Paul Mulvaney

Fabrication of a Three-Dimensional Plasmon Ruler Using an Atomic Force Microscope

Publisher: American Chemical Society (ACS)

Date: 23-07-2019

DOI: 10.1021/ACS.JPCC.9B05360

Colloidal Stability of Apolar Nanoparticles: The Role of Particle Size and Ligand Shell Structure

Publisher: American Chemical Society (ACS)

Date: 29-05-2018

DOI: 10.1021/ACSNANO.8B02202

Abstract: Being able to predict and tune the colloidal stability of nanoparticles is essential for a wide range of applications, yet our ability to do so is currently poor due to a lack of understanding of how they interact with one another. Here, we show that the agglomeration of apolar particles is dominated by either the core or the ligand shell depending on the particle size and materials. We do this by using small-angle X-ray scattering and molecular dynamics simulations to characterize the interaction between hexadecanethiol passivated gold nanoparticles in decane solvent. For smaller particles, the agglomeration temperature and interparticle spacing are determined by ordering of the ligand shell into bundles of aligned ligands that attract one another and interlock. In contrast, the agglomeration of larger particles is driven by van der Waals attraction between the gold cores, which eventually becomes strong enough to compress the ligand shell. Our results provide a microscopic description of the forces that determine the colloidal stability of apolar nanoparticles and explain why classical colloid theory fails.

Flexible Vanadium Dioxide Photodetectors for Visible to Longwave Infrared Detection at Room Temperature

Publisher: Wiley

Date: 21-06-2023

DOI: 10.1002/ADFM.202301790

Abstract: Flexible optoelectronics is a rapidly growing field, with a wide range of potential applications. From wearable sensors to bendable solar cells, curved displays, and curved focal plane arrays, the possibilities are endless. The criticality of flexible photodetectors for many of these applications is acknowledged, however, devices that are demonstrated thus far are limited in their spectral range. In this study, flexible photodetectors are demonstrated using a VO x nanoparticle ink, with an extremely broad operating wavelength range of 0.4 to 20 µm. This ink is synthesized using a simple and scalable wet‐chemical process. These photodetectors operate at room temperature and exhibit minimal variance in performance even when bent at angles of up to 100 ° at a bend radius of 6.4 mm. In addition, rigorous strain testing of 100 bend and release cycles revealed a photoresponse with a standard deviation of only 0.55%. This combination of mechanical flexibility, wide spectral response, and ease of fabrication makes these devices highly desirable for a wide range of applications, including low‐cost wearable sensors and hyperspectral imaging systems.

The Future of Layer-by-Layer Assembly: A Tribute to ACS Nano Associate Editor Helmuth Möhwald

Publisher: American Chemical Society (ACS)

Date: 24-05-2019

DOI: 10.1021/ACSNANO.9B03326

Abstract: Layer-by-layer (LbL) assembly is a widely used tool for engineering materials and coatings. In this Perspective, dedicated to the memory of ACS Nano associate editor Prof. Dr. Helmuth Möhwald, we discuss the developments and applications that are to come in LbL assembly, focusing on coatings, bulk materials, membranes, nanocomposites, and delivery vehicles.

The Degradation and Blinking of Single CsPbI3 Perovskite Quantum Dots

Publisher: American Chemical Society (ACS)

Date: 15-12-2017

DOI: 10.1021/ACS.JPCC.7B11168

Temperature Dependence of the CdS Bandgap in the Extreme Confinement Regime

Publisher: American Chemical Society (ACS)

Date: 09-10-2023

DOI: 10.1021/ACS.NANOLETT.3C02368

Room Temperature Bias-Selectable, Dual-Band Infrared Detectors Based on Lead Sulfide Colloidal Quantum Dots and Black Phosphorus

Publisher: American Chemical Society (ACS)

Date: 15-06-2023

DOI: 10.1021/ACSNANO.3C02617

Potential-Scanning Localized Plasmon Sensing with Single and Coupled Gold Nanorods

Publisher: American Chemical Society (ACS)

Date: 25-07-2017

DOI: 10.1021/ACS.JPCLETT.7B01620

Abstract: Single plasmonic nanoparticles can potentially serve as optical sensors for detecting local refractive index changes. However, simultaneous monitoring of the scattering spectra from multiple nanoparticles is not practical. Here we perform potential-scanning localized surface plasmon resonance (LSPR) sensing. Gold nanorods are immobilized on an ITO electrode. Instead of collecting the full spectrum, as is done in conventional LSPR sensing, the electrode potential is scanned while the rod spectra are monitored at a single wavelength. We demonstrate that refractive index changes can be determined from single wavelength experiments and we further find that gold nanorod (NR) dimers exhibit higher refractive index sensitivities than single NRs in both potential-scanning and conventional wavelength-scanning based LSPR sensing.

Single-Pixel Fluorescence Spectroscopy Using Near-Field Dispersion for Single-Photon Counting and Single-Shot Acquisition

Publisher: American Chemical Society (ACS)

Date: 24-08-2022

DOI: 10.1021/ACSPHOTONICS.2C00710

Polarity-Tunable Field Effect Phototransistors

Publisher: American Chemical Society (ACS)

Date: 30-05-2023

DOI: 10.1021/ACS.NANOLETT.3C00728

Ligand and solvent effects on the absorption spectra of CdS magic-sized clusters

Publisher: AIP Publishing

Date: 02-05-2023

DOI: 10.1063/5.0147609

Abstract: The absorption spectra of congenetic wurtzite (WZ) and zincblende (ZB) CdS magic-sized clusters are investigated. We demonstrate that the exciton peak positions can be tuned by up to 500 meV by varying the strong coupling between X-type ligands and the semiconductor cores, while the addition of L-type ligands primarily affects cluster midgap states. When Z-type ligands are displaced by L-type ligands, red shifts in the absorption spectra are observed, despite the fact there is a small decrease in cluster size. Density functional theory calculations are used to explain these findings and they reveal the importance of Cd and S dangling bonds on the midgap states during the Z- to L-type ligand exchange process. Overall, ZB CdS clusters show higher chemical stability than WZ clusters but their optical properties exhibit greater sensitivity to the solvent. Conversely, WZ CdS clusters are not stable in a Lewis base-rich environment, resulting in various changes in their spectra. Our findings enable researchers to select capping ligands that modulate the optical properties of semiconductor clusters while maintaining precise control over their solvent interactions.

Control of Symmetry Breaking Size and Aspect Ratio in Gold Nanorods: Underlying Role of Silver Nitrate

Publisher: American Chemical Society (ACS)

Date: 02-02-2017

DOI: 10.1021/ACS.JPCC.6B10343

Colloidal Stability of Apolar Nanoparticles: Role of Ligand Length

Publisher: American Chemical Society (ACS)

Date: 09-10-2018

DOI: 10.1021/ACS.LANGMUIR.8B02883

Abstract: Inorganic nanoparticle cores are often coated with organic ligands to render them dispersible in apolar solvents. However, the effect of the ligand shell on the colloidal stability of the overall hybrid particle is not fully understood. In particular, it is not known how the length of an apolar alkyl ligand chain affects the stability of a nanoparticle dispersion against agglomeration. Here, small-angle X-ray scattering and molecular dynamics simulations have been used to study the interactions between gold nanoparticles and between cadmium selenide nanoparticles passivated by alkanethiol ligands with 12-18 carbons in the solvent decane. We find that increasing the ligand length increases colloidal stability in the core-dominated regime but decreases it in the ligand-dominated regime. This unexpected inversion is connected to the transition from ligand-dominated to core-dominated agglomeration when the core diameter increases at constant ligand length. Our results provide a microscopic picture of the forces that determine the colloidal stability of apolar nanoparticles and explain why classical colloid theory fails.

Correction to “On the Colloidal Stability of Apolar Nanoparticles: The Role of Ligand Length”

Publisher: American Chemical Society (ACS)

Date: 03-09-2020

DOI: 10.1021/ACS.LANGMUIR.0C02478

Transient overshoot and storage of charge carriers on ligands in quantum dot LEDs

Publisher: AIP Publishing

Date: 15-08-2019

DOI: 10.1063/1.5100195

Abstract: Quantum dot light emitting diodes (QLEDs) emitting at 410 nm were studied by time-resolved electroluminescence measurements. A transient overshoot after voltage turn-off was seen, which is attributed to the accumulation and storage of charge carriers at the ligand-quantum dot interface. Shorter ligands showed a faster rise time and prevented the formation of an overshoot, whereas longer ligands caused the storage of charges, responded slower, and showed an overshoot. When the external voltage was switched off, the electric field between the injected and stored electrons and holes led to the occurrence of the overshoot. Applying a dual voltage pulse avoided this overshoot and instead a delayed luminescence was observed. As the accumulated charges were immobile and trapped in shallow states, a reverse pulse was applied to fully deplete the emissive layer. Because the transient overshoot disappeared after the device had been turned on, this can be used as a measure of the degradation of QLEDs. The ligands constitute a major obstacle for an efficient and long lasting blue urple quantum dot emitter.

Energy Transfer between CdZnS Quantum Dots and Perylene Diimide Dyes

Publisher: American Chemical Society (ACS)

Date: 25-01-2023

DOI: 10.1021/ACS.JPCC.3C00053

Ligand memory effect in purple quantum dot LEDs

Publisher: AIP Publishing

Date: 21-10-2019

DOI: 10.1063/1.5123635

Abstract: We report a ligand-dependent, trap state memory effect in a purple quantum dot light emitting diode. The measured, bistable current-voltage characteristics show a high conductance state and a low conductance state. Thereby, a memory window with an ON state and an OFF state is achieved, which can be reversed by applying a negative bias. The height of the memory window depends strongly on the length of the ligand passivating the quantum dot (QD). Together with a 5 nm thick aluminum film under the hole transport layer, charges accumulate at the charge transport/quantum dot ligand interface, leading to an increase in conductance during the forward voltage sweep. During a reverse voltage sweep, previously injected charge carriers recombine until the active layer is free of charge carriers. Voltage-capacitance measurements confirm the changes in the charge carrier population within the active layer and demonstrate that they depend on both the direction of the bias sweep and ligands surrounding the QD.

Aqueous Synthesis of Cu2ZnSnSe4 Nanocrystals

Publisher: American Chemical Society (ACS)

Date: 05-03-2019

DOI: 10.1021/ACS.CHEMMATER.9B00100

Size-Dependent Response of CdSe Quantum Dots to Hydrostatic Pressure

Publisher: American Chemical Society (ACS)

Date: 05-2023

DOI: 10.1021/ACS.JPCC.3C00998

Spectroelectrochemistry of CdSe/Cd_xZn_1–xS Nanoplatelets

Publisher: American Chemical Society (ACS)

Date: 11-01-2023

DOI: 10.1021/ACSNANO.2C09298

When Like Destabilizes Like: Inverted Solvent Effects in Apolar Nanoparticle Dispersions

Publisher: American Chemical Society (ACS)

Date: 16-04-2020

DOI: 10.1021/ACSNANO.9B03552

An ITO‐Free Kesterite Solar Cell

Publisher: Wiley

Date: 28-09-2023

DOI: 10.1002/SMLL.202307242

Advances in the Surface Functionalization of Nanodiamonds for Biological Applications: A Review

Publisher: American Chemical Society (ACS)

Date: 04-10-2021

DOI: 10.1021/ACSANM.1C02698

Tuning the Photoluminescence Anisotropy of Semiconductor Nanocrystals

Publisher: American Chemical Society (ACS)

Date: 25-09-2023

DOI: 10.1021/ACSNANO.3C05214

Electron paramagnetic resonance microscopy using spins in diamond under ambient conditions

Publisher: Springer Science and Business Media LLC

Date: 06-09-2017

DOI: 10.1038/S41467-017-00466-Y

Impact of Surface Functionalization on the Quantum Coherence of Nitrogen-Vacancy Centers in Nanodiamonds

Publisher: American Chemical Society (ACS)

Date: 20-03-2018

DOI: 10.1021/ACSAMI.7B19238

Abstract: Nanoscale quantum probes such as the nitrogen-vacancy (NV) center in diamonds have demonstrated remarkable sensing capabilities over the past decade as control over fabrication and manipulation of these systems has evolved. The biocompatibility and rich surface chemistry of diamonds has added to the utility of these probes but, as the size of these nanoscale systems is reduced, the surface chemistry of diamond begins to impact the quantum properties of the NV center. In this work, we systematically study the effect of the diamond surface chemistry on the quantum coherence of the NV center in nanodiamonds (NDs) 50 nm in size. Our results show that a borane-reduced diamond surface can on average double the spin relaxation time of in idual NV centers in nanodiamonds when compared to thermally oxidized surfaces. Using a combination of infrared and X-ray absorption spectroscopy techniques, we correlate the changes in quantum relaxation rates with the conversion of sp

Detection of Halomethanes Using Cesium Lead Halide Perovskite Nanocrystals

Publisher: American Chemical Society (ACS)

Date: 13-01-2021

DOI: 10.1021/ACSNANO.0C08794

Aqueous Synthesis of High-Quality Cu2ZnSnS4 Nanocrystals and Their Thermal Annealing Characteristics

Publisher: American Chemical Society (ACS)

Date: 19-01-2018

DOI: 10.1021/ACS.LANGMUIR.7B03885

Abstract: Copper zinc tin sulfide (CZTS) nanocrystal inks are promising candidates for the development of cheap, efficient, scalable, and nontoxic photovoltaic (PV) devices. However, optimization of the synthetic chemistry to achieve these goals remains a key challenge. Herein we describe a single-step, aqueous-based synthesis that yields high-quality CZTS nanocrystal inks while also minimizing residual organic impurities. By exploiting simultaneous redox and crystal formation reactions, square-platelet-like CZTS nanocrystals stabilized by Sn

Growth of Gold Nanorods: A SAXS Study

Publisher: American Chemical Society (ACS)

Date: 31-08-2021

DOI: 10.1021/ACS.JPCC.1C06778

A Tunable Polymer-Metal Based Anti-Reflective Metasurface.

Publisher: Wiley

Date: 29-11-2020

DOI: 10.1002/MARC.201900415

Abstract: Anti-reflective surfaces are of great interest for optical devices, sensing, photovoltaics, and photocatalysis. However, most of the anti-reflective surfaces lack in situ tunability of the extinction with respect to wavelength. This communication demonstrates a tunable anti-reflective surface based on colloidal particles comprising a metal core with an electrochromic polymer shell. Random deposition of these particles on a reflective surface results in a decrease in the reflectance of up to 99.8% at the localized surface plasmon resonance frequency. This narrow band feature can be tuned by varying the pH or by application of an electric potential, resulting in wavelength shifts of up to 30 nm. Electrophoretic particle deposition is shown to be an efficient method for controlling the interparticle distance and thereby further optimizing the overall efficiency of the anti-reflective metasurface.

Tuning Single Quantum Dot Emission with a Micromirror

Publisher: American Chemical Society (ACS)

Date: 11-01-2018

DOI: 10.1021/ACS.NANOLETT.7B04482

Abstract: The photoluminescence of single quantum dots fluctuates between bright (on) and dark (off) states, also termed fluorescence intermittency or blinking. This blinking limits the performance of quantum dot-based devices such as light-emitting diodes and solar cells. However, the origins of the blinking remain unresolved. Here, we use a movable gold micromirror to determine both the quantum yield of the bright state and the orientation of the excited state dipole of single quantum dots. We observe that the quantum yield of the bright state is close to unity for these single QDs. Furthermore, we also study the effect of a micromirror on blinking, and then evaluate excitation efficiency, biexciton quantum yield, and detection efficiency. The mirror does not modify the off-time statistics, but it does change the density of optical states available to the quantum dot and hence the on times. The duration of the on times can be lengthened due to an increase in the radiative recombination rate.

High-Performance Large-Area Luminescence Solar Concentrator Incorporating a Donor–Emitter Fluorophore System

Publisher: American Chemical Society (ACS)

Date: 08-07-2019

DOI: 10.1021/ACSENERGYLETT.9B01224

A luminescent solar concentrator ray tracing simulator with a graphical user interface: features and applications

Publisher: IOP Publishing

Date: 07-07-2020

DOI: 10.1088/2050-6120/AB993D

Negative capacitance as a diagnostic tool for recombination in purple quantum dot LEDs

Publisher: AIP Publishing

Date: 21-05-2019

DOI: 10.1063/1.5088177

Abstract: Impedance spectroscopy is a powerful and nondestructive tool for studying charge carrier dynamics in quantum dot light-emitting diodes (QLEDs). We report here that QLEDs exhibit unique capacitance behavior that strongly depends on the ligand chemistry of the quantum dots (QDs). At low frequencies and under bipolar injection, the capacitance of the QLEDs becomes negative before it returns to positive values at even lower frequencies. This behavior is fundamentally different from that observed in organic light-emitting diodes and is attributed to the accumulation of charge carriers within the ligand shells during operation. The capacitive response depends on both the conductivity and the length of the QD ligands and can be used as a diagnostic tool for understanding the luminescent recombination efficiency of a QLED. We find that short and conductive ligands result in positive device capacitances only and this correlates with enhanced device efficiency.

Two Mechanisms Determine Quantum Dot Blinking.

Publisher: American Chemical Society (ACS)

Date: 26-03-2018

DOI: 10.1021/ACSNANO.7B09052

Abstract: Many potential applications of quantum dots (QDs) can only be realized once the luminescence from single nanocrystals (NCs) is understood. These applications include the development of quantum logic devices, single-photon sources, long-life LEDs, and single-molecule biolabels. At the single-nanocrystal level, random fluctuations in the QD photoluminescence occur, a phenomenon termed blinking. There are two competing models to explain this blinking: Auger recombination and surface trap induced recombination. Here we use lifetime scaling on core-shell chalcogenide NCs to demonstrate that both types of blinking occur in the same QDs. We prove that Auger-blinking can yield single-exponential on/off times in contrast to earlier work. The surface passivation strategy determines which blinking mechanism dominates. This study summarizes earlier studies on blinking mechanisms and provides some clues that stable single QDs can be engineered for optoelectronic applications.

Synthesis of Size-Tunable Indium Nitride Nanocrystals

Publisher: American Chemical Society (ACS)

Date: 10-04-2023

DOI: 10.1021/ACS.JPCLETT.3C00024

Circular luminescent solar concentrators

Publisher: Elsevier BV

Date: 07-2017

DOI: 10.1016/J.SOLENER.2017.04.034

Tutorials and Articles on Best Practices

Publisher: American Chemical Society (ACS)

Date: 22-09-2020

DOI: 10.1021/ACSNANO.0C07588

A Mechanism for Symmetry Breaking and Shape Control in Single-Crystal Gold Nanorods

Publisher: American Chemical Society (ACS)

Date: 16-11-2017

DOI: 10.1021/ACS.ACCOUNTS.7B00313

Abstract: The phenomenon of symmetry breaking-in which the order of symmetry of a system is reduced despite manifest higher-order symmetry in the underlying fundamental laws-is pervasive throughout science and nature, playing a critical role in fields ranging from particle physics and quantum theory to cosmology and general relativity. For the growth of crystals, symmetry breaking is the crucial step required to generate a macroscopic shape that has fewer symmetry elements than the unit cell and/or seed crystal from which it grew. Advances in colloid synthesis have enabled a wide variety of nanocrystal morphologies to be achieved, albeit empirically. Of the various nanoparticle morphologies synthesized, gold nanorods have perhaps been the most intensely studied, thanks largely to their unique morphology-dependent optical properties and exciting application potential. However, despite intense research efforts, an understanding of the mechanism by which a single crystal breaks symmetry and grows anisotropically has remained elusive, with many reports presenting seemingly conflicting data and theories. A fundamental understanding of the symmetry breaking process is needed to provide a rational framework upon which future synthetic approaches can be built. Inspired by recent experimental results and drawing upon the wider literature, we present a mechanism for gold nanorod growth from the moments prior to symmetry breaking to the final product. In particular, we describe the steps by which a cuboctahedral seed particle breaks symmetry and undergoes anisotropic growth to form a nanorod. With an emphasis on the evolving crystal structure, we highlight the key geometrical and chemical drivers behind the symmetry breaking process and factors that govern the formation and growth of nanorods, including control over the crystal width, length, and surface faceting. We propose that symmetry breaking is induced by an initial formation of a new surface structure that is stabilized by the deposition of silver, thus preserving this facet in the embryonic nanorod. These new surfaces initially form stochastically as truncations that remove high-energy edge atoms at the intersection of existing {111} facets and represent the beginnings of a {011}-type surface. Crucially, the finely tuned [HAuCl

Memory in quantum dot blinking

Publisher: American Physical Society (APS)

Date: 21-07-2022

DOI: 10.1103/PHYSREVE.106.014127

CuSCN Modified Back Contacts for High Performance CZTSSe Solar Cells

Publisher: Wiley

Date: 05-01-2023

DOI: 10.1002/ADFM.202211421

Abstract: Optimization of the back contact interface is crucial for improving the performance of Cu 2 ZnSnS 4 (CZTS) thin film solar cells. In this paper, self‐depleted CuSCN is deployed as an intermediate layer at the Mo/CZTS interface to improve the quality of the back contact. This CuSCN layer, obtained via aqueous solution processing, reduces the thickness of Mo(S,Se) 2 and eliminates multi‐layer crystallization of the absorber by suppressing the undesirable reaction between Mo and Se during the selenization process. By regulating the selenium infiltration into the CZTS precursor films during the selenization process, highly crystalline, single‐layer Cu 2 ZnSn(S,Se) 4 (CZTSSe) absorber layers are realized. The single‐layer CZTSSe absorber exhibits reduced carrier recombination, enhanced carrier density and increased work function. The improved back contact and absorber layer enables 11.1% power‐conversion‐efficiency to be achieved.

An Optically Responsive Soft Etalon Based on Ultrathin Cellulose Hydrogels

Publisher: Wiley

Date: 07-08-2019

DOI: 10.1002/ADFM.201904290

A General Method for Direct Assembly of Single Nanocrystals

Publisher: Wiley

Date: 28-05-2022

DOI: 10.1002/ADOM.202200179

Abstract: Controlled nanocrystal assembly is a pre‐requisite for incorporation of these materials into solid state devices. Many assembly methods have been investigated which target precise nanocrystal positioning, high process controllability, scalability, and universality. However, most methods are unable to achieve all of these goals. Here, surface templated electrophoretic deposition (STED) is presented as a potential assembly method for a wide variety of nanocrystals. Controlled positioning and deposition of a wide range of nanocrystals into arbitrary spatial arrangements − including gold nanocrystals of different shapes and sizes, magnetic nanocrystals, fluorescent organic nanoparticles, and semiconductor quantum dots − is demonstrated. Nanoparticles with diameters nm are unable to be deposited due to their low surface charge and strong Brownian motion (low Péclet number). It is shown that this limit can be circumvented by forming clusters of nanocrystals or by silica coating nanocrystals to increase their effective size.

Linkage Projects - Grant ID: LP0669111

Start Date: 07-2006

End Date: 12-2010

Amount: $120,000.00

Funder: Australian Research Council

Linkage Projects - Grant ID: LP0454982

Start Date: 10-2004

End Date: 12-2007

Amount: $229,367.00

Funder: Australian Research Council

Linkage Projects - Grant ID: LP160100054

Start Date: 06-2017

End Date: 06-2021

Amount: $501,989.00

Funder: Australian Research Council

Federation Fellowships - Grant ID: FF0561486

Start Date: 12-2005

End Date: 12-2010

Amount: $1,551,625.00

Funder: Australian Research Council

Discovery Projects - Grant ID: DP160102754

Start Date: 05-2016

End Date: 12-2023

Amount: $770,000.00

Funder: Australian Research Council

Australian Laureate Fellowships - Grant ID: FL100100117

Start Date: 12-2010

End Date: 03-2016

Amount: $2,713,582.00

Funder: Australian Research Council

Linkage Infrastructure, Equipment And Facilities - Grant ID: LE0560722

Start Date: 2005

End Date: 12-2006

Amount: $512,744.00

Funder: Australian Research Council

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End Date: 04-2013

Amount: $690,000.00

Funder: Australian Research Council

Linkage Infrastructure, Equipment And Facilities - Grant ID: LE0989197

Start Date: 2009

End Date: 06-2010

Amount: $225,000.00

Funder: Australian Research Council

Linkage Infrastructure, Equipment And Facilities - Grant ID: LE170100118

Start Date: 2017

End Date: 12-2017

Amount: $1,800,000.00

Funder: Australian Research Council

Linkage Infrastructure, Equipment And Facilities - Grant ID: LE110100223

Start Date: 2011

End Date: 12-2014

Amount: $1,000,000.00

Funder: Australian Research Council

Linkage Infrastructure, Equipment And Facilities - Grant ID: LE0775679

Start Date: 2007

End Date: 12-2007

Amount: $700,000.00

Funder: Australian Research Council

Linkage Infrastructure, Equipment And Facilities - Grant ID: LE0989615

Start Date: 2009

End Date: 12-2009

Amount: $300,000.00

Funder: Australian Research Council

Special Research Initiatives - Grant ID: SR0354658

Start Date: 01-2004

End Date: 12-2003

Amount: $10,000.00

Funder: Australian Research Council

Learned Academies Special Projects - Grant ID: LS140100016

Start Date: 10-2014

End Date: 12-2018

Amount: $474,334.00

Funder: Australian Research Council

Linkage Infrastructure, Equipment And Facilities - Grant ID: LE0882493

Start Date: 2008

End Date: 12-2008

Amount: $700,000.00

Funder: Australian Research Council

Linkage Infrastructure, Equipment And Facilities - Grant ID: LE210100009

Start Date: 05-2021

End Date: 05-2022

Amount: $620,000.00

Funder: Australian Research Council

Linkage Infrastructure, Equipment And Facilities - Grant ID: LE140100104

Start Date: 2014

End Date: 12-2014

Amount: $500,000.00

Funder: Australian Research Council

Discovery Projects - Grant ID: DP0451651

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End Date: 12-2009

Amount: $950,000.00

Funder: Australian Research Council

Discovery Projects - Grant ID: DP0558608

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End Date: 12-2010

Amount: $1,020,000.00

Funder: Australian Research Council

Linkage Projects - Grant ID: LP110200319

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End Date: 06-2016

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Funder: Australian Research Council

Industrial Transformation Training Centres - Grant ID: IC170100020

Start Date: 07-2018

End Date: 12-2024

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Funder: Australian Research Council

Linkage Infrastructure, Equipment And Facilities - Grant ID: LE0775562

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End Date: 06-2008

Amount: $500,000.00

Funder: Australian Research Council

Linkage Infrastructure, Equipment And Facilities - Grant ID: LE0560679

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End Date: 12-2005

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Funder: Australian Research Council

Linkage Infrastructure, Equipment And Facilities - Grant ID: LE200100051

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End Date: 05-2022

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Funder: Australian Research Council

Linkage Infrastructure, Equipment And Facilities - Grant ID: LE0347970

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End Date: 05-2004

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Funder: Australian Research Council

Linkage Infrastructure, Equipment And Facilities - Grant ID: LE110100161

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End Date: 12-2011

Amount: $366,384.00

Funder: Australian Research Council

Special Research Initiatives - Grant ID: SR0354630

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End Date: 12-2004

Amount: $20,000.00

Funder: Australian Research Council

Linkage Infrastructure, Equipment And Facilities - Grant ID: LE150100001

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End Date: 12-2015

Amount: $410,000.00

Funder: Australian Research Council

ARC Centres Of Excellence - Grant ID: CE170100026

Start Date: 07-2017

End Date: 06-2024

Amount: $31,850,000.00

Funder: Australian Research Council

Research Networks - Grant ID: RN0460002

Start Date: 08-2004

End Date: 08-2009

Amount: $2,000,000.00

Funder: Australian Research Council

Special Research Initiatives - Grant ID: SR0354735

Start Date: 2003

End Date: 12-2003

Amount: $10,000.00

Funder: Australian Research Council

Linkage Infrastructure, Equipment And Facilities - Grant ID: LE210100151

Start Date: 05-2021

End Date: 05-2022

Amount: $302,154.00

Funder: Australian Research Council

Linkage Infrastructure, Equipment And Facilities - Grant ID: LE0453823

Start Date: 2004

End Date: 06-2005

Amount: $445,124.00

Funder: Australian Research Council

Linkage Infrastructure, Equipment And Facilities - Grant ID: LE120100186

Start Date: 01-2012

End Date: 12-2013

Amount: $370,000.00

Funder: Australian Research Council

Discovery Projects - Grant ID: DP0344356

Start Date: 2003

End Date: 12-2007

Amount: $141,000.00

Funder: Australian Research Council

Linkage Infrastructure, Equipment And Facilities - Grant ID: LE0668403

Start Date: 2006

End Date: 12-2007

Amount: $570,000.00

Funder: Australian Research Council

Discovery Projects - Grant ID: DP130102134

Start Date: 2013

End Date: 12-2016

Amount: $540,000.00

Funder: Australian Research Council

Research Networks - Grant ID: RN0459611

Start Date: 07-2004

End Date: 12-2010

Amount: $1,900,000.00

Funder: Australian Research Council