Insight into the High Mobility and Stability of In2 O3 :H Film.

Wide bandgap semiconductors, particularly In2 O3 :Sn (ITO), are widely used as transparent conductive electrodes in optoelectronic devices. Nevertheless, due to the strohave beenng scattering probability of high-concentration oxygen vacancy (VO ) defects, the mobility of ITO is always lower than 40 cm2  V-1  s-1 . Recently, hydrogen-doped In2 O3 (In2 O3 :H) films have been proven to have high mobility (>100 cm2  V-1  s-1 ), but the origin of this high mobility is still unclear. Herein, a high-resolution electron microscope and theoretical calculations are employed to investigate the atomic-scale mechanisms behind the high carrier mobility in In2 O3 :H films. It is found that VO can cause strong lattice distortion and large carrier scattering probability, resulting in low carrier mobility. Furthermore, hydrogen doping can simultaneously reduce the concentration of VO , which accounts for high carrier mobility. The thermal stability and acid-base corrosion mechanism of the In2 O3 :H film are investigated and found that hydrogen overflows from the film at high temperatures (>250 °C), while acidic or alkaline environments can cause damage to the In2 O3 grains themselves. Overall, this work provides insights into the essential reasons for high carrier mobility in In2 O3 :H and presents a new research approach to the doping and stability mechanisms of transparent conductive oxides.

Efficient excitation and tuning of toroidal dipoles within individual homogenous nanoparticles.

We revisit the fundamental topic of light scattering by single homogenous nanoparticles from the new perspective of excitation and manipulation of toroidal dipoles. It is revealed that besides within all-dielectric particles, toroidal dipoles can also be efficiently excited within homogenous metallic nanoparticles. Moreover, we show that those toroidal dipoles excited can be spectrally tuned through adjusting the radial anisotropy parameters of the materials, which paves the way for further more flexible manipulations of the toroidal responses within photonic systems. The study into toroidal multipole excitation and tuning within nanoparticles deepens our understanding of the seminal problem of light scattering, and may incubate many scattering related fundamental researches and applications.

Invisible nanowires with interfering electric and toroidal dipoles.

By studying the scattering of normally incident plane waves by a single nanowire, we reveal the indispensable role of toroidal multipole excitation in multipole expansions of radiating sources. It is found that for both p-polarized and s-polarized incident waves, toroidal dipoles can be effectively excited within homogenous dielectric nanowires in the optical spectrum regime. We further demonstrate that the plasmonic core-shell nanowires can be rendered invisible through destructive interference of the electric and toroidal dipoles, which may inspire many nanowire-based light-matter interaction studies, and incubate biological and medical applications that require noninvasive detections and measurements.

Ultra-directional forward scattering by individual core-shell nanoparticles.

We study the angular scattering properties of individual core-shell nanoparticles that support simultaneously both electric and optically-induced magnetic resonances of different orders. In contrast to the approach to suppress the backward scattering and enhance the forward scattering relying on overlapping electric and magnetic dipoles, we reveal that the directionality of the forward scattering can be further improved through the interferences of higher order electric and magnetic modes. Since the major contributing electric and magnetic responses can be tuned to close magnitudes, ultra-directional forward scattering can be achieved by single nanoparticles without compromising the feature of backward scattering suppression, which may offer new opportunities for nanoantennas, photovoltaic devices, bio-sensing and many other interdisciplinary researches.

Unidirectional superscattering by multilayered cavities of effective radial anisotropy.

We achieve unidirectional forward superscattering by multilayered spherical cavities which are effectively radially anisotropic. It is demonstrated that, relying on the large effective anisotropy, the electric and magnetic dipoles can be tuned to spectrally overlap in such cavities, which satisfies the Kerker's condition of simultaneous backward scattering suppression and forward scattering enhancement. We show that such scattering pattern shaping can be obtained in both all-dielectric and plasmonic multilayered cavities at different spectral positions, and believe that the mechanism we have revealed provides extra freedom for scattering shaping, which may play a significant role in many scattering related applications and also in optoelectronic devices made up of intrinsically anisotropic two dimensional materials.