scholarly journals Enhancement of Capacitive Performance in Titania Nanotubes Modified by an Electrochemical Reduction Method

2018 ◽  
Vol 2018 ◽  
pp. 1-9 ◽  
Author(s):  
Nurul Asma Samsudin ◽  
Zulkarnain Zainal ◽  
Hong Ngee Lim ◽  
Yusran Sulaiman ◽  
Sook-Keng Chang ◽  
...  
Keyword(s):  
Electrochemical Performance ◽  
Electrochemical Reduction ◽  
Photoelectron Spectroscopy ◽  
Oxygen Vacancies ◽  
Reduction Method ◽  
Titania Nanotubes ◽  
Electrochemical Anodization ◽  
Constant Current ◽  
Cyclic Voltammogram ◽  
Capacitive Performance

Highly ordered titania nanotubes (TNTs) were synthesised by an electrochemical anodization method for supercapacitor applications. However, the capacitive performance of the TNTs was relatively low and comparable to the conventional capacitor. Therefore, in order to improve the capacitive performance of the TNTs, a fast and facile electrochemical reduction method was applied to modify the TNTs (R-TNTs) by introducing oxygen vacancies into the lattice. X-ray photoelectron spectroscopy (XPS) data confirmed the presence of oxygen vacancies in the R-TNTs lattice upon the reduction of Ti4+ to Ti3+. Electrochemical reduction parameters such as applied voltage and reduction time were varied to optimize the best conditions for the modification process. The electrochemical performance of the samples was analyzed in a three-electrode configuration cell. The cyclic voltammogram recorded at 200 mV s−1 showed a perfect square-shaped voltammogram indicating the excellent electrochemical performance of R-TNTs prepared at 5 V for 30 s. The total area of the R-TNTs voltammogram was 3 times larger than the unmodified TNTs. A specific capacitance of 11.12 mF cm−2 at a current density of 20 μA cm−2 was obtained from constant current charge-discharge measurements, which was approximately 57 times higher than that of unmodified TNTs. R-TNTs also displayed outstanding cycle stability with 99% capacity retention after 1000 cycles.

scholarly journals Enhanced capacitive performance of cathodically reduced titania nanotubes pulsed deposited with Mn2O3 as supercapacitor electrode

RSC Advances ◽  
2021 ◽  
Vol 11 (43) ◽  
pp. 26700-26709
Author(s):  
Muhammad Muhammad Muzakir ◽  
Zulkarnain Zainal ◽  
Hong Ngee Lim ◽  
Abdul Halim Abdullah ◽  
Noor Nazihah Bahrudin
Keyword(s):  
Electrochemical Performance ◽  
Titania Nanotubes ◽  
Pulse Electrodeposition ◽  
Mass Loading ◽  
Supercapacitor Electrode ◽  
Capacitive Performance

The mass loading of Mn2O3 by pulse electrodeposition (PED) onto reduced titania nanotubes (R-TNTs) greatly influences the electrochemical performance of the composite.

Carbon Nanotubes/MnO2 Composite Fabricated via Laser Welding and Electrodeposition as Flexible Electrode for Supercapacitors

NANO ◽  
2019 ◽  
Vol 14 (06) ◽  
pp. 1950074 ◽  
Author(s):  
Mingping He ◽  
Jianguang Li ◽  
Wanli Xu ◽  
Zhenqiang Dong ◽  
Yuechao Wu ◽  
...  
Keyword(s):  
Carbon Nanotubes ◽  
Electrochemical Performance ◽  
Photoelectron Spectroscopy ◽  
Electrochemical Impedance ◽  
Easy Access ◽  
Cyclic Voltammogram ◽  
X Ray Diffraction ◽  
Porous Network ◽  
Flexible Electrode ◽  
X Ray

Carbon nanotubes (CNTs) were welded on the surface of thermoplastic polypropylene (PP) substrate by laser irradiation and then manganese dioxide (MnO2) was deposited on the surface of CNTs by electrochemical method to prepare CNTs/MnO2 flexible electrodes (L-CM). The microstructure and morphology of CNTs/MnO2 composites were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM). The results showed that CNTs were welded on the surface of the substrate, adhering to each other to form a porous network structure. In addition, there were distinct small protrusions on the surface of CNTs, indicating that MnO2 had been successfully deposited on the surface of CNTs. Cyclic voltammogram (CV), galvanostatic charge/discharge (GCD) and electrochemical impedance spectroscopy (EIS) techniques were employed to investigate the electrochemical performance of the composites. Compared with CNTs/MnO2 composite prepared via compaction (denoted as C-CM), L-CM composite prepared under the laser power of 0.75[Formula: see text]W (denoted as L-CM75) showed a larger capacitance of 214.6[Formula: see text]F[Formula: see text]g[Formula: see text] at the current density of 0.5[Formula: see text]A[Formula: see text]g[Formula: see text] and displayed excellent bendability, demonstrating capacitance retention of approximately 89.6% after 1000 bending cycles. The excellent performance of L-CM75 may be attributed to the fact that the CNTs welded on the substrate have formed an effective conductive network whose porous structure can facilitate easy access of electrolytes to the electrode, which results in enhancement of the electrochemical performance of L-CM75.

Investigation of Polyoxometalate-(Poly)pyrrole Heterogeneous Nanostructures as Cathodes for Rechargeable Magnesium-Ion Batteries

2018 ◽  
Author(s):  
Hakeem K. Henry ◽  
Sang Bok Lee
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Active Material ◽  
Conductive Polymer ◽  
Current Collector ◽  
Constant Current ◽  
Anodized Aluminum ◽  
Transmission Electron ◽  
Pyrrole Monomer

The PMo<sub>12</sub>-PPy heterogeneous cathode was synthesized electrochemically. In doing so, the PMo<sub>12</sub> redox-active material was impregnated throughout the conductive polymer matrix of the poly(pyrrole) nanowires. All chemicals and reagents used were purchased from Sigma-Aldrich. Anodized aluminum oxide (AAO) purchased from Whatman served as the porous hard template for nanowire deposition. A thin layer of gold of approximately 200nm was sputtered onto the disordered side of the AAO membrane to serve as the current collector. Copper tape was connected to the sputtered gold for contact and the device was sealed in parafilm with heat with an exposed area of 0.32 cm<sup>2</sup> to serve as the electroactive area for deposition. All electrochemical synthesis and experiments were conducted using a Bio-Logic MPG2 potentiostat. The deposition was carried out using a 3-electrode beaker cell setup with a solution of acetonitrile containing 5mM and 14mM of the phosphomolybdic acid and pyrrole monomer, respectively. The synthesis was achieved using chronoamperometry to apply a constant voltage of 0.8V vs. Ag/AgCl (BASi) to oxidatively polymerize the pyrrole monomer to poly(pyrrole). To prevent the POM from chemically polymerizing the pyrrole, an injection method was used in which the pyrrole monomer was added to the POM solution only after the deposition voltage had already been applied. The deposition was well controlled by limiting the amount of charge transferred to 300mC. Following deposition, the AAO template was removed by soaking in 3M sodium hydroxide (NaOH) for 20 minutes and rinsed several times with water. After synthesis, all cathodes underwent electrochemical testing to determine their performance using cyclic voltammetry and constant current charge-discharge cycling in 0.1 M Mg(ClO<sub>4</sub>)<sub>2</sub>/PC electrolyte. The cathodes were further characterized using scanning electron microscopy (SEM), transmission electron microscopy (TEM), scanning transmission electron microscopy (STEM), and x-ray photoelectron spectroscopy (XPS).

scholarly journals Study on Synthesis and Photocatalytic Activity of Porous Titania Nanotubes

2016 ◽  
Vol 2016 ◽  
pp. 1-10 ◽  
Author(s):  
Huang Liu ◽  
Yanhua Zhang ◽  
Hongtao Yang ◽  
Wei Xiao ◽  
Lanlan Sun
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Filter Paper ◽  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance Spectroscopy ◽  
Cellulose Nanofibers ◽  
Titania Nanotubes ◽  
Tetrabutyl Titanate ◽  
X Ray ◽  
Porous Titania

Using the common natural cellulose substance (filter paper) and triblock copolymer (Pluronic P123) micelles as dual templates, porous titania nanotubes with enhanced photocatalytic activity have been successfully synthesized through sol-gel methods. Firstly, P123 micelles were adsorbed onto the surfaces of cellulose nanofibers of filter paper, followed by hydrolysis and condensation of tetrabutyl titanate around these micelles to form titania layer. After calcination to remove the organic templates, hierarchical titania nanotubes with pores in the walls were obtained. The sample was characterized by X-ray diffraction pattern (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), nitrogen adsorption/desorption, Fourier Transform Infrared Spectroscopy (FT-IR), Ultraviolet-Visible Diffuse Reflectance Spectroscopy (UV-Vis DRS), and X-ray photoelectron spectroscopy (XPS). As compared with commercial P25 catalyst, the porous titania nanotubes prepared by this method displayed significantly enhanced photocatalytic activity for degrading methyl orange under UV irradiation. Within 10 minutes, the porous titania nanotubes are able to degrade over 70% of the original MO, while the value for the commercial Degussa P25 is only about 33%.

Engineering the geometric and electronic structure of Ru via Ru-TiO2 interaction for enhanced selective hydrogenation

2022 ◽  
Author(s):  
Jian-guo Wang ◽  
Qiang Zhou ◽  
Zijiang Zhao ◽  
Zihao Yao ◽  
Zhongzhe Wei ◽  
...  
Keyword(s):  
Electronic Structure ◽  
Chemical Reactions ◽  
Selective Hydrogenation ◽  
Oxygen Vacancies ◽  
Reduction Method ◽  
Support Interaction ◽  
Important Chemical ◽  
Metal Support Interaction ◽  
Metal Support

Modulation of the metal-support interaction plays a key role in many important chemical reactions. Here, by adjusting the reduction method of the catalyst and introducing oxygen vacancies in TiO2 to...

scholarly journals Hydrothermal Synthesis of Iodine-Doped Nanoplates with Enhanced Visible and Ultraviolet-Induced Photocatalytic Activities

2012 ◽  
Vol 2012 ◽  
pp. 1-12 ◽  
Author(s):  
Jiang Zhang ◽  
Zheng-Hong Huang ◽  
Yong Xu ◽  
Feiyu Kang
Keyword(s):  
Photocatalytic Activity ◽  
Photoelectron Spectroscopy ◽  
Oxygen Vacancies ◽  
Diffuse Reflectance Spectroscopy ◽  
Synergetic Effect ◽  
X Ray Diffraction ◽  
X Ray ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
Photocatalytic Activities

The iodine-doped Bi2WO6(I-BWO) photocatalyst was prepared via a hydrothermal method using potassium iodide as the source of iodine. The samples were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscopy (TEM) and selected area electron diffraction (SAED), X-ray photoelectron spectroscopy (XPS), UV-vis diffuse reflectance spectroscopy (DRS), and photoluminescence (PL) spectroscopy. The photocatalytic activity of I-BWO for the degradation of rhodamine B (RhB) was higher than that of pure BWO and I2-BWO regardless of visible light (>420 nm) or ultraviolet light (<400 nm) irradiation. The results of DRS analysis showed that the I-BWO and I2-BWO catalysts had narrower band gaps. XPS analysis proved that the multivalent iodine species including I0and were coadsorbed on the defect surface of Bi2WO6in I-BWO. The enhanced PL intensity revealed that a large number of defects of oxygen vacancies were formed by the doping of iodine. The enhanced photocatalytic activity of I-BWO for degradation of RhB was caused by the synergetic effect of a small crystalline size, a narrow band gap, and plenty of oxygen vacancies.

scholarly journals Ferromagnetic Properties of N-Doped and Undoped TiO2 Rutile Single-Crystal Wafers with Addition of Tungsten Trioxide

Materials ◽  
2018 ◽  
Vol 11 (10) ◽  
pp. 1934 ◽  
Author(s):  
Jing Xu ◽  
Haiying Wang ◽  
Zhongpo Zhou ◽  
Zhaorui Zou
Keyword(s):  
Magnetic Properties ◽  
Single Crystal ◽  
Saturation Magnetization ◽  
Photoelectron Spectroscopy ◽  
Oxygen Vacancies ◽  
Tio2 Surface ◽  
Doped Tio2 ◽  
X Ray ◽  
N Doping ◽  
Tio2 Rutile

In this work, undoped, N-doped, WO3-loaded undoped, and WO3-loaded with N-doped TiO2 rutile single-crystal wafers were fabricated by direct current (DC) magnetron sputtering. N-doping into TiO2 and WO3 loading onto TiO2 surface were used to increase and decrease oxygen vacancies. Various measurements were conducted to analyze the structural and magnetic properties of the samples. X-ray diffraction results showed that the N-doping and WO3 loading did not change the phase of all samples. X-ray photoelectron spectroscopy results revealed that W element loaded onto rutile single-crystal wafers existed in the form of WO3. UV-Vis spectrometer results showed that the absorption edge of WO3-loaded undoped and WO3-loaded with N-doped TiO2 rutile single-crystal wafers had red shift, resulting in a slight decrease in the corresponding band gap. Photoluminescence spectra indicated that oxygen vacancies existed in all samples due to the postannealing atmosphere, and oxygen vacancies density increased with N-doping, while decreasing with WO3 loading onto TiO2 surface. The magnetic properties of the samples were investigated, and the saturation magnetization values were in the order N-doped > WO3-loaded with N-doped > undoped > WO3-loaded undoped rutile single-crystal wafers, which was the same order as the oxygen vacancy densities of these samples. N-doping improved the saturation magnetization values, while WO3-loaded decreased the saturation magnetization values. This paper reveals that the magnetic properties of WO3-loaded with N-doped rutile single-crystal wafers originate from oxygen vacancies.

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