ORCID Profile
0000-0003-2085-5148
Current Organisation
James Cook University
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In Research Link Australia (RLA), "Research Topics" refer to ANZSRC FOR and SEO codes. These topics are either sourced from ANZSRC FOR and SEO codes listed in researchers' related grants or generated by a large language model (LLM) based on their publications.
Atomic, Molecular, Nuclear, Particle and Plasma Physics | Nanotechnology | Nanoscale Characterisation | Plasma Physics; Fusion Plasmas; Electrical Discharges | Condensed Matter Characterisation Technique Development | Chemical Characterisation of Materials | Atomic and Molecular Physics
Expanding Knowledge in the Physical Sciences | Scientific Instruments | Expanding Knowledge in Engineering |
Publisher: Wiley
Date: 03-03-2023
Abstract: Atmospheric pressure microwave plasma has the lead in synthesizing freestanding and scalable graphene within seconds without the need for high vacuum and temperature. However, the process is limited in utilizing chemical sources for synthesis, such as methane and ethanol. Herein, the usage of an extract of a sustainable precursor, that is, Melaleuca alternifolia , commonly known as tea tree, is for the first time reported to synthesize graphene nanosheets in atmospheric pressure microwave plasma. The synthesis is carried out in a single step at a remarkably low microwave power of 200 W. The morphology, structure, and electrochemical properties of graphene are studied using state‐of‐the‐art characterization techniques such as Raman spectroscopy, X‐ray diffraction, transmission electron microscopy (TEM) and electrochemical impedance spectroscopy. The TEM images reveal the presence of a combination of nanostructures such as nano‐horns, nano‐rods, or nano‐onions consisting of multi‐layer graphitic architectures. An excellent sensing capability of as‐synthesized graphene is demonstrated through the detection of diuron herbicide. A commendable linear range of 20 µ m to 1 m m and a limit of detection of 5 µ m of diuron is recorded.
Publisher: Royal Society of Chemistry (RSC)
Date: 2020
DOI: 10.1039/D0AN00823K
Abstract: Electrochemical determination of nitrate: an overview from the perspective of s le matrices.
Publisher: Elsevier BV
Date: 06-2021
Publisher: American Chemical Society (ACS)
Date: 26-08-2009
DOI: 10.1021/CG900217T
Publisher: American Chemical Society (ACS)
Date: 08-04-2015
DOI: 10.1021/ACS.ANALCHEM.5B00461
Abstract: In this work, the ion-transfer voltammetric detection of the protonated β-blocker propranolol was explored at arrays of nanoscale interfaces between two immiscible electrolyte solutions (ITIES). Silicon nitride nanoporous membranes with 400 pores in a hexagonal arrangement, with either 50 or 17 nm radius pores, were used to form regular arrays of nanoITIES. It was found that the aqueous-to-organic ion-transfer current continuously increased steadily rather than reaching a limiting current plateau after the ion-transfer wave the slope of this limiting current region was concentration dependent and associated with the high ion flux at the nanointerfaces. Electrochemical data were examined in terms of an independent nanointerface approach and an equivalent microdisc approach, supported by finite element simulation. In comparison to the larger interface configuration (50 nm radius), the array of 17 nm radius nanoITIES exhibited a 6.5-times higher current density for propranolol detection due to the enhanced ion flux arising from the convergent diffusion to smaller electrochemical interfaces. Both nanoITIES arrays achieved the equivalent limits of detection, 0.8 μM, using cyclic voltammetry. Additionally, the effect of scan rate on the charging and faradaic currents at these nanoITIES arrays, as well as their stability over time, was investigated. The results demonstrate that arrays of nanoscale liquid-liquid interfaces can be applied to study electrochemical drug transfer, and provide the basis for the development of miniaturized and integrated detection platforms for drug analysis.
Publisher: Elsevier BV
Date: 12-2008
DOI: 10.1016/J.BIOS.2008.06.011
Abstract: Palladium nanoparticle-loaded carbon nanofibers (Pd/CNFs) were prepared by electrospinning and subsequent thermal treatment processes. Pd/CNFs modified carbon paste electrode (Pd/CNF-CPE) displayed excellent electrochemical catalytic activities towards dopamine (DA), uric acid (UA) and ascorbic acid (AA). The oxidation overpotentials of DA, UA and AA were decreased significantly compared with those obtained at the bare CPE. Differential pulse voltammetry was used for the simultaneous determination of DA, UA and AA in their ternary mixture. The peak separation between UA and DA, DA and AA was 148 mV and 244 mV, respectively. The calibration curves for DA, UA and AA were obtained in the range of 0.5-160 microM, 2-200 microM, and 0.05-4mM, respectively. The lowest detection limits (S/N=3) were 0.2 microM, 0.7 microM and 15 microM for DA, UA and AA, respectively. With good selectively and sensitivity, the present method was applied to the determination of DA in injectable medicine and UA in urine s le.
Publisher: The Chemical Society of Japan
Date: 05-07-2007
DOI: 10.1246/CL.2007.924
Publisher: Elsevier BV
Date: 10-2008
Publisher: American Chemical Society (ACS)
Date: 24-05-2023
Publisher: Royal Society of Chemistry (RSC)
Date: 2010
DOI: 10.1039/C0AY00098A
Publisher: Wiley
Date: 26-01-2023
Abstract: The detection of dopamine (DA) has received enormous attention since it is widely recognized as an important neurotransmitter associated with nerve signaling and some diseases. In this work, glucose‐derived carbon nanospheres (CNs) are synthesized by the green hydrothermal approach and are served to modify electrodes for the detection of DA. The CNs were successfully synthesized and were investigated in detail by various characterization technologies. The CNs modified glassy carbon electrode (CNs/GCE) exhibits better electrochemical sensing performance with a wide linear range of 0.05–1600 μM and a low limit of 8.3 nM for determination of DA, as compared with the modified electrodes reported previously. The CNs/GCE was successfully applied to detect DA in human serum s les, which makes it promising for a variety of biomedical applications. More importantly, this work shows a novel green and simple strategy for the development of cost‐effective and high‐performance sensing materials, which provides more opportunities for design of electrochemical sensors with future capabilities of mass production in practical applications.
Publisher: American Chemical Society (ACS)
Date: 15-12-2020
Publisher: Elsevier BV
Date: 03-2012
Publisher: Elsevier BV
Date: 11-2020
Publisher: Wiley
Date: 21-03-2013
Publisher: Elsevier BV
Date: 04-2020
DOI: 10.1016/J.JHAZMAT.2019.122001
Abstract: Accurately monitoring of aflatoxin B1 (AFB1), the most hazardous mycotoxin in agricultural products, is essential for the public health, but various testing demands (e.g. detection range, sensitivity) for different s les can be challenging for sensors. Here, we developed a sensitivity-programmable ratiometric electrochemical aptasensor for AFB1 analysis in peanut. Thionine functionalized reduced graphene oxide (THI-rGO) served as reference signal generator, ferrocene-labelled aptamer (Fc-apt) output the response signal. During analysis, the formation of Fc-apt-AFB1 complex led to its stripping from the electrode and faded the current intensity of Fc (I
Publisher: Wiley
Date: 05-11-2012
Publisher: Elsevier BV
Date: 02-2012
DOI: 10.1016/J.JCIS.2011.10.040
Abstract: Pt/carbon nanofiber (Pt/CNF) nanocomposites were facilely synthesized by the reduction of hexachloroplatinic acid (H(2)PtCl(6)) using formic acid (HCOOH) in aqueous solution containing electrospun carbon nanofibers at room temperature. The obtained Pt/CNF nanocomposites were characterized by TEM and EDX. The Pt nanoparticles could in situ grow on the surface of CNFs with small particle size, high loading density, and uniform dispersion by adjusting the concentration of H(2)PtCl(6) precursor. The electrocatalytic activities of the Pt/CNF nanocomposites were also studied. These Pt/CNF nanocomposites exhibited higher electrocatalytic activity toward methanol oxidation reaction compared with commercial E-TEK Pt/C catalyst. The results presented may offer a new approach to facilely synthesize direct methanol fuel cells (DMFCs) catalyst with enhanced electrocatalytic activity and low cost.
Publisher: American Chemical Society (ACS)
Date: 18-02-2016
Publisher: American Chemical Society (ACS)
Date: 19-01-2022
Abstract: Single-step, single-precursor synthesis of nitrogen-doped graphene oxide (N-GO) was demonstrated in this work. By choosing aniline as the sole source of carbon and nitrogen, N-GO films were fabricated using microwave plasma at a power as low as 80 W in atmospheric conditions. The aniline vapor dissociated under plasma formed islands of N-GO nanosheets on the substrates or walls of the quartz deposition chamber. The interplanar spacing in the pristine N-GO films was observed to be lower than that of GO films, which indicated a lower concentration of oxygen and other species present in the space between the N-GO layers. The as-fabricated N-GO demonstrated superior antiscaling and algicidal properties that are deemed imperative for water purification applications.
Publisher: Springer Science and Business Media LLC
Date: 06-08-2020
Publisher: CSIRO Publishing
Date: 2020
DOI: 10.1071/CH19532
Publisher: Elsevier BV
Date: 07-2011
DOI: 10.1016/J.BIOS.2011.05.034
Abstract: A facile wet-chemical method was developed to prepare a novel Pt nanoparticle-loaded carbon nanofiber (Pt/CNF) electrode. Without using any stabilizer or pretreatment procedure, large amounts of Pt nanoparticles could be well deposited on the surface of the electrospun CNF electrode at room temperature, as revealed by scanning electron microscopy (SEM). The effect of the precursor concentration on the formation of Pt catalysts was investigated to optimize the performance of the proposed hybrid electrode. When applied to the electrochemical detection of hydrogen peroxide (H₂O₂), the Pt/CNF electrode exhibited low overpotential, fast response and high sensitivity. A low detection limit of 0.6 μM with wide linear range of 1-800 μM (R=0.9991) was achieved at the Pt/CNF electrode, which was superior to that obtained with other H₂O₂ electrochemical sensors reported previously. In addition, the Pt/CNF electrode showed good selectivity for H₂O₂ detection in the presence of ascorbic acid (AA), acetaminophenol (AP) and uric acid (UA) under physiological pH condition. The attractive analytical performances and facile preparation method made this novel hybrid electrode promising for the development of effective H₂O₂ sensors.
Publisher: MDPI AG
Date: 16-04-2022
DOI: 10.3390/BIOS12040253
Abstract: Thrombin plays a central role in hemostasis and its imbalances in coagulation can lead to various pathologies. It is of clinical significance to develop a fast and accurate method for the quantitative detection of thrombin. Electrochemical aptasensors have the capability of combining the specific selectivity from aptamers with the extraordinary sensitivity from electrochemical techniques and thus have attracted considerable attention for the trace-level detection of thrombin. Nanomaterials and nanostructures can further enhance the performance of thrombin aptasensors to achieve high sensitivity, selectivity, and antifouling functions. In highlighting these material merits and their impacts on sensor performance, this paper reviews the most recent advances in label-free electrochemical aptasensors for thrombin detection, with an emphasis on nanomaterials and nanostructures utilized in sensor design and fabrication. The performance, advantages, and limitations of those aptasensors are summarized and compared according to their material structures and compositions.
Publisher: Elsevier BV
Date: 08-2010
Publisher: Springer Science and Business Media LLC
Date: 11-07-2010
Publisher: No publisher found
Date: 2016
DOI: 10.1146/ANNUREV-ANCHEM-071015-041415
Abstract: Ion transfer at the interface between immiscible electrolyte solutions offers many benefits to analytical chemistry, including the ability to detect nonredox active ionized analytes, to detect ions whose redox electrochemistry is accompanied by complications, and to separate ions based on electrocontrolled partition. Nanoscale miniaturization of such interfaces brings the benefits of enhanced mass transport, which in turn leads to improved analytical performance in areas such as sensitivity and limits of detection. This review discusses the development of such nanoscale interfaces between immiscible liquids and examines the analytical advances that have been made to date, including prospects for trace detection of ion concentrations.
Publisher: Elsevier BV
Date: 02-2020
DOI: 10.1016/J.BIOS.2019.111814
Abstract: A novel ratiometric electrochemical aptasensor was developed for Ochratoxin A (OTA) detection based on the binding of methylene blue (MB) to DNA with a dual signal lification strategy. The formation of dsDNA structures between ferrocene-labeled complementary DNA (Fc-cDNA), the OTA aptamer, and complementary helper DNA (hDNA) caused Fc away from the electrode, and allowed dsDNA to bind with a certain amount of MB. Here, a small oxidation current of Fc (I
Publisher: American Chemical Society (ACS)
Date: 17-06-2016
DOI: 10.1021/ACS.ANALCHEM.6B00513
Abstract: The direct experimental characterization of diffusion processes at nanoscale remains a challenge that could help elucidate processes in biology, medicine and technology. In this report, two experimental approaches were employed to visualize ion diffusion profiles at the orifices of nanopores (radius (ra) of 86 ± 6 nm) in array format: (1) electrochemically assisted formation of silica deposits based on surfactant ion transfer across nanointerfaces between two immiscible electrolyte solutions (nanoITIES) (2) combined atomic force - scanning electrochemical microscopy (AFM-SECM) imaging of topography and redox species diffusion through the nanopores. The nature of the diffusion zones formed around the pores is directly related to the interpore distance within the array. Nanopore arrays with different ratios of pore center-to-center separation (rc) to pore radius (ra) were fabricated by focused ion beam (FIB) milling of silicon nitride (SiN) membranes, with 100 pores in a hexagonal arrangement. The ion diffusion profiles determined by the two visualization methods indicated the formation of overlapped or independent diffusion profiles at nanopore arrays with rc/ra ratios of 21 ± 2 and 91 ± 7, respectively. In particular, the silica deposition method resulted in formation of a single deposit encompassing the complete array with closer nanopore arrangement, whereas in idual silica deposits were formed around each nanopore within the more widely spaced array. The methods reveal direct experimental evidence of diffusion zones at nanopore arrays and provide practical illustration that the pore-pore separation within such arrays has a significant impact on diffusional transport as the pore size is reduced to the nanoscale. These approaches to nanoscale diffusion zone visualization open up possibilities for better understanding of molecular transport processes within miniaturized systems.
Publisher: Elsevier BV
Date: 2202
Publisher: Elsevier BV
Date: 2020
DOI: 10.1016/J.BIOS.2019.111735
Abstract: Design of suitable nanocomposites with tailored structures was significant in the fabrication of effective and reliable electrochemical sensors. Herein, the copper-nickel@nitrogen, boron-doped reduced graphene oxide (Cu-Ni@N,B-rGO) was successfully synthesized, which exhibited superior electrocatalytic performance towards guanine (G) and adenine (A) oxidation. The Cu-Ni NPs were sequentially decorated on N,B-rGO substrate via an environmentally friendly reduction strategy, which utilized glucose as reducer and stabilizing agent. The nanocomposites with large specific surface area, remarkable conductivity and high catalytic activity showed prominent synergistic effect owning to the uniform dispersion of Cu-Ni NPs on the surface of N,B-rGO. When applied to analysis of G and A using DPV, the wide linear ranges of 1.0-160.0 μM and 1.0-120.0 μM with the determination limits of 0.118 μM and 0.134 μM were obtained, respectively. The sensor was successfully applied to the detection of G and A in calf-thymus DNA with G/A ratio of 0.80. The facile preparation process and attractive sensing properties of the Cu-Ni@N,B-rGO nanocomposites made it a promising candidate for the development of advanced electrochemical sensor.
Publisher: Wiley
Date: 14-08-2016
Publisher: Wiley
Date: 08-2008
Publisher: Springer Science and Business Media LLC
Date: 06-09-2013
Publisher: Elsevier BV
Date: 04-2017
Publisher: American Chemical Society (ACS)
Date: 29-10-2015
Abstract: Ru(bpy)3(2+)-doped silica (Ru-SiO2) nanoparticles and gold-nanoparticle-decorated graphene (P-RGO@Au) were combined to form a P-RGO@Au@Ru-SiO2 composite. The composite was used to develop a novel sandwich-type electrochemiluminescence immunosensor for the analysis of HIV-1 p24 antigen. The composite worked as carrier to immobilize target antibody and to build a sandwich-type electrochemiluminescence immunosensor through an interaction between antigen and antibody. Importantly, high ECL signal could be obtained due to the large amounts of Ru(bpy)3(2+) molecules per Ru-SiO2 nanoparticle. The P-RGO@Au composite with good conductivity and high surface area not only accelerated the electron transfer rate but also improved the loading of both ECL molecules and capture antibody, which could further increase the ECL response and result in high sensitivity. Taking advantage of both Ru-SiO2 nanoparticles and the P-RGO@Au composite, the proposed immunosensor exhibited a linear range from 1.0 × 10(-9) to 1.0 × 10(-5) mg mL(-1) with a detection limit of 1.0 × 10(-9) mg mL(-1) for HIV-1 p24 antigen. The proposed ECL immunosensor was used to analyze HIV-1 p24 antigen in human serum, and satisfactory recoveries were obtained, indicating that the proposed method is promising for practical applications in the clinical diagnosis of HIV infection.
Publisher: Elsevier BV
Date: 10-2019
Publisher: Wiley
Date: 02-09-2018
DOI: 10.1111/ANS.13278
Publisher: Elsevier BV
Date: 10-2019
Publisher: Elsevier BV
Date: 03-2010
DOI: 10.1016/J.ACA.2010.01.061
Abstract: We have developed a novel nickel nanoparticle-loaded carbon fiber paste (NiCFP) electrode for enzyme-free determination of ethanol. An electrospinning technique was used to prepare the NiCF composite with large amounts of spherical nanoparticles firmly embedded in carbon fibers (CF). In application to electroanalysis of ethanol, the NiCFP electrode exhibited high erometric response and good operational stability. The calibration curve was linear up to 87.5 mM with a detection limit of 0.25 mM, which is superior to that obtained with other transition metal based electrodes. For detection of ethanol present in liquor s les, the values obtained with the NiCFP electrode were in agreement with the ones declared on the label. The attractive analytical performance and simple preparation method make this novel material promising for the development of effective enzyme-free sensors.
Publisher: Elsevier BV
Date: 07-2009
DOI: 10.1016/J.BIOS.2009.04.032
Abstract: A novel nonenzymatic glucose sensor was developed based on the renewable Ni nanoparticle-loaded carbon nanofiber paste (NiCFP) electrode. The NiCF nanocomposite was prepared by combination of electrospinning technique with thermal treatment method. The scanning electron microscopy (SEM) and transmission electron microscopy (TEM) images showed that large amounts of spherical nanoparticles were well dispersed on the surface or embedded in the carbon nanofibers. And the nanoparticles were composed of Ni and NiO, as revealed by energy dispersive X-ray spectroscopy (EDX) and X-ray powder diffraction (XRD). In application to nonenzymatic glucose determination, the renewable NiCFP electrodes, which were constructed by simply mixing the electrospun nanocomposite with mineral oil, exhibited strong and fast erometric response without being poisoned by chloride ions. Low detection limit of 1 microM with wide linear range from 2 microM to 2.5 mM (R=0.9997) could be obtained. The current response of the proposed glucose sensor was highly sensitive and stable, attributing to the electrocatalytic performance of the firmly embedded Ni nanoparticles as well as the chemical inertness of the carbon-based electrode. The good analytical performance, low cost and straightforward preparation method made this novel electrode material promising for the development of effective glucose sensor.
Publisher: Royal Society of Chemistry (RSC)
Date: 2010
DOI: 10.1039/C0CE00096E
Publisher: Royal Society of Chemistry (RSC)
Date: 2010
DOI: 10.1039/B9AY00312F
Publisher: Elsevier BV
Date: 2020
Publisher: American Chemical Society (ACS)
Date: 15-05-2015
DOI: 10.1021/ACS.ANALCHEM.5B01162
Abstract: In this work, independent radial diffusion at arrayed nanointerfaces between two immiscible electrolyte solutions (nanoITIES) was achieved. The arrays were formed at nanopores fabricated by focused ion beam milling of silicon nitride (SiN) membranes, enabling the reproducible and systematic design of five arrays with different ratios of pore center-to-center distance (rc) to pore radius (ra). Voltammetry across water-1,6-dichlorohexane nanoITIES formed at these arrays was examined by the interfacial transfer of tetrapropylammonium ions. The diffusion-limited ion-transfer current increased with the ratio rc/ra, reaching a plateau for rc/ra ≥ 56, which was equivalent to the theoretical current for radial diffusion to an array of independent nanoITIES. As a result, mass transport to the nanoITIES arrays was greatly enhanced due to the decreased overlap of diffusion zones at adjacent nanoITIES, allowing each interface in the array to behave independently. When the rc/ra ratio increased from 13 to 56, the analytical performance parameters of sensitivity and limit of detection were improved from 0.50 (±0.02) A M(-1) to 0.76 (±0.02) A M(-1) and from 0.101 (±0.003) μM to 0.072 (±0.002) μM, respectively. These results provide an experimental basis for the design of arrayed nanointerfaces for electrochemical sensing.
Publisher: American Chemical Society (ACS)
Date: 10-01-2022
Publisher: Elsevier BV
Date: 02-2019
DOI: 10.1016/J.SAA.2019.117716
Abstract: A fluorescent nanoprobe based on carbon dots (CDs) has been facilely synthesized by a one-step hydrothermal pyrolysis of salicylic acid and utilized for the sequential detection of Fe
Publisher: Elsevier BV
Date: 11-2021
Publisher: Elsevier BV
Date: 15-03-2010
DOI: 10.1016/J.TALANTA.2009.11.027
Abstract: A novel and simple method for the direct and quantitative determination of L-tryptophan (Trp), L-tyrosine (Tyr) and L-cysteine (Cys) was proposed in this work. Carbon nanofibers (CNFs), made by electrospinning technique, were used to modify carbon paste electrode (CPE) without any treatment to study the electrochemical behaviors of the three amino acids using cyclic voltammetry (CV) and constant potential erometric method. The results demonstrated that the CNFs modified carbon paste electrode (CNF-CPE) exhibited high electrocatalytic activity and good analytical performance towards the oxidation of the three amino acids. The linear ranges of Trp, Tyr and Cys were 0.1-119, 0.2-107 and 0.15-64 microM with correlation coefficients of 0.9994, 0.9985 and 0.9996, respectively. All the detection limits of the analytes were 0.1 mM (S/N=3). In addition, the CNF-CPE displayed good reproducibility, high sensitivity and good selectivity towards the determination of the amino acids, making it suitable for the determination of Trp, Tyr and Cys in clinical and medicine.
Publisher: CSIRO Publishing
Date: 10-06-2021
DOI: 10.1071/CH21075
Abstract: Glucose oxidase (GOx) was immobilized between aligned carbon nanotube films (ACNTFs) using a cross-stacking method without any purification and functionalization processes. Direct electron transfer of GOx was achieved on the ACNTFs with reversible redox peaks observed at the formal potential of –0.448 V. When applied to the determination of glucose by cyclic voltammetry, the prepared enzymatic electrode exhibited a linear range from 1 to 5 mM under mediator-free physiological conditions, which makes it a promising candidate for the development of third-generation glucose biosensors.
Publisher: Hindawi Limited
Date: 2010
DOI: 10.1155/2010/659207
Abstract: A novel sonochemical process, using hydrogen peroxide in a laboratory ultrasonic bath, was employed to pretreat the carbon nanofiber (CNF) for creating oxygen-rich groups on the surface of CNF. After the sonochemical process, the CNF showed good hydrophilicity and high electrochemical activity. Compared to normal pretreatment process, this sonochemical process is timesaving and effective for dispersion and functionalization of CNF. The resulting CNF showed high catalytic activity toward the oxidation of DA. A carbon paste electrode modified by CNF (CPE-CNF) was used to determine the dopamine (DA) in the presence of ascorbic acid (AA). The detection limit is 0.05 μ M, with the linear range from 0.05 μ M to 6.4 μ M.
Publisher: Elsevier BV
Date: 02-2022
DOI: 10.1016/J.TALANTA.2010.11.019
Abstract: Xanthine (Xa) determination is of considerable importance in clinical analysis and food quality control. Therefore, a sensitive nonenzymatic erometric sensor for Xa based on carbon nanofibers (CNFs) has been proposed. The CNFs, which were prepared by electrospinning technique and subsequent thermal treatment, were used to modify carbon paste electrode (CNF-CPE) to construct the erometric sensor device without any oxidation pretreatment. In application to Xa electrochemical determination, the CNF-CPE exhibited high electrocatalytic activity and fast erometric response. Various experimental parameters, such as pH and applied potential were optimized. Under the optimal conditions, the dynamic linear range of Xa was 0.03-21.19 μM (R=0.9992) with the detection limit low to 20 nM (S/N=3). With good selectivity and sensitivity, the present system was successfully applied to estimate the freshness of fish and determine Xa in human urine, which provides potential application in food quality control and clinical analysis.
Publisher: American Chemical Society (ACS)
Date: 06-2020
Start Date: 07-2021
End Date: 12-2023
Amount: $950,000.00
Funder: Australian Research Council
View Funded ActivityStart Date: 07-2023
End Date: 06-2026
Amount: $360,000.00
Funder: Australian Research Council
View Funded Activity