Preparation and photoelectrochemical performance of nano Bi2S3–TiO2 composites

2018 ◽  
Vol 11 (03) ◽  
pp. 1850055 ◽  
Author(s):  
Senlin Li ◽  
Jinliang Huang ◽  
Xiangmei Ning ◽  
Yongchao Chen ◽  
Qingkui Shi

TiO2 nanorod (NR) arrays were prepared on FTO by the simple hydrothermal synthesizing method. On this basis, a layer of Bi2S3 quantum dots (QDs) was covered on the surface of TiO2 NRs array by solvothermal method, by which the Nano Bi2S3/TiO2 NRs composites films were obtained. The phase structure, morphologies, optical absorptions and photoelectrochemical (PEC) properties of the as-prepared materials were characterized by X-ray diffraction (XRD), Scanning Electron Microscope (SEM), High Resolution Transmission Electron Microscopy (HRTEM), Ultraviolet–visible spectroscopy (UV-Vis), Photoluminescence (PL) and electrochemical workstation. The results indicate that the concentration of tetrabutyl titanate (TBT) has a great influence on the morphology of the film, with the increase of TBT content, the array of TiO2 NRs changed from loose to tight, and the thin films were cracked when the TBT volume is up to 0.7[Formula: see text]mL; The absorption of the TiO2 NRs array film to the visible light is enhanced significantly when sensitized with Bi2S3 and the absorption wavelength is increased from 400[Formula: see text]nm to 800[Formula: see text]nm. Compared with the pure TiO2, the fluorescence intensity of the TiO2/Bi2S3 NRs is weakened, and there is no obvious fluorescence diffraction peak. Under the irradiation of standard (AM1.5[Formula: see text]G 100[Formula: see text]mW/cm[Formula: see text], the photocurrent density of the composite film increased significantly. When the external bias voltage is 1.2[Formula: see text]V, the current density of the composite films is five times of that of the pure TiO2.

2010 ◽  
Vol 663-665 ◽  
pp. 965-968
Author(s):  
Yue Hui Wang ◽  
Dong Jun Wang ◽  
Ai Jun Song ◽  
Zhi Gang Zhang ◽  
Shi Tao Song

TiO2/Ga2O3 nanowires were successfully prepared by a sol–gel-solvothermal method using tetrabutyl titanate as precursor, alcohol as solvent, Ga2O3 as templet and dopants, alginate as dispersant. The structures, morphologies,compositions and catalytic activity of products have been characterized by powder X-ray diffraction (XRD), transmission electron microscopy (TEM), field emission scanning electron microscopy ( FESEM ), nitrogen adsorption test, ultraviolet-visible near-infrared spectroscopy (UV–vis–NIR ),energy dispersive X-ray (EDX) analysis and spectrophotometer. The results revealed that the as-synthesized TiO2/Ga2O3 nanowires grew along [001] direction,which is reported for the first time, and the as-prepared product had better optical activity than TiO2 nanoparticles. Finally, the nanowires have a good adsorption capacity of 128.2 m2/g tested through nitrogen adsorption.


2022 ◽  
Author(s):  
Xing Zhang ◽  
Hao Chen ◽  
Wei Zhang ◽  
Lina Zhang ◽  
Xinyu Liu ◽  
...  

Abstract Exploring and fabricating a suitable photoanode with high catalytic activity is critical for enhancing photoelectrochemical (PEC) performance. Herein, a novel 3D hierarchical Fe2O3/SnO2 photoanode was fabricated by a hydrothermal route, combining with an annealing process. The morphology, crystal structure were studied by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photon spectroscopy (XPS), and X-ray diffraction (XRD), respectively. The results reveal the successful preparation of Fe2O3 nanothorns on the surface of SnO2 nanosheets. The as-fabricated 3D Fe2O3/SnO2 photoanode yields obviously promoted PEC performance with a photocurrent density of approximate 5.85 mA cm-2, measured in a mixture of Na2S (0.25 M) and Na2SO3 (0.35 M) aqueous solution at 1.23 V (vs. reversible hydrogen electrode, RHE). This value of photocurrent is about 53 times higher than that of the bare SnO2 photoanode. The obvious improved PEC properties can be attributed to the 3D Fe2O3/SnO2 heterostructures that offer outstanding light harvesting ability as well as improved charge transport and separation. These results suggest that exploring a suitable 3D hierarchical photoanode is an effective approach to boost PEC performance.approach to boost PEC performance.


2021 ◽  
Author(s):  
Yan Chen ◽  
Yuemei Lan ◽  
Dong Wang ◽  
Guoxing Zhang ◽  
Wenlong Peng ◽  
...  

A series of Gd2-xMoO6:xEu3+(x=0.18-0.38) nanophosphors were synthesized by the solvothermal method. The properties of this nanophosphor were characterized by x-ray diffraction (XRD), transmission electron microscope (TEM), fluorescence spectra and diffuse...


2011 ◽  
Vol 236-238 ◽  
pp. 1712-1716 ◽  
Author(s):  
Hai Tao Liu ◽  
Jun Dai ◽  
Jia Jia Zhang ◽  
Wei Dong Xiang

Bismuth selenide (Bi2Se3) hexagonal nanosheet crystals with uniform size were successfully prepared via a solvothermal method at 160°C for 22 h using bismuth trichloride(BiCl3) and selenium powder(Se) as raw materials, sodium bisulfite(NaHSO3) as a reducing agent, diethylene glycol(DEG) as solvent, and ammonia as pH regulator. Various techniques such as X-ray diffraction (XRD), field-emission scanning electron microscope (FESEM), high-resolution transmission electron microscope (HRTEM), and selected area electron diffraction (SAED) were used to characterize the obtained products. Results show that the as-synthesized samples are pure Bi2Se3 hexagonal nanosheet crystals. A possible growth mechanism for Bi2Se3 hexagonal nanosheet crystals is also discussed based on the experiment.


Author(s):  
Xianxue Li

Abstract Well-dispersed cerium-doped Y2SiO5 (Ce:YSO) phosphor particles with spherical morphology and good luminescence intensity have been achieved by a solvothermal method with ethanol and water as solvent media. X-ray diffraction, Fourier transform infrared spectroscopy, fluorescence spectrophotometry and transmission electron microscopy were employed to characterize the as-synthesized Ce:YSO precursor and powders. The results showed that pure-phase Ce:YSO powders with a mean particle size of about 162 nm were accurately available at 310°C and above. The fluorescence ability and persistent luminescence decay properties of the Ce:YSO powders were also studied, and the excellent fluorescence properties could be attributed to the homogeneous Ce:YSO particles obtained through the solvothermal method.


2014 ◽  
Vol 997 ◽  
pp. 359-362 ◽  
Author(s):  
Chun Hong Ma ◽  
Xue Lin ◽  
Liang Wang ◽  
Yong Sheng Yan

Nanocrystalline bismuth titanate (Bi4Ti3O12; BTO) powders were successfully prepared by the sol-gel method, using bismuth nitrate (Bi(NO3)3·5H2O) and tetrabutyl titanate (Ti(OC4H9)4) as source materials, acetic anhydride and ethanediol as solvents. The thermal decomposition and phase inversion process of the gel precursors were studied by using differential thermal analysis (DTA). The crystal structures and microstructures of BTO powders were investigated by using x-ray diffraction (XRD), and transmission electron microscope (TEM). The crystallization of amorphous bismuth titanate has been discussed. The effect of sintering temperature on the structure and morphology of BTO was investigated. At 644 oC and above, BTO powder undergoes a phase transformation from tetragonal to orthorhombic. At 900 oC, the purified orthorhombic BTO nanocrystals were obtained.


2020 ◽  
Vol 12 (6) ◽  
pp. 810-814 ◽  
Author(s):  
Xiao-Lei Song ◽  
Yi-Lin Wu ◽  
Si-Ran Zhang ◽  
Zhi Chen ◽  
Yong-Gui Li

Multi-structured NdFe2O4 magnetic nanoparticles (NPs) were successfully prepared at different reaction times through a convenient solvothermal method. The microstructure and elemental composition of the NPs were characterized using powder X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) technique. An energy dispersive spectrometer (EDS) was connected to a scanning electron microscope to determine the weight and atomic percent of the prepared products. Subsequently, high-resolution transmission electron microscopy (HR/TEM) and TEM were performed at 3, 7, 11, and 15 h to elucidate the synthetic mechanism of the rare-earth element Nd doped in Fe3O4. The magnetic activities of the NPs were evaluated using a vibrating sample magnetometer (VSM). XRD, EDS, and XPS analyses show that Nd was successfully doped into Fe3O4 without breaking its crystal structure. Procedural single-crystal nanosheets and final spherical particles of NdFe2O4 were verified by TEM. The magnetic parameters of the products were further analyzed using the VSM.


2010 ◽  
Vol 03 (02) ◽  
pp. 125-129 ◽  
Author(s):  
CAIQUAN ZHANG ◽  
YALI CUI ◽  
DIDI ◽  
KUNPING YAN ◽  
CHAO CHEN ◽  
...  

Facile procedures to synthesize large quantities of uniform and well dispersed magnetite particles in water were developed through a solvothermal method. Magnetite microspheres were obtained by using FeCl 3 · 6H 2 O , urea and polyethylene glycol as the starting materials in ethylene glycol at 200°C for 8 h. The samples were characterized by using X-ray diffraction, transmission electron microscopy, scanning electron microscopy and vibrating sample magnetometry. Experimental results revealed that the particles were well dispersed with uniform particle size and diameters in the range 260 to 280 nm. The saturation magnetization value was 71.5 emu/g with negligible remanence.


2011 ◽  
Vol 233-235 ◽  
pp. 1954-1957
Author(s):  
Xiao Yan Yan ◽  
Zhi Qiang Wei ◽  
Li Gang Liu ◽  
Xiao Juan Wu ◽  
Ge Zhang

Helical structure ZnS were successfully prepared via solvothermal method by the reaction of zinc acetate and sodium sulphide. The composition, morphology, and microstructure of the sample were characterized by X-ray diffraction (XRD), high resolution transmission electron microscopy (HRTEM), the corresponding selected area electron diffraction (SAED) and X-ray energy spectrum (EDS). The experiment results show that the sample is 1-D hexagonal crystal ZnS and grows along the [002] direction, and is helical structure, with lengths in the range of 100-200 nm, the diameter about 5-15 nm, and pitch about 20nm.


2016 ◽  
Vol 697 ◽  
pp. 706-709
Author(s):  
Ming Gong ◽  
Chang An Wang

V2O5 hollow microspheres were synthesized by a one-step solvothermal method, with the assistance of PVP as the soft template, ethylene glycol (EG) as the solvent, and vanadium (iii) acetylacetonate (acac) as the metal-ions source. The samples were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), transmission electron microscopy (TEM). The size of V2O5 hollow microspheres, which can be easily tuned by using PVP of different molecular weights, was about 2.5μm, 4.5μm and 6μm when using PVP-K17, PVP-K30 and PVP-K60 as the template, respectively.


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