High-Quality FeTe_(1-x)Se_x Monolayer Films on SrTiO_3(001) Substrates Grown by Molecular Beam Epitaxy

We report the growth process of FeTe1-xSex （0 〈 x 〈 1） monolayer films on SrTi03 （STO） substrates through molecular beam epitaxy and discuss the possible ways to improve the film quality. By exploring the parameters of substrate treatment, growth control and post growth annealing, we successfully obtain a series of FeTe1-xSex monolayer films. In the whole growth process, we find the significance of the temperature control through surface roughness monitored by the reflection high-energy electron diffraction and scanning tunneling microscopy. We obtain the best quality of FeSe monolayer films with the STO substrate treated at T = 900 950℃ before growth, the FeSe deposited at T = 310℃ during growth and annealed at T = 380℃ after growth. For FeTe1-xSex （x-1）, both the growth temperature and annealing temperature decrease to T=260℃. According to the angle- resolved photoemission spectroscopy measurements, the superconductivity of the FeTe1-xSex film is robust and insensitive to Se concentration. All the above are instructive for further investigations of the superconductivity in FeTe1-xSex films.

Electron Transport Properties of Two-Dimensional Monolayer Films from Au-P-Au to Au-Si-Au Molecular Junctions

We investigate the electronic-transport properties of two-dimensional monolayer films from Au-P-Au molecular junction to Au-Si-Au molecular junction using elastic scattering Green＇s function theory. In the process of replacing the P atoms with Si atoms every other line from the middle of monolayer blue phosphorus molecular structure, the substitution of Si atoms changes the properties of Au-P-Au molecular junction significantly. Interestingly, the current value has a symmetric change as a parabolic curve with the peak appearing in Au-Si_1P_1-Au molecular junction, which provides the most stable current of 15.00 nA in a wide voltage range of 0.70-2.70 V.Moreover, the current-voltage characteristics of the structures indicate that the steps tend to disappear revealing the property similar to metal when the Si atoms dominate the molecular junction.

Large-scale area of magnetically anisotropic nanoparticle monolayer films deposited by MAPLE

Magnetically anisotropic nanoparticle monolayer films are of great interest for the development of ap-plications such as high-density data storage,sensors.However,the formation of large-scale magnetically anisotropic monolayer film is a challenging task.Here,we provide a new way to fabricate large-scale area of Fe_(3)O_(4) nanoparticle monolayer films by vacuum deposition technique(matrix-assisted pulsed laser evaporation,MAPLE).During the deposition process,only interactions between nanoparticles influence nanoparticle self-assembly behaviors.A strong magnetic anisotropy,characterized by in-plane and out-of-plane coercivity and saturation field obtained by DCM(dynamic cantilever magnetometry),was obtained both in cubic and spherical Fe_(3)O_(4) nanoparticle monolayer films.The inter-particle dipolar interaction but not crystal anisotropy is responsible for this effective magnetic anisotropy,which has been proved by Monte-Carlo simulations.

Influence of pigment substitution on the electrochemical properties of Rhodobacter sphaeroides 601 reaction centers

With the help of pigment substitution, self-assembled monolayer film and square wave voltammetry, the influence of pigment substitution on the electrochemical properties of Rhodobacter sphaeroides 601 reaction centers was investigated. Results showed that the charge separation could also be driven by externally electric field, similar to the primary photochemical reaction in purple bacterial reaction center. On the surface of Au electrode, a self-assembled monolayer film (the RC-PDDA-DMSA film) was made up of 2,3-dimercaptosuccinic acid (DMSA), poly-dimeth-yldiallylammonium chloride (PDDA) and reaction center (RC). When square wave voltammetry was used to study the RC-PDDA-DMSA film, four redox pairs in the photochemical reaction of RC were observed by changing frequency. With nonlinear fitting, the standard potential of P/P+ and the corresponding electrode reaction rate constant were determined to be 0.522 V and 13.04 S-1, respectively. It was found that the redox peak at -0.02 V changed greatly when bacteriopheophytin was substituted by plant pheophytin in the reaction center. Further studies indicated that this change resulted from the decrease in electron transfer rate between Bphe-/Bphe (Phe-/Phe) and QA-/QA after pigment substitution. After investigations of spectra and electrochemical properties of different RCs and comparisons of different function groups of pigments, it was indicated that the phytyl tail, similar to other substituted groups of pheophytin, affected the efficiencies of pigment substitution.