changes in optical properties and electronic structures of SrTiO3 films have been investigated by using spectroscopic ellipsometry and x-ray photoemission spectroscopy. Combined with the first-principles calculations, it is found that the localized N 2p states above O 2p states are attributed to the new absorption edge at 500nm and the photoactivity in the visible light region. Our results are consistent with both recent experimental and theoretical studies on nitrogen-doped TiO2, where the visible light responses arise from the localized N 2p states slightly above the valence-band edge rather than the band gap narrowing.

First-principles study on ferromagnetism in nitrogen-doped In2O3

We report stable room temperature ferromagnetism in nitrogen doped In2O3 (N–In2O3) based on density functional theory. Our investigation on the electronic and magnetic properties of N–In2O3 suggests that N dopant introduces spin-polarized hole states in the band gap generating a total magnetic moment of 1.0μB per N, which is mainly localized on the doped N atoms. The ferromagnetic interaction in N–In2O3 system is mainly driven by the occurrence of coupling chains between a first N (N1)-2p to a second N (N2)-2p via a bridging In 5p and 4d orbitals.

Charge transfer dynamics in Cu-doped ZnO nanowires

Time resolved photoluminescence (TRPL) and transient absorption (TA) spectroscopy reveal an ultrafast charge transfer (CT) process, with an electron localization time constant 39±9 ps, between the ZnO host and the Cu dopants in Cu-doped ZnO nanowires. This CT process effectively competes with the ZnO band edge emission, resulting in the quenching of the ZnO UV emission. TRPL measurements show that the UV decay dynamics coincides with the buildup of the Cu-related green emission. TA measurements probing the state-filling of the band edge and defect states provide further support to the CT model where the bleaching dynamics concur with the TRPL lifetimes.

Energy level alignment at the methylammonium lead iodide/copper phthalocyanine interface

The energy level alignment at the CH3NH3PbI3/copper phthalocyanine (CuPc) interface is investigated by X-ray photoelectron spectroscopy (XPS) and ultraviolet photoelectron spectroscopy (UPS). XPS reveal a 0.3 eV downward band bending in the CuPc film. UPS validate this finding and further reveal negligible interfacial dipole formation – verifying the viability of vacuum level alignment. The highest occupied molecular orbital of CuPc is found to be closer to the Fermi level than the valance band maximum of CH3NH3PbI3, facilitating hole transfer from CH3NH3PbI3 to CuPc. However, subsequent hole extraction from CuPc may be impeded by the downward band bending in the CuPc layer.

Morphology-controlled synthesis and a comparative study of the physical properties of SnO2 nanostructures: from ultrathin nanowires to ultrawide nanobelts.

Controlled synthesis of one-dimensional materials, such as nanowires and nanobelts, is of vital importance for achieving the desired properties and fabricating functional devices. We report a systematic investigation of the vapor transport growth of one-dimensional SnO(2) nanostructures, aiming to achieve precise morphology control. SnO(2) nanowires are obtained when SnO(2) mixed with graphite is used as the source material; adding TiO(2) into the source reliably leads to the formation of nanobelts. Ti-induced modification of crystal surface energy is proposed to be the origin of the morphology change. In addition, control of the lateral dimensions of both SnO(2) nanowires (from approximately 15 to approximately 115 nm in diameter) and nanobelts (from approximately 30 nm to approximately 2 microm in width) is achieved by adjusting the growth conditions. The physical properties of SnO(2) nanowires and nanobelts are further characterized and compared using room temperature photoluminescence, resonant Raman scattering, and field emission measurements.