Abdoulie A. Jallow
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Abdoulie A. Jallow has a total of 13 co-authors. Here are the top co-authors by number of shared publications:
- Lane Allen Baker
Texas A&M University
2 shared publications - Debjani Paul
Indian Institute of Technology Bombay
1 shared publication - Despina Moschou
University of Bath
1 shared publication - Gabriel C. Halford
University of Virginia
1 shared publication - Gorachand Dutta
NanoBiosensors and Biodevices Lab, School of Medical Sciences and Technology, Indian Institute of Technology Kharagpur, Kharagpur-721302, India
1 shared publication K. L. Vernon
Department of Chemistry, Texas A&M University, College Station, Texas 77845, United States
1 shared publication
Latest Publications
- Open Access
- 10 May 2024
- Published by American Chemical Society (ACS) in Analytical Chemistry
- Vol. 96 (20) , 8036-8055
Recent Developments in Single-Entity Electrochemistry
- 10 May 2024
- Published by American Chemical Society (ACS) in Analytical Chemistry
- Vol. 96 (20) , 8036-8055
Open AccessRecent Developments in Single-Entity Electrochemistry
- Open Access
- 14 March 2024
- Published by American Chemical Society (ACS) in Chemistry of Materials
- Vol. 36 (6) , 3034-3041
Nanomaterials Synthesis Discovery via Parallel Electrochemical Deposition
Electrodeposition of nanoparticles is investigated with a multichannel potentiostat in electrochemical and chemical arrays. De novo deposition and shape control of palladium nanoparticles are explored in arrays with a two-stage strategy. Initial conditions for electrodeposition of materials are discovered in a first stage and then used in a second stage to logically expand chemical and electrochemical parameters. Shape control is analyzed primarily with scanning electron microscopy. Using this approach, optimized conditions for the electrodeposition of cubic palladium nanoparticles were identified from a set of previously untested electrodeposition conditions. The parameters discovered through the array format were then successfully extrapolated to a traditional bulk three-electrode electrochemical cell. Electrochemical arrays were also used to explore electrodeposition parameters reported in previous bulk studies, further demonstrating the correspondence between the array and bulk systems. These results broadly highlight opportunities for electrochemical arrays, both for discovery and for further investigations of electrodeposition in nanomaterials synthesis.
- 14 March 2024
- Published by American Chemical Society (ACS) in Chemistry of Materials
- Vol. 36 (6) , 3034-3041
Open AccessNanomaterials Synthesis Discovery via Parallel Electrochemical Deposition
Electrodeposition of nanoparticles is investigated with a multichannel potentiostat in electrochemical and chemical arrays. De novo deposition and shape control of palladium nanoparticles are explored in arrays with a two-stage strategy. Initial conditions for electrodeposition of materials are discovered in a first stage and then used in a second stage to logically expand chemical and electrochemical parameters. Shape control is analyzed primarily with scanning electron microscopy. Using this approach, optimized conditions for the electrodeposition of cubic palladium nanoparticles were identified from a set of previously untested electrodeposition conditions. The parameters discovered through the array format were then successfully extrapolated to a traditional bulk three-electrode electrochemical cell. Electrochemical arrays were also used to explore electrodeposition parameters reported in previous bulk studies, further demonstrating the correspondence between the array and bulk systems. These results broadly highlight opportunities for electrochemical arrays, both for discovery and for further investigations of electrodeposition in nanomaterials synthesis.
- Open Access
- 30 August 2019
- Published by MDPI AG in Micromachines
- Vol. 10 (9) , 575
Label-Free Electrochemical Detection of S. mutans Exploiting Commercially Fabricated Printed Circuit Board Sensing Electrodes
This paper reports for the first time printed-circuit-board (PCB)-based label-free electrochemical detection of bacteria. The demonstrated immunosensor was implemented on a PCB sensing platform which was designed and fabricated in a standard PCB manufacturing facility. Bacteria were directly captured on the PCB sensing surface using a specific, pre-immobilized antibody. Electrochemical impedance spectra (EIS) were recorded and used to extract the charge transfer resistance (Rct) value for the different bacteria concentrations under investigation. As a proof-of-concept, Streptococcus mutans (S. mutans) bacteria were quantified in a phosphate buffered saline (PBS) buffer, achieving a limit of detection of 103 CFU/mL. Therefore, the proposed biosensor is an attractive candidate for the development of a simple and robust point-of-care diagnostic platform for bacteria identification, exhibiting good sensitivity, high selectivity, and excellent reproducibility.
- 30 August 2019
- Published by MDPI AG in Micromachines
- Vol. 10 (9) , 575
Open AccessLabel-Free Electrochemical Detection of S. mutans Exploiting Commercially Fabricated Printed Circuit Board Sensing Electrodes
This paper reports for the first time printed-circuit-board (PCB)-based label-free electrochemical detection of bacteria. The demonstrated immunosensor was implemented on a PCB sensing platform which was designed and fabricated in a standard PCB manufacturing facility. Bacteria were directly captured on the PCB sensing surface using a specific, pre-immobilized antibody. Electrochemical impedance spectra (EIS) were recorded and used to extract the charge transfer resistance (Rct) value for the different bacteria concentrations under investigation. As a proof-of-concept, Streptococcus mutans (S. mutans) bacteria were quantified in a phosphate buffered saline (PBS) buffer, achieving a limit of detection of 103 CFU/mL. Therefore, the proposed biosensor is an attractive candidate for the development of a simple and robust point-of-care diagnostic platform for bacteria identification, exhibiting good sensitivity, high selectivity, and excellent reproducibility.