scholarly journals Hydrothermal synthesis of ZnO quantum dot/KNb3O8 nanosheet photocatalysts for reducing carbon dioxide to methanol

2017 ◽  
Vol 8 ◽  
pp. 2264-2270 ◽  
Author(s):  
Xiao Shao ◽  
Weiyue Xin ◽  
Xiaohong Yin

ZnO quantum dots and KNb3O8 nanosheets were synthesized by a two-step hydrothermal method for the photocatalytic reduction of CO2 to methanol where isopropanol is simultaneously oxidized to acetone . The as-prepared photocatalysts were characterized by X-ray diffraction (XRD), energy dispersive X-ray spectroscopy (EDS), scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM) and UV–vis absorption spectroscopy (UV–vis). The photocatalytic activity of the materials was evaluated by formation rate of methanol under UV light irradiation at ambient temperature and pressure. The methanol formation rate of pure KNb3O8 nanosheets was found to be 1257.21 μmol/g/h, and after deposition of 2 wt % ZnO quantum dots on the surface of KNb3O8 nanosheets, the methanol production rate was found to increase to 1539.77 μmol/g/h. Thus, the ZnO quantum dots obviously prompted separation of charge carriers, which was explained by a proposed mechanism for this photocatalytic reaction.

2009 ◽  
Vol 1207 ◽  
Author(s):  
Xi Zhang ◽  
Dazhi Sun ◽  
Hung-Jue Sue

AbstractMonodisperse ZnO quantum dots (QDs) with a particle size of about 5 nm have been synthesized. Isopropanol together with hexane were utilized to precipitate ZnO nanoparticles to form condensed phases, ranging from white flocculation, to gel-like fluid, and to transparent solid. The morphology and structure in the transparent ZnO solid was characterized by UV-vis, X-ray diffraction, small-angle X-ray scattering, transmission electron microscopy, and scanning electron microscopy. The mechanisms for the formation of transparent ZnO QDs close-packed structure were monitored via UV-vis spectra, and found likely to be a colloidal crystal. The colloidal crystal is transparent and absorbs UV light efficiently. Possible conditions for the formation of the ZnO QDs colloidal crystal are discussed.


Author(s):  
Nguyen Ca ◽  
N. D Vinh ◽  
Phan Van Do ◽  
N. T. Hien ◽  
Xuan Hoa Vu ◽  
...  

Tb3+-doped ZnSe quantum dots (QDs) with Tb content in the range of 0.5 - 7% were successfully synthesized by a wet chemical method. X-ray diffraction (XRD) and transmission electron microscopy...


CrystEngComm ◽  
2020 ◽  
Vol 22 (21) ◽  
pp. 3644-3655
Author(s):  
Stefan Neumann ◽  
Christina Menter ◽  
Ahmed Salaheldin Mahmoud ◽  
Doris Segets ◽  
David Rafaja

Capability of TEM and XRD to reveal scale-bridging information about the microstructure of non-monodisperse quantum dots is illustrated on the CdSe quantum dots synthesized using an automated hot-injection method.


Nanomaterials ◽  
2019 ◽  
Vol 9 (7) ◽  
pp. 999
Author(s):  
Yi-An Chen ◽  
Kuo-Hsien Chou ◽  
Yi-Yang Kuo ◽  
Cheng-Ye Wu ◽  
Po-Wen Hsiao ◽  
...  

To the best of our knowledge, this report presents, for the first time, the schematic of the possible chemical reaction for a one-pot synthesis of Zn0.5Cd0.5Se alloy quantum dots (QDs) in the presence of low/high oleylamine (OLA) contents. For high OLA contents, high-resolution transmission electron microscopy (HRTEM) results showed that the average size of Zn0.5Cd0.5Se increases significantly from 4 to 9 nm with an increasing OLA content from 4 to 10 mL. First, [Zn(OAc)2]–OLA complex can be formed by a reaction between Zn(OAc)2 and OLA. Then, Fourier transform infrared (FTIR) spectroscopy and X-ray diffraction (XRD) data confirmed that ZnO is formed by thermal decomposition of the [Zn(OAc)2]–OLA complex. The results indicated that ZnO grew on the Zn0.5Cd0.5Se surface, thus increasing the particle size. For low OLA contents, HRTEM images were used to estimate the average sizes of the Zn0.5Cd0.5Se alloy QDs, which were approximately 8, 6, and 4 nm with OLA loadings of 0, 2, and 4 mL, respectively. We found that Zn(OAc)2 and OLA could form a [Zn(OAc)2]–OLA complex, which inhibited the growth of the Zn0.5Cd0.5Se alloy QDs, due to the decreasing reaction between Zn(oleic acid)2 and Se2−, which led to a decrease in particle size.


NANO ◽  
2018 ◽  
Vol 13 (05) ◽  
pp. 1850056 ◽  
Author(s):  
Yugan He ◽  
Qi Yan ◽  
Xiaoyu Chang ◽  
Meiying Zhu ◽  
Weiwei Wang ◽  
...  

A TiO2 photocatalyst with peony-like microstructures and a large percentage of exposed {001} facets was synthesized using a facile solvethermal method. The peony-like TiO2 was obtained using HF as a capping agent, TiCl4 as the precursor and ethanol as the solvothermal agent. The parameters which influence the mophology and formation mechanism of the products including the HF concentration, the reaction time and temperature and the solvothermal solvent, were investigated. The samples were characterized using field emission scanning electron microscopy, transmission electron microscopy, X-ray diffraction and N2 adsorption and desorption analysis. As the reaction time or reaction temperature increased, the morphology TiO2 changed from hexagonally assembled microspheres to peony-like microflowers which were composed of stacks of ultrathin nanosheets. The other reaction parameters also play a crucial role in the formation of the TiO2 microstuctures. Photocatalytic experiments showed that the synthesized TiO2 outperformed Degussa P25 in the photodegradation of methelene blue under a very weak UV light irradiation (power: 8[Formula: see text]W, light intensity: 0.4[Formula: see text]mW[Formula: see text]cm[Formula: see text]).


2016 ◽  
Vol 2016 ◽  
pp. 1-7 ◽  
Author(s):  
Manoj Pudukudy ◽  
Zahira Yaakob

α-Mn2O3 microspheres with high phase purity, crystallinity, and surface area were synthesized by the thermal decomposition of precipitated MnCO3 microspheres without the use of any structure directing agents and tedious reaction conditions. The prepared Mn2O3 microspheres were characterized by Fourier transform infrared (FTIR) spectroscopy, powder X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), transmission electron microscopy (TEM), and Brunauer-Emmett-Teller (BET) and photoluminescence (PL) studies. The complete thermal transformation of MnCO3 to Mn2O3 was clearly shown by the FTIR and XRD analysis. The electron microscopic images clearly confirmed the microsphere-like morphology of the products with some structural deformation for the calcined Mn2O3 sample. The mesoporous texture generated from the interaggregation of subnanoparticles in the microstructures is visibly evident from the TEM and BET studies. Moreover, the Mn2O3 microstructures showed a moderate photocatalytic activity for the degradation of methylene blue dye pollutant under UV light irradiation, using air as the potential oxidizing agent.


2011 ◽  
Vol 335-336 ◽  
pp. 460-463 ◽  
Author(s):  
Hong Mei Wang ◽  
Da Peng Zhou ◽  
Yuan Lian ◽  
Ming Pang ◽  
Dan Liu

Hexagonal flower-like CdS nanostructures were successfully synthesized through a facile hydrothermal method with thiourea as sulfur source. By combining the results of X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), field-emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), the structural and morphological characterizations of the products were performed. The photocatalytic activity of CdS nanostructures had been tested by degradation of Rhodamine B (RB) under UV light compared to commercial CdS powders, which indicated that the as-syntherized CdS nanostructures exhibited enhanced photocatalytic activity for degradation of RB. The possible growth mechanism of CdS nanostructures was proposed in the end.


2011 ◽  
Vol 374-377 ◽  
pp. 956-959
Author(s):  
Li Yun Yang ◽  
Gui Peng Feng ◽  
Yong Cai Zhang

ZnO2 nanorods were synthesized via hydrothermal treatment of 2ZnCO3•3Zn(OH)2 powder in 30 mass% H2O2 aqueous solution at 170 °C for 12 h, and characterized by means of X-ray diffraction, transmission electron microscopy and UV–vis diffuse reflectance spectra. Besides, the photocatalytic activity of the as-synthesized ZnO2 nanorods was tested for the degradation of methyl orange in distilled water under UV light irradiation.


1993 ◽  
Vol 8 (9) ◽  
pp. 2170-2176 ◽  
Author(s):  
B. Heeb ◽  
L.J. Gauckler ◽  
H. Heinrich ◽  
G. Kostorz

The 2212 phase formation during annealing of melt textured Bi–2212 (Bi2Sr2CaCu2Ox) was investigated using differential thermal analysis, thermal gravimetric analysis, x-ray diffraction, scanning electron microscopy, energy dispersive x-ray analysis, and high resolution transmission electron microscopy. After zone melting, the material is multiphase consisting of 2212, 2201, Sr1−xCaxCuO2, and the eutectic. The 2212 phase formed is highly perfect with less than 5% intergrowths of 2201 layers; the 2201 phase shows no intergrowth of 2212 at all. In the first period of the annealing, remelting of the eutectic leads to fast oxygen diffusion and a high 2212 formation rate. The 2201 → 2212 transformation proceeds via intermediate states of high defect density. The 2212 grains contain up to 30–70% 2201 intergrowths. Further heat treatments lead to an annihilation of the great majority of intergrown 2201 layers. We propose a model for the formation of 2212 grains with a low planar defect density, based on frequent stacking faults, that allows diffusion of Ca- and Cu-atoms over a short distance. The model provides a schematic description of this solid-state process and correlates it to the characteristic microstructural features of melt-processed Bi–2212.


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