Preparation of TiO2 Nanocrystals/Graphene Composite and Its Photocatalytic Performance

TiO2 nanocrystals/graphene （TiO2/GR） composite are prepared by combining flocculation and hydrothermal reduction technology using graphite oxide and TiO2 colloid as precursors. The obtained materials are examined by scanning electron microscopy, transition electron microscopy, X-ray diffraction, N2 adsorption desorption, and ultraviolet-visible diffuse spectroscopy. The results suggest that the presence of TiO2 nanocrystals with diameter of about 15 nm prevents GR nanosheets from agglomeration. Owing to the uniform distribution of TiO2 nanocrystals on the GR nanosheets, TiO2/GR composite exhibits stronger light absorption in the visible region, higher adsorption capacity to methylene blue and higher efficiency of charge separation and transportation compared with pure TiO2. Moreover, the TiO2/GR composite with a GR content of 30% shows higher photocatalytic removal efficiency of MB from water than that of pure TiO2 and commercial P25 under both UV and sunlight irradiation.

(N,F)-codoped TiO_2 Nanocrystals as Visible Light-activated Photocatalyst

（N, F）-codoped anatase TiO2 nanocrystals with active visible light response were prepared by using a simple sol-gel approach. X-ray photoelectron spectroscopy measurements suggested that the substitutional N and F species replaced the lattice oxygen atoms in TiO2 nanocrystals. Such nanocrystals showed strong absorption from 400 to 550 nm, which was mainly induced by nitrogen doping. The phase transformation from anatase to rutile was hindered by fluorine doping at high calcination temperatures, which was verified by XRD patterns. The N2 adsorption-desorption isotherms revealed the absence of mesopores in these nanocrystals. The （N, F）- codoped TiO2 nanocrystals showed satisfying photocatalytic activity on the photo-degradation of methylene blue under visible light.

Preparation, characterization and photocatalytic activity of N-doped TiO_2 nanocrystals

N-doped TiO2 nanocrystals were prepared using titanium alkoxide as precipitant with different proportional materials. The products were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, and UV-vis diffuse reflectance spectra. It is confirmed experimentally that the photocatalytic activity of N-doped TiO2 is much higher than that of Degussa P25, when used for the degradation of crystal violet. The degradation kinetics follows an apparent first-order reaction, which is consistent with a generally observed Langmuir-Hinshelwood mechanism. The doping of TiO2 with nitrogen significantly increases the absorption in the region of visible light. The energy of the band gap of N-doped TiO2 is 2.92 eV. The better performance of N-doped TiO2 can be explained by the fact that it is also excited with longer-wavelength light.

Importance of ligands on TiO_2 nanocrystals for perovskite solar cells

The fabrication of high-quality electron-selective layers at low temperature is a prerequisite to realizing efficient flexible and tandem perovskite solar cells （PSCs）. A colloidal-quantum-dot ink that contains TiO2 nanocrystals enables the deposition of a flat film with matched energy level for PSCs; however, the selection of ligands on the TiO2 surface is still unexplored. Here, we systematically studied the effect of the titanium diisopropoxide bis（acetylacetonate） （TiAc2） ligand on the performance of PSCs with a planar n-i-p architecture. We prepared TiO2 nanocrystals from TiCI4 and ethyl alcohol with C1- ligands attached on its surface and we found that a tiny amount of TiAc2 treatment of as-prepared TiO2 nanocrystals in a mixed solution of chloroform and methyl alcohol can enhance PSC power conversion efficiency （PCE） from 14.7% to 18.3%. To investigate the effect of TiAc2 ligand on PSCs, TiO2 samples with different TiAc2 content were prepared by adding TiAc2 into the as-obtained TiO2 nanocrystal solution. We use x-ray photoelectron spectroscopy to identify the content of C1 so as to reveal that C1 ligands can be substituted by TiAc2. We speculate that the improvement in PCE originates from amorphous TiO2 formation on the TiO2 nanocrystal surface, whereby a single-molecule layer of amorphous TiO2 facilitates charge transfer between the perovskite film and the TiO2 electronic transport layer, but excessive TiAc2 lowers the PSC performance dramatically. We further prove our hypothesis by x-ray diffraction measurements. We believe the PCE of PSCs can be further improved by carefully choosing the type and changing the content of surface ligands on TiO2 nanocrystal.

Is Water Physisorption Reversible for TiO_2 Nanocrystals? A Combinational Spectral Study

In this work,the nature of physisorbed water and its impacts on the structure,surface chemistry,and proton conduction properties of TiO2 nanocrystals were investigated by a combinational spectral technique.All TiO2 nanocrystals were directly prepared by a hydrothermal method,which showed highly hydrated and sulfated surfaces.The surface water molecules were indicated to exist in a wide set of energetically nonequivalent surface hydration groups,leading to the removal of physisorbed and chemisorbed water in sequence with increasing temperature.After heating treatment at 100 ℃ in air,physisorbed water layers were recovered with no significant impacts on the TiO2 nanostructure.On the other hand,when treated at the same temperature in vacuum,the recovery of physisorbed water layers was partially reversible,while a new hydration state appeared due to the filling of the high-energy adsorption sites by water molecules,which led to a significant increase in the amount of water molecules for surface hydration and an accelerated dehydration process toward lower temperature.As a result,an abnormal increase was observed in proton conductivity.These observations were explained in terms of thermally induced changes of surface chemistry and the amount of hydrated water.The results reported in this work are important,which may help understand the roles that the physisorbed water plays in stabilizing the nanostructures and therefore could have a broad class of implications.

TiO_2对镁碳复合纳米材料吸放氢性能的影响研究

将TiO2引入镁碳复合材料中反应球磨,在快速纳米化的过程中,TiO2纳米颗粒较容易镶嵌到金属Mg和碳的基体中,对复合材料的吸放氢性能具有良好的催化作用。DSC分析表明,(70Mg30C)2TiO2材料的初始放氢温度比MgH2降低了95℃,高峰放氢温度也降低了80℃。当TiO2的添加量为2%(质量分数,下同)时,(70Mg30C)2TiO2反应球磨储氢密度达到最大值4.78%,300℃放氢量达到3.75%。

16MnR钢焊缝表面纳米复合电镀及抗湿H2S应力腐蚀试验研究

采用Ni-纳米TiO2复合电镀对16MnR钢焊缝进行表面处理,运用均匀设计方法,研究了镀液温度、阴极电流密度、搅拌速度、纳米TiO2浓度等对复合电镀过程的影响,优选出Ni-纳米TiO2复合电镀的最佳工艺配方。借助金相显微镜、扫描电镜(SEM)与能谱仪(EDS)对复合镀层的微观形貌、组织结构及成分组成进行测试分析。恒载荷拉伸试验结果表明:普通电镀层的抗湿H2S应力腐蚀性能是无镀层的1.9倍,而Ni-纳米TiO2复合电镀层的抗湿H2S应力腐蚀性能是无镀层的4.1倍;镀层中纳米材料的引入,使得金属表面局部晶粒纳米化,提高了16MnR焊缝抗湿H2S应力腐蚀的能力。

Controllable hydrothermal synthesis of nanocrystal TiO_2 particles and their use in dye-sensitized solar cells

A simple method for the controllable hydrothermal synthesis of nanocrystalline anatase TiO2(nc-TiO2) particles involving the selection of suitable organic alkali peptizing agents is reported.A dye-sensitized solar cell(DSSC) with square-like nc-TiO2 particles with side lengths about 8-13 nm-prepared using tetraethylammonium hydroxide(TEAOH)-in the photoelectrode showed higher photovoltaic performance than two other DSSCs with square-like nc-TiO2 particles with side lengths about 7-10 nm-prepared using tetrabutylammonium hydroxide-or elongated nc-TiO2 particles with lengths about 18-35 nm and width about 10 18 nm-prepared using tetramethylammonium hydroxide(TMAOH)-in the photoelectrodes.When a scattering layer prepared from sub-micron size spheres or cone-like nc-TiO2 particles-synthesized using a higher concentration of TMAOH-was added on top of the photoelectrode fabricated from nc-TiO2 synthesized with TEAOH,the energy conversion efficiency of the DSSC was markedly increased from 6.77% to 8.18%.