Transmission electron microscopy (TEM) and scanning near-field optical microscopy (SNOM) techniques were used to provide simultaneous investigation on the micro-structure and crystallinity, micro-PL spectrum, and

mode-selected mapping image. Both near-bandgap emission and trapped-state emission of ZnSe are observed in Mn-ZnSe nanobelts obtained using Mn powder as dopant. However, the Mn ion transition emission cannot be observed in this ZnSeMn nanobelt. Using manganese chloride (MnCl2) as dopant, strong Mn ion transition emission and weak near-bandgap emission are selleck kinase inhibitor observed. We can also observe the strong Mn ion transition emission and weak near-bandgap emission in the Mn-ZnSe nanobelts obtained using manganese acetate as dopant. More interestingly, the Mn ion transition emission can split into multi-mode emission due to multi-Fabry-Pérot cavity effect in the nanobelt. Raman spectrum was used to confirm the effective doping. These results are helpful in understanding the effect of dopant on the optical micro-cavities and multi-mode emission. These Mn-ZnSe nanostructures can find promising applications in multicolor emitter or wavelength selective photodetector. Methods The 1D Mn-ZnSe nanobelts were synthesized by a simple thermal evaporation method. Commercial grade mixed powder of ZnSe and Mn or MnCl2 or manganese acetate (Mn(CH3COO)2) with a

weight ratio of 5:1 was used as Selleckchem CDK inhibitor source material. The obtained samples were labeled Selleckchem Entospletinib as ZnSeMn, , , respectively. The other synthesis processes are similar with our previous report [16]. The evaporation temperature, growth temperature, and growth time are set to 900°C, 600°C, and 45 min, respectively. A yellow product deposited on the silicon wafer after the furnace cools down to room temperature. For comparison, the pure ZnSe nanobelts were also synthesized using ZnSe powder as source material. XRD (D/max-5000, Rigaku Corporation, Tokyo, Japan), E-SEM (QUANTA 200, FEI, Hillsboro, OR, USA), energy dispersive X-ray spectroscopy (EDS; attached to SEM), and TEM

(JEM-3010, JEOL Ltd., Tokyo, Japan) were used to examine the phase structure, crystallinity, and composition of the as-prepared nanobelts. Raman spectroscopy was performed in a confocal microscope (LABRAM-010, HORIBA Ltd., Kyoto, Japan) using He-Ne laser (632.8 nm) as excitation light source. The Baricitinib PL and corresponding mapping were obtained by SNOM (alpha 300 series, WITec GmbH, Ulm, Germany) with He-Cd laser (325 nm) as excitation source at room temperature. In all optical experiments, the excitation signal illuminated perpendicularly onto the sample surface. Results and discussion The XRD patterns of pure and doped ZnSe nanobelts are shown in Figure 1. All of the XRD pattern peaks of pure and doped ZnSe nanobelts are in agreement with the standard values (JCPDS card no. 37–1463), see Figure 1a. There are no diffraction peaks of Mn or MnSe in the doped samples.