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STUDI PREPARASI TIO2 NANOTUBE SERBUK DENGAN TEKNIK RAPID BREAKDOWN ANODIZATION Linda J Kusumawardanil; Ivandini Tribidasari; Jarnuzi Gunlazuardi
Ekologia: Jurnal Ilmiah Ilmu Dasar dan Lingkungan Hidup Vol 16, No 1 (2016): Ekologia : Jurnal Ilmiah Ilmu Dasar dan Lingkungan Hidup
Publisher : Universitas Pakuan

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.33751/ekol.v16i1.56

Abstract

Technique of Rapid Breakdown Anodization (RBA) is the new anodisasi technique introduced in 2009 as super fast synthesis methods for producing TiO2 powder. The development of this technique continues to be done in order to obtain the best quality of TiO2 powders according to the needs of the application. At this time the experiment reported the existence of the influence the granting of potential anodisasi currently underway against TiO2 powder produced good particle size, surface area and shape of the morfologinya. In addition, observations on the reaction time is also conducted to take into account the efficiency. From the results of the experiment, potential variations below 20 V, i.e., 10, 13, 14 and 15 V, it can be reported that the plate It can be transformed into the perfect TiO2 powder on electrochemical reaction of potential system 15 V for approximately 3 hours in perchloric acid media 0.15 M. Whereas the process of potential reactions on 10, 13 and 14 V does not produce TiO2 powder significantly in the time of observation for 7 hours. So further study focused on the synthesis of TiO2 powder results in a potential 15 V which will be compared with the potential 20 V, which is a potential that is used when this technique was first introduced. From the results of the experiment, reported on the potential RBA engineering 15 V produces TiO2 powder with a size outer diameter are smaller, i.e. an average of 84 nm with a more uniform particle size and surface area of the Crystal results kalsinasi at 500oC generated on 15 potential V is wider with a more uniform morphology, i.e. 69.723 g/m2 compared to 20 V , i.e. 63.824 g/m2. This will provide a significant influence in the activity of the fotokatalitik used for the fotodegradasi, as well as its application as DSSC (Dye Sensitized Solar Cells).  KeyWord  :Rapid Breakdown Anodization (RBA), Anodisasi, TiO2, TiO2 Nanotube-Serbuk
Development of BiOBr/TiO2 nanotubes electrode for conversion of nitrogen to ammonia in a tandem photoelectrochemical cell under visible light Prita Amelia; Jarnuzi Gunlazuardi
International Journal of Renewable Energy Development Vol 12, No 4 (2023): July 2023
Publisher : Center of Biomass & Renewable Energy, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14710/ijred.2023.51314

Abstract

Ammonia (NH3) is one of the important chemicals for human life. The demand for ammonia is expected to increase every year. Conventionally, the fixation process of N2 to produce NH3 in the industrial sector is carried out through the Haber−Bosch process, which requires extreme temperature and pressure conditions that consume a high amount of energy and emit a considerable amount of CO2. Therefore, it is necessary to develop alternative technology to produce ammonia using environmentally friendly methods. Many studies have developed the photo-electrochemical conversion of nitrogen to ammonia in the presence of semiconductor materials, but the resulting efficiency is still not as expected. In this research, the development of the tandem system of Dye-Sensitized Solar Cell - Photoelectrochemistry (DSSC - PEC) was carried out for the conversion of nitrogen to ammonia. The DSSC cell was prepared using N719/TiO2 nanotubes as photoanode, Pt/FTO as cathode, and electrolyte I-/I3-. The DSSC efficiency produced in this research was 1.49%. PEC cell at the cathode and anode were prepared using BiOBr/TiO2 nanotubes synthesized by the SILAR (Successive Ionic Layer Adsorption and Reaction) method. The resulting ammonia levels were analyzed using the phenate method. In this study, ammonia levels were obtained at 0.1272 µmol for 6 hours of irradiation with an SCC (Solar to Chemical Conversion) percentage of 0.0021%.
Development of Microfluidic Paper-Based Analytical Devices (µPADs) for Determination of Cd2+, Pb2+, and Cu2+ Ions in Mineral Water Andri Hermansyah; Neil V. Rees; Jarnuzi Gunlazuardi; Rahmat Wibowo
Jurnal Kimia Sains dan Aplikasi Vol 26, No 9 (2023): Volume 26 Issue 9 Year 2023
Publisher : Chemistry Department, Faculty of Sciences and Mathematics, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14710/jksa.26.9.353-362

Abstract

Microfluidic paper-based analytical devices (µPADs) have been successfully developed using dual detection: electrochemical and colorimetric systems. The µPADs have the potential to be used as Pb(II), Cd(II), and Cu(II) sensors to test the quality of water. The fabrication process uses hot embossing and screen-printing methods. The working electrode in the electrochemical zone was enhanced by the bismuth metal deposition process, while in the colorimetric zone, the gold nanoparticles modified with thioctic acid and dansylhydrazine (TA-Au-DNS) were used as a colorimetric sensor to detect Cu. The basic material of µPADs was characterized using a Fourier-transform infrared (FTIR) and a contact angle meter (CAM). In the electrochemical zone, the signals of square wave anodic stripping voltammetry (SWASV) resulted in good detection of Pb(II) and Cd(II) (from 0 to 100 ppb) with a limit of detection of 1.588 and 1.42 ppb, respectively. In the colorimetric zone, the performance of TA-Au-DNS for detecting Cu metal was obtained from readings through the red-green-blue (RGB) sensor as a miniature of µPADs reader. The LOD, LOQ, and average Vx0 (linearity values) in the detection of Cu(II) (from 58 to 100 ppb) are 8.51 ppb, 28.36 ppb, and 0.41%, respectively.
Light-Harvesting Metal-Organic Frameworks (MOFs) La-PTC for Photocatalytic Dyes Degradation Agustino Zulys; Adawiah Adawiah; Jarnuzi Gunlazuardi; Muhammad Derry Luthfi Yudhi
Bulletin of Chemical Reaction Engineering & Catalysis 2021: BCREC Volume 16 Issue 1 Year 2021 (March 2021)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.16.1.10309.170-178

Abstract

A novel porous metal organic framework, La-PTC was synthesized by solvothermal method using a perylene-3,4,9,10-tetracarboxylate ligand and lanthanum metal ion. The FTIR analysis showed that La-PTC has a different structure with PTCDA and Na4PTC. The La-PTC MOF has high crystallinity, bandgap energy of 2.21 eV with a maximum absorption area at 561 nm. A rod shape structure of La-PTC has been obtained with the surface area of 22.2364 m2.g−1 and classified into mesoporous material. The La-PTC was relative stable up to 376.93 °C. The La-PTC can degrade 64.76% of MO within ca. 240 min under visible light irradiation with the amount of 30 mg La-PTC. The addition of H2O2 improved the photocatalytic activity of La-PTC with degradation efficiency of 67.02%, 70.00%, and 99.60% for MB, RhB, and MO, respectively. This study presents the fabrication of the light-harvesting metal organic framework, La-PTC and its potential in dyes degradation. Copyright © 2021 by Authors, Published by BCREC Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0). 
Comparative Study of Bismuth Ferrite Deposition Method on TiO2 Nanotube and Performance of Hydrogen Evolution in a Photoelectrochemical Dye-Sensitized Solar Cell Tandem System Yunita, Yunita; Syauqi, Muhammad Iqbal; Gunlazuardi, Jarnuzi
Makara Journal of Science
Publisher : UI Scholars Hub

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Abstract

Hydrogen is a renewable and environmentally friendly energy source that can replace fossil fuels by utilizing solar energy through water splitting. The hydrogen production was conducted in this research by using a tandem system of dye-sensitized solar cell–photoelectrochemical cell (DSSC–PEC) and a TiO2 nanotube coated with BiFeO3 (BiFeO3/TNT) as a photoanode in the PEC. The deposition of BiFeO3 on TNT was prepared using the following three methods: successive ionic layer adsorption and reaction (SILAR), ultrasonication-assisted SILAR, and ultrasonic– immersion method by varying the number of deposition cycles in each method. In this study, the optimum cycles for SILAR, ultrasonication-assisted SILAR, and ultrasonic–immersion methods were 15, 5, and 3, respectively. Results show that the BiFeO3 deposited on TNT using the ultrasonic–immersion method with three cycles (BiFeO3/TNT_UI3) demonstrates the best photoelectrochemical activity. The tandem system comprises BiFeO3/TNT_UI3 photoanode and Pt-coated TNT dark cathode PEC cell connected to TNT/N719-based DSSC with an efficiency of 1.27%. The constructed DSSC–PEC system could produce 3.11 × 10−6 mol hydrogen in 6 h with a solar-to-hydrogen (STH) efficiency of 0.0033% in an H-type reactor filled with 0.5 M H2SO4 electrolyte.
Modification of Gold Nanoparticles at Carbon Electrodes and the Applications for Arsenic (III) Detections Ivandini, Tribidasari Anggraningrum; Wijaya, Lany; Gunlazuardi, Jarnuzi
Makara Journal of Science Vol. 16, No. 1
Publisher : UI Scholars Hub

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Abstract

TiO2 Crystallization at Room Temperature and Preparation of Transparent Carbon Counter Electrode for Low-Cost Dye-Sensitized Solar Cells Syauqi, Muhammad Iqbal; Sanjaya, Afiten Rahmin; Madiabu, Mohammad Jihad; Khalil, Munawar; Gunlazuardi, Jarnuzi
Makara Journal of Science Vol. 27, No. 2
Publisher : UI Scholars Hub

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Abstract

We developed a low-cost dye-sensitized solar cell (DSSC) using TiO2 fabricated via rapid breakdown anodization (RBA) and ultrafast room-temperature crystallization (URTC). The prepared TiO2 was deposited on a self-made fluorine-doped tin oxide (FTO) conductive glass, and the FTO/TiO2 system was sensitized using curcumin dye. The DSSC was constructed by sandwiching the FTO/TiO2/curcumin electrode with an I−/I2 electrolyte and a transparent carbon counter electrode prepared using a liquid–liquid interface system. The characterization results showed that the TiO2 freshly prepared via URTC was transformed into an anatase crystalline phase, which exhibited a 3.10 eV band gap and a 10.08 nm average crystallite size, comparable to those of the TiO2 prepared via the conventional 450 °C annealing treatment (3.13 eV, 11.60 nm). The photocurrent activity of the URTC-prepared TiO2 under ultraviolet light (0.10 mA/cm2) was also comparable to that of the annealed TiO2 (0.12 mA/cm2). In addition, a transparent carbon electrode (FTO/Ct) was prepared successfully; it exhibited a ±58.26% transparency under visible light and comparable electrocatalytic activity to Pt-coated FTO. The DSSC based on FTO/TiO2-URTC/curcumin and FTO/Ct showed front and back illumination efficiencies of 0.47% and 0.26%, respectively. These results are only slightly lower than those of the conventional DSSC with FTO/annealed TiO2/curcumin//FTO/Pt, which exhibited front and back illumination efficiencies of 0.52% and 0.36%, respectively.
Effect of Precursors Concentration on The Optical and Photoelectrochemical Properties of Bi₂S₃/TiO₂ Nanotubes Arrays Photoanode Synthesized by the SILAR Technique Eko Martin Sinaga; Muhammad Iqbal Syauqi; Jarnuzi Gunlazuardi
Jurnal Kimia Sains dan Aplikasi Vol 27, No 6 (2024): Volume 27 Issue 6 Year 2024
Publisher : Chemistry Department, Faculty of Sciences and Mathematics, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14710/jksa.27.6.265-270

Abstract

The use of robust solar energy-driven photocatalysis materials to address the global energy and environmental crisis has gained significant attention in recent years. However, the wide band gaps in many robust semiconductor photocatalysts hinder their absorption of visible light from the solar spectrum. To address this issue, the modification of the large band gap semiconductor with the lower band gap material using the Successive Ionic Layers Adsorption and Reaction (SILAR) technique has emerged as an economical, accessible, and reproducible method for depositing nanoscale materials onto semiconductor substrates. This research aims to know how the concentration variation of cation and anion precursors in the SILAR technique affects the optical and photoelectrochemical properties of the resulting composite materials. Bi₂S₃ serves as a modifier for TiO₂ nanotube arrays (NTAs). The result shows that the cation-anion concentration ratio of 1:1.5 mM with five SILAR cycles gives the best photoelectrochemical performance, with a stable current density of 0.12 mA/cm², compared to pristine TiO₂ NTAs the current density of Bi₂S₃/TiO₂ NTAs is 15-fold. In addition, at each variation, the concentration ratio of cation and anion precursors decreases bandgap energy with each increase in the SILAR cycle.
Glycine-modulated Zirconium Perylene-based Metal-Organic Framework for Rhodamin B Photocatalytic Degradation Zulys, Agustino; Defania, Mella; Gunlazuardi, Jarnuzi; Adawiah, Adawiah
Molekul Vol 18 No 3 (2023)
Publisher : Universitas Jenderal Soedirman

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.20884/1.jm.2023.18.3.9126

Abstract

Photocatalysis employing Metal-Organic Framework (MOF) material may degrade Rhodamin B pollutant. MOF photocatalytic activity can be adjusted by altering the ligands, metal ions, and modulators. This research aims to synthesize glycine-modulated zirconium perylene-based metal organic framework (Zr-PTCA-Gly) for Rhodamin B photocatalytic degradation under visible light irradiation. The activated Zr-PTCA-Gly exhibits good catalytic activity to degrade Rhodamine B with a 95% degradation efficiency.
Synthesis and characterization silica-MB@GO-NH2 particle as fluorescence-based chlorine sensor Fatah, Fadhlir Rahman Aufar Al; Rahmawati, Isnaini; Gunlazuardi, Jarnuzi; Sanjaya, Afiten Rahmin
Environmental and Materials Vol. 1 No. 2: (December) 2023
Publisher : Institute for Advanced Science, Social, and Sustainable Future

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.61511/eam.v1i2.2023.399

Abstract

In this research, we developed a fluorescence-based sensor to determine the sodium hypochlorite concentration (NaOCl) in tap water and swimming pool water samples. The detection of NaOCl was conducted by measuring the luminescence response of analyte in the paper-based sensor modified Silica-MB@GO-NH2 material were synthesized using Hummer's and Stober's methods under UV Light irradiation. Additionally, the prepared material exposed a couple peak 2D and 2G at 2938 cm-1 and 3286 cm-1 with ID/IG ratio 0.98 using Raman characterization which appropriate with the presence of GO structure in the mixture. This result was validated by the appearance of several functional groups like Si-O-Si, NH, OH, and C-C at 1079, 1391, 1611, and 3457 cm-1, respectively. Moreover, the existence of Si-O-Si bond indicates that the silica-MB interaction was perfectly formed, which plays the main role to absorb ultraviolet light that is used as sensor probe. The morphology of particles depicted an aggregated formation of spherical structure with 288 nm particle size, indicating the existence of silica-coated methylene blue. In this work, the paper-based sensor modified Silica-MB@GO-NH2 can detect the NaOCl species with concentration range 10-150 µM (R2 = 0.9757), a detection limit at 2.60 µM and quantification limit at 7.88 µM. Furthermore, this developed sensor has stable measurement with recovery performance 3.65%-6.67% for tap water and 0.05%–0.14% for swimming pool water. This result indicates that the prepared sensor can be potentially applied to calculate the hypochlorite species in the aquatic environment.