Recyclable adsorbent of BiFeO_3/Carbon for purifying industrial dye wastewater via photocatalytic reproducible

It is essential to prepare highly-efficiency reproducible adsorbent for purifying industrial dye wastewater. In this work, biscuit with a layered porous structure as a template is applied to prepare a photocatalytic recyclable adsorbent of BiFeO3/Carbon nanocomposites for purifying simulative industrial dye wastewater. It is found that the structure of the prepared BiFeO3/Carbon nanocomposite is related to the natural structure of the biscuit, annealing temperatures and immersing times, demonstrated by XRD, TEM, UV-Vis and adsorptive activities. Kinetics data shows that the adsorption rate of the adsorbent to the dye is rapid and fitted well with the pseudo-second-order model, that more than 80% of dyes can be removed in the beginning 30 min. The adsorption isotherm can be perfectly described by the Langmuir model as well. It can be seen from the adsorption data that the adsorption performance can reach over 90% at pH ? 2–12, which can imply its universal utilization. The prepared BiFeO_3/Carbon nanocomposites have also displayed excellent capacities(over 90% within 30 min) for adsorption of seven different dyes and their mixed one. According to the five times photocatalytic reproducible experiments, it is proved that BiFeO_3/Carbon nanocomposites show the excellent stability and reproduction for purifying simulative industrial dyes, even the sample have been placed for one year. These research results indicate that the adsorbent BiFeO_3/Carbon can be a suitable material used in treating industrial dye wastewater potentially.

Efficient singlet oxygen generation by excitonic energy transfer on ultrathin g-C_(3)N_(4) for selective photocatalytic oxidation of methyl-phenyl-sulfide with O_(2)

Efficient generation of singlet oxygen(1 O_(2)) by an excitonic ene rgy transfer process is highly desired on a semiconductor photocatalyst for selective oxidation of methyl phenyl sulfide(MPS).Herein,it is demonstrated that a large amount of 1 O_(2) is produced on pristine graphitic carbon nitride(CN) nanosheet compared with bismuth oxybromide(BiOBr) and comme rcial P25 titanium dioxide(TiO_(2)).This leads to a certain photoactivity of CN for MPS oxidation.The observed ~77% selectivity for CN depends on the competitive results of excitonic energy transfer for 1 O_(2) formation and charge carrier separation for superoxide radical(O_(2)·) production,which are based on the phosphorescence spectra and electron paramagnetic resonance signals,respectively.Moreover,ultrathin CN nanosheets are synthesized by thermal treatment with the cyanuric acid-melamine hydrogen bonded aggregates as precursors.It is confirmed that the amount of produced 1 O_(2) could be increased by decreasing the thickness of resultant CN nanosheets.The optimized ultrathin CN nanosheet(~4 nm) exhibits excellent photoactivity with high selectivity(~99%).It is suggested that the excitonic energy transfer for 1 O_(2) formation is close related to the intrinsic exciton binding energy and the two-dimensional quantum confinement effect.This work establishes a basic mechanistic understanding on the excitonic processes in CN,and develops a feasible route to design CN-based photocatalysts for efficient 1 O_(2) generation.

Prolonged lifetime and enhanced separation of photo- generated charges of nanosized α-Fe2O3 by coupling SnO2 for efficient visible-light photocatalysis to convert C02 and degrade acetaldehyde

To develop efficient visible-light photocatalysis on α-Fe2O3, it is highly desirable to promote visible-light-excited high-energy-level electron transfer to a proper energy platform thermodynamically. Herein, based on the transient-state surface photovoltage responses and the atmosphere-controlled steady-state surface photovoltage spectra, it is demonstrated that the lifetime and separation of photogenerated charges of nanosized α-Fe2O3 are increased after coupling a proper amount of nanocrystalline SnO2. This naturally leads to greatly improved photocatalytic activities for CO2 reduction and acetaldehyde degradation. It is suggested that the enhanced charge separation results from the electron transfer from α-Fe2O3 to SnO2, which acts as a proper energy platform. Based on the photocurrent action spectra, it is confirmed that the coupled SnO2 exhibits longer visible-light threshold wavelength （-590 nm） compared with the coupled TiO2 （-550 nm）, indicating that the energy platform introduced by SnO2 would accept more photogenerated electrons from α-Fe2O3. Moreover, electrochemical reduction experiments proved that the coupled SnO2 possesses better catalytic ability for reducing CO2 and O2. These are well responsible for the much efficient photocatalysis on SnO2-coupled α-Fe2O3.

Progress of super-resolution near-field structure and application in optical data storage

The era of big data has necessitated the use of ultra-high density optical storage devices. Super-resolution near-field structure （super-RENS）, which has successfully surpassed the fundamental optical diffraction limit, is one of the promising next generation high-density optical storage technologies. This technology combines the traditional super-resolution optical disk with a near-field structure, and has the advantages of structural simplicity, strong practicability, and, more importantly, compatibility with the current optical storage pickup. The mask layer in super-RENS functions as the key to realizing superresolution. Development of suitable materials and stack designs has greatly been improved in the last decade. This paper described several types of super-RENS, such as aperture-type, light scattering center-type, bubble-type, and other types （e.g., WOx and ZnO）, particularly the newly proposed super-RENS technology and research achievements. The paper also reviews the applications of super-RENS in high-density optical data storage in recent years. After analyzing and comparing various types of super-RENS technology, the paper proposes the aperturetype based on the mechanism of nonlinear optics as the most suitable candidate for practical applications in the near future.

Nanoscale-resolved patterning on metal hydrazone complex thin films using diode-based maskless laser writing in the visible light regime

Metal hydrazone complex thin films are used as laser patterning materials, and the patterns with a minimum resolution of about 78 nm are successfully obtained by the laser writing setup （λ = 405 nm, NA = 0.9）. The minimum resolution is only about 1/8 of the writing spot size. In the formation of patterns, there is only a single step for forming patterns by the laser heating-induced clear thermal gasification threshold effect without any other development processes such as wet etching. This work provides an effective method for directly achieving nanoscale-resolved pattern structures with diode-based maskless laser writing lithography at visible light wavelengths.