scholarly journals Polymer/Graphene oxide nanocomposite thin film for NO2 sensor: An in situ investigation of electronic, morphological, structural, and spectroscopic properties

2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Praveen Kumar Sahu ◽  
Rajiv K. Pandey ◽  
R. Dwivedi ◽  
V. N. Mishra ◽  
R. Prakash
2008 ◽  
Vol 62 (17-18) ◽  
pp. 2654-2656 ◽  
Author(s):  
H.H. Liu ◽  
X.K. Duan ◽  
R.C. Che ◽  
Z.F. Wang ◽  
X.F. Duan

2020 ◽  
Vol 10 (21) ◽  
pp. 7703
Author(s):  
Woo Hyun Nam ◽  
Hyung Mo Jeong ◽  
Jong-Hyeong Lim ◽  
Jong-Min Oh ◽  
Hiesang Sohn ◽  
...  

ZnO is utilized as a promising material for various electronic and energy areas due to its outstanding chemical stability, abundance, non-toxicity, and low cost. However, controlling electronic transport properties of ZnO by facile strategy is still necessary for wider applications. Here, we synthesized reduced graphene oxide incorporated Al-doped ZnO nanocomposite thin film prepared by the electrospray deposition method and investigated the electronic transport behavior. The electron transport in pristine Al-doped ZnO thin film is strongly affected by grain boundary scattering, but significant enhancement of carrier mobility is observed in reduced graphene oxide-incorporated Al-doped ZnO nanocomposite thin film. The results demonstrate that this hybrid strategy with graphene has an important effect on the charge transport behavior in ZnO polycrystalline materials.


2017 ◽  
Vol 5 (31) ◽  
pp. 7746-7752 ◽  
Author(s):  
Xueliang Ye ◽  
Zhen Yuan ◽  
Huiling Tai ◽  
Weizhi Li ◽  
Xiaosong Du ◽  
...  

A novel strain sensor based on reduced graphene oxide with ultra-sensitive and ultra-durable performance was fabricated by the chemical layer-by-layer self-assembly method.


Author(s):  
Moritz Doering ◽  
Jochen Kieninger ◽  
Gerald Urban ◽  
Andreas Weltin

Abstract Objective. The stability of platinum and other noble metal electrodes is critical for neural implants, electrochemical sensors, and energy sources. Beyond the acidic or alkaline environment found in most electrochemical studies, the investigation of electrode corrosion in neutral pH and chloride containing electrolytes is essential, particularly regarding the long-term stability of neural interfaces, such as brain stimulation electrodes or cochlear implants. In addition, the increased use of microfabricated devices demands the investigation of thin-film electrode stability. Approach. We developed a procedure of electrochemical methods for continuous tracking of electrode degradation in situ over the complete life cycle of platinum thin-film microelectrodes in a unique combination with simultaneous chemical sensing. We used chronoamperometry and cyclic voltammetry to measure electrode surface and analyte redox processes, together with accelerated electrochemical degradation. Main results. We compared degradation between thin-film microelectrodes and bulk electrodes, neutral to acidic pH, different pulsing schemes, and the presence of the redox active species oxygen and hydrogen peroxide. Results were confirmed by mechanical profilometry and microscopy to determine material changes on a nanometer scale. We found that electrode degradation is mainly driven by repeated formation and removal of the platinum surface oxide, also within the electrochemical stability window of water. There was no considerable difference between thin-film micro- and macroscopic bulk electrodes or in the presence of reactive species, whereas acidic pH or extending the potential window led to increased degradation. Significance. Our results provide valuable fundamental information on platinum microelectrode degradation under conditions found in biomedical applications. For the first time, we deployed a unified method to report quantitative data on electrode degradation up to a defined endpoint. Our method is a widely applicable framework for comparative long-term studies of sensor and neural interface stability.


2011 ◽  
Vol 415-417 ◽  
pp. 715-719 ◽  
Author(s):  
Akhmad Herman Yuwono ◽  
Yu Zhang ◽  
John Wang

Nanocomposite thin film containing TiO2nanoparticles in polymethyl methacrylate (PMMA) is a new class of potential materials for optoelectronic applications. Among the various processing techniques for these nanocomposites, in situ sol−gel process is well known to be versatile as it enables control of the inorganic-organic interaction at various molecular, nanometer and micrometer scales. However, the resulting TiO2phase is largely amorphous, as a consequence of the relatively low processing temperatures. Therefore, the current research is aimed at enhancing the nanocrystallinity of TiO2nanoparticles in nanocomposites. For this purpose, pre-hydrothermal treatment was carried on the inorganic sols. The nanocrystallinity degree of the resulting TiO2nanoparticles was studied by XRD and FTIR. The studies showed that the nanocrystallinity of TiO2nanoparticles synthesized from the inorganic sol can be enhanced significantly by the pre-hydrothermal treatment, as a result of the completion of hydrolysis stage during sol-gel process.


1997 ◽  
Vol 485 ◽  
Author(s):  
D. Wolf ◽  
G. Müller

AbstractStudies of the reaction path during annealing of Cu-In-Se thin films for solar cell absorbers have been limited up to now to ex-situ analyses of the phase composition by X-Ray Diffraction (XRD) after processing by a specific temperature-time program. As an indirect method, the application of ex-situ XRD is not sufficient for the determination of reaction temperatures and reaction times for setting up a general model of CIS-formation.We show in this paper that the use of a calorimetric method (Thin Film Calorimetry, TFC) offers the advantage of a direct (in-situ) observation of thin film reactions. Special care is taken to use film thicknesses of practical interest for industrial application (1.5 – 3 μm). In a first step we show results of binary reactions in the Cu-In, In-Se and Cu-Se systems. Their knowledge is necessary for understanding the processes involved in the ternary CIS-layers. It turned out that thin Cu-In and Cu-Se films react already at room temperature and behave as predicted by the bulk equilibrium phase diagrams during heating. In-Se thin films show prominent exothermic reactions starting with the melting of In. The first phase to be formed is generally In2Se which is then converted to more Se-rich compounds. In ternary Cu-In-Se films (Cu/In = 1.00) we observe transitions of the Cu-Se-system which can be attributed to the decomposition of CuSe2 and CuSe. Consequences for the model of improved CIS-growth by a Cu-Se flux agent are discussed.


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