No abstract

We propose a simple analytical formula that can quantitatively predict resonant light scattering from metal nanoparticles of arbitrary shape, whose sizes are too large for Rayleigh approximation to be applicable. The formula has been derived as an empirical extension of Mie’s rigorous calculation for light scattering from spheres. It can very well reproduce the experimental characteristics of light scattering from Au nanorods.

Light scattering by individual Ag nanoparticles and structures have been studied spectroscopically. Individual particles were selected and manipulated with a micromanipulator installed inside a scanning electron microscope (SEM). With typical particle dimensions of some 100 nm, the plasma resonances of particles and the coupled modes of particle pairs were observed in the visible region. The polarization dependence of the resonance frequencies strongly reflects the shape anisotropy; the effect that would be averaged out for experiments on ensembles. With a simple approximation to take the glass substrate into account, the results are in good agreement with the analytical calculations by Mie scattering, and with numerical calculations by the finite-difference time-domain method, both of which are performed with the morphological parameters obtained from the SEM observation for the corresponding particle or particle pair.

In this study, highly stable, low-temperature-processed planar lead halide perovskite (MAPbI 3– x Cl x ) solar cells with NiO x interfaces have been developed. Our solar cells maintain over 85% of the initial efficiency for more than 670 h, at the maximum power point tracking (MPPT) under 1 sun illumination (no UV-light filtering) at 30 °C, and over 73% of the initial efficiency for more than 1000 h, at the accelerating aging test (85 °C) under the same MPPT condition. Storing the encapsulated devices at 85 °C in dark over 1000 h revealed no performance degradation. The key factor for the prolonged lifetime of the devices was the sputter-deposited polycrystalline NiO x hole transport layer (HTL). We observed that the properties of NiO x are dependent on its composition. At a higher Ni 3+ /Ni 2+ ratio, the conductivity of NiO x is higher, but at the expense of optical transmittance. We obtained the highest power conversion efficiency of 15.2% at the optimized NiO x condition. The sputtered NiO x films were used to fabricate solar cells without annealing or any other treatments. The device stability enhanced significantly compared to that of the devices with PEDOT:PSS HTL. We clearly demonstrated that the illumination-induced degradation depends heavily on the nature of the HTL in the inverted perovskite solar cells (PVSCs). The sputtered NiO x HTL can be a good candidate to solve stability problems in the lead halide PVSCs.

Photoinduced phase transitions are of special interest in condensed matter physics because they can be used to change complex macroscopic material properties on the ultrafast timescale. Cooperative interactions between microscopic degrees of freedom greatly enhance the number and nature of accessible states, making it possible to switch electronic, magnetic or structural properties in new ways. Photons with high energies, of the order of electron volts, in particular are able to access electronic states that may differ greatly from states produced with stimuli close to equilibrium. In this study we report the photoinduced change in the lattice structure of a charge and orbitally ordered Nd(0.5)Sr(0.5)MnO(3) thin film using picosecond time-resolved X-ray diffraction. The photoinduced state is structurally ordered, homogeneous, metastable and has crystallographic parameters different from any thermodynamically accessible state. A femtosecond time-resolved spectroscopic study shows the formation of an electronic gap in this state. In addition, the threshold-like behaviour and high efficiency in photo-generation yield of this gapped state highlight the important role of cooperative interactions in the formation process. These combined observations point towards a 'hidden insulating phase' distinct from that found in the hitherto known phase diagram.

The light-induced insulator-metal transition in the "colossal magnetoresistance" compound Pr0.7Ca0.3MnO3 is shown to generate a well-localized conducting path while the bulk of the sample remains insulating. The path can be visualized through a change of reflectivity that accompanies the phase transition. Its visibility provides a tool for gaining insight into electronic transport in materials with strong magnetic correlations. For example, a conducting path can be generated or removed at an arbitrary position just because of the presence of another path. Such manipulation may be useful in the construction of optical switches.

Persistent and reversible optical phase control has been achieved in a manganite thin film through a careful choice of the composition of Pr1-x(Ca1-ySr(y))xMnO3 near a multicritical point. Pulsed laser light brings the lower temperature metallic phase out of the higher temperature charge-ordered insulator, while a cw light reverses the effect by heating. We clearly demonstrate the two competing roles played by light, heating, and excitation across the charge gap, which are important in both the application and the understanding of the physics of electron correlation.

Strain effect in charge- and orbital-ordered state has been investigated for Nd0.5Sr0.5MnO3 thin films deposited on (100), (110), and (111)-oriented substrates of SrTiO3. Films on (001) and (111) substrates have a monotonous temperature dependence for magnetic and transport properties showing no first-order phase transition. On the other hand, films on (110) substrate show a clear ferromagnetic-antiferromagnetic and metal-insulator transition around 170K similar to that in a bulk single crystal, which is a manifestation of the charge and orbital order. Precise control of the hole concentration was also demonstrated around half doping.