Three-dimensional chiral metasurfaces for circular-polarized anomalous beam steering.

Metasurfaces offer unprecedented possibilities for developing versatile ultracompact photonic devices with unique functions, e.g., for linear- or circular-polarized light beam steering. Here we report a three-dimensional (3D) chiral metasurface for phase controlling and beam steering, which consists of periodically arranged double-layer circular arc chiral nanostructures. By tuning the central angle of the lower circular arc, the left- and right-circularly polarized light (LCP and RCP) induce different spatial phases, which have been designed as a beam steering device to realize the abnormal reflection of LCP and the mirror reflection of RCP in the near-infrared (NIR) spectrum from 900 nm to 1150 nm, providing a potential device for chiral molecule detection.

Photoluminescence enhancement in monolayer MoS2 and self-assembled 3D photonic crystal heterostructures.

Self-assembled photonic crystals (PCs) have promising applications in enhancing and directional manipulation of the photoemission due to their photonic bandgaps. Here, we employed self-assembled 3D polystyrene PCs to enhance the photoluminescence (PL) of monolayer molybdenum disulfide (MoS2). Through tuning the photonic bandgap of the polystyrene crystals to overlap with the direct emission band of monolayer MoS2, the MoS2/3D-PC heterostructure showed a maximum 12-fold PL enhancement, and Rabi splitting was also observed in the reflection spectrum. The heterostructure is expected to be useful in nanophotonic emitting devices.

Organic sensitizers featuring thiophene derivative based donors with improved stability and photovoltaic performance.

Thiophene derivatives, including thieno[3,2-b][1]benzothiophene (TBT), benzo[b]thiophene (BT), 2-phenylthieno[3,2-b]thiophene (PTT) and 2-phenylthiophene (PT), have been introduced as donors for the construction of triarylamine organic dyes (M52, M53, M56, M57 and M52A). The absorption, electrochemical and photovoltaic properties as well as the stabilities of these dyes are systematically investigated and compared with the reference dye (M55), whose donor is composed of the hexyloxybenzene (HOB) unit. It is found that introducing the TBT, BT, PTT or PT donors positively shifted the HOMO and LUMO levels of the organic dyes, providing a larger driving force for regeneration and reducing the energy loss for electron injection. In addition, we found that M52, which contains the TBT unit, exhibited better photovoltaic performance and photostability as compared to the reference dye. In contrast, M53 displayed the lowest efficiency and stability of these dyes, indicating that the BT unit is not a good building block for donors. Interestingly, upon the incorporation of the mixed donor (TBT-HOB), M52A achieved a desirable driving force for regeneration without a loss in light absorption, thus resulting in a further improved photovoltaic performance with respect to that of M52. This work demonstrates that introducing donors based on thiophene derivatives is a good strategy for tuning the energy levels and thereby enhancing the efficiency of the resulting devices.

Influence of the Terminal Electron Donor in D-D-π-A Organic Dye-Sensitized Solar Cells: Dithieno[3,2-b:2',3'-d]pyrrole versus Bis(amine).

With respect to the electron-withdrawing acceptors of D-A-π-A organic dyes, reports on the second electron-donating donors for D-D-π-A organic dyes are very limited. Both of the dyes have attracted significant attention in the field of dye-sensitized solar cells (DSCs). In this work, four new D-D-π-A organic dyes with dithieno[3,2-b:2',3'-d]pyrrole (DTP) or bis(amine) donor have been designed and synthesized for a investigation of the influence of the terminal electron donor in D-D-π-A organic dye-sensitized solar cells. It is found that DTP is a promising building block as the terminal electron donor when introduced in the dithiophenepyrrole direction, but not just a good bridge, which exhibits several characteristics: (i) efficiently increasing the maximum molar absorption coefficient and extending the absorption bands; (ii) showing stronger charge transfer interaction as compared with the pyrrole direction; (iii) beneficial to photocurrent generation of DSCs employing cobalt electrolytes. DSCs based on M45 with the Co-phen electrolyte exhibit good light-to-electric energy conversion efficiencies as high as 9.02%, with a short circuit current density (JSC) of 15.3 mA cm(-2), open circuit voltage (VOC) of 867 mV and fill factor (FF) of 0.68 under AM 1.5 illumination (100 mW cm(-2)). The results demonstrate that N,S-heterocycles such as DTP unit could be promising candidates for application in highly efficient DSCs employing cobalt electrolyte.