Surface-enhanced Raman spectroscopy (SERS), which utilizes nanogaps between noble-metal nanostructures as hot spots to yield ultrasensitive SERS signals, is an outstanding label-free and straightforward tool for DNA methylation analysis. Herein, a plasmonic gold nanohole array (PGNA) with well-controlled hot spots and an open surface was designed as a SERS substrate for DNA methylation detection. A finite-difference time-domain (FDTD) simulation was first employed to investigate the electric field distributions of the PGNA as a function of the geometric parameters. The plasmonic response was tuned to 785 cm −1 to match the ring breathing vibrational band of cytosine, the intensity change of which was revealed to be a marker of DNA methylation. Then, guided by the FDTD simulation results, the PGNA was fabricated via the electron beam lithography (EBL) technique. The fabricated PGNA had an open and easily accessible surface topology, a SERS enhancement factor of ∼10 6 , and a relative standard deviation (RSD) of 7.1% for 500 repetitions over an area of 20 × 20 μm 2 using 1 μM Rhodamine 6G as the Raman reporter. The fabricated PGNA was further used as a platform for determining DNA methylation. The proposed method exhibited a sensitivity for detecting 1% of methylation changes. Moreover, insight into the dynamic information on methylation events was obtained by combining principal component analysis (PCA) with 2D correlation spectroscopy analysis. Finally, clear discrimination of the different methylation sites, such as 5-methylcytosine and N6-methyladenine, was demonstrated.

In this work, methylammonium lead trichloride (CH3NH3PbCl3) perovskite thin films were fabricated via a two-step spin coating and solvent-vapor-assisted thermal annealing method under low temperature. The films exhibited cubic crystalline structure and pinhole-free morphologies.The possible charge traps were investigated via the analysis of photoluminescence (PL) spectra of perovskite films prepared with different lead chloride (PbCl2) precursor concentrations while maintaining the same concentration of methylammonium chloride (CH3NH3Cl). Prototypical ultraviolet (UV) photodetectors with the structure of ITO/CH3NH3PbCl3/Poly (triaryl amine) (PTAA)/Al were fabricated and showed low dark current density 1.60 × 10 -5 mA/cm 2 under -1 V reverse bias, strong photoresponse in 300-400 nm region, and a high UV-visible rejection ratio up to 500 under 0 or -0.5 V bias. All the results demonstrated that low-temperature solution-processed CH3NH3PbCl3 perovskite thin films offer a great potential for making flexible, lightweight visible-blind UV-A photodetectors.

Lightweight and flexible ultraviolet (UV) photodetectors (PDs) have wide applications and have attracted more attention. PDs using organic and inorganic nanocomposites as active layers with a photodiode configuration could achieve photomultiplication and narrowband photoresponse via the control of microstructure and thickness of active layers. Here, we fabricated flexible UV PDs on indium tin oxide-coated poly(ethylene terephthalate) substrates with a nanocomposite active layer composed of ZnO nanoparticles blended with a wide band gap conjugated polymer, poly[(9,9-dioctylfluorenyl-2,7-diyl)- alt- co-(bithiophene)] (F8T2). As a result of the wavelength-dependent penetration depth of light in the active layer, the fabricated flexible UV PDs showed two narrow response peaks at 360 and 510 nm under reverse biases in the external quantum efficiency (EQE) spectra with full width at half maximum (FWHM) less than 20 nm. Both responses exhibited greater than 100% EQE, indicating a photomultiplication effect, whereas the UV response at 360 nm was 10 times stronger under -15 V bias. The fabricated flexible UV PDs were bent under both tensile and compressive stress to a curvature of 2.1 cm, each with 50 repetitions. The peak specific detectivity ( D*) only decreased by about 5% in total, the FWHM was well retained below 20 nm and the response speed remained almost constant after two types of bending, demonstrating mechanical flexibility and photoresponse stability of the fabricated flexible UV PDs. The photodiode configuration with nanocomposite active layers offers a promising route to make flexible and conformable narrowband, photomultiplication-type photodetectors for modern applications.

Csx(MA0.17FA0.83)1−xPb1−ySny(I0.83Br0.17)3 perovskites with cubic-phase morphologies were deployed in solar cells, achieving high efficiencies and improved stability for high Sn-containing devices.