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Chiral light-matter interactions have emerged as a promising area in biophysics and quantum optics. Great progress in enhancing chiral light-matter interactions have been investigated through passive resonators or spontaneous emission. Nevertheless, the interaction between chiral biomolecules and stimulated emission remains unexplored. Here we introduce the concept of a biological chiral laser by amplifying chiral light-matter interactions in an active resonator through stimulated emission process. Green fluorescent proteins or chiral biomolecules encapsulated in Fabry-Perot microcavity served as the gain material while excited by either left-handed or right-handed circularly polarized pump laser. Owing to the nonlinear pump energy dependence of stimulated emission, significant enhancement of chiral light-matter interactions was demonstrated. Detailed experiments and theory revealed that a lasing dissymmetry factor is determined by molecular absorption dissymmetry factor at its excitation wavelength. Finally, chirality transfer was investigated under a stimulated emission process through resonance energy transfer. Our findings elucidate the mechanism of stimulated chiral light-matter interactions, providing better understanding of light-matter interaction in biophysics, chiral sensing, and quantum biophotonics. Agency for Science, Technology and Research (A*STAR) Ministry of Education (MOE) Nanyang Technological University This research is supported by A*STAR under its AME IRG Grant (Project No. A20E5c0085) and the Ministry of Education Singapore (Tier 1- RG 158/19(S)). We thank the Internal Grant NAP SUG - M4082308.040 from NTU.

Optofluidic lasers are emerging building blocks with immense potential in the development of miniaturized light sources, integrated photonics, and sensors. The capability of on-demand lasing output with programmable and continuous wavelength tunability over a broad spectral range enables key functionalities in wavelength-division multiplexing and manipulation of light-matter interactions. However, the ability to control multicolor lasing characteristics within a small mode volume with high reconfigurability remains challenging. The color gamut is also restricted by the number of dyes and emission wavelength of existing materials. In this study, we introduce a fully programmable multicolor laser by encapsulating organic-dye-doped cholesteric liquid crystal microdroplet lasers in an optofluidic fiber. A mechanism for tuning laser emission wavelengths was proposed by manipulating the topologically induced nanoshell structures in microdroplets with different chiral dopant concentrations. Precision control of distinctive lasing wavelengths and colors covering the entire visible spectra was achieved, including monochromatic lasing, dual-color lasing, tri-color lasing, and white colored lasing with tunable color temperatures. Our findings revealed a CIE color map with 145% more perceptible colors than the standard RGB space, shedding light on the development of programmable lasers, multiplexed encoding, and biomedical detection. Agency for Science, Technology and Research (A*STAR) Nanyang Technological University This research is supported by A*STAR under its AME IRG Grant (Project No. A20E5c0085). We would like to thank the Centre of Bio-Devices and Bioinformatics and Internal Grant NAP SUG -M4082308.040 from NTU for the lab support.

This work demonstrates a self-powered and broadband photodetector using a heterojunction formed by camphor-based chemical vaper deposition (CVD) bilayer graphene on p-Si substrates. Here, graphene/p-Si heterostructures and graphene layers serve as ultra-shallow junctions for UV absorption and zero bandgap junction materials (&lt, Si bandgap (1.1 eV)) for long-wave near-infrared (LWNIR) absorption, respectively. According to the Raman spectra and large-area (16 &times, 16 &mu, m2) Raman mapping, a low-defect, &gt, 95% coverage bilayer and high-uniformity graphene were successfully obtained by camphor-based CVD processes. Furthermore, the carrier mobility of the camphor-based CVD bilayer graphene at room temperature is 1.8 &times, 103 cm2/V&middot, s. Due to the incorporation of camphor-based CVD graphene, the graphene/p-Si Schottky junctions show a good rectification property (rectification ratio of ~110 at &plusmn, 2 V) and good performance as a self-powered (under zero bias) photodetector from UV to LWNIR. The photocurrent to dark current ratio (PDCR) value is up to 230 at 0 V under white light illumination, and the detectivity (D*) is 8 &times, 1012 cmHz1/2/W at 560 nm. Furthermore, the photodetector (PD) response/decay time (i.e., rise/fall time) is ~118/120 &mu, s. These results support the camphor-based CVD bilayer graphene/Si Schottky PDs for use in self-powered and ultra-broadband light detection in the future.

We report the fabrication and characterization of large-area reduced graphene oxide (rGO) photodetectors by a cost-effective solution process. To meet the requirement of high-sensitivity and low-power consumption, the photodetectors are operated under low-light intensity and low-driving voltage conditions. The photodetectors show low dark current and great light current under 0.41W cm−2 light illumination at the bias of 0.5V. Our study provides a useful method to construct rGO-based samples through a simple way and has a potential for the future applications of green devices operated under a low-bias voltage.

Solution processing of metal oxide semiconductors (MOS) is widely used for electronic and optoelectronic applications. However, the high-temperature annealing process that is required for device-quality films is incompatible with a flexible substrate because plastics can be thermally damaged. This study fabricates a p-type Cu2O flexible photodetector (PD) with a metal-semiconductor-metal structure on a polyethylene terephthalate (PET) substrate by irradiating a preheated precursor film with ultraviolet (UV) light. High-quality Cu2O crystals are formed on PET substrates by the charge transfer transition that is excited by the UV-irradiation at room temperature. An extremely high photo-to-dark current ratio (PDCR) of 1590 is achieved for a solution-processed Cu2O flexible PD. This flexible PD exhibits a relatively fast photoresponse (~0.2 s) and folds reproducibly after repeated bending for 500 cycles. This process does not require conventional high-temperature thermal annealing and is applicable to other solution-processed MOS, particularly those that are used for flexible electronic applications.

A highly efficient electron transport layer (ETL) is an essential constituent for good performance and stability in planar perovskite solar cells. Among n-type metal oxide materials, zinc oxide (ZnO) is a promising candidate for an electron transport layer due to its relatively high electron mobility, high transparency, and versatile nanostructures. However, it was found that several disadvantages could occur at the ZnO/perovskite interface, such as decomposition of CH3NH3PbI3 and poorly aligned energy levels. To overcome these issues, we present a design based on staircase band alignment of a low-temperature solution-processed ZnO/Al-doped ZnO (AZO) bilayer thin film as electron transport layers in planar perovskite solar cells. Experimental results revealed that the power conversion efficiency (PCE) of perovskite solar cells was significantly increased from 12.3% to 16.1% by employing the AZO thin film as the buffer layer. Meanwhile, the short-circuit current density (Jsc), open-circuit voltage (Voc), a...

A cost-effective approach of building graphene-based photodetectors with Ag nanowires (AgNWs) as the contact electrode on the glass substrate via solution process has been developed. The transmittance of the graphene/glass and the AgNWs/graphene/glass at a wavelength of 550 nm is 74% and 67%, respectively. To further improve the performance of the graphene photodetector, Ag nanoparticles are applied on the graphene to obtain the enhanced photocurrent and the improved ON/OFF ratio of 505 by the surface plasmon resonance effect. This semi-transparent graphene photodetector shows the superior optical and electrical performance and it paves the way to the future development of graphene-based devices by costly and high-throughput techniques.

The emerged demand for high-performance systems promotes the development of two-dimensional (2D) graphene-based photodetectors. However, these graphene-based photodetectors are usually fabricated by an expensive photolithography and complicated transferred process. Here, a semi-transparent reduced graphene oxide (rGO) photodetector on a polyethylene terephthalate (PET) substrate with ultra-low power operation by simple processes is developed. The photodetector has achieved a transmittance about 60%, a superior responsivity of 375 mA/W and a high detectivity of 1012 Jones at a bias of -1.5 V. Even the photodetector is worked at zero bias, the photodetector exhibits a superior on/off ratio of 12. Moreover, the photoresponse of such photodetector displays little reduction after hundred times bending, revealing that the photodetector is reliable and robust. The proposed fabrication strategy of the photodetector will be beneficial to the integration of semi-transparent and low-power wearable devices in the future.

In article number 1903707, Yu‐Cheng Chen and co‐workers demonstrate an approach to amplify bio‐nano‐electricity through the encapsulation of living algae in an optical micro‐cavity. The strong energy coupling between the cavity mode and photosynthetic resonance reveal the potential of exploiting optical resonators to amplify biological photocurrent generation and energy‐harvesting efficiency. Potential applications include photocatalysis, electrochemistry, and sustainable biophotonics. [Image: see text]

The unique and outstanding electrical and optical properties of graphene make it a potential material to be used in the construction of high-performance photosensors. However, the fabrication process of a graphene photosensor is usually complicated and the size of the device also is restricted to micrometer scale. In this work, we report large-area photosensors based on reduced graphene oxide (rGO) implemented with Ag nanoparticles (AgNPs) via a simple and cost-effective method. To further optimize the performance of photosensors, the absorbance and distribution of the electrical field intensity of graphene with AgNPs was simulated using the finite-difference time-domain (FDTD) method through use of the surface plasmon resonance effect. Based on the simulated results, we constructed photosensors using rGO with 60&ndash, 80 nm AgNPs and analyzed the characteristics at room temperature under white-light illumination for outdoor environment applications. The on/off ratio of the photosensor with AgNPs was improved from 1.166 to 9.699 at the bias voltage of &minus, 1.5 V, which was compared as a sample without AgNPs. The proposed photosensor affords a new strategy to construct cost-effective and large-area graphene films which raises opportunities in the field of next-generation optoelectronic devices operated in an outdoor environment.

This manuscript describes how to design and fabricate efficient inverted solar cells, which are based on a two-dimensional conjugated small molecule (SMPV1) and [6,6]-phenyl-C71-butyric acid methyl ester (PC(71)BM), by utilizing ZnO nanorods (NRs) grown on a high quality Al-doped ZnO (AZO) seed layer. The inverted SMPV1:PC(71)BM solar cells with ZnO NRs that grew on both a sputtered and sol-gel processed AZO seed layer are fabricated. Compared with the AZO thin film prepared by the sol-gel method, the sputtered AZO thin film exhibits better crystallization and lower surface roughness, according to X-ray diffraction (XRD) and atomic force microscope (AFM) measurements. The orientation of the ZnO NRs grown on a sputtered AZO seed layer shows better vertical alignment, which is beneficial for the deposition of the subsequent active layer, forming better surface morphologies. Generally, the surface morphology of the active layer mainly dominates the fill factor (FF) of the devices. Consequently, the well-aligned ZnO NRs can be used to improve the carrier collection of the active layer and to increase the FF of the solar cells. Moreover, as an anti-reflection structure, it can also be utilized to enhance the light harvesting of the absorption layer, with the power conversion efficiency (PCE) of solar cells reaching 6.01%, higher than the sol-gel based solar cells with an efficiency of 4.74%.

By employing graphene quantum dots (GQDs), we have achieved a high efficiency of 16.55% in n-type Si heterojunction solar cells. The efficiency enhancement is based on the photon downconversion phenomenon of GQDs to make more photons absorbed in the depletion region for effective carrier separation, leading to the enhanced photovoltaic effect. The short circuit current and the fill factor are increased from 35.31 to 37.47 mA/cm(2) and 70.29% to 72.51%, respectively. The work demonstrated here holds the promise for incorporating graphene-based materials in commercially available solar devices for developing ultrahigh efficiency photovoltaic cells in the future.

This study aims to explore the effects and mechanisms of hepcidin, a potential antimicrobial peptide from Tilapia, and epirubicin (Epi), an antineoplastic agent, on the generation of reactive oxygen species (ROS) and link the ROS levels to the reversal mechanisms of multidrug resistance (MDR) by epirubicin and hepcidin in human squamous cell carcinoma SCC15 and human embryonal carcinoma NT2D1 cells. The cells, pretreated with hepcidin, epirubicin, or a combination of these compounds in PEGylated liposomes, were used to validate the molecular mechanisms involved in inhibiting efflux transporters and inducing apoptosis as evaluated by cytotoxicity, intracellular accumulation, mRNA levels, cell cycle distribution, and caspase activity of this combination. We found that hepcidin significantly enhanced the cytotoxicity of epirubicin in liposomes. The co-incubation of epirubicin with hepcidin in liposomes intensified the ROS production, including hydrogen peroxide and superoxide free radicals. Hepcidin significantly increased epirubicin intracellular uptake into NT2D1 and SCC15 cells, as supported by the diminished mRNA expressions of MDR1, MDR-associated protein (MRP) 1, and MRP2. Hepcidin and/or epirubicin in liposomes triggered apoptosis, as verified by the reduced mitochondrial membrane potential, increased sub-G1 phase of cell cycle, incremental populations of apoptosis using annexin V/PI assay, and chromatin condensation. As far as we know, this is the first example showing that PEGylated liposomal TH1-5 and epirubicin gives rise to cell death in human squamous carcinoma and testicular embryonic carcinoma cells through the reduced epirubicin efflux via ROS-mediated suppression of P-gp and MRPs and concomitant initiation of mitochondrial apoptosis pathway. Hence, hepcidin in PEGylated liposomes may function as an adjuvant to anticancer drugs, thus demonstrating a novel strategy for reversing MDR.

Polycrystalline CuCl films were fabricated by chemical bath deposition (CBD) on a Cu substrate at a low solution temperature of 90 °C. Continuous CuCl films were prepared using the copper (II) chloride (CuCl2) compound as the precursor for both the Cu2 + and Cl− sources, together with repeated HCl dip treatments. An HCl dip pretreatment of the substrate favored the nucleation of CuCl crystallites. Further, interrupting the film deposition and including an HCl dip treatment of the film growth surface facilitated the deposition of a full-coverage CuCl film. A dual beam (FIB/SEM) system with energy dispersive spectrometry facilities attached revealed a homogeneous CuCl layer with a flat-top surface and an average thickness of about 1 μm. Both the excitonic and biexcitonic emission lines were well-resolved in the 6.4 K photoluminescence spectra. In particular, the free exciton emission line was observable at room temperature, indicating the good quality of the CuCl films prepared by CBD.

A three-dimensional display system based on metal nano-grating structure is modeled. The aluminum based nano-grating structures are designed and fabricated by nano-imprint as a linear polarizer to select the transverse magnetic wave in the wavelength range of 400–700 nm. The average transmission of the nano-grating for the transverse magnetic wave is around 80% and the polarization ratio of the emission light can reach as high as 97.1%. The polarization characteristics are studied theoretically, simulated by rigorous coupled wave analysis, and verified experimentally in detail.

We report an interfacial modification of sol-gel ZnO/A1-doped ZnO (AZO) bilayer thin film as the electron transport layer (ETL) in the perovskite solar cells. We found that the power conversion efficiency (PCE) of perovskite solar cells was significantly increased from 11.28% to 14.24% with short-circuit current density (J sc ) of 19.53 rnA cm−2,open-circuit voltage (V oc ) of 1.12 V, and fill factor (FF) of 65.1% by employing the AZO thin film as the buffer layer. Moreover, the enhancement in performance was obtained through energy-level offset adjustment of AZO thin film, which allows the better charge separation of perovskite solar cells.

In the study, the chemically-derived reduced graphene oxide flakes on the pyramidal Si substrate to construct the heterojunction solar cells via simple spin-coating process have been presented. The total reflectance of chemically-derived graphene on pyramidal Si is ~12% at the wavelength of 550 nm which is remarkably reduced compared with that of reduced graphene oxide on planar Si. By modifying the density and distribution of reduced graphene oxide flakes on Si, the power conversion efficiency of 5.20% is achieved. Additionally, the simulated absorbance of different-thick graphene is implemented to optimize the performance of graphene/pyramidal Si devices. The fabrication technique for rGO-based devices has the merits of simplicity, large scale, high throughput and low cost, which is a new starting point in the direction of graphene-based material for the applications of next generation optoelectronics.

The ITO-free inverted SMPV1:PCsub71/subBM solar cells with an Al doped ZnO (AZO) transparent electrodes are fabricated. The AZO thin film prepared by pulsed laser deposition (PLD) technique exhibits high transmission (85%) and low sheet resistance (~30 Ω/sq) and the power conversion efficiency (PCE) of devices based on AZO electrode can reach around 4%. To further enhance the light harvesting of the absorption layer of solar cells, ZnO nanorods interlayer is grown on the AZO layer before the deposition the active layer. The absorption spectrums of devices under various conditions are also simulated by RCWA method to identify the optical saturation length of the ZnO nanorods. The PCE of ITO-free inverted small molecule solar cell improved with ZnO nanorods can reach 6.6%.

Flexible indium tin oxide (ITO)-free poly(3-hexylthiophene):[6,6]-phenyl C61-butyric acid methyl ester (P3HT:PC61BM) solar cells with a spin-coated silver nanowire transparent electrode are demonstrated. The solution-processed silver nanowire thin film not only exhibits high transmission (~87%), but also shows low sheet resistance R s (~25 Ω/sq). For solar cells with a conventional structure, the power conversion efficiency (PCE) of devices based on silver nanowires can reach around 2.29%. For the inverted structure, the PCE of devices can reach 3.39%. Conventional and inverted flexible ITO-based P3HT:PC61BM solar cells are also fabricated as a reference for comparison. For both types of solar cells, the PCE of ITO-free devices is very close that of an ITO-based polymer solar cell.

Chrysophsin-1, an amphipathic alpha-helical antimicrobial peptide, is isolated from the gills of the red sea bream and possesses different structure and mechanism(s) in comparison with traditional multidrug resistance (MDR) modulators. For the purpose of reducing off-target normal cell toxicity, it is rational to incorporate chrysophsin-1 and epirubicin in a PEGylated liposomal formulation. In the present study, we report a multifunctional liposomes with epirubicin as an antineoplastic agent and an apoptosis inducer, as well as chrysophsin-1 as a MDR transporter inhibitor and an apoptosis modulator in human cervical cancer HeLa cells. Co-incubation of HeLa cells with PEGylated liposomal formulation of epirubicin and chrysophsin-1 resulted in a significant increase in the cytotoxicity of epirubicin. The liposomal formulations of epirubicin and/or chrysophsin-1 were shown to considerably improve the intracellular H2O2 and O2(-) levels of HeLa cells. Furthermore, these treatments were found to extensively reduce mRNA expression levels of MDR1, MRP1, and MRP2. The addition of chrysophsin-1 in liposomes was demonstrated to substantially enhance the intracellular accumulation of epirubicin in HeLa cells. Moreover, the PEGylated liposomes of epirubicin and chrysophsin-1 were also found to significantly increase the mRNA expressions of p53, Bax, and Bcl-2. The ratio of Bax to Bcl-2 was noticeably amplified in the presence of these formulations. Apoptosis induction was also validated by chromatin condensation, a reduction in mitochondrial membrane potential, the increased sub-G1 phase of cell cycle, and more populations of apoptosis using annexin V/PI assay. These formulations were verified to increase the activity and mRNA expression levels of caspase-9 and caspases-3. Collectively, our findings provide the first evidence that cotreatment with free or liposomal chrysophsin-1 and epirubicin leads to cell death in human cervical cancer cells through the ROS-mediated inhibition of P-gp and MRPs and concerted activation of mitochondrial apoptosis pathway. Thus, chrysophsin-1 represents a potential antimicrobial peptide to function as a new generation of MDR-reversing agent to enhance the activity of cancer chemotherapeutics.

Developing a transparent and cost-effective electrode for a textured and large-scale optoelectronic device is an important requirement for high-throughput products. Here, we propose a costly fabrication procedure using reduced graphene oxide (rGO) hybrid materials composed of rGO, Au nanoparticles (AuNPs) and Ag nanowires (AgNWs) top electrodes for structured Si solar cells via a spin coating method. This work overcomes the obstacle of graphene damage during the transferred process and provides a simple way to form large-scale graphene-based films on textured surfaces. Due to the spin-coated rGO being uniform along with AgNW frameworks and plasmonic AuNPs, the pyramidal Si solar cell exhibits a significant improved efficiency of 10.75% compared with solar cells using pure rGO flakes as the top electrodes. Our study realizes the rGO hybrid materials deposited on a textured surface and has great potential for integration into transparent and structured devices for next-generation industrial production.