Publications

This contribution places emphasis on tuning pore architecture and film thickness of mesoporous Pd–Cu–Si thin films sputtered on Si/SiO2 substrates for enhanced electrocatalytic and hydrogen sorption/desorption activity and their comparison with the state-of-the-art thin film electrocatalysts. Small Tafel slope of 43 mV dec–1 for 1250 nm thick coatings with 2 µm diameter pores with 4.2 µm interspacing (H2) electrocatalyst with comparable hydrogen overpotentials to the literature suggests its use for standard fuel cells. The largest hydrogen sorption has been attained for the 250 nm thick electrocatalyst on 5 µm pore diameter and 12 µm interspacing (2189 µC cm–2 per CV cycle) making it possible for rapid storage systems. Moreover the charge transfer resistance described by an equivalent circuit model has an excellent correlation with Tafel slopes. Along with its very low Tafel slope of 42 mV dec–1 10 nm thick H2 pore design electrocatalyst has the highest capacitive response of ∼0.001 S sn cm–2 and is promising to be used as a nano-charger and hydrogen sensor.

A detailed thermodynamic analysis of the sorption enhanced chemical looping reforming of methane (SE-CL-SMR) using CaO and NiO as CO2 sorbent and oxygen transfer material (OTM) respectively was conducted. Conventional reforming (SMR) and sorption enhanced reforming (SE-SMR) were also investigated for comparison reasons. The results of the thermodynamic analysis show that there are significant advantages of both sorption enhanced processes compared to conventional reforming. The presence of CaO leads to higher methane conversion and hydrogen purity at low temperatures. Addition of the OTM in the SECL-SMR process concept minimizes the thermal requirements and results in superior performance compared to SE-SMR and SMR in a two-reactor concept with use of pure oxygen as oxidant/sweep gas.

A comprehensive investigation on diesel pilot spray ignited methane-hydrogen (CH₄–H₂) combustion tri-fuel combustion (TF) is performed in a single-cylinder compression ignition (CI) engine. The experiments provide a detailed analysis of the effect of H₂ concentration (based on mole fraction M_H2) and charge-air temperature (Tair) on the ignition behavior combustion stability cycle-to-cycle (CCV) and engine performance. The results indicate that adding H₂ from 0 to 60% shortens the ignition delay time (IDT) and combustion duration (based on CA90) up to 33% and 45% respectively. Thereby H₂ helps to increase the indicated thermal efficiency (ITE) by as much as 10%. Furthermore to gain an insight into the combustion stability and CCV the short-time Fourier transform (STFT) and continuous wavelet transform (CWT) methodologies are applied to estimate the combustion stability and CCV of the TF combustion process. The results reveal that the pressure oscillation can be reduced up to 4 dB/Hz and the CCV by 50% when M_H2 < 60% and Tair < 55 °C. However when M_H2 > 60% and Tair > 40 °C abnormal combustion and knocking are observed.

Managing the concentration of atmospheric CO₂ requires a multifaceted engineering strategy which remains a highly challenging task. Reducing atmospheric CO₂ (CO2R) by converting it to value-added chemicals in a carbon neutral footprint manner must be the ultimate goal. The latest progress in CO2R through either abiotic (artificial catalysts) or biotic (natural enzymes) processes is reviewed herein. Abiotic CO2R can be conducted in the aqueous phase that usually leads to the formation of a mixture of CO formic acid and hydrogen. By contrast a wide spectrum of hydrocarbon species is often observed by abiotic CO2R in the gaseous phase. On the other hand biotic CO2R is often conducted in the aqueous phase and a wide spectrum of value-added chemicals are obtained. Key to the success of the abiotic process is understanding the surface chemistry of catalysts which significantly governs the reactivity and selectivity of CO2R. However in biotic CO2R operation conditions and reactor design are crucial to reaching a neutral carbon footprint. Future research needs to look toward neutral or even negative carbon footprint CO2R processes. Having a deep insight into the scientific and technological aspect of both abiotic and biotic CO2R would advance in designing efficient catalysts and microalgae farming systems. Integrating the abiotic and biotic CO2R such as microbial fuel cells further diversifies the spectrum of CO2R.

The report “Hydrogen for Net Zero” presents an ambitious yet realistic deployment scenario until 2030 and 2050 to achieve Net Zero emissions considering the uses of hydrogen in industry power mobility and buildings. The scenario is described in terms of hydrogen demand supply infrastructure abatement potential and investments required and then compared with current momentum and investments in the industry to identify the investment gaps across value chains and geographies.

The report is based on the technoeconomic data of cost and performance of hydrogen technologies provided by Hydrogen Council members and McKinsey & Company as well as the Hydrogen Council investment tracker which covers all large-scale investments into hydrogen globally.

Link to their website

Deployment and investments in hydrogen have accelerated rapidly in response to government commitments to deep decarbonisation establishing hydrogen as a key component in the energy transition.

To help guide regulators decision-makers and investors the Hydrogen Council collaborated with McKinsey & Company to release the report ‘Hydrogen Insights 2021: A Perspective on Hydrogen Investment Deployment and Cost Competitiveness’. The report offers a comprehensive perspective on market deployment around the world investment momentum as well as implications on cost competitiveness of hydrogen solutions.

The document can be downloaded from their website

The present study investigates a process for the selective production of hydrogen from the catalytic decomposition of formic acid in the presence of iridium and iridium–palladium nanoparticles under various conditions. It was found that a loading of 1 wt.% of 2% palladium in the presence of 1% iridium over activated charcoal led to a 43% conversion of formic acid to hydrogen at room temperature after 4 h. Increasing the temperature to 60 °C led to further decomposition and an improvement in conversion yield to 63%. Dilution of formic acid from 0.5 to 0.2 M improved the decomposition reaching conversion to 81%. The reported process could potentially be used in commercial applications.

The virtual energy storage system (VESS) is one of the emerging novel concepts among current energy storage systems (ESSs) due to the high effectiveness and reliability. In fact VESS could store surplus energy and inject the energy during the shortages at high power with larger capacities compared to the conventional ESSs in smart grids. This study investigates the optimal operation of a multi-carrier VESS including batteries thermal energy storage (TES) systems power to hydrogen (P2H) and hydrogen to power (H2P) technologies in hydrogen storage systems (HSS) and electric vehicles (EVs) in dynamic ESS. Further demand response program (DRP) for electrical and thermal loads has been considered as a tool of VESS due to the similar behavior of physical ESS. In the market three participants have considered such as electrical thermal and hydrogen markets. In addition the price uncertainties were calculated by means of scenarios as in stochastic programming while the optimization process and the operational constraints were considered to calculate the operational costs in different ESSs. However congestion in the power systems is often occurred due to the extreme load increments. Hence this study proposes a bi-level formulation system where independent system operators (ISO) manage the congestion in the upper level while VESS operators deal with the financial goals in the lower level. Moreover four case studies have considered to observe the effectiveness of each storage system and the simulation was modeled in the IEEE 33-bus system with CPLEX in GAMS.

The hazardous effects of pollutants from conventional fuel vehicles have caused the scientific world to move towards environmentally friendly energy sources. Though we have various renewable energy sources the perfect one to use as an energy source for vehicles is hydrogen. Like electricity hydrogen is an energy carrier that has the ability to deliver incredible amounts of energy. Onboard hydrogen storage in vehicles is an important factor that should be considered when designing fuel cell vehicles. In this study a recent development in hydrogen fuel cell engines is reviewed to scrutinize the feasibility of using hydrogen as a major fuel in transportation systems. A fuel cell is an electrochemical device that can produce electricity by allowing chemical gases and oxidants as reactants. With anodes and electrolytes the fuel cell splits the cation and the anion in the reactant to produce electricity. Fuel cells use reactants which are not harmful to the environment and produce water as a product of the chemical reaction. As hydrogen is one of the most efficient energy carriers the fuel cell can produce direct current (DC) power to run the electric car. By integrating a hydrogen fuel cell with batteries and the control system with strategies one can produce a sustainable hybrid car

It is a common belief that embedded expanding inclusions are subjected to an internal homogeneous compressive hydrostatic stress. Still cracks that appear in precipitates that occupy a larger volume than the original material are frequently observed. The appearance of cracks has since long been regarded as a paradox. In the present study it is shown that matrix materials that increases its volume even several percent during the precipitation process develop a tensile hydrostatic stress in the centre of the precipitate. This is the result of a complicated mechanical-chemical phase transformation process. The process is here studied using a Landau phase feld model. Before the material is transformed and incorporated in a precipitate it undergoes stretching beyond the elastic strain limit because of the presence of already expanded material. During the phase transformation the accompanying volumetric expansion cannot be fully accommodated which instead creates an internal compressive stress and adds tension in the surrounding material. As the growth of the precipitate proceeds a region with increasing tensile stress develops in the interior of the precipitate. This is suggested to be the most probable cause of the observed cracks. First the mechanics that lead to the tension is computed. The infuence of elastic-plastic properties is studied both for cases both with and without cracks. The growth history from microscopic to macroscopic precipitates is followed and the result is compared with observations of so called hydride blisters that are formed on surfaces of zirconium alloys in the presence of hydrogen. A common practical situation is when the zirconium is in contact with an object of lower temperature. Then the cooled spot attracts hydrogen that make the zirconium transform to a metal hydride with the shape of a blister. The simulations predicts a final size and position of the growing crack that compares well with the experimental observations.

To address the climate emergency France is committed to achieving carbon neutrality by 2050. It plans to significantly increase the contribution of renewable energy in its energy mix. The share of renewable energy in its electricity production which amounts to 25.5% in 2020 should reach at least 40% in 2030. This growth poses several new challenges that require policy makers and regulators to act on the technological changes and expanding need for flexibility in power systems. This document presents the main strategies and projects developed in France as well as various recommendations to accompany and support its energy transition policy.

In this paper the implications of the use of hydrogen on product yield and conversion efficiency as well as on economic performance of a hydrogen enhanced Biomass-to-Liquid (BtL) process are analyzed. A process concept for the synthesis of fuel (gasoline and LPG) from biomass-derived synthesis gas via Methanol-to-Gasoline (MtG) route with utilization of carbon dioxide from gasification by feeding additional hydrogen is developed and modeled in Aspen Plus. The modeled process produces 0.36 kg fuel per kg dry straw. Additionally 99 MW electrical power are recovered from purge and off gases from fuel synthesis in CCGT process covering the electricity consumption of fuel synthesis and synthesis gas generation. The hydrogen enhanced BtL procces reaches a combined chemical and electrical efficiency of 48.2% and overall carbon efficiency of 69.5%. The total product costs (TPC) sum up to 3.24 €/kg fuel. Raw materials (hydrogen and straw) make up the largest fraction of TPC with a total share of 75%. The hydrogen enhanced BtL process shows increased chemical energy and carbon efficiencies and thus higher product yields. However economic analysis shows that the process is unprofitable under current conditions due to high costs for hydrogen provision.

Insufficient active sites and fast charge carrier recombination are detrimental to photocatalytic activity of graphitic carbon nitride (g-C3N4). In this work a combination of pore creating with thermal exfoliation was employed to prepare porous g-C3N4 nanosheets for photocatalytic water splitting into hydrogen. Hexadecyl trimethyl ammonium chloride (CTAC) as the soft template promoted the formation of porous g-C3N4 during the thermal condensation of melamine. On further post-synthesis calcination the porous g-C3N4 aggregates were exfoliated into discrete nanosheets accompanied by an increase in specific surface area and defects. Optimal porous g-C3N4 nanosheets achieved 3.6 times the photocatalytic hydrogen evolution rate for bulk counterpart. The enhanced photocatalytic activity may be ascribed to TCN-1%CTAC has larger specific surface area stronger optical absorption intensity and higher photogenerated electron–hole separation efficiency. The external quantum efficiency of TCN-1%CTAC was measured to be 3.4% at 420 nm. This work provides a simple combinatorial strategy for the preparation of porous g-C3N4 nanosheets with low cost environmental friendliness and enhanced photocatalytic activity.

Hydrogen production from biomass pyrolysis is economically and technologically attractive from the perspectives of energy and the environment. The two-stage catalytic pyrolysis of pine sawdust for hydrogen-rich gas production is investigated using nano-NiO/Al2O3 as the catalyst at high temperatures. The influences of residence time (0–30 s) and catalytic temperature (500–800 ◦C) on pyrolysis performance are examined in the distribution of pyrolysis products gas composition and gas properties. The results show that increasing the residence time decreased the solid and liquid products but increased gas products. Longer residence times could promote tar cracking and gas-phase conversion reactions and improve the syngas yield H2/CO ratio and carbon conversion. The nano-NiO/A12O3 exhibits excellent catalytic activity for tar removal with a tar conversion rate of 93% at 800 ◦C. The high catalytic temperature could significantly improve H2 and CO yields by enhancing the decomposition of tar and gas-phase reactions between CO2 and CH4 . The increasing catalytic temperature increases the dry gas yield and carbon conversion but decreases the H2/CO ratio and low heating value.

A joint experimental and numerical investigation of turbulent flame anchoring at externally heated walls is presented. The phenomenon has primarily been studied for laminar flames and micro-combustion while this study focuses on large-scale applications and elevated Reynolds number flows. Therefore a novel burner design is developed and examined for a diverse set of operating conditions. Hydroxyl radical chemiluminescence measurements are employed to validate the numerical method. The numerical investigation evaluates the performance of various hydrogen/air kinetics Reynolds-averaged turbulence models and the eddy dissipation concept (EDC) as a turbulence-chemistry interaction model. Simulation results show minor differences between detailed chemical mechanisms but pronounced deviations for a reduced kinetic. The baseline k-ω turbulence model is assessed to most accurately predict flame front position and shape. Universal applicability of EDC modelling constants is contradicted. Conclusively the flame anchoring concept is considered a promising approach for pilot flames in continuous combustion devices.

In this study indentations were made on Zr-2.5%Nb pressure tube material to induce multi-axial stress field. An I-shaped punch mark was indented on the Pressure tube material with predefined punch load. Later material was charged with 50 wppm of hydrogen. The samples near the punch mark were metallographically examined for hydrides orientation. It was observed that hydrides exhibited preferentially circumferential orientation far away from the indent to mixed orientation containing both circumferential and radial hydrides near the indent. This is probably as a result of stress field generated by indentation. Extent of radial hydride formation was observed to be varying with indentation load.

Introduction of hydrogen into the UK gas main has been reviewed in terms of how materials within the Keele G3 gas distribution network (G3 GDN) on the Keele University network may be affected by contact with natural gas (NG):hydrogen blends up to a limit of 20 % mol/mol hydrogen.<br/>This work has formed part of the supporting evidence for a 1 year hydrogen blending trial on the Keele G3 GDN coordinated by the HyDeploy consortium (formed of representatives of Cadent Northern Gas Networks ITM Power Progressive Energy HSL and Keele University).<br/>A wide range of materials were identified and assessed via a combination of literature review and practical test programmes. No significant changes to material properties in terms of accelerated material degradation or predicted efficiency of gas confinement were identified which would cause concern for the year-long trial at Keele.<br/>It can be concluded that materials on the Keele G3 GDN should be acceptable to provide a safe operating network the HyDeploy demonstrator project up to a level of 20 % mol/mol hydrogen.<br/>Check the supplements tab for the other documents in this report

Over the last decade’s magnesium and magnesium based compounds have been intensively investigated as potential hydrogen storage as well as thermal energy storage materials due to their abundance and availability as well as their extraordinary high gravimetric and volumetric storage densities. This review work provides a broad overview of the most appealing systems and of their hydrogenation/dehydrogenation properties. Special emphasis is placed on reviewing the efforts made by the scientific community in improving the material’s thermodynamic and kinetic properties while maintaining a high hydrogen storage capacity.

This study focuses on structural imperfections caused by hydrogen impurities in AlN thin films obtained using atomic layer deposition method (ALD). Currently there is a severe lack of studies regarding the presence of hydrogen in the bulk of AlN films. Fourier-transform infrared spectroscopy (FTIR) is one of the few methods that allow detection bonds of light elements in particular - hydrogen. Hydrogen is known to be a frequent contaminant in AlN films grown by ALD method it may form different bonds with nitrogen e.g. amino (–NH2) or imide (–NH) groups which impair the quality of the resulting film. Which is why it is important to investigate the phenomenon of hydrogen as well as to search for the suitable methods to eliminate or at least reduce its quantity. In this work several samples have been prepared using different precursors substrates and deposition parameters and characterized using FTIR and additional techniques such as AFM XPS and EDS to provide a comparative and comprehensive analysis of topography morphology and chemical composition of AlN thin films.

Global energy sources are being transformed from hydrocarbon-based energy sources to renewable and carbon-free energy sources such as wind solar and hydrogen. The biggest challenge with hydrogen as a renewable energy carrier is the storage and delivery system’s complexity. Therefore other media such as ammonia for indirect storage are now being considered. Research has shown that at reasonable pressures ammonia is easily contained as a liquid. In this form energy density is approximately half of that of gasoline and ten times more than batteries. Ammonia can provide effective storage of renewable energy through its existing storage and distribution network. In this article we aimed to analyse the previous studies and the current research on the preparation of ammonia as a next-generation renewable energy carrier. The study focuses on technical advances emerging in ammonia synthesis technologies such as photocatalysis electrocatalysis and plasmacatalysis. Ammonia is now also strongly regarded as fuel in the transport industrial and power sectors and is relatively more versatile in reducing CO₂ emissions. Therefore the utilisation of ammonia as a renewable energy carrier plays a significant role in reducing GHG emissions. Finally the simplicity of ammonia processing transport and use makes it an appealing choice for the link between the development of renewable energy and demand.

Stress corrosion cracking (SCC) of steels can reduce the structural integrity of gas pipelines. To simulate in-service degradation of pipeline steels in laboratory the method of accelerated degradation consisted in subjecting specimens to electrolytic hydrogenation to loading up the certain plastic deformation and heating of specimen at 250°C was recently developed. The purpose of this paper was to analyse mechanical and SCC behaviour of in-service and in-laboratory degraded gas pipeline steels and to reveal some fractographic features of SCC. Three pipeline steels of the different strength (17H1S which is equivalent of API X52 API X60 and API X70) were investigated. The characteristics of the as-received pipeline steels with different strength were compared with the properties of pipeline steels after in-service and in-laboratory degradation. An influence of the NS4 solution on SCC resistance of 17H1S and API X60 steels in the as-received state and after the accelerated degradation using slow strain rate tension method was analysed. The noticeable decrease of plasticity for 17H1S and API X60 steels after long-term operation was shown. Deep microdelaminations revealed in the central part of fracture surfaces for the operated steels can be considered as the signs of dissipated damaging in the metal caused by texture and hydrogen absorbed by metal. Comparison of the SCC tests results showed that the characteristics of both steels in the as-received state were insignificantly changed under the influence of the environment. At the same time the degraded steels were characterized by a high sensitivity to SCC. It was shown fractographically that it associated with cracking along interfaces of ferrite and pearlite grains with secondary deep intergranular cracks formation and also by delamination between ferrite and cementite inside pearlite grains. The similar fracture mechanism at SCC tests was revealed for near the outer surface of the specimens and in the central part of the fracture surfaces of in-laboratory degraded specimens. These results demonstrated the key role of hydrogen during SCC and in-bulk cracking as well.

Experimental tests of flat titanium samples at a temperature of 450 °C stretched with a constant force up to destruction were carried out. Titanium samples were hydrogenated in the Moscow Aviation Institute laboratory to a hydrogen content of 0.1 % 0.3 % and 0.6 % by weight of the specimen and then tested in the laboratory of Lomonosov Moscow State University. From the experiments the time to failure the localization time of the deformations and the stress distribution along the longitudinal coordinate of the sample over time were obtained. A metallographic study was conducted and the phase composition was investigated in Moscow Aviation Institute. The effect of hydrogen on long-term strength mechanical characteristics and phase composition has been elucidated.

This report is part of DNV’s suite of Energy Transition Outlook publications for 2021. It focuses on how key energy transition technologies will develop compete and interact in the coming five years.

Debate and uncertainty about the energy transition tend to focus on what technology can and can’t do. All too often such discussions involve wishful thinking advocacy of a favoured technology or reference to outdated information. Through this report we bring insights derived from our daily work with the world’s leading energy players including producers transporters and end users. Each of the ten chapters that follow are written by our experts in the field – or in the case of maritime technologies on the ocean.

Because the pace of the transition is intensifying describing any given technology is like painting a fast-moving train. We have attempted to strike a balance between technical details and issues of safety efficiency cost and competitiveness. Transition technologies are deeply interlinked and in some cases interdependent; any discussion on green hydrogen for example must account for developments in renewable electricity hydrogen storage and transport systems and end-use technologies such as fuels cells.

Our selection of ten technologies is not exhaustive but each of these technologies is of particular interest for the pace and direction of the energy transition. They range from relatively mature technologies like solar PV to technologies like nuclear fusion which are some distance from commercialization but which have current R&D and prototyping worth watching. Together they cover most but not all key sectors. We describe expected developments for the coming five years which to a large extent will determine how the energy transition unfolds through to mid-century. As such this Technology Progress report is an essential supplement to our main Energy Transition Outlook forecast.

Our aim is to make an objective and realistic assessment of the status of these technologies and evaluate how they contribute to the energy transition ahead. Attention to progress in these technologies will be critical for anyone concerned with energy.

Several alternative fuel–vehicle combinations are being considered for replacement of the internal combustion engine (ICE) vehicles to reduce greenhouse gas (GHG) emissions and the dependence on fossil fuels. The International Energy Agency has proposed the inclusion of low carbon alternatives such as electricity hydrogen and biofuels in the transport sector for reducing the GHG emissions and providing a sustainable future. This paper compares the use of these alternative fuels viz. electricity hydrogen and bio-ethanol in combination with battery electric vehicle (BEV) and fuel cell electric vehicle (FCEV) technologies on the basis of their overall efficiency and GHG emissions involved in the conversion of the primary energy source to the actual energy required at wheels through a well-to-wheel analysis. The source of energy for electricity production plays a major role in determining the overall efficiency and the GHG emissions of a BEV. Hence electricity production mix of Germany (60% fossil fuel energy) France (76% nuclear energy) Sweden and Austria (60 and 76% renewable energy respectively) the European Union mix (48% fossil fuel energy) and the United States of America (68% fossil fuel energy) are considered for the BEV analysis. In addition to the standard hydrogen based FCEVs CNG and bio-ethanol based FCEVs are analysed. The influence of a direct ethanol fuel cell (DEFC) on GHG emissions and overall chain efficiency is discussed. In addition to the standard sources of bio-ethanol (like sugarcane corn etc.) sources like wood waste and wheat straw are included in the analysis. The results of this study suggest that a BEV powered by an electricity production mix dominated by renewable energy and bio-ethanol based DEFC electric vehicles offer the best solution in terms of GHG emissions efficiency and fossil fuel dependency. Bio-ethanol as a fuel has the additional advantage to be implemented readily in ICE vehicles followed by advancements through reformer based FCEVs and DEFC electric vehicles. Although important this analysis does not include the health effects of the alternative vehicles. Bio-ethanol used in an ICE may lead to increased emission of acetaldehydes which however might not be the case if it is used in fuel cells.

Now it is time to set up reliable water electrolysis stacks with active and robust electro‐ catalysts to produce green hydrogen. Compared with catalytic kinetics much less attention has been paid to catalyst stability and the weak understanding of the catalyst deactivation mechanism restricts the design of robust electrocatalysts. Herein we discuss the issues of catalysts’ stability evaluation and characterization and the degradation mechanism. The systematic understanding of the degradation mechanism would help us to formulate principles for the design of stable catalysts. Particularly we found that the dissolution rate for different 3d transition metals differed greatly: Fe dissolves 114 and 84 times faster than Co and Ni. Based on this trend we designed Fe@Ni and FeNi@Ni core‐shell structures to achieve excellent stability in a 1 A cm−2 current density as well as good catalytic activity at the same time