ITO/Poly-3-Methylaniline/Au Electrode for Electrochemical Water Splitting and Dye Removal

Author(s):  
Ahmed Adel A. Abdelazeez ◽  
Gehad Abd El-Fatah ◽  
Mohamed Shaban ◽  
Ashour M. Ahmed ◽  
Mohamed Rabia

Abstract Application of aniline derivative semiconductor nanopolymer and its Au composite for H2 generation and dye removal were investigated. Electrochemical polymerization of poly-3-methylaniline (P3MA) on ITO glass was carried out for acid medium. Au nanoparticles with crystal sizes of 15 and 30 nm were sputter coated on the surface. Chemical structure of the polymer and its composite was characterized using FTIR, XRD, 1HNMR, SEM, and UV-Vis. All function groups were confirmed using FTIR analyses. XRD confirmed the formation of nanopolymer with a crystal size of ~15 nm. SEM confirmed the formation of smooth lamellar surface feature with a <20 nm nanoporous structure. Porosity and particle sizes increases with Au coating, confirmed using the modeling Image J program. Optical analysis also demonstrated that the strength of P3MA absorption peaks increases with rising Au coating time, in which the bandgap values changed from 1.64 to 1.63 eV for 15 and 30 nm Au, respectively. The photoelectrode ITO/PMT/30 nm Au was applied for H2 generation and dye removal. The current density (Jph) values were -0.3 and -1.6 mA.cm-2 in the absence and presence of the Congo red dye, respectively. The incident photon-to-current conversion efficiency (IPCE%) for the electrode was 2.3 at 390 nm. The activation energy (Ea) was 31.49 KJ mol-1. The enthalpy (∆H*) and entropy (∆S*) values were 114.49 and 160.46 JK-1 mol-1, respectively. A simple mechanism for the H2 generation and dye removal is mentioned

2021 ◽  
Vol 765 (1) ◽  
pp. 012089
Author(s):  
R Taufik ◽  
M Mohamad ◽  
R Wannahari ◽  
N F Shoparwe ◽  
WHW Osman ◽  
...  

2021 ◽  
pp. 111492
Author(s):  
Dang Le Tri Nguyen ◽  
Quach An Binh ◽  
Xuan Cuong Nguyen ◽  
Thi Thanh Huyen Nguyen ◽  
Quang Nha Vo ◽  
...  

Processes ◽  
2020 ◽  
Vol 8 (6) ◽  
pp. 653 ◽  
Author(s):  
Nina Mladenovic ◽  
Petre Makreski ◽  
Anita Tarbuk ◽  
Katia Grgic ◽  
Blazo Boev ◽  
...  

To improve the ability of the rice husk to purify colored wastewater, effluent from the alkaline scouring of cotton yarn was used immediately after the scouring (without cooling and additionally added chemicals) in order to remove the non-cellulosic silicon-lignin shield from the rice husk’s surface. This rice husk, with 93.8 mg/g adsorption capacity, behaves similarly as the rice husk treated with an optimized alkaline scouring recipe consisting of 20 g/L NaOH, 2 mL/L Cotoblanc HTD-N and 1 mL/L Kemonecer NI at 70 °C for 30 min with an adsorption capacity of 88.9 mg/g of direct Congo red dye. Treating one form of waste (rice husk) with another (effluent from the alkaline scouring of cellulosic plant fibers), in an effort to produce a material able to purify colored effluent, is an elegant environment-friendly concept based on the circular economy strategy. This will result in a closed-loop energy-efficient process of the pre-treatment of cotton (alkaline scouring), modification of rice husk using effluent from the alkaline scouring, dyeing cotton fabrics and cleaning its colored effluents with modified rice husk without adding chemicals and energy for heating.


2020 ◽  
Vol 8 (1) ◽  
pp. 103618 ◽  
Author(s):  
Ana Carolina de Lima Barizão ◽  
Marcela Fernandes Silva ◽  
Murilo Andrade ◽  
Fernanda Caroline Brito ◽  
Raquel Guttierres Gomes ◽  
...  

2019 ◽  
Vol 2019 ◽  
pp. 1-11 ◽  
Author(s):  
H. Letifi ◽  
Y. Litaiem ◽  
D. Dridi ◽  
S. Ammar ◽  
R. Chtourou

In this paper, we have reported a novel photocatalytic study of vanadium-doped SnO2 nanoparticles (SnO2: V NPs) in rhodamine B degradation. These NPs have been prepared with vanadium concentrations varying from 0% to 4% via the coprecipitation method. Structural, morphological, and optical properties of the prepared nanoparticles have been investigated by X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, transmission electron microscope (TEM), and UV-Vis and photoluminescence (PL) spectroscopy. Structural properties showed that both undoped and SnO2: V NPs exhibited the tetragonal structure, and the average crystal size has been decreased from 20 nm to 10 nm with the increasing doping level of vanadium. Optical studies showed that the absorption edge of SnO2: V NPs showed a redshift with the increasing vanadium concentration. This redshift leads to the decrease in the optical band gap from 3.25 eV to 2.55 eV. A quenching in luminescence intensity has been observed in SnO2: V NPs, as compared to the undoped sample. Rhodamine B dye (RhB) has been used to study the photocatalytic degradation of all synthesized NPs. As compared to undoped SnO2 NPs, the photocatalytic activity of SnO2: V NPs has been improved. RhB dye was considerably degraded by 95% within 150 min over on the SnO2: V NPs.


2013 ◽  
Vol 832 ◽  
pp. 333-337 ◽  
Author(s):  
Zainovia Lockman ◽  
Dede Miftahul Anwar ◽  
Monna Rozana ◽  
Syahriza Ismail ◽  
Ehsan Ahmadi ◽  
...  

Anodic oxidation of titanium (Ti), zirconium (Zr) and niobium (Nb) foils in fluoride ethylene glycol (EG) added to it 1 H2O2 as oxidant was done to produce oxide film with nanostructures at 40 V. Whilst arrays of aligned nanotubes were successfully formed on the surface of Ti and Zr respectively, anodic Nb2O5 was found to consist of nanoporous structure with pore size of ~ 20 nm. Despite long nanotubes were formed on both Ti (2 μm) and Zr (3 μm), the surface of the nanotubes suffered from severe dissolution, thinning the wall and collapsing them. Well defined, ordered surface structure of the nanotubes is required as they will be used as template for subsequent deposition of nanoparticles. This was achieved when Ti anodised in 5 ml H2O2 fluoride EG. With excess H2O2 etching at the surface occur more uniformly forming homogenous surface structure. α-Fe2O3 were then electrodeposited on this surface at-3 V from chloride solution and the mode of formation is believed to be due to electrogeneration of base at the surface of the TiO2.


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