ORCID Profile
0000-0002-7042-2976
Current Organisation
Curtin 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.
Functional Materials | Nanomaterials | Electrochemistry | Materials Engineering | Colloid and Surface Chemistry | Physical Chemistry (Incl. Structural) | Nanotechnology | Surfaces and Structural Properties of Condensed Matter | Catalysis and Mechanisms of Reactions | Physical Chemistry of Materials | Biochemistry and Cell Biology | Synthesis of Materials | Geochemistry | Powder and Particle Technology | Microelectronics and Integrated Circuits | Photodetectors, Optical Sensors and Solar Cells | Nanochemistry and Supramolecular Chemistry | Materials Engineering not elsewhere classified | Structural Chemistry and Spectroscopy | Nanoscale Characterisation | Structural Biology (incl. Macromolecular Modelling) | Organic Geochemistry | Isotope Geochemistry | Plant Cell and Molecular Biology | Compound Semiconductors |
Expanding Knowledge in Engineering | Expanding Knowledge in the Chemical Sciences | Fuel Cells (excl. Solid Oxide) | Solid Oxide Fuel Cells | Management of Greenhouse Gas Emissions from Electricity Generation | Expanding Knowledge in the Biological Sciences | Emerging Defence Technologies | Mineral Exploration not elsewhere classified | Manufacturing not elsewhere classified | Hydrogen Storage | Expanding Knowledge in Technology | Hydrogen Production from Renewable Energy | Biofuel (Biomass) Energy | Oil and Gas Exploration | Industrial Chemicals and Related Products not elsewhere classified | Expanding Knowledge in the Physical Sciences | Integrated Circuits and Devices
Publisher: Wiley
Date: 08-2021
Publisher: Elsevier BV
Date: 05-2016
DOI: 10.1016/J.JCIS.2016.02.013
Abstract: Brookite titanium dioxide (TiO2) is rarely studied, as compared with anatase and rutile phases TiO2, due to its comparatively lower photoactivity. It has been recently reported that brookite TiO2 with active facets exhibits excellent performance, however, synthesis of such faceted brookite TiO2 is difficult because of its low thermodynamic phase stability and low structural symmetric. Furthermore, like faceted anatase and rutile TiO2, faceted brookite TiO2 is not responsive to visible light due to its wide bandgap. In this study, a novel dopant, hydrazine, was introduced in the development of nitrogen doping. By applying this dopant, nitrogen doped brookite nanorods with active {120}, {111} and {011¯} facets were successfully synthesized. The resultant materials exhibited remarkably enhanced visible-light photoactivity in photodegradation.
Publisher: Elsevier BV
Date: 2022
Publisher: Royal Society of Chemistry (RSC)
Date: 2022
DOI: 10.1039/D1EE03311E
Abstract: The in situ atomization of carbon supported metal oxide nanoparticles provides a novel strategy to synthesize atomic sites supported on highly graphitized carbon materials with high metal loading and controlled atomic layers.
Publisher: Elsevier BV
Date: 2016
Publisher: Wiley
Date: 21-06-2019
Publisher: Royal Society of Chemistry (RSC)
Date: 2021
DOI: 10.1039/D0TA11503G
Abstract: A Co single-atom catalyst on g-C 3 N 4 support was prepared for the selective oxidation of ethylbenzene (EB) to acetophenone (AcPO) by peroxymonosulfate (PMS). The Co atoms bonded with N were robust active sites for EB oxidation via the radical pathway.
Publisher: Royal Society of Chemistry (RSC)
Date: 2020
DOI: 10.1039/D0QI00737D
Abstract: Schematic illustration of the formation process and performance of overall water splitting for NiFe-NCNT@MoS 2 s les.
Publisher: Elsevier BV
Date: 11-2015
Publisher: Elsevier BV
Date: 12-2013
Publisher: Elsevier BV
Date: 09-2023
Publisher: Elsevier BV
Date: 11-2018
Publisher: Elsevier BV
Date: 03-2017
Publisher: Royal Society of Chemistry (RSC)
Date: 2022
DOI: 10.1039/D2TA02187K
Abstract: An ultrathin carbon quantum dots modified hydrogenated mesoporous SrTiO 3 heterostructure (CQDs/STO) has been developed as a bifunctional catalyst for enhanced photoelectrochemical nitrogen reduction, resulting in a ∼50% increase in the ammonia yield.
Publisher: Elsevier BV
Date: 2014
Publisher: Elsevier BV
Date: 09-2021
Publisher: Royal Society of Chemistry (RSC)
Date: 2022
DOI: 10.1039/D2CC03877C
Abstract: Solid oxide cell (SOC) is one of the most important candidates for efficient storage and conversion of renewable energies from solar and wind power and the performance and stability of SOC is critically dependent on the synthesis methods and characteristics of nano-scaled electrodes.
Publisher: Elsevier BV
Date: 04-2019
Publisher: American Chemical Society (ACS)
Date: 19-01-2018
Publisher: Elsevier BV
Date: 2021
Publisher: Elsevier BV
Date: 09-2018
Publisher: American Chemical Society (ACS)
Date: 30-05-2023
Publisher: American Chemical Society (ACS)
Date: 03-02-2023
Publisher: Royal Society of Chemistry (RSC)
Date: 2019
DOI: 10.1039/C9TA01951K
Abstract: A new one-dimensional hierarchical hollow MnO 2 nanotubes@NiCo-LDH/CoS 2 nanocage supercapacitor, MnO 2 @NiCo-LDH/CoS 2 , achieves a high specific capacitance and high stability.
Publisher: American Chemical Society (ACS)
Date: 17-12-2022
Abstract: The lack of low-cost catalysts with high activity leads to the unsatisfactory electrochemical performance of Li-CO
Publisher: Royal Society of Chemistry (RSC)
Date: 2016
DOI: 10.1039/C6TA08396J
Abstract: Cathode/electrolyte interface could be formed by electrochemical polarization, offering new opportunities for direct application of double perovskites to YSZ-based SOFCs.
Publisher: Elsevier BV
Date: 08-2019
Publisher: Elsevier BV
Date: 07-2014
Publisher: American Chemical Society (ACS)
Date: 22-02-2017
Abstract: Rechargeable Zn-air battery is limited by the sluggish kinetics and poor durability of the oxygen catalysts. In this Research Article, a new bifunctional oxygen catalyst has been developed through embedding the ultrafine NiFeO nanoparticles (NPs) in a porous amorphous MnO
Publisher: Royal Society of Chemistry (RSC)
Date: 2020
DOI: 10.1039/C9TA13288K
Abstract: In situ selenization is a potential method to repair the defects of metal selenide films for enhancing their photoelectrochemical performance and environmental stability.
Publisher: Wiley
Date: 13-01-2022
Abstract: Nonprecious group metal (NPGM)‐based single atom catalysts (SACs) hold a great potential in electrocatalysis and dopant engineering has been extensively exploited to boost their catalytic activity, while the coordination environment of dopant, which also significantly affects the electronic structure of SACs, and consequently their electrocatalytic performance, have been largely ignored. Here, by adopting a precursor modulation strategy, the authors successfully synthesize single cobalt atom catalysts embedded in nitrogen‐doped carbon, Co–N/C, with similar overall Co and N concentrations but different N types, that is, pyridinic N (N P ), graphitic N (N G ), and pyrrolic N (N PY ). Co–N/C with the Co–N 4 moieties coordinated with N G displays far superior activity for oxygen reduction (ORR) and evolution reactions, and superior activity and stability in both zinc–air batteries and proton exchange membrane fuel cells. Density functional theory calculation indicates that coordinated N species in particular N G functions as electron donors to the Co core of Co–N 4 active sites, leading to the downshift of d ‐band center of Co–N 4 and weakening the binding energies of the intermediates on Co–N 4 sites, thus, significantly promoting catalytic kinetics and thermodynamics for ORR in a full pH range condition.
Publisher: American Chemical Society (ACS)
Date: 23-11-2020
Publisher: American Chemical Society (ACS)
Date: 23-03-2023
Publisher: Springer Science and Business Media LLC
Date: 07-11-2022
DOI: 10.1007/S41918-022-00160-8
Abstract: Solid-state electrochemistry (SSE) is an interdisciplinary field bridging electrochemistry and solid-state ionics and deals primarily with the properties of solids that conduct ions in the case of ionic conducting solid electrolytes and electrons and/or electron holes in the case of mixed ionic and electronic conducting materials. However, in solid-state devices such as solid oxide fuel cells (SOFCs), there are unique electrochemical features due to the high operating temperature (600–1 000 °C) and solid electrolytes and electrodes. The solid-to-solid contact at the electrode/electrolyte interface is one of the most distinguished features of SOFCs and is one of the fundamental reasons for the occurance of most importance phenomena such as shift of the equipotential lines, the constriction effect, polarization-induced interface formation, etc. in SOFCs. The restriction in placing the reference electrode in solid electrolyte cells further complicates the SSE in SOFCs. In addition, the migration species at the solid electrode/electrolyte interface is oxygen ions, while in the case of the liquid electrolyte system, the migration species is electrons. The increased knowledge and understanding of SSE phenomena have guided the development of SOFC technologies in the last 30–40 years, but thus far, no up-to-date reviews on this important topic have appeared. The purpose of the current article is to review and update the progress and achievements in the SSE in SOFCs, largely based on the author’s past few decades of research and understanding in the field, and to serve as an introduction to the basics of the SSE in solid electrolyte devices such as SOFCs. Graphical abstract
Publisher: Royal Society of Chemistry (RSC)
Date: 2019
DOI: 10.1039/C9TA01275C
Abstract: A new Cr incorporation mechanism involving preferential formation of nanometre size Fe–Co–Cr–O spinel particles was found to be responsible for a reduced Cr poisoning effect at 900 °C under cathodic polarization for the La 0.6 Sr 0.4 Co 0.2 Fe 0.8 O 3−δ solid oxide fuel cell cathode.
Publisher: Wiley
Date: 14-11-2020
Publisher: Elsevier BV
Date: 02-2018
Publisher: Wiley
Date: 27-04-2020
Publisher: Wiley
Date: 03-12-2021
Publisher: American Chemical Society (ACS)
Date: 05-11-2018
Abstract: Bismuth-based oxides exhibit outstanding oxygen ionic conductivity and fast oxygen surface kinetics and have shown great potential as a highly active component for electrode materials in solid oxide fuel cells (SOFCs). Herein, a Nb-doped La
Publisher: Royal Society of Chemistry (RSC)
Date: 2018
DOI: 10.1039/C8TA00370J
Abstract: Nanostructured bismuth oxide–cobaltite is developed as a high performance and durable oxygen electrode for reversible solid oxide cells.
Publisher: Royal Society of Chemistry (RSC)
Date: 2019
DOI: 10.1039/C8CC09633C
Abstract: New g-C 3 N 4 crystalline/amorphous lateral-like homostructures show excellent photocatalytic activity due to the effective separation of photogenerated carriers.
Publisher: Elsevier BV
Date: 09-2020
Publisher: American Chemical Society (ACS)
Date: 23-01-2023
Publisher: Royal Society of Chemistry (RSC)
Date: 2018
DOI: 10.1039/C7CP08683K
Abstract: Remarkable differences in the electrocatalytic activity and reversibility were observed among CNTs with wall numbers for the VO 2 + /VO 2+ redox.
Publisher: Elsevier BV
Date: 04-2021
Publisher: Wiley
Date: 29-10-2019
Publisher: Elsevier BV
Date: 02-2015
Publisher: American Chemical Society (ACS)
Date: 30-12-2020
DOI: 10.1021/ACS.NANOLETT.9B04719
Abstract: Lithium-sulfur (Li-S) batteries are promising next-generation energy storage technologies due to their high theoretical energy density, environmental friendliness, and low cost. However, low conductivity of sulfur species, dissolution of polysulfides, poor conversion from sulfur reduction, and lithium sulfide (Li
Publisher: Wiley
Date: 29-04-2020
Publisher: Wiley
Date: 07-2019
Publisher: American Chemical Society (ACS)
Date: 18-10-2019
Publisher: Elsevier BV
Date: 08-2022
Publisher: Wiley
Date: 09-02-2018
Abstract: Single‐atom catalysts (SACs) are the smallest entities for catalytic reactions with projected high atomic efficiency, superior activity, and selectivity however, practical applications of SACs suffer from a very low metal loading of 1–2 wt%. Here, a class of SACs based on atomically dispersed transition metals on nitrogen‐doped carbon nanotubes (MSA‐N‐CNTs, where M = Ni, Co, NiCo, CoFe, and NiPt) is synthesized with an extraordinarily high metal loading, e.g., 20 wt% in the case of NiSA‐N‐CNTs, using a new multistep pyrolysis process. Among these materials, NiSA‐N‐CNTs show an excellent selectivity and activity for the electrochemical reduction of CO 2 to CO, achieving a turnover frequency (TOF) of 11.7 s −1 at −0.55 V (vs reversible hydrogen electrode (RHE)), two orders of magnitude higher than Ni nanoparticles supported on CNTs.
Publisher: Elsevier BV
Date: 11-2018
Publisher: Elsevier BV
Date: 09-2018
Publisher: Elsevier BV
Date: 04-2021
Publisher: American Chemical Society (ACS)
Date: 31-01-2023
Publisher: Elsevier BV
Date: 09-2015
Publisher: Elsevier BV
Date: 10-2021
Publisher: Elsevier BV
Date: 12-2018
Publisher: Wiley
Date: 15-12-2017
Publisher: Elsevier BV
Date: 2021
Publisher: American Association for the Advancement of Science (AAAS)
Date: 2020
Abstract: Elevation of operational temperatures of polymer electrolyte membrane fuel cells (PEMFCs) has been demonstrated with phosphoric acid-doped polybenzimidazole (PA/PBI) membranes. The technical perspective of the technology is simplified construction and operation with possible integration with, e.g., methanol reformers. Toward this target, significant efforts have been made to develop acid-base polymer membranes, inorganic proton conductors, and organic-inorganic composite materials. This report is devoted to updating the recent progress of the development particularly of acid-doped PBI, phosphate-based solid inorganic proton conductors, and their composite electrolytes. Long-term stability of PBI membranes has been well documented, however, at typical temperatures of 160°C. Inorganic proton-conducting materials, e.g., alkali metal dihydrogen phosphates, heteropolyacids, tetravalent metal pyrophosphates, and phosphosilicates, exhibit significant proton conductivity at temperatures of up to 300°C but have so far found limited applications in the form of thin films. Composite membranes of PBI and phosphates, particularly in situ formed phosphosilicates in the polymer matrix, showed exceptionally stable conductivity at temperatures well above 200°C. Fuel cell tests at up to 260°C are reported operational with good tolerance of up to 16% CO in hydrogen, fast kinetics for direct methanol oxidation, and feasibility of nonprecious metal catalysts. The prospect and future exploration of new proton conductors based on phosphate immobilization and fuel cell technologies at temperatures above 200°C are discussed.
Publisher: Elsevier BV
Date: 04-2018
Publisher: Elsevier BV
Date: 2020
Publisher: Elsevier BV
Date: 02-2023
Publisher: Royal Society of Chemistry (RSC)
Date: 2016
DOI: 10.1039/C6TA07067A
Abstract: Cobaltite based perovskites can be directly applied on the YSZ electrolyte via an in situ polarization induced electrode/electrolyte interface.
Publisher: American Chemical Society (ACS)
Date: 14-10-2021
Publisher: Royal Society of Chemistry (RSC)
Date: 2019
DOI: 10.1039/C9EE00524B
Abstract: The efficiency and stability of narrow-gap semiconductor-based photoelectrodes are two fundamental factors for realizing their industrial solar-to-fuel conversion.
Publisher: Wiley
Date: 03-2019
Publisher: Royal Society of Chemistry (RSC)
Date: 2017
DOI: 10.1039/C7TA00276A
Abstract: A metal–organic framework (MOF) seed-mediated deposition route is developed to synthesize graphene oxide/core–shell structured MOF nano-sandwiches.
Publisher: Wiley
Date: 24-08-2018
Abstract: An acid pretreatment strategy is developed to enhance the proton transport of polysulfone-polyvinylpyrrolidone (PSF-PVP) membranes for application in vanadium redox flow batteries (VRFB). The acid pretreatment leads to the formation of ionic conducting clusters with a size of around d=15.41 nm in the membrane (p-PSF-PVP). As a result, the proton conductivity and proton/vanadium ion selectivity of the p-PSF-PVP membrane increases to 6.60×10
Publisher: Royal Society of Chemistry (RSC)
Date: 2018
DOI: 10.1039/C7TA09208C
Abstract: The Fe center in FePc can be electrochemically substituted by Co and Ni, achieving high activity and stability for CO 2 reduction.
Publisher: American Chemical Society (ACS)
Date: 20-09-2018
Publisher: American Chemical Society (ACS)
Date: 13-02-2019
Publisher: Elsevier BV
Date: 12-2021
Publisher: Wiley
Date: 21-02-2017
Abstract: Direct assembly is a newly developed technique in which a cobaltite-based perovskite (CBP) cathode can be directly applied to a barrier-layer-free Y
Publisher: Elsevier BV
Date: 08-2020
Publisher: Royal Society of Chemistry (RSC)
Date: 2017
DOI: 10.1039/C7NR00978J
Abstract: A “MOF genetic” strategy was developed to form hollow metal–organic structures from MOF crystals and dopamine, providing a simple and effective way to synthesize hollow metal/N carbon materials as high-performance oxygen reduction reaction electrocatalysts.
Publisher: Wiley
Date: 2023
DOI: 10.1002/IDM2.12068
Abstract: Solid oxide cells (SOCs) are all solid ceramic devices with the dual functionality of solid oxide fuel cells (SOFCs) to convert the chemical energy of fuels like H 2 , natural gas and other hydrocarbons to electricity and of solid oxide electrolysis cells (SOECs) to store renewable electric energy of sun and wind in hydrogen fuel. Among the electrochemical energy conversion and storage devices, SOCs are the most clean and efficient technology with unique dual functionality. Due to the high operation temperature (typically 600–800°C), SOCs exhibit many advantages over other energy conversion devices, such as low material cost, high efficiency and fuel flexibility. There has been rapid development of SOC technologies over the last decade with significant advantages and progress in key materials and a fundamental understanding of key issues such as an electrode, electrolyte, performance degradation, poisoning, and stack design. The reversible polarization also has a critical effect on the surface segregation and stability of the electrode and electrode/electrolyte interface. This critical review starts with a brief introduction, working principles and thermodynamics of SOC technology to readers with interests in this rapidly developing and emerging field. Then the key materials currently used in SOCs are summarized, followed by the discussion of the most advanced electrode modification methods and critical issues of SOCs, including the surface chemistry, segregation, electrode/electrolyte interface and varying material degradation mechanisms under reversible operations. The challenges and prospects of SOC technology for future developments are discussed.
Publisher: Elsevier BV
Date: 12-2015
Publisher: Elsevier BV
Date: 10-2022
Publisher: Wiley
Date: 16-06-2020
Publisher: Elsevier BV
Date: 02-2020
Publisher: Wiley
Date: 13-03-2019
Publisher: Elsevier BV
Date: 2023
Publisher: Wiley
Date: 30-03-2023
Abstract: As a widely used commodity chemical, ammonia is critical for producing nitrogen‐containing fertilizers and serving as the promising zero‐carbon energy carrier. Photoelectrochemical nitrogen reduction reaction (PEC NRR) can provide a solar‐powered green and sustainable route for synthesis of ammonia (NH 3 ). Herein, an optimum PEC system is reported with an Si‐based hierarchically‐structured PdCu/TiO 2 /Si photocathode and well‐thought‐out trifluoroethanol as the proton source for lithium‐mediated PEC NRR, achieving a record high NH 3 yield of 43.09 µg cm −2 h −1 and an excellent faradaic efficiency of 46.15% under 0.12 MPa O 2 and 3.88 MPa N 2 at 0.07 V versus lithium(0/+) redox couple (vs Li 0/+ ). PEC measurements coupled with operando characterization reveal that the PdCu/TiO 2 /Si photocathode under N 2 pressures facilitate the reduction of N 2 to form lithium nitride (Li 3 N), which reacts with active protons to produce NH 3 while releasing the Li + to reinitiate the cycle of the PEC NRR. The Li‐mediated PEC NRR process is further enhanced by introducing small amount of O 2 or CO 2 under pressure by accelerating the decomposition of Li 3 N. For the first time, this work provides mechanistic understanding of the lithium‐mediated PEC NRR process and opens new avenues for efficient solar‐powered green conversion of N 2 ‐to‐NH 3 .
Publisher: Elsevier BV
Date: 11-2017
Publisher: Wiley
Date: 22-03-2018
Publisher: Elsevier BV
Date: 08-2015
Publisher: Springer Science and Business Media LLC
Date: 10-09-2022
DOI: 10.1038/S41467-022-33066-6
Abstract: Electrocatalytic urea synthesis emerged as the promising alternative of Haber–Bosch process and industrial urea synthetic protocol. Here, we report that a diatomic catalyst with bonded Fe–Ni pairs can significantly improve the efficiency of electrochemical urea synthesis. Compared with isolated diatomic and single-atom catalysts, the bonded Fe–Ni pairs act as the efficient sites for coordinated adsorption and activation of multiple reactants, enhancing the crucial C–N coupling thermodynamically and kinetically. The performance for urea synthesis up to an order of magnitude higher than those of single-atom and isolated diatomic electrocatalysts, a high urea yield rate of 20.2 mmol h −1 g −1 with corresponding Faradaic efficiency of 17.8% has been successfully achieved. A total Faradaic efficiency of about 100% for the formation of value-added urea, CO, and NH 3 was realized. This work presents an insight into synergistic catalysis towards sustainable urea synthesis via identifying and tailoring the atomic site configurations.
Publisher: Elsevier BV
Date: 03-2019
Publisher: Elsevier BV
Date: 02-2021
Publisher: The Electrochemical Society
Date: 2019
DOI: 10.1149/2.0841912JES
Publisher: Royal Society of Chemistry (RSC)
Date: 2017
DOI: 10.1039/C7TA02950K
Abstract: A directly assembled ESB decorated LSM nanostructured electrode exhibits high electrocatalytic activity and excellent stability in reversible solid oxide cell mode.
Publisher: Elsevier BV
Date: 05-2023
Publisher: IOP Publishing
Date: 07-2020
Publisher: American Chemical Society (ACS)
Date: 07-05-2019
Abstract: It is highly attractive but challenging to develop transition-metal electrocatalysts for direct hydrazine fuel cells (DHzFCs). In this work, a nickel crystalline core@nickel phosphide amorphous shell heterostructured electrocatalyst supported by active carbon (Ni@NiP/C) is developed. Ni@NiP/C with a P/Ni molar ratio of 3:100, Ni@NiP
Publisher: Elsevier BV
Date: 08-2022
Publisher: Royal Society of Chemistry (RSC)
Date: 2021
DOI: 10.1039/D1CC00209K
Abstract: Type II heterostructures consisting of red/yellow g-C 3 N 4 nanosheets prepared via edge-epitaxial growth revealed superior photocatalytic activities for enhanced H 2 generation and CO 2 reduction.
Publisher: American Chemical Society (ACS)
Date: 14-06-2022
Publisher: IOP Publishing
Date: 05-02-2021
Abstract: Conventional two-dimensional (2D) graphitic carbon nitride, 2D g-C
Publisher: Elsevier BV
Date: 04-2020
Publisher: Wiley
Date: 07-04-2020
Publisher: American Chemical Society (ACS)
Date: 07-09-2017
Abstract: As differentiated from conventional synthetic processes, amino-functionalized hollow mesoporous silica (NH
Publisher: Springer Science and Business Media LLC
Date: 10-08-2020
DOI: 10.1007/S41918-020-00078-Z
Abstract: Solid oxide cells (SOCs) are highly efficient and environmentally benign devices that can be used to store renewable electrical energy in the form of fuels such as hydrogen in the solid oxide electrolysis cell mode and regenerate electrical power using stored fuels in the solid oxide fuel cell mode. Despite this, insufficient long-term durability over 5–10 years in terms of lifespan remains a critical issue in the development of reliable SOC technologies in which the surface segregation of cations, particularly strontium (Sr) on oxygen electrodes, plays a critical role in the surface chemistry of oxygen electrodes and is integral to the overall performance and durability of SOCs. Due to this, this review will provide a critical overview of the surface segregation phenomenon, including influential factors, driving forces, reactivity with volatile impurities such as chromium, boron, sulphur and carbon dioxide, interactions at electrode/electrolyte interfaces and influences on the electrochemical performance and stability of SOCs with an emphasis on Sr segregation in widely investigated (La,Sr)MnO 3 and (La,Sr)(Co,Fe)O 3− δ . In addition, this review will present strategies for the mitigation of Sr surface segregation.
Publisher: American Chemical Society (ACS)
Date: 25-07-2017
DOI: 10.1021/ACS.JPCLETT.7B01557
Abstract: It is known that hierarchical structure plays a key role in many unique material properties such as self-cleaning effect of lotus leaves and the antifogging property of the compound eyes of mosquitoes. This study reports a series of highly ordered mesoporous Nafion membranes with unique hierarchical structural features at the nanometer scale. Using NMR, we show for the first time that, at low RH conditions, the proton in the ionic domains migrates via a surface diffusion mechanism and exhibits approximately 2 orders of magnitude faster transport than that in the nanopores, whereas the nanopores play a role of reservoir and maintain water and thereby conductivity at higher temperature and lower humidities. Thereby creating hierarchical nanoscale structures is a feasible and promising strategy to develop PEMs that would enable efficient electrochemical performance in devices such as fuel cells, even in the absence of high humidity and at elevated temperatures.
Publisher: Elsevier BV
Date: 04-2018
Publisher: Elsevier BV
Date: 03-2018
Publisher: Wiley
Date: 23-12-2022
Abstract: Development of high temperature polymer electrolyte membrane fuel cells (HT‐PEMFCs) at elevated temperatures is important for the enhancement of tolerance toward CO impurities and for the development of non‐precious metal catalysts. The key challenge in such HT‐PEMFCs is the high temperature polymer electrolyte membranes. Herein, the development of in situ formed metal pyrophosphates (MP 2 O 7 , where M = Sn, Ti, and Zr) in phosphoric acid doped polybenzimidazole (PA/PBI) composite membranes for HT‐PEMFCs is reported. The formation mechanism of MP 2 O 7 , and characteristics of MP 2 O 7 /PA/PBI composite membranes are studied in detail. In contrast to the rapid decay in performance of pristine PA/PBI membrane cells, the in situ formed MP 2 O 7 /PA/PBI composite membranes show significantly higher proton conductivity, improved performance, and stability at elevated temperatures of 200–250 °C. The best results are obtained on the in situ formed SnP 2 O 7 /PA/PBI composite membrane cells, exhibiting a high peak power density of 476 mW cm −2 and proton conductivity of 51.3 mS cm −1 at 250 °C. The excellent durability of SnP 2 O 7 /PA/PBI composite membrane is due to the uniform distribution of in situ formed SnP 2 O 7 nanoparticles in PBI membranes and the formation of a gel‐like region, thin and irregular amorphous layer on the SnP 2 O 7 with the high acid retention ability. This effectively alleviates the PA leaching at elevated temperatures of the new HT‐PEMFCs.
Publisher: Elsevier BV
Date: 11-2014
Publisher: Elsevier BV
Date: 03-2017
Publisher: Royal Society of Chemistry (RSC)
Date: 2018
DOI: 10.1039/C8CC07095D
Abstract: Ni single atoms encapsulated in carbon nanotubes substantially enhance the activity of Pd nanoparticles for oxidation of alcohols in alkaline media.
Publisher: Elsevier BV
Date: 03-2021
Publisher: The Electrochemical Society
Date: 2018
DOI: 10.1149/2.0151807JES
Publisher: American Chemical Society (ACS)
Date: 17-08-2023
Publisher: Royal Society of Chemistry (RSC)
Date: 2016
DOI: 10.1039/C6RA23286H
Abstract: Polarization can induce an LSM/YSZ interface which is electrochemically compatible with the one formed under high temperature sintering.
Publisher: Wiley
Date: 16-09-2022
Abstract: Green hydrogen production by renewables‐powered water electrolysis holds the key to energy sustainability and a carbon‐neutral future. The sluggish kinetics of water‐splitting reactions, namely, hydrogen evolution reaction (HER) and oxygen evolution reaction (OER), however, remains a bottleneck to the water electrolysis technology. High‐entropy materials, due to their compositional flexibility, structural stability, and synergy between various elemental components, have recently aroused considerable interest in catalyzing the water‐splitting reactions. Herein, a timely review of the recent achievements is provided in high‐entropy materials for water electrolysis. An overview of different kinds of high‐entropy materials for catalyzing the HER and OER half‐reactions is introduced, followed by a discussion of theoretical and experimental efforts in understanding the fundamental origins of the enhanced catalytic performance observed on high‐entropy catalysts. Various materials design strategies, including control of size and shape, construction of a porous structure, engineering of defect, and formation of hybrid/composite structure, to develop high‐entropy catalysts with improved catalytic performance are highlighted. Finally, the remaining challenges are pointed out and the corresponding perspectives to address these challenges are put forward to promote the development of the research field of high‐entropy water‐splitting catalysts.
Start Date: 2015
End Date: 12-2017
Amount: $330,900.00
Funder: Australian Research Council
View Funded ActivityStart Date: 02-2012
End Date: 02-2015
Amount: $270,000.00
Funder: Australian Research Council
View Funded ActivityStart Date: 10-2011
End Date: 10-2014
Amount: $200,000.00
Funder: Australian Research Council
View Funded ActivityStart Date: 01-2012
End Date: 12-2013
Amount: $480,000.00
Funder: Australian Research Council
View Funded ActivityStart Date: 07-2018
End Date: 12-2021
Amount: $564,124.00
Funder: Australian Research Council
View Funded ActivityStart Date: 2015
End Date: 12-2017
Amount: $375,500.00
Funder: Australian Research Council
View Funded ActivityStart Date: 07-2013
End Date: 04-2014
Amount: $670,000.00
Funder: Australian Research Council
View Funded ActivityStart Date: 2012
End Date: 06-2015
Amount: $420,000.00
Funder: Australian Research Council
View Funded ActivityStart Date: 2018
End Date: 12-2021
Amount: $412,916.00
Funder: Australian Research Council
View Funded ActivityStart Date: 2019
End Date: 06-2020
Amount: $1,267,674.00
Funder: Australian Research Council
View Funded ActivityStart Date: 04-2017
End Date: 12-2018
Amount: $700,000.00
Funder: Australian Research Council
View Funded Activity