Md. Rakibul Hasan
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Md. Rakibul Hasan has a total of 14 co-authors. Here are the top co-authors by number of shared publications:
- Sharifah Bee Abd Hamid
Nanotechnology and Catalysis Research Center (NANOCAT), University of Malaya, Kuala Lumpur 50603, Malaysia
3 shared publications - Syazwan Hanani Meriam Suhaimy
Nanotechnology and Catalysis Research Centre (NANOCAT), Institute of Graduate Studies, University of Malaya, Kuala Lumpur 50603, Malaysia
2 shared publications - Wan Jefrey Basirun
Department of Chemistry, Faculty of Science, University Malaya, Kuala Lumpur 50603, Malaysia
2 shared publications - Ahmad Esmaielzadeh Kandjani
CSIRO, Manufacturing Research Unit (MRU), Research Way, Clayton, Melbourne, Victoria 3168, Australia
1 shared publication - Ahmad Hazri Ab Rashid
Industrial Biotechnology Research Centre, SIRIM Berhad, No.1, Persiaran Dato’ Menteri, Section 2, P.O. Box 7035, 40700 Shah Alam, Malaysia
1 shared publication - Ahmad Nazeer Che Mat
Department of Chemistry, Faculty of Science, University of Malaya, Kuala Lumpur, Malaysia
1 shared publication
Latest Publications
- Open Access
TiO2 Nanotubes Supported Cu Nanoparticles for Improving Photocatalytic Degradation of Simazine under UV Illumination
Nano size Copper (Cu) incorporated TiO2 nanotubes was successfully synthesized via the anodic oxidation technique in ethylene glycol (EG) containing 0.5 wt % NH4F and 1.6 wt % KOH for the photocatalytic degradation of Simazine (2-chloro-4, 6-diethylamino-1,3,5-triazine) under Ultraviolet (UV) illumination. In the present study, the influence of different loading Cu concentrations on the formation of Cu-TiO2 nanotubes film towards the photocatalytic degradation of Simazine is reported. Based on our study, it was found that the optimum Cu loading concentration was about 0.45 wt % on TiO2 nanotubes film for approximately 64% photocatalytic degradation of Simazine after 4 h under UV illumination. This finding was mainly attributed to the uniform surface covering of the Cu loaded TiO2NTs which acted as electron traps, preventing the recombination of electron hole pairs, eventually leading to higher photocatalytic activity of our photocatalyst in degrading the targeted organic pollutant, Simazine. Moreover, an increased kinetic rate of the degradation to 0.0135 h−1 was observed in the presence of Cu in TiO2NTs.
Open AccessTiO2 Nanotubes Supported Cu Nanoparticles for Improving Photocatalytic Degradation of Simazine under UV Illumination
Nano size Copper (Cu) incorporated TiO2 nanotubes was successfully synthesized via the anodic oxidation technique in ethylene glycol (EG) containing 0.5 wt % NH4F and 1.6 wt % KOH for the photocatalytic degradation of Simazine (2-chloro-4, 6-diethylamino-1,3,5-triazine) under Ultraviolet (UV) illumination. In the present study, the influence of different loading Cu concentrations on the formation of Cu-TiO2 nanotubes film towards the photocatalytic degradation of Simazine is reported. Based on our study, it was found that the optimum Cu loading concentration was about 0.45 wt % on TiO2 nanotubes film for approximately 64% photocatalytic degradation of Simazine after 4 h under UV illumination. This finding was mainly attributed to the uniform surface covering of the Cu loaded TiO2NTs which acted as electron traps, preventing the recombination of electron hole pairs, eventually leading to higher photocatalytic activity of our photocatalyst in degrading the targeted organic pollutant, Simazine. Moreover, an increased kinetic rate of the degradation to 0.0135 h−1 was observed in the presence of Cu in TiO2NTs.
- Open Access
- 29 June 2016
- Published by MDPI AG in Biosensors
- Vol. 6 (3) , 31
Amperometric Biosensor Based on Zirconium Oxide/Polyethylene Glycol/Tyrosinase Composite Film for the Detection of Phenolic Compounds
A phenolic biosensor based on a zirconium oxide/polyethylene glycol/tyrosinase composite film for the detection of phenolic compounds has been explored. The formation of the composite film was expected via electrostatic interaction between hexacetyltrimethylammonium bromide (CTAB), polyethylene glycol (PEG), and zirconium oxide nanoparticles casted on screen printed carbon electrode (SPCE). Herein, the electrode was treated by casting hexacetyltrimethylammonium bromide on SPCE to promote a positively charged surface. Later, zirconium oxide was mixed with polyethylene glycol and the mixture was dropped cast onto the positively charged SPCE/CTAB. Tyrosinase was further immobilized onto the modified SPCE. Characterization of the prepared nanocomposite film and the modified SPCE surface was investigated by scanning electron microscopy (SEM), Electrochemical Impedance Spectroscopy (EIS), and Cyclic voltamogram (CV). The developed biosensor exhibits rapid response for less than 10 s. Two linear calibration curves towards phenol in the concentrations ranges of 0.075–10 µM and 10–55 µM with the detection limit of 0.034 µM were obtained. The biosensor shows high sensitivity and good storage stability for at least 30 days.
- 29 June 2016
- Published by MDPI AG in Biosensors
- Vol. 6 (3) , 31
Open AccessAmperometric Biosensor Based on Zirconium Oxide/Polyethylene Glycol/Tyrosinase Composite Film for the Detection of Phenolic Compounds
A phenolic biosensor based on a zirconium oxide/polyethylene glycol/tyrosinase composite film for the detection of phenolic compounds has been explored. The formation of the composite film was expected via electrostatic interaction between hexacetyltrimethylammonium bromide (CTAB), polyethylene glycol (PEG), and zirconium oxide nanoparticles casted on screen printed carbon electrode (SPCE). Herein, the electrode was treated by casting hexacetyltrimethylammonium bromide on SPCE to promote a positively charged surface. Later, zirconium oxide was mixed with polyethylene glycol and the mixture was dropped cast onto the positively charged SPCE/CTAB. Tyrosinase was further immobilized onto the modified SPCE. Characterization of the prepared nanocomposite film and the modified SPCE surface was investigated by scanning electron microscopy (SEM), Electrochemical Impedance Spectroscopy (EIS), and Cyclic voltamogram (CV). The developed biosensor exhibits rapid response for less than 10 s. Two linear calibration curves towards phenol in the concentrations ranges of 0.075–10 µM and 10–55 µM with the detection limit of 0.034 µM were obtained. The biosensor shows high sensitivity and good storage stability for at least 30 days.
- 8 September 2015
- Published by Royal Society of Chemistry (RSC) in RSC Advances
- Vol. 5 (95) , 77803-77813
A sol–gel derived, copper-doped, titanium dioxide–reduced graphene oxide nanocomposite electrode for the photoelectrocatalytic reduction of CO 2 to methanol and formic acid
Highly efficient photoelectrocatalytic reduction of CO 2 into methanol and formic acid at Cu doped RGO–TiO 2 photoelectrode.
- 8 September 2015
- Published by Royal Society of Chemistry (RSC) in RSC Advances
- Vol. 5 (95) , 77803-77813
A sol–gel derived, copper-doped, titanium dioxide–reduced graphene oxide nanocomposite electrode for the photoelectrocatalytic reduction of CO 2 to methanol and formic acid
Highly efficient photoelectrocatalytic reduction of CO 2 into methanol and formic acid at Cu doped RGO–TiO 2 photoelectrode.
- 17 October 2014
- Published by Royal Society of Chemistry (RSC) in New Journal of Chemistry
- Vol. 39 (1) , 369-376
Ga doped RGO–TiO 2 composite on an ITO surface electrode for investigation of photoelectrocatalytic activity under visible light irradiation
Ga doping in RGO–TiO 2 nanocomposite photoelectrode shows enhanced photocurrent density (4.6 mA cm −2 ) in CO 2 photoelectrocatalysis.
- 17 October 2014
- Published by Royal Society of Chemistry (RSC) in New Journal of Chemistry
- Vol. 39 (1) , 369-376
Ga doped RGO–TiO 2 composite on an ITO surface electrode for investigation of photoelectrocatalytic activity under visible light irradiation
Ga doping in RGO–TiO 2 nanocomposite photoelectrode shows enhanced photocurrent density (4.6 mA cm −2 ) in CO 2 photoelectrocatalysis.