Growth and Characterization of Uniform Carbon Nanotube Arrays on Active Substrates

2015 ◽  
Vol 1752 ◽  
pp. 3-14
Author(s):  
Qiuhong Zhang ◽  
Betty T. Quinton ◽  
Bang-Hung Tsao ◽  
James Scofield ◽  
Neil Merrett ◽  
...  

ABSTRACTCarbon nanotubes (CNTs) have unique thermal/electrical/mechanical properties and high aspect ratios. Growth of CNTs directly onto reactive material substrates (such as metals and carbon based foam structures, etc.) to create a micro-carbon composite layer on the surface has many advantages: possible elimination of processing steps and resistive junctions, provision of a thermally conductive transition layer between materials of varying thermal expansion coefficients, etc. Compared to growing CNTs on conventional inert substrates such as SiO2, direct growth of CNTs onto reactive substrates is significantly more challenging. Namely, control of CNT growth, structure, and morphology has proven difficult due to the diffusion of metallic catalysts into the substrate during CNT synthesis conditions. In this study, using a chemical vapor deposition method, uniform CNT layers were successfully grown on copper foil and carbon foam substrates that were pre-coated with an appropriate buffer layer such as Al2O3 or Al. SEM images indicated that growth conditions and, most notably, substrate surface pre-treatment all influence CNT growth and layer structure/morphology. The SEM images and pull-off testing results revealed that relatively strong bonding existed between the CNT layer and substrate material, and that normal interfacial adhesion (0.2‒0.5 MPa) was affected by the buffer layer thickness. Additionally, the thermal properties of the CNT/substrate structure were evaluated using a laser flash technique, which showed that the CNT layer can reduce thermal resistance when used as a thermal interface material between bonded layers.

Materials ◽  
2021 ◽  
Vol 14 (4) ◽  
pp. 806
Author(s):  
Michalina Ehlert ◽  
Aleksandra Radtke ◽  
Katarzyna Roszek ◽  
Tomasz Jędrzejewski ◽  
Piotr Piszczek

The surface modification of titanium substrates and its alloys in order to improve their osseointegration properties is one of widely studied issues related to the design and production of modern orthopedic and dental implants. In this paper, we discuss the results concerning Ti6Al4V substrate surface modification by (a) alkaline treatment with a 7 M NaOH solution, and (b) production of a porous coating (anodic oxidation with the use of potential U = 5 V) and then treating its surface in the abovementioned alkaline solution. We compared the apatite-forming ability of unmodified and surface-modified titanium alloy in simulated body fluid (SBF) for 1–4 weeks. Analysis of the X-ray diffraction patterns of synthesized coatings allowed their structure characterization before and after immersing in SBF. The obtained nanolayers were studied using Raman spectroscopy, diffuse reflectance infrared Fourier transform spectroscopy (DRIFT), and scanning electron microscopy (SEM) images. Elemental analysis was carried out using X-ray energy dispersion spectroscopy (SEM EDX). Wettability and biointegration activity (on the basis of the degree of integration of MG-63 osteoblast-like cells, L929 fibroblasts, and adipose-derived mesenchymal stem cells cultured in vitro on the sample surface) were also evaluated. The obtained results proved that the surfaces of Ti6Al4V and Ti6Al4V covered by TiO2 nanoporous coatings, which were modified by titanate layers, promote apatite formation in the environment of body fluids and possess optimal biointegration properties for fibroblasts and osteoblasts.


2019 ◽  
Vol 507 ◽  
pp. 288-294 ◽  
Author(s):  
Mitsuru Imaizumi ◽  
Masumi Hirotani ◽  
Tetsuo Soga ◽  
Masayoshi Umeno

2016 ◽  
Vol 2016 (1) ◽  
pp. 000038-000043
Author(s):  
James E. Webb ◽  
Roger McCleary

Abstract Increasing volume using larger substrates with decreasing process margins continues to create new challenges for advanced packaging applications. Key step and repeat camera technology continues evolving for the mass production of microstructures used for 2.5D and 3D technologies. Printing dense arrays of smaller features with high aspect ratios requires higher sidewall angles in thick photoresists and polyimides. To help solve these imaging challenges we have leveraged resist modeling software and guided the adjustment of optical parameters needed for better performance. Higher contrast films have also been evaluated to help achieve the improvements in performance needed. Resist models that can include the effects of flare have been critical to understand the requirement for printing in thick negative resists and has aided in printing features on varying topography and film thicknesses. Special chucks help improve the flatness of warped wafers and real-time auto-focusing provides good image fidelity. Printing microstructures over larger formats with higher throughput has been accomplished using large magnification adjustment for improving overlay and validated by characterizing image placement errors over large substrates. Examples of resist models that are created using resist parameters and optimized using SEM images of printed features are compared. Extrapolations of the resist models have shown that guide improvements can be achieved by varying optical parameters. SEM images confirm that the modeled result of the optimal solution was achieved. Reduction in large substrate overlay error was achieved after the stage corrections were applied. Examples show that topographical errors of warped wafers can be reduced and how real-time auto-focusing for each exposure minimizes focus errors.


Membranes ◽  
2019 ◽  
Vol 9 (6) ◽  
pp. 70 ◽  
Author(s):  
Nancy Li ◽  
Jackie Zheng ◽  
Pejman Hadi ◽  
Mengying Yang ◽  
Xiangyu Huang ◽  
...  

Despite the advantages of membrane processes, their high energy requirement remains a major challenge. Fabrication of nanocomposite membranes by incorporating various nanomaterials in the polymer matrix has shown promise for enhancing membrane flux. In this study, we embed functionalized cellulose nanofibers (CNFs) with high aspect ratios in the polymer matrix to create hydrophilic nanochannels that reduce membrane resistance and facilitate the facile transport of water molecules through the membrane. The results showed that the incorporation of 0.1 wt % CNF into the polymer matrix did not change the membrane flux (~15 L · m − 2 · h − 1 ) and Bovine Serum Albumin (BSA) Fraction V rejection, while increasing the CNF content to 0.3 wt % significantly enhanced the flux by seven times to ~100 L · m − 2 · h − 1 , but the rejection was decreased to 60–70%. Such a change in membrane performance was due to the formation of hydrophilic nanochannels by the incorporation of CNF (corroborated by the SEM images), decreasing the membrane resistance, and thus enhancing the flux. When the concentration of the CNF in the membrane matrix was further increased to 0.6 wt %, no further increase in the membrane flux was observed, however, the BSA rejection was found to increase to 85%. Such an increase in the rejection was related to the electrostatic repulsion between the negatively-charged CNF-loaded nanochannels and the BSA, as demonstrated by zeta potential measurements. SEM images showed the bridging effect of the CNF in the nanochannels with high CNF contents.


1998 ◽  
Vol 13 (12) ◽  
pp. 3378-3388
Author(s):  
Y. Huang ◽  
B. V. Vuchic ◽  
M. Carmody ◽  
P. M. Baldo ◽  
K. L. Merkle ◽  
...  

The sputter-induced epitaxy change of in-plane orientation occurring in YBa2Cu3O7-x (001) thin films grown on MgO (001) substrates by pulsed organo-metallic beam epitaxy (POMBE) is investigated by a series of film growth and characterization experiments, including RBS and TEM. The factors influencing the orientation change are systematically studied. The experimental results suggest that the substrate surface morphology change caused by the ion sputtering and the Ar ion implantation in the substrate surface layer are not the major factors that affect the orientation change. Instead, the implantation of W ions, which come from the hot filament of the ion gun, and the initial Ba deposition layer in the YBCO film growth play the most important roles in controlling the epitaxy orientation change. Microstructure studies show that a BaxMg1-xO buffer layer is formed on top of the sputtered substrate surface due to Ba diffusion into the W implanted layer. It is believed that the formation of this buffer layer relieves the large lattice mismatch and changes the YBCO film from the 45° oriented growth to the 0° oriented growth.


2021 ◽  
Vol 59 ◽  
pp. 473-481
Author(s):  
Youzhang Huang ◽  
Xueshuang Zhu ◽  
Daoping Cai ◽  
Zhixiang Cui ◽  
Qianting Wang ◽  
...  

1993 ◽  
Vol 334 ◽  
Author(s):  
K. Yamane ◽  
M. Murahara

AbstractThe patterned Zn nucleation and the ZnS growth onto the Zn seeds on a thermal oxidized silicon substrate was demonstrated at room temperature with the excimer laser chemical vapor deposition method.The formation of ZnS films was realized by the method based on the two—step process consisting of the nucleation and the subsequent ZnS growth. In the nucleation, a gaseous dimethylzinc was sealed in a reaction chamber and was then evacuated immediately. Then, the substrate surface which was uniformly adsorbed by dimethylzinc molecules was exposed with a single shot irradiation of a patterned KrF laser; Zn seeds were created only on the irradiated parts by a photodecomposition. And the subsequent growth of ZnS was performed by the parallel or perpendicular irradiation methods. As a result, in the perpendicular irradiation method, the high selectivity and crystallinity of the film were performed by irradiating the whole substrate surface with very low fluence of the KrF laser such as 3 mJ/cm2.


2013 ◽  
Vol 20 (03n04) ◽  
pp. 1350039 ◽  
Author(s):  
YUDI GUO ◽  
DONGYAN TANG ◽  
SHUO GU

The dependence of particulate Langmuir–Blodgett (LB) monolayer quality on the surface nature of the substrate was investigated by pretreating the substrates with different methods, and the optimal withdrawal speed was determined by detecting the quality of particulate monolayers deposited at different withdrawal speeds. Furthermore, the effects of stearic acid (SA) concentration on the quality of particulate monolayers were discussed. Results indicated that surface amination would favor the transfer of the floating particulate monolayer from the interface to the substrate, which would be attributed to the formation of chemical bonds between the – NH 2 groups on the substrate surface and the functional groups of – COOH and Si – OH groups on surfaces of particles floating at the interface. And the withdrawal speed of 1 mm ⋅ min-1 was appropriate for the fabrication of high-quality particulate LB monolayer because low withdrawal speed can offer sufficient time to form chemical bonds and expel the subphase from the substrate. Additionally, SEM images illustrated that the SA concentration of 0.40 mg ⋅ mL-1 was suitable for the fabrication of well-ordered particulate LB monolayers composed by the particles of 380 nm.


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