Incorporation of Sb in ZnO Nanostructures Through Hydrothermal Process

2008 ◽  
Vol 8 (12) ◽  
pp. 6551-6557 ◽  
Author(s):  
A. Escobedo Morales ◽  
U. Pal ◽  
M. Herrera Zaldivar

Incorporation of dopants in optoelectronic semiconductor nanostructures has been a matter of great interest in recent times. While such doping has been performed almost routinely using physical methods, use of low-cost chemical techniques for that purpose is still rare. We incorporated antimony in zinc oxide (ZnO) nanostructures through a low temperature hydrothermal method. In as-grown nanostructures, antimony remains partially in Sb2O3 phase. On thermal annealing at 500 °C, it dissociates and antimony incorporates into ZnO mainly by substituting zinc from the crystal lattice. Incorporation of Sb drastically modifies the morphology of the ZnO nanostructures. While incorporation of Sb in low concentration promotes the formation of uniform prismatic ZnO nanorods probably due to catalytic effect, high concentration of Sb causes the formation of rounded shaped nanoparticles due to high interfacial compressive stress. Incorporated Sb in the ZnO nanostructures remains inhomogeneously distributed. The optical band gap of the ZnO nanostructures increases a bit for lightly doped samples but it decreases for heavy doping.

2021 ◽  
Author(s):  
Yanyan Dong ◽  
Xiaojie Zhu ◽  
Fei Pan ◽  
Baiwen Deng ◽  
Zhicheng Liu ◽  
...  

Abstract Inspired by the nature, biomass-derived carbon attracts many attentions as the electromagnetic wave absorption (EMA) material owing to its advantages including abundant, low cost, renewable and environmentally friendly. However, it is difficult to make further breakthrough in effective absorption bandwidth (EAB) due to the impedance mismatch. In this work, mace-like carbon fibers/ZnO nanorods composites (BDCFs@ZnO) derived from Typha orientalis were prepared via a carbonization process and a subsequent hydrothermal process for the first time. The unique hollow structure of BDCFs and the construction of 3D interconnected conductive network led to the strong conduction loss and multiple reflection. The BDCFs sample possesses an excellent EMA performance with an ultralow filling ratio of only 5wt%. After directionally growing of the ZnO nanorods, an exceptional RL of -62.35 dB at 14.12 GHz and the EAB achieves 6.8 GHz at the thickness of 2.29 mm at a filling ratio of 15wt% were revealed. Mace-like ZnO with suitable permittivity effectively avoid the reflection result from direct contraction between EMW and carbon fiber, further improving impedance match. Simultaneously, a dielectric sum-quotient model was proposed to analyze the EMA performance of the samples. This work not only offers an inspiration for the development of dielectric loss-type EMA materials with lightweight and strong EMA performance by a sustainable, low-cost and easily available approach, but also provides an important strategy toward biomass-derived carbon-fiber-based composites in other fields.


Nanomaterials ◽  
2020 ◽  
Vol 10 (10) ◽  
pp. 1940
Author(s):  
Abderrahim Moumen ◽  
Navpreet Kaur ◽  
Nicola Poli ◽  
Dario Zappa ◽  
Elisabetta Comini

Recently, one-dimensional (1D) nanostructures have attracted the scientific community attention as sensitive materials for conductometric chemical sensors. However, finding facile and low-cost techniques for their production, controlling the morphology and the aspect ratio of these nanostructures is still challenging. In this study, we report the vapor-liquid-solid (VLS) synthesis of one dimensional (1D) zinc oxide (ZnO) nanorods (NRs) and nanowires (NWs) by using different metal catalysts and their impact on the performances of conductometric chemical sensors. In VLS mechanism, catalysts are of great interest due to their role in the nucleation and the crystallization of 1D nanostructures. Here, Au, Pt, Ag and Cu nanoparticles (NPs) were used to grow 1D ZnO. Depending on catalyst nature, different morphology, geometry, size and nanowires/nanorods abundance were established. The mechanism leading to the VLS growth of 1D ZnO nanostructures and the transition from nanorods to nanowires have been interpreted. The formation of ZnO crystals exhibiting a hexagonal crystal structure was confirmed by X-ray diffraction (XRD) and ZnO composition was identified using transmission electron microscopy (TEM) mapping. The chemical sensing characteristics showed that 1D ZnO has good and fast response, good stability and selectivity. ZnO (Au) showed the best performances towards hydrogen (H2). At the optimal working temperature of 350 °C, the measured response towards 500 ppm of H2 was 300 for ZnO NWs and 50 for ZnO NRs. Moreover, a good selectivity to hydrogen was demonstrated over CO, acetone and ethanol.


2012 ◽  
Vol 1439 ◽  
pp. 39-44 ◽  
Author(s):  
Thushara J. Athauda ◽  
Umaiz Butt ◽  
Parameswar Harikumar ◽  
Ruya R. Ozer

ABSTRACTZnO nanostructures such as nanorods and nanoneedles were prepared on both cotton textiles and electrospun cellulosic nanofibers by a simple, two-step hydrothermal process at low temperature in aqueous solution. Commercially available cotton fabrics were used. Cellulosic nanofibers (average diameters of 100 nm) were obtained by electrospinning of cellulose acetate/polyvinyl acetate/polyethylene glycol mixture on glass slides to form non-woven mats.On cotton textiles, the systematic change of the seed-to-growth solution concentration ratio caused a noticeable variation on the morphology of the nanostructures. The loading ratio of ZnO nanorods and nanoneedles were 37.5% and 18.1 wt%, respectively. Durable superhydrophobicity was achieved with a static water contact angle of 160.7° upon fluorosilane treatment, even after prolonged exposure to UV and plasma irradiation. The surface wettability was found to slightly vary from nanorods (160.7°) to nanoneedles (159.8°). The ZnO nanostructures did not lose their superhydrophobicity after 1 h of agitation in DI water. Excellent UV blocking activities were observed for nanorods and nanoneedles in the wavelength region analyzed. On electrospun cellulosic nanofibers of approximately 100 nm diameter, the loading ratio of ZnO nanorods were found to be 33.3 wt% which are densely and uniformly distributed the entirety of the nanofibers. Although diameters of the nanofibers and cotton fibers are very different in size (around 100 nm and 15-20 micron, respectively) the ZnO loading on electrospun fibers are very close to that of cotton fabric due to the high surface area and coiled nature of electrospun fibers, resulting in high packing density. ZnO nanorods grown on electrospun nanofibers exhibited hydrophilic behavior.


2014 ◽  
Vol 2014 ◽  
pp. 1-6 ◽  
Author(s):  
Le Thuy Hoa ◽  
Huynh Ngoc Tien ◽  
Seung Hyun Hur

Fabrication of 3D structures composed of 1D n-type ZnO nanorods (NRs) and 2D p-type NiO nanosheets (NSs) by a low-cost, low-temperature, and large-area scalable hydrothermal process and its use in highly sensitive NO2gas sensors were studied. The p-n heterojunctions formed by NiO-ZnO interfaces as well as large area two-dimensional NiO NSs themselves increased the adsorption of NO2. Moreover, the charge transfer between NiO and ZnO enhanced the responsivity and sensitivity of NO2sensing even at a concentration of 1 ppm. The 30-min NiO NS growth on ZnO NRs in the hybrid sensor showed the highest sensitivity due to the formation of optimum p-n heterojunctions between ZnO NRs and NiO NSs for gas adsorption and carrier transport. Low responsivity toward reducing gases was also observed.


Chemosphere ◽  
2021 ◽  
Vol 274 ◽  
pp. 129689
Author(s):  
Jianpei Feng ◽  
Xiaolei Zhang ◽  
Guan Zhang ◽  
Ji Li ◽  
Wei Song ◽  
...  

2021 ◽  
pp. 096739112110245
Author(s):  
Amrita Sharma ◽  
PP Pande

It has been observed that acrylate monomers are very difficult to polymerize with the low cost nitroxide catalyst 2,2,6,6-tetramethylpiperidinyl-1-oxyl (TEMPO). Therefore, costly acyclic nitroxides such as N-tert-butyl-N-(1-diethylphosphono-2,2-dimethyl)-N-oxyl, (SG1), 2,2,5-Trimethyl-4-phenyl-3-azahexane-3-nitroxide (TIPNO) and TIPNO derivatives have to be used for the polymerization of the acrylic acid derivatives. There are very few reports on the use of TEMPO-derivatives toward the polymerization of n-butyl acrylate. Generally different reducing agents viz. glucose, ascorbic acid, hydroxyacetone etc. have been used to destroy excess TEMPO during the polymerization reaction. The acrylate polymerizations fail in the presence of TEMPO due to the strong C–O bond formed between the acrylate chain end and nitroxide. To the best of our knowledge, no literature report is available on the use of TEMPO without reducing agent or high temperature initiators, toward the polymerization of n-butyl acrylate. The present study has been carried out with a view to re-examine the application of low cost nitroxide TEMPO, so that it can be utilized towards the polymerization of acrylate monomers (e.g. n-butyl acrylate). We have been able to polymerize n-butyl acrylate using the nitroxide TEMPO as initiator (via a macroinitiator). In this synthesis, a polystyrene macroinitiator was synthesized in the first step from TEMPO, after this TEMPO end-capped styrene macroinitiator (PSt-TEMPO) is used to polymerize n-butyl acrylate monomer. The amount of macroinitiator taken was varied from 0.05% to 50% by weight of n-butyl acrylate monomer. The polymerization was carried out at 120°C by bulk polymerization method. The experimental findings showed a gradual increase in molecular weight of the polymer formed and decrease in the polydispersity index (PDI) with increase in amount of PSt-TEMPO macroinitiator taken. In all experiments conversion was more than 80%. These results indicate that the polymerization takes place through controlled polymerization process. Effect of different solvents on polymerization has also been investigated. In the following experiments TEMPO capped styrene has been used as macroinitiator leading to the successful synthesis of poly n-Butyl acrylate. It has been found that styrene macroinitiator is highly efficient for the nitroxide mediated polymerization, even in very small concentration for the synthesis of poly n-butyl acrylate. High concentration of macroinitiator results in the formation of block copolymers of polystyrene and poly ( n-butyl acrylate) viz. polystyrene-block-poly-( n-butyl acrylate). The use of TEMPO toward controlled polymerization is of much importance, because it is the nitroxide commercially available at the lowest cost.


Author(s):  
Hanh

In this work, ZnO nanorods (NRs) were successfully grown on printed circuit board substrates (PCBs) by utilizing a one-step, seedless, low-cost hydrothermal method. It was shown that by implementing a galvanic cell structure in an aqueous solution of 80 mM of zinc nitrate hexahydrate and hexamethylenetetramine, ZnO NRs can directly grow on the PCBs substrate without the assistance of a seed layer. The effect of hydrothermal time on the surface morphologies, and the crystallinity of the as-grown ZnO nanorods (NRs) was also investigated. The as-grown ZnO NRs also exhibited a significant enhancement in vertical growth and their crystallinity with 5 hour growth.


RSC Advances ◽  
2017 ◽  
Vol 7 (56) ◽  
pp. 35004-35011 ◽  
Author(s):  
Suling Yang ◽  
Gang Li ◽  
Chen Qu ◽  
Guifang Wang ◽  
Dan Wang

A new kind of ZnO nanoparticle/N-doped reduced graphene oxide nanocomposite (ZnONPs/N-rGO) was synthesized through a low temperature, low-cost and one step hydrothermal process.


2018 ◽  
Vol 23 (2) ◽  
Author(s):  
Patricia María Perillo ◽  
Mariel Nahir Atia ◽  
Daniel Fabián Rodríguez

ABSTRACT ZnO nanostructures were synthesized through a chemical method using different Zn precursors and hexamethylenetetramine (HMTA) at 90 °C. The effects of the reactants on the morphological evolution of ZnO nanorods were investigated. The samples were characterized by using XRD, SEM, EDX and BET. The hexagonal wurtzite phase of ZnO was confirmed by X-ray diffraction (XRD). The performed analysis indicated that different morphologies were obtained by changing the reactants.


2020 ◽  
Vol 9 (4) ◽  
pp. 117-122
Author(s):  
Vuong Nguyen Minh ◽  
Dung Dinh Tien ◽  
Hieu Hoang Nhat ◽  
Nghia Nguyen Van ◽  
Truong Nguyen Ngoc Khoa ◽  
...  

The volatile organic compounds (VOCs) sensing layers were studied using ZnO nanomaterials with different morphologies including hierarchical nanostructure (ZnO-H), nanorods (ZnO-NRs), commercial nanoparticles (ZnO-CNPs) and wet chemical synthesized nanoparticles (ZnO-HNPs). ZnO hierarchical structure was fabricated by an electrospinning technique followed by hydrothermal process. ZnO vertical nanorods structure was fabricated by hydrothermal method, while ZnO nanoparticles based sensors were prepared from commercial powder and wet chemical method. The morphology and properties of the fabricated samples were examined by scanning electron microscopy (SEM), X-ray diffraction (XRD) and transmission electron microscopy (TEM). VOCs sensing responses toward acetone, ethanol and methanol with respect to altered ZnO nanostructureswas systematically compared at different working temperatures. The enhanced response at low working temperatures induced by theopen space hierarchical structure was observed. The VOCs sensing mechanisms of the ZnO nanostructures based sensing layer were also explained and discussed in detail. 


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