198 results found
Park JY, Kwak DH, Ma KB, et al., 2018, Enhanced oxygen reduction reaction of Pt deposited Fe/N-doped bimodal porous carbon nanostructure catalysts, Journal of Catalysis, Vol: 359, Pages: 46-54, ISSN: 0021-9517
© 2018 Elsevier Inc. For commercialization of proton exchange membrane fuel cells (PEMFCs), the loading amount of Pt-based cathode catalysts for oxygen reduction reaction (ORR) needs be significantly reduced. In this study, we propose Pt catalysts supported by an iron/nitrogen-doped porous carbon (FeNC) nanostructure having a catalytic activity for ORR in order to significantly reduce the utilization of Pt. The FeNC nanostructure was prepared using a template method with 50 and 500 nm SiO 2 beads and phthalocyanine as a dopant and carbon source. The nanosized Pt catalysts with different loading weights (5, 10, 20, 30 wt%) were uniformly deposited on the FeNC with a bimodal porous crystalline doped carbon nanostructure using an electron beam radiation method. In particular, the cathode catalyst having 5 wt% Pt on FeNC (Pt5/FeNC) exhibited enhanced ORR mass activities of 2.19 and 2.58 A mg Pt −1 at 0.9 V measured by electrochemical half cells in acidic and alkaline media, respectively, compared to a commercial Pt(20 wt%)/C (Pt20/C). Furthermore, Pt5/FeNC showed a higher mass activity of 18.76 A mg Pt −1 at 0.6 V as a unit cell performance than that of the commercial catalyst. The improved ORR activity of Pt/FeNC might be synergistically attributed to the homogeneous dispersion of Pt nanoparticles on the bimodal porous doped carbon nanostructure, the interaction (electronic effect) between the metallic catalyst and the doped support, and the dual catalytic effect of both Pt and the doped carbon nanostructure.
zalitis C, Kucernak ARJ, sharman J, et al., 2017, Design principles for platinum nanoparticles catalysing electrochemical hydrogen evolution and oxidation reactions: edges are much more active than facets, Journal of Materials Chemistry A, Vol: 5, Pages: 23328-23338, ISSN: 2050-7496
Improving the performance of hydrogen evolution and oxidation reactions using precious metal catalysts is key in reducing the cost of electrolysers and fuel cells. By considering the performance of these reactions as a function of platinum particle size (2.1–15 nm) under high mass transport conditions in acids, we find that the activity is composed of two components which vary in a defined way with the particle size. Geometrical considerations and electrokinetic modelling suggest that these two components correspond to the response of edges/vertices and the response of facets (Pt(100) and Pt(111)). Edges and vertices are much more active towards the hydrogen reaction. This assignment also rationalises the poor performance of platinum in alkaline environments. We predict that “ideal” particles made up of only edges/vertices would allow fuel cells and electrolysers to operate with only 1 μgPt cm−2 – about two to three orders of magnitude lower than what is currently used.
Beruski O, Lopes T, Kucernak ARJ, et al., 2017, Investigation of convective transport in the so-called “gas diﬀusion layer” used in polymer electrolyte fuel cell, Physical Review Fluids, Vol: 2, ISSN: 2469-990X
Recent experimental data on a fuel-cell-like system revealed insights into the fluid flow in both free and porous media. A computational model is used to investigate the momentum and species transport in such a system, solved using the finite element method. The model consists of a stationary, isothermal, diluted species transport in free and porous media flow. The momentum transport is treated using different formulations, namely, Stokes-Darcy, Darcy-Brinkman, and hybrid Stokes-Brinkman formulations. The species transport is given by the advection equation for a reactant diluted in air. The formulations are compared to each other and to the available experimental data, where it is concluded that the Darcy-Brinkman formulation reproduces the data appropriately. The validated model is used to investigate the contribution of convection in reactant transport in porous media of fuel cells. Convective transport provides a major contribution to reactant distribution in the so-called diffusion media. For a serpentine channel and flow with Re=260–590, convection accounts for 29–58% of total reactant transport to the catalyst layer.
Recently, there has been a drive to design and develop fully tunable metamaterials for applications ranging from new classes of sensors to superlenses among others. Although advances have been made, tuning and modulating the optical properties in real time remains a challenge. We report on the first realization of a reversible electrotunable liquid mirror based on voltage-controlled self-assembly/disassembly of 16 nm plasmonic nanoparticles at the interface between two immiscible electrolyte solutions. We show that optical properties such as reflectivity and spectral position of the absorption band can be varied in situ within ±0.5 V. This observed effect is in excellent agreement with theoretical calculations corresponding to the change in average interparticle spacing. This electrochemical fully tunable nanoplasmonic platform can be switched from a highly reflective ‘mirror’ to a transmissive ‘window’ and back again. This study opens a route towards realization of such platforms in future micro/nanoscale electrochemical cells, enabling the creation of tunable plasmonic metamaterials.
Malko D, Kucernak ARJ, 2017, Kinetic isotope effect in the oxygen reduction reaction (ORR) over Fe-N/C catalysts under acidic and alkaline conditions., Electrochemistry Communications, Vol: 83, Pages: 67-71, ISSN: 1388-2481
Heat treated Fe-N/C materials which are highly effective oxygen reduction catalysts in alkaline and acid, show a significant kinetic isotope effect (KIE). The values in acid (~3.4) and alkaline (~2.5) are much larger than the value for the metal free catalyst in acid (~1.8) suggesting that the rate determining step (RDS) is a proton coupled electron transfer in acid with a significant pathway involving a proton independent step under an alkaline environment
Bazant M, Bennewitz R, Bocquet L, et al., 2017, Electrotunable wetting, and micro- and nanofluidics: general discussion, Publisher: ROYAL SOC CHEMISTRY
Symianakis E, Kucernak A, 2017, Embedded atom method interatomic potentials fitted upon density functional theory calculations for the simulation of binary Pt-Ni nanoparticles, Computational Materials Science, Vol: 133, Pages: 185-193, ISSN: 0927-0256
Embedded Atom Method (EAM) potentials have been fitted for the atomistic simulation of small, 2–5 nm, binary, PtANi, nanoparticles completely from Density Functional Theory (DFT) total energy calculations.The overall quality of the DFT calculations and the final potential is obtained through the independentcalculation of an array of properties of the pure metals and the stable alloys, which arenormally used for the fitting of interatomic potentials. The ability of the fitted potentials to simulatenanostructures is evaluated by the reproduction of binary nanoslabs with thickness 1 nm, and nanoparticlesin the extreme case of the smallest icosahedrons possible, with diameter 0.6 nm. The usedapproach requires high quality of convergence but otherwise low cost DFT as it is based on static totalenergy calculations. It also provides objective criteria for the evaluation of the fitted potentials during fittingand has been implemented with the open source code GULP
Cousens N, Kucernak ARJ, 2017, Reversible ultralow-voltage liquid-liquid electrowetting without a dielectric layer, Faraday Discussions, Vol: 199, Pages: 63-73, ISSN: 1364-5498
Electrowetting-on-dielectric devices typically have operating voltages of 10-20 V. A reduction in the operating voltage could greatly reduce the energy consumption of these devices. Here, the fully reversible one electrolyte electrowetting of a droplet on a solid metal surface is reported for the first time. A reversible change of 29o for an 800 mV step is achieved. The effect of surface roughness, electrolyte composition, electrolyte concentration and droplet composition is investigated. It is found that there is a dramatic dependence of the reversibility and hysteresis of the system on these parameters, contrary to theoretical predictions. When a 3-chloro-1-propanol droplet is used, a system with no hysteresis and a 40o change in angle is achieved.
Velleman L, Sikdar D, Turek V, et al., 2016, Tuneable 2D self-assembly of plasmonic nanoparticles at liquid | liquid interfaces, Nanoscale, Vol: 8, Pages: 19229-19241, ISSN: 2040-3372
Understanding the structure and assembly of nanoparticles at liquid | liquid interfaces is paramount to their integration into devices for sensing, catalysis, electronics and optics. However, many difficulties arise when attempting to resolve the structure of such interfacial assemblies. In this article we use a combination of X-ray diffraction and optical reflectance to determine the structural arrangement and plasmon coupling between 12.8 nm diameter gold nanoparticles assembled at a water | 1,2-dichloroethane interface. The liquid | liquid interface provides a molecularly flat and defect-correcting platform for nanoparticles to self-assemble. The amount of nanoparticles assembling at the interface can be controlled via the concentration of electrolyte within either the aqueous or organic phase. At higher electrolyte concentration more nanoparticles can settle at the liquid | liquid interface resulting in a decrease in nanoparticle spacing as observed from X-ray diffraction experiments. The coupling of plasmons between the nanoparticles as they come closer together is observed by a red-shift in the optical reflectance spectra. The optical reflectance and the X-ray diffraction data are combined to introduce a new ‘plasmon ruler’. This allows extraction of structural information from simple optical spectroscopy techniques, with important implications in understanding the structure of nanoparticle films at liquid interfaces and their self-assembly.
Kucernak ARJ, kakati, Fahy KF, 2016, Using corrosion-like processes to remove poisons from electrocatalysts: a viable strategy to chemically regenerate irreversibly poisoned polymer electrolyte fuel cells, Electrochimica Acta, Vol: 222, Pages: 888-897, ISSN: 1873-3859
Poisoning of Pt/C catalysts due to SO2 on a rotating disk electrode (RDE), and as part of the cathode layer in a single cell fuel cell and fuel cell stack are studied in terms of the system performance, and the effect of electrochemical and chemical post treatment to remove the adsorbed sulphur containing species. It is found that external polarisation can only recover the ORR performance of catalyst on an RDE after SO2 poisoning when an applied potential of 1.6 V(RHE) is used for 1 ks. An alternative approach is to use ozone, as in the presence of this species, the electrode potential is raised to ~1.6V(RHE) due to the high potential of the ozone reduction reaction. The high open circuit potential leads to a mixed potential and was found also to be highly efficient at removing the poison via coupled ozone reduction and poison oxidation. The ozone process is found to work efficiently at the catalyst level as shown through rotating disk electrode studies and also in single cell fuel cells. Furthermore we demonstrate for the first time the recovery of a SO2 poisoned fuel cell stack using the mixed-potential approach and ozone as a reactant. The cleaning process is fast (~10 minutes), occurs at room temperature, and does not require any special modification to the fuel cell. The process may be applicable to a wide range of poisons which can be oxidatively removed from platinum at high potentials.
Kucernak A, Malko D, Lopes T, 2016, Performance of Fe-N/C oxygen reduction electrocatalysts towards NO−₂, NO, and NH₂OH electroreduction from fundamental insights into the active center to a new method for environmental nitrite destruction, Journal of the American Chemical Society, Vol: 138, Pages: 16056-16068, ISSN: 1520-5126
Although major progress has recently been achieved through ex situ methods, there is still a lack of understanding of the behavior of the active center in non-precious metal Fe–N/C catalysts under operating conditions. Utilizing nitrite, nitric oxide, and hydroxylamine as molecular probes, we show that the active site for the oxygen reduction reaction (ORR) is different under acidic and alkaline conditions. An in-depth investigation of the ORR in acid reveals a behavior which is similar to that of iron macrocyclic complexes and suggests a contribution of the metal center in the catalytic cycle. We also show that this catalyst is highly active toward nitrite and nitric oxide electroreduction under various pH values with ammonia as a significant byproduct. This study offers fundamental insight into the chemical behavior of the active site and demonstrates a possible use of these materials for nitrite and nitric oxide sensing applications or environmental nitrite destruction.
Chakrabarti BK, Nir DP, Yufit V, et al., 2016, Studies of performance enhancement of rGO-modified carbon electrodes for Vanadium Redox Flow Systems, ChemElectroChem, Vol: 4, Pages: 194-200, ISSN: 2196-0216
Reduced graphene oxide (rGO) suspended in an N,N′-dimethylformamide (DMF) solvent underwent electrophoretic deposition (EPD) on carbon paper (CP) electrodes. X-ray computed micro-tomography (XMT) indicates a 24 % increase in the specific surface area of CP modified with rGO in comparison to the untreated sample. Furthermore, XMT confirms that the deposition also penetrates into the substrate. Raman analysis shows that the rGO deposited is more amorphous than the CP electrode. A significant reduction in charge-transfer resistance of the VO2+/VO2+ reaction is also observed (from impedance measurements) in modified samples in comparison to untreated CP electrodes.
Malko D, Kucernak A, Lopes T, 2016, In-situ electrochemical quantification of active sites in Fe-N/C non-precious metal catalysts, Nature Communications, Vol: 7, ISSN: 2041-1723
The economic viability of low temperature fuel cells as clean energy devices is enhanced by the development of inexpensive oxygen reduction reaction catalysts. Heat treated iron and nitrogen containing carbon based materials (Fe–N/C) have shown potential to replace expensive precious metals. Although significant improvements have recently been made, their activity and durability is still unsatisfactory. The further development and a rational design of these materials has stalled due to the lack of an in situ methodology to easily probe and quantify the active site. Here we demonstrate a protocol that allows the quantification of active centres, which operate under acidic conditions, by means of nitrite adsorption followed by reductive stripping, and show direct correlation to the catalytic activity. The method is demonstrated for two differently prepared materials. This approach may allow researchers to easily assess the active site density and turnover frequency of Fe–N/C catalysts.
Lopes T, Kucernak A, Malko D, et al., 2016, Mechanistic Insights into the Oxygen Reduction Reactionon Metal–N–C Electrocatalysts under Fuel Cell Conditions, ChemElectroChem, Vol: 3, Pages: 1580-1590, ISSN: 2196-0216
Three different transition metal-C-N catalysts are tested under a range of fuel cell conditions. It is found that common features of the polarisation curve can be explained by a change in electrocatalytic mechanism. Utilising a simple model to quantify the change in mechanisms, iR free results of the fuel cell experiments are fit and found to be represented by a common set of parameters. The change in mechanism is assumed to be a switch from four electron reduction of oxygen to water to a two electron reduction to hydrogen peroxide followed by disproportionation of the hydrogen peroxide to water and oxygen. The data is used to estimate a mass specific exchange current density towards the ORR in the range 10-11-10-13 A g-1 depending on the catalyst. For the reduction of oxygen to hydrogen peroxide, the mass specific exchange current density is estimated to be in the range 10-2-10-3 A g-1. Utilising the electrokinetic model, it is shown how the mass transport losses can be extracted from the polarisation curve. For all three catalyst layers studied, these mass transport losses reach about 100mV at a current density of 1 A cm-2. Finally a discussion of the performance and site density requirements of the non-precious metal catalysts are provided, and it is estimated that the activity towards the ORR needs to be increased by an order of magnitude, and the site density by two/three orders of magnitude in order to compete with platinum as an ORR electrocatalyst.
Malko D, lopes T, Ticianelli E, et al., 2016, A catalyst layer optimisation approach using electrochemical impedance spectroscopy for PEM fuel cells operated with pyrolysed transition metal-N-C catalysts, Journal of Power Sources, Vol: 323, Pages: 189-200, ISSN: 0378-7753
The effect of the ionomer to carbon (I/C) ratio on the performance of single cell polymer electrolyte fuel cells is investigated for three different types of non-precious metal cathodic catalysts. Polarisation curves as well as impedance spectra are recorded at different potentials in the presence of argon or oxygen at the cathode and hydrogen at the anode. It is found that a optimised ionomer content is a key factor for improving the performance of the catalyst. Non-optimal ionomer loading can be assessed by two different factors from the impedance spectra. Hence this observation could be used as a diagnostic element to determine the ideal ionomer content and distribution in newly developed catalyst-electrodes. An electrode morphology based on the presence of inhomogeneous resistance distribution within the porous structure is suggested to explain the observed phenomena. The back-pressure and relative humidity effect on this feature is also investigated and supports the above hypothesis. We give a simple flowchart to aid optimisation of electrodes with the minimum number of trials.
Kucernak ARJ, Zalitis CM, 2016, General Models for the Electrochemical Hydrogen Oxidation and Hydrogen Evolution Reactions – Theoretical Derivation and Experimental Results Under Near Mass-Transport Free Conditions, Journal of Physical Chemistry C, Vol: 120, Pages: 10721-10745, ISSN: 1932-7455
Full derivations of Heyrovsky-Volmer (HV), Tafel-Volmer(TV), Heyrovsky-Tafel(HT), and Heyrovsky-Tafel-Volmer(HTV) mechanisms under steady state conditions are provided utilising a new theoretical framework which allows better understanding of the each of the mechanistic currents and part currents. Simple and easily implemented equations are presented, which provide both the hydrogen coverage and electrochemical current as a function of overpotential and relevant kinetic parameters. It is shown how these responses are governed by a set of dimensionless parameters associated with the ratio of electrokinetic parameters. For each of the different mechanisms, an “atlas” of Hads coverage with overpotential and corresponding current density is provided, allowing an understanding of all possible responses depending on the dimensionless parameters. Analysis of these mechanisms provides the limiting reaction orders of the exchange current density for protons and bimolecular hydrogen for each of the different mechanisms, as well as the possible Tafel slopes as a function of the molecular symmetry factor, . Only the HV mechanism is influenced by pH whereas the TV,HT, and HTV mechanisms are not. The cases where the equations simplify to limiting forms are discussed. Analysis of the exchange current density from experimental data is discussed, and it is shown that fitting the linear region around the equilibrium potential underestimates the true exchange current density for all of the mechanisms studied. Furthermore, estimates of exchange current density via back-extrapolation from large overpotentials is also shown to be highly inaccurate. Analysis of Tafel slopes is discussed along with the mechanistic information which can and cannot be determined. The new models are used to simultaneously fit sixteen experimental responses of Pt/C electrodes in acid towards the her/hor as a function of , pH, p(H2), and temperature, using a consistent set of electrokinetic parame
Beruski O, Lopes T, Kucernak A, et al., 2016, Comparison between Darcy's law and Darcy-Brinkman formulation for reactant transport in PEFC porous media, Publisher: AMER CHEMICAL SOC, ISSN: 0065-7727
Kucernak ARJ, kakati, Unnikrishnan A, et al., 2016, Recovery of Polymer Electrolyte Fuel Cell exposed to sulfur dioxide, International Journal of Hydrogen Energy, Vol: 41, Pages: 5598-5604, ISSN: 1879-3487
Sulfur dioxide (SO2) is a common atmospheric contaminant which has a deleterious effect on fuel cells. The performance of a Polymer Electrolyte Fuel Cell (PEFC) utilising a Pt on nitrogen doped graphene support as the cathode catalyst was studied in the presence of air contaminated with known levels of SO2. The nitrogen doped graphene supported platinum was synthesized by a hydrothermal method. At levels of 25ppm SO2 in air there was within 15 minutes a 28 % reduction in the PEFC performance at 0.5 V. The performance degradation was more severe at higher SO2 concentrations. At 100 ppm SO2 in air the performance degraded by 91% at the same potential. The power loss of the fuel cell could not be recovered by externally polarising the PEFC at 1.6 V. Even after continuous potential cycling of the cell for 9 h only 80% of the initial performance could be recovered. However, a 15 minute treatment with 0.4% O3 in air showed almost a 100% performance recovery of the 100ppm SO2 contaminated fuel cell. The enhanced recovery of the fuel cell is related both to the chemical reaction of O3 with the adsorbed sulphur contaminant, and an increase of cathode potential during the electrochemical treatment.
Edel JB, Kornyshev AA, Kucernak AR, et al., 2016, Fundamentals and applications of self-assembled plasmonic nanoparticles at interfaces, Chemical Society Reviews, Vol: 45, Pages: 1581-1596, ISSN: 1460-4744
This tutorial review will introduce and explore fundamental and applied aspects of using electrolytic interfaces incorporating nanoscale building blocks for use in novel applications such as sensors, and tunable optics. In order to do this, it is important to be able to understand the principles behind even the simplest of immiscible interfaces such as that of the Liquid | Liquid and Solid | Liquid Qualitatively, the picture is simple however the complexity is easily compounded by the addition of electrolyte, and further compounded by addition of more complex entities such as nanoparticles. Nevertheless combining all these components surprisingly results in an elegant solution, where the nanoparticles have the ability to self assemble at the interface with a high level of control. Importantly, this opens up the door to development of new types of materials with a range of applications which have only recently been exploited. As such initially we begin with a description of the fundamentals related to liquid | Liquid and Solid | Liquid interfaces both with and without electrolyte. The discussions then shifts to a description of biasing the interface by application of an electric field. This is followed by an exploration of nanoparticle assembly and disassembly at the interface by controlling parameters such as ligand composition, charge, pH, and electric field. Finally a description of the state-of-the-art is given in terms of current applications and possible future directions. It is perhaps fair to say that these new frontiers have caused great excitement within the sensing community not only due to the simplicity of the technique but also due to the unprecedented levels of sensitivity
Malko D, Lopes T, Symianakis E, et al., 2016, The intriguing poison tolerance of non-precious metal oxygen reduction reaction (ORR) catalysts, Journal of Materials Chemistry A, Vol: 4, Pages: 142-152, ISSN: 2050-7496
Electrochemical devices such as fuel cells are key to a sustainable energy future. However the applicability of such underrealistic conditions is not viable to date. Expensive precious metals are used as electrocatalysts and contaminants presentin the operating media poison the utilized catalysts. Here the one pot synthesis of a highly active, self-supporting andsurprisingly poison tolerant catalyst is reported. The polymerisation of 1,5-Diaminonaphthalene provides self-assemblednanospheres, which upon pyrolysis form a catalytically active high surface area material. Tolerance to a wide range ofsubstances that poison precious metal based catalysts combined with high electrocatalytic activity might enable numerousadditional technological applications. In addition to fuel cells these could be metal-air batteries, oxygen-depolarized chloralkalicathodes, oxygen sensors, medical implantable devices, waste water treatment and as counter electrodes for manyother sensors where the operating medium is a complex and challenging mixture.
Kucernak ARJ, Fahy KF, Naranammalpuram Sundaram VN, 2015, Facile synthesis of palladium phosphide electrocatalysts and their activity for the hydrogen oxidation, hydrogen evolutions, oxygen reduction and formic acid oxidation reactions, Catalysis Today, Vol: 262, Pages: 48-56, ISSN: 1873-4308
We demonstrate a new approach for producing highly dispersed supported metal phosphide powders with small particle size, improved stability and increased electrocatalytic activity towards some useful reactions. The approach involves a one-step conversion of metal supported on high surface area carbon to the metal phosphide utilising a very simple and scalable synthetic process. We use this approach to produce PdP₂ and Pd₅P₂ particles dispersed on carbon with a particle size of 4.5–5.5 nm by converting a commercially available Pd/C powder. The metal phosphide catalysts were tested for the oxygen reduction, hydrogen oxidation and evolution, and formic acid oxidation reactions. Compared to the unconverted Pd/C material, we find that alloying the P at different levels shifts oxide formation on the Pd to higher potentials, leading to greater stability during cycling studies (20% more ECSA retained, 5k cycles) and in thermal treatment under air. Hydrogen absorption within the PdP₂ and Pd₅P₂ particles is enhanced. The phosphides compare favourably to the most active catalysts reported to date for formic acid oxidation, especially PdP₂, and there is a significant decrease in poisoning of the surface compared to Pd alone. The mechanistic changes in the reactions studied are rationalised in terms of increased water activation on the surface phosphorus atoms of the catalyst. One of the catalysts, PdP₂/C is tested in a fuel cell as anode and cathode catalyst and shows good performance.
Markiewicz M, Zalitis C, Kucernak A, 2015, Performance measurements and modelling of the ORR on fuel cell electrocatalysts - the modified double trap model, Electrochimica Acta, Vol: 179, Pages: 126-136, ISSN: 1873-3859
Experimental results for the ORR (oxygen reduction reaction) in perchloric acid for ultra low loading Pt/Celectrodes have been fitted to a number of different ORR mechanisms. These were accomplished as afunction of temperature (280–330 K), oxygen partial pressure(0:01 < po2p0o2< 1) and potential (0.3–1.0V vs.RHE). A reaction exponent for oxygen of 1 0.1 across the potential range 0.3–0.85V vs. RHE is confirmed.From the experimental results it is clear that the surface becomes increasingly blocked towards the ORRas overpotential increases (i.e. as the potential decreases from 0.6 to 0.3 V vs. RHE). The double trap model[J.X. Wang, J. Zhang, R.R. Adzic, J. Phys. Chem. A, 111 (2007) 12,702] fails to account for this observation,although we have produced a modified version to include the formation of OOHad intermediates. Theseintermediates block the electrode at larger overpotentials and lead to a decrease in electrocatalystperformance compared to a Tafel type approximation. Furthermore these intermediates can lead to theformation of hydrogen peroxide at large overpotentials, an experimental observation which is currentlypoorly described by models.The decreased activity at large overpotentials suggests that blocking of active catalyst sites may be asimportant to catalyst activity in an operating fuel cell as the absolute performance of the electrode in thelow overpotential region as typically measured on an RDE. It may also offer an explanation to theincreased losses seen in fuel cell electrodes at lower catalyst loadings – i.e. the loses, which are typicallyascribed to increased mass transport loses, may instead result from decreased electrocatalyticperformance at high overpotentials.
Ahmad EA, Tileli V, Kramer D, et al., 2015, Optimizing Oxygen Reduction Catalyst Morphologies from First Principles, Journal of Physical Chemistry C, Vol: 119, Pages: 16804-16810, ISSN: 1932-7455
Catalytic activity of perovskites for oxygen reduction (ORR) wasrecently correlated with bulk d-electron occupancy of the transition metal. Weexpand on the resultant model, which successfully reproduces the high activity ofLaMnO3 relative to other perovskites, by addressing catalyst surface morphology asan important aspect of the optimal ORR catalyst. The nature of reaction sites onlow index surfaces of orthorhombic (Pnma) LaMnO3 is established from FirstPrinciples. The adsorption of O2 is markedly influenced by local geometry andstrong electron correlation. Only one of the six reactions sites that result from experimentally confirmed symmetry-breakingJahn−Teller distortions is found to bind O2 with an intermediate binding energy while facilitating the formation of superoxide, animportant ORR intermediate in alkaline media. As demonstrated here for LaMnO3, rational design of the catalyst morphology topromote specific active sites is a highly effective optimization strategy for advanced functional ORR catalysts.
Kucernak ARJ, zalitis C, Sharman J, et al., 2015, Properties of the hydrogen oxidation reaction on Pt/C catalysts at optimised high mass transport conditions and its relevance to the anode reaction in PEFCs and cathode reactions in electrolysers, Electrochimica Acta, Vol: 176, Pages: 763-776, ISSN: 1873-3859
Using a high mass transport floating electrode technique with an ultra-low catalyst loading (0.84-3.5 gPt cm-2) of commonly used Pt/C catalyst (HiSPEC 9100, Johnson Matthey), features in the hydrogen oxidation reaction (HOR) and hydrogen evolution reaction (HER) were resolved and defined, which have rarely been previously observed. These features include fine structure in the hydrogen adsorption region between 0.18 < V vs. RHE < 0.36 V vs. RHE consisting of two peaks, an asymptotic decrease at potentials greater than 0.36 V vs. RHE, and a hysteresis above 0.1 V vs. RHE which corresponded to a decrease in the cathodic scan current by up to 50 % of the anodic scan. These features are examined as a function of hydrogen and proton concentration, anion type and concentration, potential scan limit, and temperature. We provide an analytical solution to the Heyrovsky-Volmer equation and use it to analyse our results. Using this model we are able to extract catalytic properties (without mass transport corrections; a possible source of error) by simultaneously fitting the model to HOR curves in a variety of conditions including temperature, hydrogen partial pressure and anion/H+ concentration. Using our model we are able to rationalise the pH and hydrogen concentration dependence of the hydrogen reaction. This model may be useful in application to fuel cell and electrolyser simulation studies.
edel, turek, cecchini, et al., 2015, METHOD OF DETECTING AN ANALYTE IN A SAMPLE USING RAMAN SPECTROSCOPY, INFRA RED SPECTROSCOPY AND/OR FLUORESCENCE SPECTROSCOPY
The invention relates to a method of detecting the presence of an analyte associated with a nanoparticle layer formed at a liquid-liquid interface. The method comprises removing a portion of one of the liquid phases; and detecting the presence of the analyte by Raman spectroscopy, Infra Red spectroscopy and/or fluorescence spectroscopy. The invention further relates to a kit for use in the method, comprising a sample vessel for receiving in use, a first and second liquid phase; wherein said phases are immiscible and wherein one or both of the first or the second liquid phase comprise nanoparticles, and instructions to allow analysis of an analyte in a sample according to the claimed method
Kucernak ARJ, edel, turek, et al., 2015, Document METHOD OF DETECTING AN ANALYTE IN A SAMPLE USING RAMAN SPECTROSCOPY, INFRA RED SPECTROSCOPY AND/OR FLUORESCENCE SPECTROSCOPY | [VERFAHREN ZUM NACHWEIS EINES ANALYTEN IN EINER PROBE MITTELS RAMAN-SPEKTROSKOPIE, INFRAROTSPEKTROSKOPIE UND/ODER FLUORESZENZSPEKTROSKOPIE], EP2880425
Kucernak ARJ, 2015, Electrochemical Characterization and Quantified Surface Termination Obtained by LEIS and XPS of Orthorhombic and Rhombohedral LaMnO<sub>3</sub> Powders, Journal of Physical Chemistry C, Vol: 119, Pages: 12209-12217, ISSN: 1932-7455
LaMnO3 powder synthesized by glycine combustion synthesis with the rhombohedral and orthorhombic structures has been characterized by the combination of low energy ion scattering (LEIS) and X-ray photoelectron spectroscopy (XPS), while the electrocatalytic activity for the oxygen reduction reaction is measured with the rotating disk electrode (RDE) method. Quantification of the surface terminations obtained by LEIS suggests that the orthorhombic LaMnO3 crystallites are near thermodynamic equilibrium as surface atomic ratios compare well with those of equilibrium morphologies computed by a Wulff construction based on computed surface energies. Both rhombohedral and orthorhombic structures present the same La/Mn atomic ratio on the surface. Electrochemical activity of the two structures is found to be the same within the error bar of our measurements. This result is in disagreement with results previously reported on the activity of the two structures obtained by the coprecipitation method [Suntivich et al. Nat. Chem. 2011, 3 (7), 546], and it indicates that the preparation method and the resulting surface termination might play a crucial role for the activity of perovskite catalysts.
Kucernak ARJ, malko, lopes, 2015, OXYGEN REDUCTION CATALYSTS | [CATALYSEURS DE RÉDUCTION D'OXYGÈNE], WO2015049318
The present invention relates to a method for preparing a catalyst which can be used to catalyse the oxygen reduction reaction (ORR). The invention also provides a catalyst obtained from the method and its use as an electrode, for example, in a galvanic cell, an electrolytic cell or an oxygen sensor.
Stockford C, Brandon N, Irvine J, et al., 2015, H2FC SUPERGEN: An overview of the Hydrogen and Fuel Cell research across the UK, International Journal of Hydrogen Energy, Vol: 40, Pages: 5534-5543, ISSN: 1879-3487
The United Kingdom has a vast scientific base across the entire Hydrogen and Fuel Cell research landscape, with a world class academic community coupled with significant industrial activity from both UK-based Hydrogen and Fuel Cell companies and global companies with a strong presence within the country. The Hydrogen and Fuel Cell (H2FC) SUPERGEN Hub, funded by the Engineering and Physical Sciences Research Council (EPSRC), was established in 2012 as a five-year programme to bring the UK's H2FC research community together. Here we present the UK's current Hydrogen and Fuel Cell activities along with the role of the H2FC SUPERGEN Hub.
Kucernak ARJ, 2015, Fuel Cell
A fuel cell assembly is disclosed comprising a fuel cell electrode component and a reactant gas flow component ink bonded thereto. In one aspect direct bonding of a gas diffusion layer with a flow field is achieved allowing a simplified structural configuration. In another aspect improved component printing techniques reduce corrosion effects. In a further aspect flow fields are described providing reactant channels extending in both the horizontal and vertical directions, i.e. providing three dimensional flow. In a further aspect an improved wicking material allows wicking away and reactant humidification. In a further aspect improved mechanical fastenings and connectors are provided. In a further aspect improved humidification approaches are described. Further improved aspects are additionally disclosed.
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