ORCID Profile
0000-0002-5935-3287
Current Organisations
Australian National University
,
National Renewable Energy Laboratory
,
Northumbria University
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Publisher: Wiley
Date: 22-09-2022
Abstract: Photoelectrochemical (PEC) water splitting is considered a promising technology to produce renewable hydrogen, a clean fuel or energy carrier to replace conventional carbon‐based fossil‐fuel sources. Nevertheless, the overall solar‐to‐hydrogen efficiency and the cost‐effectiveness of this technology are still unsatisfactory for practical implementation. This can be primarily attributed to the sluggish kinetics of the anodic oxygen evolution reaction (OER) and the relatively low economic value of cogenerated O 2 production. Over the past decades, there are extensive efforts to explore more kinetically favorable photooxidation reactions, which coupled with hydrogen evolution reaction (HER) can simultaneously improve H 2 production yield and produce higher valuable alternatives to conventional O 2 . This review aims to present recent progress on the alternative anodic choices to OER. Here, the fundamental of PEC water splitting and the critical components required for this system are first shortly summarized. Then the benefits and issues of alternative photooxidation reactions including photooxidation of water to hydrogen peroxide, chlorine, alcohol, 5‐hydroxymethylfurfural, or urea oxidation when combined with the concurrent HER, are reviewed and analyzed. This review is concluded by presenting a critical evaluation of the challenges and opportunities of these alternative HER‐coupled photooxidation reactions for solar energy production and environmental treatment.
Publisher: American Physiological Society
Date: 08-2018
Publisher: Elsevier BV
Date: 11-2013
DOI: 10.1016/J.JSAMS.2012.12.005
Abstract: This study examined distances covered at low (1-2 ms(-2)), moderate (2-3 ms(-2)) and high (>3 ms(-2)) acceleration (L(ACC), M(ACC) and H(ACC) respectively) and deceleration (L(DEC), M(DEC), and H(DEC) respectively) during competitive football games. Temporal and transient patterns of acceleration and deceleration were also examined. Observational, repeated measures. Thirty-six professional male professional footballers were monitored using a 10 Hz non-differential global positioning system (NdGPS). Match data was organised into six 15 min periods (P1: 1-15 min, P2: 16-30 min, P3: 31-45 min, P4: 46-60 min, P5: 61-75 min, and P6: 76-90 min) for analysis of temporal patterns, and into eighteen 5 min periods for analysis of transient patterns. ANOVA with Bonferroni post hoc tests were used to identify significant (p<0.05) differences between periods. Distance covered at L(ACC), M(ACC), H(ACC), L(DEC), M(DEC), and H(DEC) was 424±75 m, 242±25 m, 178±38 m, 365±54 m, 210±23 m and 162±29 m respectively. Between period decrements ranged from 8.0% to 13.2% from P1 to P3, 9.2% to 16.3% from P4 to P6, and from 14.9% to 21.0% from P1 to P6. Following PEAK H(ACC) (148% of mean 5 min H(ACC)), H(ACC) at 5POST was 10.4% lower than mean (p<0.01). Time-dependent reductions in distances covered suggest that acceleration and deceleration capability are acutely compromised during match play. Further, the occurrence of transient fatigue may be supported by the findings that HACC and HDEC performance following PEAK was approximately 10% lower than mean values.
Publisher: Elsevier BV
Date: 04-2008
DOI: 10.1016/J.RESP.2008.02.001
Abstract: We tested the hypothesis that priming exercise would speed V(O2) kinetics during treadmill running. Eight subjects completed a square-wave protocol, involving two bouts of treadmill running at 70% of the difference between the running speeds at lactate threshold (LT) and V(O2) max, separated by 6-min of walking at 4 km h(-1), on two occasions. Oxygen uptake was measured breath-by-breath and subsequently modelled using non-linear regression techniques. Heart rate and blood lactate concentration were significantly elevated prior to the second exercise bout compared to the first. However, V(O2) kinetics was not significantly different between the first and second exercise bouts (mean+/-S.D., phase II time constant, Bout 1: 16+/-3s vs. Bout 2: 16+/-4s V(O2) slow component litude, Bout 1: 0.24+/-0.10 L min(-1)vs. Bout 2: 0.20+/-0.12 L min(-1) mean response time, Bout 1: 34+/-4s vs. Bout 2: 34+/-6s P>0.05 for all comparisons). These results indicate that, contrary to previous findings with other exercise modalities, priming exercise does not alter V(O2) kinetics during high-intensity treadmill running, at least in physically active young subjects. We speculate that the relatively fast V(O2) kinetics and the relatively small V(O2) slow component in the control ('un-primed') condition negated any enhancement of V(O2) kinetics by priming exercise in this exercise modality.
Publisher: Wiley
Date: 03-10-2021
Abstract: Geometrical structuring of monolithic metal‐organic frameworks (MOFs) components is required for their practical implementation in many areas, including electronic devices, gas storage/separation, catalysis, energy storage as well as bio‐medical applications. Despite progress in structuring MOFs, an approach for the precise patterning of MOF functional geometries in the millimeter‐ to micro‐meter depth is lacking. Here, a facile and flexible concept for the microfabrication of complex MOF patterns on large surfaces is reported. The method relies on the engineering of easily‐writable sheets of precursor metal oxide nanoparticles. The gas‐phase conversion of these patterned ceramic nanoparticle sheets results in monolithic MOF objects with arbitrarily shaped geometries and thicknesses of up to hundreds of micrometers. The writing of complex patterns of zeolitic imidazolate framework‐8 (ZIF‐8) is demonstrated by a variety of approaches including ion beam, laser, and hand writing. Nanometer‐scale patterns are achieved by focused ion beam (FIB). Artless handwritings are obtained by using a pen in a similar fashion to writing on a paper. The pure ZIF‐8 composition of the resulting patterns is confirmed by a series of physical and chemical characterization. This facile MOF precursor‐writing approach provides novel opportunities for the design of MOF‐based devices with applications ranging from micro‐fluidics to renewable energy systems.
Publisher: Royal Society of Chemistry (RSC)
Date: 2016
DOI: 10.1039/C5NR08604C
Publisher: Wiley
Date: 24-04-2019
Publisher: Wiley
Date: 22-10-2019
Publisher: Wiley
Date: 16-04-2018
Abstract: Photoelectrochemical water splitting is a promising approach for the carbon-free production of hydrogen using sunlight. Here, robust and efficient WO
Publisher: Elsevier BV
Date: 09-2014
DOI: 10.1016/J.JSAMS.2013.08.005
Abstract: To examine the validity and inter-unit reliability of 10 Hz GPS for measuring instantaneous velocity during maximal accelerations. Experimental. Two 10 Hz GPS devices secured to a sliding platform mounted on a custom built monorail were towed whilst sprinting maximally over 10 m. Displacement of GPS devices was measured using a laser s ling at 2000 Hz, from which velocity and mean acceleration were derived. Velocity data was pooled into acceleration thresholds according to mean acceleration. Agreement between laser and GPS measures of instantaneous velocity within each acceleration threshold was examined using least squares linear regression and Bland-Altman limits of agreement (LOA). Inter-unit reliability was expressed as typical error (TE) and a Pearson correlation coefficient. Mean bias ± 95% LOA during accelerations of 0-0.99 ms(-2) was 0.12 ± 0.27 ms(-1), decreasing to -0.40 ± 0.67 ms(-1) during accelerations >4 ms(-2). Standard error of the estimate ± 95% CI (SEE) increased from 0.12 ± 0.02 ms(-1) during accelerations of 0-0.99 ms(-2) to 0.32 ± 0.06 ms(-1) during accelerations >4 ms(-2). TE increased from 0.05 ± 0.01 to 0.12 ± 0.01 ms(-1) during accelerations of 0-0.99 ms(-2) and >4 ms(-2) respectively. The validity and reliability of 10 Hz GPS for the measurement of instantaneous velocity has been shown to be inversely related to acceleration. Those using 10 Hz GPS should be aware that during accelerations of over 4 ms(-2), accuracy is compromised.
Publisher: Wiley
Date: 26-04-2022
Abstract: Aiming to design a catalyst for stable electrooxidation of water at low pH, the present work explores the properties and structural features of electrodeposited composite oxides based on Bi and Co, which were anticipated to provide stability and catalytical activity, respectively. Materials deposited as very thin ( ca 50 nm) films on F‐doped SnO 2 (FTO) substrate do not initially exhibit high activity in 0.1 M H 2 SO 4 , but are activated during operation through the electrooxidatively‐induced enrichment of the catalytic surface with Co and Sn oxides. The latter originate from the FTO support and are identified as an important component of the catalyst through control experiments with a Sn‐free substrate and with Sn 2+ intentionally added at the electrodeposition stage. A distinctive feature of the Co−Bi−Sn‐based electrocatalyst is the slow but persistent improvement in the activity during operation in 0.1 M H 2 SO 4 at both ambient and elevated (60 °C) temperatures, which contrasts with the continuously degrading behaviour of state‐of‐the‐art oxygen evolution catalysts at low pH. This is demonstrated by 9‐day‐long galvanostatic tests at 10 mA cm −2 , during which the Co−Bi−Sn‐based thin film catalyst shows no degradation and sustains stable water oxidation at ca 1.9 V vs . reversible hydrogen electrode. The effects of tin leaching from the support detected herein might have implications to other acidic water oxidation catalysts supported on high‐surface area doped SnO 2 materials.
Publisher: Wiley
Date: 20-10-2023
Publisher: Wiley
Date: 20-11-2019
Publisher: American Chemical Society (ACS)
Date: 20-09-2019
Publisher: Royal Society of Chemistry (RSC)
Date: 2016
DOI: 10.1039/C5CY01685A
Abstract: Ordered meso–macroporous silica (MMS) was applied for the cobalt-based FTS reaction, and the enhanced activity on the Co/MMS was mainly due to the larger macropore cavity by enhancing the mass transfer rate which can be easily regenerated by in situ feeding of liquid hydrocarbons.
Publisher: Georg Thieme Verlag KG
Date: 21-11-2014
Abstract: This study examined the acceleration demands associated with changing direction and the subsequent physiological consequences of acceleration during running at 3 submaximal speeds. 10 male professional footballers completed four 600 m running bouts at 3 speeds (2.50, 3.25 & 4.00 m·s(-1)). Each bout was in the format of either: i) 3 laps of a 200 m track (CON), ii) ten 60 m shuttles (S60), iii) twenty 30 m shuttles (S30), or iv) thirty 20 m shuttles (S20). Peak heart rate (HRPEAK), blood lactate concentration (BLa) and RPE (Borg CR-10) were recorded for each bout. A single change of direction required 1.2, 1.5 and 2.0 s of acceleration at running speeds of 2.50, 3.25 and 4.00 m s(-1) respectively. An increase in time spent accelerating produced a linear increase in BLa (r=0.43-0.74) and RPE (r=0.81-0.93) at all speeds. Acceleration increases linearly with change of direction frequency during submaximal shuttle running. Increased time spent accelerating elicits proportional increases in perceived exertion, BLa and HRPEAK. The current study further underlines the need to consider acceleration when quantifying training load during activities involving numerous changes of direction.
Publisher: Wiley
Date: 15-09-2023
Publisher: Wiley
Date: 29-01-2023
Abstract: Photoelectrochemical water splitting is a promising approach to produce green hydrogen using solar energy. A primary bottleneck remains the lack of efficient photoanodes to catalyze the sluggish water photooxidation reaction. Engineering photoabsorbers with a narrow bandgap and suitable band edge can boost the photoelectrochemical performance. Herein, nanostructured iron tungstate (FeWO 4 ) photoanodes are engineered directly on a fluorine doped tin oxide glass substrate via a scalable and ultra‐fast flame synthesis route in 13 seconds. Physiochemical, optoelectronic, and electrochemical properties of these photoanodes are systematically investigated. The key roles of charge transport, transfer, and dissolution of W and Fe ions from the FeWO 4 matrix within long‐term performance are revealed. Optimal FeWO 4 photoanode with a bandgap of 1.82 eV and a FeOOH/NiOOH co‐catalyst coating shows an improved water photooxidation performance, reaching a photocurrent density of 0.23 mA cm −2 at 1.4 V versus reversible hydrogen electrode in 1 m potassium hydroxide. It further demonstrates relatively good photostability, maintaining ≈96% of photocurrent density after 1‐hour continuous photooxidation, albeit some trace of Fe, W and Ni elements dissolution. Insights on the photooxidation performance of nanostructured FeWO 4 provide promising directions for the engineering of small band‐gap catalysts for a variety of photoelectrochemical applications.
Publisher: Royal Society of Chemistry (RSC)
Date: 2019
DOI: 10.1039/C9NR08901B
Abstract: The rapid development of smart wearable electronics is driving the engineering of novel miniaturized sensing materials that can rapidly respond to very small changes in the concentration of biomarkers at room temperature. Carbon-based nanomaterials offer numerous attractive properties such as low resistivity, good mechanical robustness and integration potential, but lack a strong detection and transduction mechanism for the measurement of chemical molecules or photons. Here, we present a three-dimensional nanostructured architecture comprising optimally integrated graphene oxide (GO)-ZnO heterojunctions for the room temperature sensing of volatile biomarkers. We show that this layout also provides excellent response to UV light showcasing its applicability as a visible-blind photodetector. Notably, the optimal integration of well-dispersed GO nanodomains in a 3D ZnO network significantly enhances the room-temperature chemical sensitivity and light responsivity, while higher GO contents drastically worsen the material performance. This is attributed to the different roles of GO at low and high contents. Small amounts of GO lead to the formation of electron depleted nano-heterojunctions with excellent electron-hole separation efficiency. In contrast, large amounts of GO form a percolating electrical network that inhibits the light and chemical-sensing properties of the ZnO nanoparticles. Our optimal GO-ZnO demonstrates 33 A W
Publisher: American Chemical Society (ACS)
Date: 05-02-2020
Publisher: Wiley
Date: 10-12-2022
Abstract: Environmentally friendly routes from “Power‐to‐X” (P2X) technologies to sustainably harvest and store renewable energy with net‐zero CO 2 emission are imperative. The concept of P2X relies on (photo)electrolysis of earth‐abundant molecules into value‐added products. For practical utilization, engineering robust, active, albeit inexpensive (photo)electrocatalysts via industrially compatible technologies is indeed crucial. In this context, flame spray pyrolysis (FSP) stands as an emerging approach for one‐step synthesis of ready‐to‐use (photo)electrocatalysts with production rates of Kg h ‐1 in lab‐scales. While features of FSP to engineer nanomaterials have been summarised, there is a need for more critical discussions on key factors, modulating properties of flame‐made catalysts. Therefore, this review article will first provide an overview about the concept of the P2X and catalyst development strategies. Unique characteristic of flame‐synthesized nano‐catalysts including compositions, fractal morphologies, defects, and active sites will be then critically discussed. Furthermore, a potential of FSP as an electrode‐assembly technique for one‐step preparation of catalysts on gas diffusion layers for industry‐relevant electrolyser testing will be presented. Finally, perspectives on challenges and opportunities of FSP for renewable energies will be raised. This will provide insights into the versatility and commercial viability of the FSP route for engineering novel nanostructured catalysts for renewable energy applications.
Publisher: American Chemical Society (ACS)
Date: 05-02-2015
DOI: 10.1021/AM506797D
Abstract: Polyethylene (PE) separators have been the most popular option for commercial Li-ion batteries because of their uniform pore size, high tensile strength, low cost, and electrochemical stability. Unfortunately, PE separators generally suffer from significant dimensional changes at high temperatures, which frequently results in serious safety problems. In this regard, the integration of inorganic nanoparticles with PE separators has been considered to be a promising approach. Here, inorganic nanoparticles with a hierarchical pore structure were coated on a conventional polymer separator. The resultant composite separator exhibited superior Li ion transportation compared with separators coated with mesopore-only nanoparticles or conventional nonporous nanoparticles. The mesopores and macropores act synergistically to improve the electrolyte uptake and ionic conductivity of the inorganic nanoparticles, while other positive aspects such as their thermal and mechanical properties are still maintained.
Location: United States of America
Location: United Kingdom of Great Britain and Northern Ireland
No related grants have been discovered for Thanh Tran-Phu.