China, People’s Republic

In some areas the problem of wind and solar power curtailment is prominent. Hydrogen energy has the advantage of high storage density and a long storage time. Multi-energy hybrid systems including renewable energies batteries and hydrogen are designed to solve this problem. In order to reduce the power loss of the converter an AC-DC hybrid bus is proposed. A multi-energy experiment platform is established including a wind turbine photovoltaic panels a battery an electrolyzer a hydrogen storage tank a fuel cell and a load. The working characteristics of each subsystem are tested and analyzed. The multi-energy operation strategy is based on state monitoring and designed to enhance hydrogen utilization energy efficiency and reliability of the system. The hydrogen production is guaranteed preferentially and the load is reliably supplied. The system states are monitored such as the state of charge (SOC) and the hydrogen storage level. The rated and ramp powers of the battery and fuel cell and the pressure limit of the hydrogen storage tank are set as safety constraints. Eight different operation scenarios comprehensively evaluate the system’s performance and via physical experiments the proposed operation strategy of the multi-energy system is verified as effective and stable.

This paper designs the integrated charging station of PV and hydrogen storage based on the charging station. The energy storage system includes hydrogen energy storage for hydrogen production and the charging station can provide services for electric vehicles and hydrogen vehicles at the same time. To improve the independent energy supply capacity of the hybrid charging station and reduce the cost the components are reasonably configured. To minimize the configuration cost of the integrated charging station and the proportion of power purchase to the demand of the charging station the energy flow strategy of the integrated charging station is designed and the optimal configuration model of optical storage capacity is constructed. The NSGA-II algorithm optimizes the non-inferior Pareto solution set and a fuzzy comprehensive evaluation evaluates the optimal configuration.

Compact-tension (CT) specimens made of low alloy 30CrMo steels were hydrogen-charged and then subjected to the fracture toughness test. The experimental results revealed that the higher crack propagation and the lower crack growth resistance (CTOD-R curve) are significantly noticeable with increasing hydrogen embrittlement (HE) indexes. Moreover the transition in the microstructural fracture mechanism from ductile (microvoid coalescence (MVC)) without hydrogen to a mixed quasi-cleavage (QC) fracture and QC + intergranular (IG) fracture with hydrogen was observed. The hydrogen-enhanced decohesion (HEDE) mechanism was characterized as the dominant HE mechanism. According to the experimental testing the coupled problem of stress field and hydrogen diffusion field with cohesive zone stress analysis was employed to simulate hydrogen-assisted brittle fracture behavior by using ABAQUS software. The trapezoidal traction-separation law (TSL) was adopted and the initial TSL parameters from the best fit to the load-displacement and J-integral experimental curves without hydrogen were calibrated for the critical separation of 0.0393 mm and the cohesive strength of 2100 MPa. The HEDE was implemented through hydrogen influence in the TSL and to estimate the initial hydrogen concentration based on matching numerical and experimental load-line displacement curves with hydrogen. The simulation results show that the general trend of the computational CTOD-R curves corresponding to initial hydrogen concentration is almost the same as that obtained from the experimental data but in full agreement the computational CTOD values being slightly higher. Comparative analysis of numerical and experimental results shows that the coupled model can provide design and prediction to calculate hydrogen-assisted fracture behavior prior to extensive laboratory testing provided that the material properties and properly calibrated TSL parameters are known.

This study presents an overview of the current status of hydrogen production in relation to the global requirement for energy and resources. Subsequently it symmetrically outlines the advantages and disadvantages of various production routes including fossil fuel/biomass conversion water electrolysis microbial fermentation and photocatalysis (PC) in terms of their technologies economy energy consumption and costs. Considering the characteristics of hydrogen energy and the current infrastructure issues it highlights that onsite production is indispensable and convenient for some special occasions. Finally it briefly summarizes the current industrialization situation and presents future development and research directions such as theoretical research strengthening renewable raw material development process coupling and sustainable energy use.

Liquid hydrogen is the main fuel of large-scale low-temperature heavy-duty rockets and has become the key direction of energy development in China in recent years. As an important application carrier in the large-scale storage and transportation of liquid hydrogen liquid hydrogen cryogenic storage and transportation containers are the key equipment related to the national defense security of China’s aerospace and energy fields. Due to the low temperature of liquid hydrogen (20 K) special requirements have been put forward for the selection of materials for storage and transportation containers including the adaptability of materials in a liquid hydrogen environment hydrogen embrittlement characteristics mechanical properties and thermophysical properties of liquid hydrogen temperature which can all affect the safe and reliable design of storage and transportation containers. Therefore it is of great practical significance to systematically master the types and properties of cryogenic materials for the development of liquid hydrogen storage and transportation containers. With the wide application of liquid hydrogen in different occasions the requirements for storage and transportation container materials are not the same. In this paper the types and applications of cryogenic materials commonly used in liquid hydrogen storage and transportation containers are reviewed. The effects of low-temperature on the mechanical properties of different materials are introduced. The research progress of cryogenic materials and low-temperature performance data of materials is introduced. The shortcomings in the research and application of cryogenic materials for liquid hydrogen storage and transportation containers are summarized to provide guidance for the future development of container materials. Among them stainless steel is the most widely used cryogenic material for liquid hydrogen storage and transportation vessel but different grades of stainless steel also have different applications which usually need to be comprehensively considered in combination with its low temperature performance corrosion resistance welding performance and other aspects. However with the increasing demand for space liquid hydrogen storage and transportation the research on high specific strength cryogenic materials such as aluminum alloy titanium alloy or composite materials is also developing. Aluminum alloy liquid hydrogen storage and transportation containers are widely used in the space field while composite materials have significant advantages in being lightweight. Hydrogen permeation is the key bottleneck of composite storage and transportation containers. At present there are still many technical problems that have not been solved.

Fully decarbonizing global industry is essential to achieving climate stabilization and reaching net zero greenhouse gas emissions by 2050–2070 is necessary to limit global warming to 2 °C. This paper assembles and evaluates technical and policy interventions both on the supply side and on the demand side. It identifies measures that employed together can achieve net zero industrial emissions in the required timeframe. Key supply-side technologies include energy efficiency (especially at the system level) carbon capture electrification and zero-carbon hydrogen as a heat source and chemical feedstock. There are also promising technologies specific to each of the three top-emitting industries: cement iron & steel and chemicals & plastics. These include cement admixtures and alternative chemistries several technological routes for zero-carbon steelmaking and novel chemical catalysts and separation technologies. Crucial demand-side approaches include material-efficient design reductions in material waste substituting low-carbon for high-carbon materials and circular economy interventions (such as improving product longevity reusability ease of refurbishment and recyclability). Strategic well-designed policy can accelerate innovation and provide incentives for technology deployment. High-value policies include carbon pricing with border adjustments or other price signals; robust government support for research development and deployment; and energy efficiency or emissions standards. These core policies should be supported by labeling and government procurement of low-carbon products data collection and disclosure requirements and recycling incentives. In implementing these policies care must be taken to ensure a just transition for displaced workers and affected communities. Similarly decarbonization must complement the human and economic development of low- and middle-income countries.

Supercritical water gasification is a promising technology for wet biomass utilization. In this paper Ni and other metal catalysts were synthesized by wet impregnation. The stability and catalytic activities of Ni catalysts were evaluated. Firstly catalytic activities of Ni Fe Cu catalysts supported on MgO were tested using wheat straw as raw material in a batch reactor at 723 K and water density of 0.07 cm³/g. Experimental results showed that the order of metal catalyst activity for hydrogen generation was Ni/MgO > Fe/MgO > Cu/MgO. Secondly the influence of different supports on Ni catalysts performance was investigated. The results showed that the order of the Ni catalysts’ activity with different supports was Ni/MgO > Ni/ZnO > Ni/Al2O3 > Ni/ZrO2. Finally the effects of Ni loading and the amount of Ni catalyst addition on hydrogen production and the stability of Ni/MgO catalyst were studied. It was found that serious deactivation of Ni catalyst in the process of supercritical water gasification took place. Even if carbon deposited on the catalyst surface was removed by high temperature calcination and the catalyst was reduced with hydrogen the activity of used catalyst was only partially restored.

From the perspective of risk control when hydrogen fuel and fuel cells are used on ships there is a possibility of low-flash fuel leakage leading to the risk of explosion. Since the fuel cell space (cabin for fuel cell installations) is an enclosed space any small amount of leakage must be handled properly. In ship design area classification is a method of analyzing and classifying the areas where explosive gas atmospheres may occur. If the fuel cell space is regarded as a hazardous area all the electrical devices inside it must be explosion-proof type which will make the ship’s design very difficult. This paper takes a Chinese fuel cell powered ship as an example to analyze its safety. Firstly the leakage rates of fuel cell modules valves and connectors are calculated. Secondly the IEC60079-10-1 algorithm is used to calculate the risk level of the fuel cell space. Finally the ship and fuel cells are optimized and redesigned and the risk level of the fuel cell space is recalculated and compared. The result shows that the optimized fuel space risk level could be reduced to the level of the non-hazardous zone.

Magnesium hydride (MgH₂) is a potential material for solid-state hydrogen storage. However the thermodynamic and kinetic properties are far from practical application in the current stage. In this work two-dimensional vanadium carbide (V₂C) MXene with layer thickness of 50−100 nm was fist synthesized by selectively HF-etching the Al layers from V₂AlC MAX phase and then introduced into MgH2 to improve the hydrogen sorption performances of MgH2. The onset hydrogen desorption temperature of MgH₂ with V2C addition is significantly reduced from 318 °C for pure MgH2 to 190 °C with a 128 °C reduction of the onset temperature. The MgH₂+ 10 wt% V₂C composite can release 6.4 wt% of H₂ within 10 min at 300 °C and does not loss any capacity for up to 10 cycles. The activation energy for the hydrogen desorption reaction of MgH₂ with V₂C addition was calculated to be 112 kJ mol−1 H₂ by Arrhenius's equation and 87.6 kJ mol−1 H₂ by Kissinger's equation. The hydrogen desorption reaction enthalpy of MgH₂ + 10 wt% V₂C was estimated by van't Hoff equation to be 73.6 kJ mol−1 H₂ which is slightly lower than that of the pure MgH₂ (77.9 kJ mol−1 H₂). Microstructure studies by XPS TEM and SEM showed that V₂C acts as an efficient catalyst for the hydrogen desorption reaction of MgH₂. The first-principles density functional theory (DFT) calculations demonstrated that the bond length of Mg−H can be reduced from 1.71 Å for pure MgH₂ to 2.14 Å for MgH₂ with V₂C addition which contributes to the destabilization of MgH₂. This work provides a method to significantly and simultaneously tailor the hydrogen sorption thermodynamics and kinetics of MgH₂ by two-dimensional MXene materials.

The study on temper embrittlement and hydrogen embrittlement of a test block from a 3Cr1Mo1/4V hydrogenation reactor after ten years of service was carried out by small punch test (SPT) at different temperatures. The SPT fracture energy Esp (derived from integrating the load-displacement curve) divided by the maximum load (Fm) of SPT was used to fit the Esp/Fm versus-temperature curve to determine the energy transition temperature (Tsp) which corresponded to the ductile-brittle transition temperature of the Charpy impact test. The results indicated that the ratio of Esp/Fm could better represent the energy of transition in SPT compared with Esp. The ductile-to-brittle transition temperature of the four different types of materials was measured using the hydrogen charging test by SPT. These four types of materials included the base metal and the weld metal in the as-received state and the base metal and the weld metal in the de-embrittled state. The results showed that there was a degree of temper embrittlement in the base metal and the weld metal after ten years of service at 390 °C. The specimens became slightly more brittle but this was not obvious after hydrogen charging. Because the toughness of the material of the hydrogenation reactor was very good the flat samples of SPT could not characterize the energy transition temperature within the liquid nitrogen temperature. Additionally there was no synergetic effect of temper embrittlement and hydrogen embrittlement found in 3Cr1Mo1/4V steel.

The hydrogen fuel cell (HFC) vehicle is an important clean energy vehicle which has prospects for development. The behavior of the hydrogen fuel cell (HFC) vehicle power system and in particular the proton-exchange membrane fuel cell has been extensively studied as of recent. The development of the dynamic system modeling technology is of paramount importance for HFC vehicle studies; however it is hampered by the separation of the electrochemical properties and dynamic properties. In addition the established model matching the follow-up control method lacks applicability. In attempts to counter these obstructions we proposed an improved fuzzy (Proportional Integral Derivative) PID control method considering HFC voltage-output characteristics. By developing both the electrochemical and dynamic model for HFC vehicle we can realize the coordinated control of HFC and power cell. The simulation results are in good agreement with the experimental results in the two models. The proposed control algorithm has a good control effect in all stages of HFC vehicle operation.

Regarding the problem of hydrogen diffusion of the fuel cell vehicle (HFCV) when its hydrogen supply system leaks this research uses the FLUENT software to simulate numerical values in the process of hydrogen leakage diffusion in both open space and closed space. This paper analyzed the distribution range and concentration distribution characteristics of hydrogen in these two different spaces. Besides this paper also took a survey about the effects of leakage rate wind speed wind direction in open space and the role the air vents play on hydrogen safety in closed space which provides a reference for the hydrogen safety of HFCV. In conclusion the experiment result showed that: In open space hydrogen leakage rate has a great influence on its diffusion. When the leakage rate doubles the hydrogen leakage range will expand about 1.5 times simultaneously. The hydrogen diffusion range is the smallest when the wind blows at 90 degrees which is more conducive to hydrogen diffusion. However when the wind direction is against the direction of the leakage of hydrogen the range of hydrogen distribution is maximal. Under this condition the risk of hydrogen leakage is highest. In an enclosed space when the vent is set closest to the leakage position the volume fraction of hydrogen at each time is smaller than that at other positions so it is more beneficial to safety.

In this paper a kind of on-board liquid hydrogen (LH2 ) cold energy utilization system for a heavy-duty fuel cell hybrid truck is proposed. Through this system the cold energy of LH2 is used for cooling the inlet air of a compressor and the coolant of the accessories cooling system sequentially to reduce the parasitic power including the air compressor water pump and radiator fan power. To estimate the cold energy utilization ratio and parasitic power saving capabilities of this system a model based on AMESim software was established and simulated under different ambient temperatures and fuel cell stack loads. The simulation results show that cold energy utilization ratio can keep at a high level except under extremely low ambient temperature and light load. Compared to the original LH2 system without cold energy utilization the total parasitic power consumption can be saved by up to 15% (namely 1.8 kW).

Hydrogen storage in solid-state materials is believed to be a most promising hydrogen-storage technology for high efficiency low risk and low cost. Mg(BH4)2 is regarded as one of most potential materials in hydrogen storage areas in view of its high hydrogen capacities (14.9 wt% and 145–147 kg cm3 ). However the drawbacks of Mg(BH4)2 including high desorption temperatures (about 250 C–580 C) sluggish kinetics and poor reversibility make it difficult to be used for onboard hydrogen storage of fuel cell vehicles. A lot of researches on improving the dehydrogenation reaction thermodynamics and kinetics have been done mainly including: additives or catalysts doping nanoconfining Mg(BH4)2 in nanoporous hosts forming reactive hydrides systems multi-cation/anion composites or other derivatives of Mg(BH4)2. Some favorable results have been obtained. This review provides an overview of current research progress in magnesium borohydride including: synthesis methods crystal structures decomposition behaviors as well as emphasized performance improvements for hydrogen storage.

China is the world’s largest carbon emitter and suffers from severe air pollution which results in approximately one million premature deaths/year. Alternative energy vehicles (AEVs) (electric hydrogen fuel cell and natural gas vehicles) can reduce carbon emissions and improve air quality. However climate air quality and health benefits of AEVs powered with deeply decarbonized power generation are poorly quantified. Here we quantitatively estimate the air quality health carbon emission and economic benefits of replacing internal combustion engine vehicles with various AEVs. We find co-benefits increase dramatically as the electricity grid decarbonizes and hydrogen is produced from non-fossil fuels. Relative to 2015 a conversion to AEVs using largely non-fossil power can reduce air pollution and associated premature mortalities and years of life lost by 329000 persons/year and 1611000 life years/year. Thus maximizing climate air quality and health benefits of AEV deployment in China requires rapid decarbonization of the power system.

With the development of high-altitude and long-endurance unmanned aerial vehicles (UAVs) optimization of the coordinated energy dispatch of UAVs’ energy management systems has become a key target in the research of electric UAVs. Several different energy management strategies are proposed herein for improving the overall efficiency and fuel economy of fuel cell/battery hybrid electric power systems (HEPS) of UAVs. A rule-based (RB) energy management strategy is designed as a baseline for comparison with other strategies. An energy management strategy (EMS) based on fuzzy logic (FL) for HEPS is presented. Compared with classical rule-based strategies the fuzzy logic control has better robustness to power fluctuations in the UAV. However the proposed FL strategy has an inherent defect: the optimization performances will be determined by the heuristic method and the past experiences of designers to a great extent rather than a specific cost function of the algorithm itself. Thus the paper puts forward an improved fuzzy logic-based strategy that uses particle swarm optimization (PSO) to track the optimal thresholds of membership functions and the equivalent hydrogen consumption minimization is considered as the objective function. Using a typical 30 min UAV mission profile all the proposed EMS were verified by simulations and rapid controller prototype (RCP) experiments. Comprehensive comparisons and analysis are presented by evaluating hydrogen consumption system efficiency and voltage bus stability. The results show that the PSO-FL algorithm can further improve fuel economy and achieve superior overall dynamic performance when controlling a UAV’s fuel-cell powertrain.

The ever-increasing demand for energy coupled with dwindling fossil fuel resources make the establishment of a clean and sustainable energy system a compelling need. Hydrogen-based energy systems offer potential solutions. Although in the long-term the ultimate technological challenge is large-scale hydrogen production from renewable sources the pressing issue is how to store hydrogen efficiently on board hydrogen fuel-cell vehicles.

Implementation of non-precious electrocatalysts is key-enabling for water electrolysis to relieve challenges in energy and environmental sustainability. Self-supporting Ni-V₂O₃.electrodes consisting of nanostrip-like V₂O₃.perpendicularly anchored on Ni meshes are herein constructed via the electrochemical reduction of soluble NaVO₃ in molten salts for enhanced electrocatalytic hydrogen evolution. Such a special configuration in morphology and composition creates a well confined interface between Ni and V₂O₃. Experimental and Density-Functional-Theory results confirm that the synergy between Ni and V₂O₃.accelerates the dissociation of H₂O for forming hydrogen intermediates and enhances the combination of H* for generating H₂.

Energy requirements push the shipping industry towards more energy-efficient ships while environmental regulations influence the development of environmentally friendly ships by replacing fossil fuels with alternatives. Current mathematical models for ship energy efficiency which set the analysis boundaries at the level of the ship power system are not able to consider alternative fuels as a powering option. In this paper the energy efficiency and emissions index are formulated for ships with alternative power systems considering three different impacts on the environment (global warming acidification and eutrophication) and realistic fuel pathways and workloads. Besides diesel applications of alternative powering options such as electricity methanol liquefied natural gas hydrogen and ammonia are considered. By extending the analysis boundaries from the ship power system to the complete fuel cycle it is possible to compare different ships within the considered fleet or a whole shipping sector from the viewpoint of energy efficiency and environmental friendliness. The applicability of the model is illustrated on the Croatian ro-ro passenger fleet. A technical measure of implementation of alternative fuels in combination with an operational measure of speed reduction results in an even greater emissions reduction and an increase in energy efficiency. Analysis of the impact of voluntary speed reduction for ships with different power systems resulted in the identification of the optimal combination of alternative fuel and speed reduction by a specific percentage from the ship design speed.

As a promising hydrogen storage material the practical application of magnesium is obstructed by the stable thermodynamics and sluggish kinetics. In this paper three kinds of NiTiO₃ catalysts with different mole ratio of Ni to Ti were successfully synthesized and doped into nanocrystalline Mg to improve its hydrogen storage properties. Experimental results indicated that all the Mg-NiTiO₃ composites showed prominent hydrogen storage performance. Especially the Mg-NiTiO3/TiO₂ composite could take up hydrogen at room temperature and the apparent activation energy for hydrogen absorption was dramatically decreased from 69.8 ± 1.2 (nanocrystalline Mg) kJ/mol to 34.2 ± 0.2 kJ/mol. In addition the hydrogenated sample began to release hydrogen at about 193.2 °C and eventually desorbed 6.6 wt% H₂. The desorption enthalpy of the hydrogenated Mg-NiTiO₃ -C was estimated to be 78.6 ± 0.8 kJ/mol 5.3 kJ/mol lower compared to 83.9 ± 0.7 kJ/mol of nanocrystalline Mg. Besides the sample revealed splendid cyclic stability during 20 cycles. No obvious recession occurred in the absorption and desorption kinetics and only 0.3 wt% hydrogen capacity degradation was observed. Further structural analysis demonstrates that nanosizing and catalyst doping led to a synergistic effect on the enhanced hydrogen storage performance of Mg-NiTiO₃ -C composite which might serve as a reference for future design of highly effective hydrogen storage materials.

Synthetic natural gas (SNG) is one of the promising energy carriers for the excessive electricity generated from variable renewable energy sources. SNG production from renewable H₂ and CO₂  via catalytic CO₂ methanation has gained much attention since CO₂ emissions could be simultaneously reduced. In this study Ni–Fe/(MgAl)O_x alloy catalysts for CO₂ methanation were prepared via hydrotalcite precursors using a rapid coprecipitation method. The effect of total metal concentration on the physicochemical properties and catalytic behavior was investigated. Upon calcination the catalysts showed high specific surface area of above 230 m² g⁻¹. Small particle sizes of about 5 nm were obtained for all catalysts even though the produced catalyst amount was increased by 10 times. The catalysts exhibited excellent space-time yield under very high gas space velocity (34000 h⁻¹) irrespective of the metal concentration. The CO₂ conversions reached 73–79% at 300 °C and CH₄ selectivities were at 93–95%. Therefore we demonstrated the potential of large-scale production of earth-abundant Ni–Fe based catalysts for CO₂ methanation and the Power-to-Gas technology.

The global energy crisis and environmental pollution have caused great concern. Hydrogen is a renewable and environmentally friendly source of energy and has potential to be a major alternative energy carrier in the future. Due to its high capacity and relatively low cost of raw materials alanate has been considered as one of the most promising candidates for hydrogen storage. Among them LiAlH₄ and NaAlH₄ as two representative metal alanates have attracted extensive attention. Unfortunately the high desorption temperature and sluggish kinetics restrict its practical application. In this paper the basic physical and chemical properties as well as the hydrogenation/dehydrogenation reaction mechanism of LiAlH₄ and NaAlH₄ are briefly reviewed. The recent progress on strategic optimizations toward tuning the thermodynamics and kinetics of the alanate including nanoscaling doping catalysts and compositing modification are emphatically discussed. Finally the coming challenges and the development prospects are also proposed in this review.

Designing nanostructured electrocatalysts for selective transfer hydrogenation of α β-unsaturated aldehydes with water as the hydrogen source is highly desirable. Here a facile self-templating strategy is designed for the synthesis of CoS₂ and CoS₂-x nanocapsules (NCs) as efficient cathodes for selective transfer hydrogenation of cinnamaldehyde a model α β-unsaturated aldehyde. The hollow porous structures of NCs are rich in active sites and improve mass transfer resulting in high turnover frequency. The specific adsorption of the styryl block on pristine CoS₂ NCs is conducive to the selective formation of half-hydrogenated hydrocinnamaldehyde with 91.7% selectivity and the preferential adsorption of the C = O group induced by sulfur vacancies on defective CoS₂-x NCs leads to the full-hydrogenated hydrocinnamyl alcohol with 92.1% selectivity. A cross-coupling of carbon and hydrogen radicals may be involved in this electrochemical hydrogenation reaction. Furthermore this selective hydrogenation method is also effective for other α β-unsaturated aldehydes illustrating the universality of the method.

A compact air-breathing jet hybrid-electric engine coupled with solid oxide fuel cells (SOFC) is proposed to develop the propulsion system with high power-weight ratios and specific thrust. The heat exchanger for preheating air is integrated with nozzles. Therefore the exhaust in the nozzle expands during the heat exchange with compressed air. The nozzle inlet temperature is obviously improved. SOFCs can directly utilize the fuel of liquid natural gas after being heated. The performance parameters of the engine are acquired according to the built thermodynamic and mass models. The main conclusions are as follows. 1) The specific thrust of the engine is improved by 20.25% compared with that of the traditional jet engine. As pressure ratios rise the specific thrust increases up to 1.7 kN/(kg·s⁻¹). Meanwhile the nozzle inlet temperature decreases. However the temperature increases for the traditional combustion engine. 2) The power-weight ratio of the engine is superior to that of internal combustion engines and inferior to that of turbine engines when the power density of SOFC would be assumed to be that predicted for 2030. 3) The total pressure recovery coefficients of SOFCs combustors and preheaters have an obvious influence on the specific thrust of the engine and the power-weight ratio of the engine is strongly affected by the power density of SOFCs.

The effects of temperature on bulk hydrogen concentration and diffusion have been tested with the Devanathan–-Stachurski method. Thus a model based on hydrogen potential diffusivity loading frequency and hydrostatic stress distribution around crack tips was applied in order to quantify the temperature’s effect. The theoretical model was verified experimentally and confirmed a temperature threshold of 320 K to maximize the crack growth. The model suggests a nanoscale embrittlement mechanism which is generated by hydrogen atom delivery to the crack tip under fatigue loading and rationalized the ΔK dependence of traditional models. Hence this work could be applied to optimize operations that will prolong the life of the pipeline.