Molecular simulation of copper based metal-organic framework (Cu-MOF) for hydrogen adsorption

Metal organic framework (MOF) are widely used in adsorption and separation due to their porous nature, high surface area, structural diversity and lower crystal density. Due to their exceptional thermal and chemical stability, Cu-based MOF are considered excellent hydrogen storage materials in the world of MOFs. Efforts to assess the effectiveness of hydrogen storage in MOFs with molecular simulation and theoretical modeling are crucial in identifying the most promising materials before extensive experiments are undertaken. In the current work, hydrogen adsorption in four copper MOFs namely, MOF-199, MOF 399, PCN-6′, and PCN-20 has been analyzed. These MOFs have a similar secondary building unit (SBU) structure, i.e., twisted boracite (tbo) topology. The Grand Canonical Monte Carlo (GCMC) simulation was carried at room temperature (298 K) as well as at cryogenic temperature (77 K) and pressures ranging from 0 to 1 bar and 0–50 bar. These temperatures and pressure were selected to comply with the conditions set by department of energy (DOE) and to perform a comparative study on hydrogen adsorption at two different temperatures. The adsorption isotherm, isosteric heat, and the adsorption sites were analyzed in all the MOFs. The findings revealed that isosteric heat influenced hydrogen uptake at low pressures, while at high pressures, porosity and surface area affected hydrogen storage capacity. PCN-6′ is considered viable material at 298 K and 77 K due to its high hydrogen uptake.     

A review on current trends in potential use of metal-organic framework for hydrogen storage

Hydrogen can be a promising clean energy carrier for the replenishment of non-renewable fossil fuels. The set back of hydrogen as an alternative fuel is due to its difficulties in feasible storage and safety concerns. Current hydrogen adsorption technologies, such as cryo-compressed and liquefied storage, are costly for practical applications. Metal-organic frameworks (MOFs) are crystalline materials that have structural versatility, high porosity and surface area, which can adsorb hydrogen efficiently. Hydrogen is adsorbed by physisorption on the MOFs through weak van der Waals force of attraction which can be easily desorbed by applying suitable heat or pressure. The strategies to improve the MOFs surface area, hydrogen uptake capacities and parameters affecting them are studied. Hydrogen spill over mechanism is found to provide high-density storage when compared to other mechanisms. MOFs can be used as proton exchange membranes to convert the stored hydrogen into electricity and can be used as electrodes for the fuel cells. In this review, we addressed the key strategies that could improve hydrogen storage properties for utilizing hydrogen as fuel and opportunities for further growth to meet energy demands.     

A comprehensive review on water management strategies and developments in anion exchange membrane fuel cells

In spite of significant achievements in alkaline exchange membrane fuel cells (AEMFCs) in recent years, they are still lagging behind proton exchange membrane fuel cells (PEMFCs) due to performance instability. Among the relevant operational parameters of AEMFC, the researchers have found that poor water management within the cell was the main reason for failure of the system. In the past five years, numerous modeling and experimental works were reported proposing different strategies to improve water management of AEMFC. With proper water management, the achievable power output in AEMFCs is comparable with that of PEMFCs or even more. Efforts have to be continued, but AEMFCs can become a strong competitor in the market place. This review paper discusses the strategies and developments impacting water management of AEMFCs providing knowledge source for upcoming studies.     

Recent advances in artificial neural network research for modeling hydrogen production processes

Artificial Neural Networks (ANN) have been widely used by scientists in a variety of energy modes (biomass, wind, solar, geothermal, and hydroelectric). This review highlights the assistance of ANN for researchers in the quest for discovering more advanced materials/processes for efficient hydrogen production (HP). The review is divided into two parts in this context. The first section briefly mentions, in terms of technologies, economy, energy consumption, and costs symmetrically outlined the advantages and disadvantages of various HP routes such as fossil fuel/biomass conversion, water electrolysis, microbial fermentation, and photocatalysis. Subsequently, ANN and ANN hybrid studies implemented in HP research were evaluated. Finally, statistics of hybrid studies with ANN are given, and future research proposals and hot research topics are briefly discussed. This research, which touches upon the types of ANNs applied to HP methods and their comparison with other modeling techniques, has an essential place in its field.     

Evaluating influences of impurities on hydrogen production in the reaction of Si with water using Si sludge

Hydrogen has attracted much attention as a next-generation energy resource. Among various technologies, one of the promising approaches for hydrogen production is the use of the reaction between Si and water, which does not require any heat, electricity, and light energy as an input. Notwithstanding the usefulness of Si as a prospective raw material of hydrogen production, the manufacturing process of Si requires a significant amount of energy. Therefore, as an alternative to pure Si, this study used a wasted Si sludge, generated though the manufacturing process of Si wafer, for the direct reuse. Thus, the Si-water reaction for the hydrogen generation was investigated in comparison with pure Si and Si sludge by employing X-ray absorption near edge structure (XANES) to evaluate the feasibility of hydrogen production with the use of Si sludge and to identify the influence of impurities contained in Si sludge. As a result, hydrogen was not produced with the use of Si sludge because of containing Al compound as the impurity. Through the XANES analysis, the formation of SiO(OH)₂ was found as core-shell structure, which potentially would hinder the hydrogen generation.     

Sustainable biohydrogen production by Chlorella sp. microalgae: A review

The use of fossil fuels is causing a huge environmental impact due to the emission of air pollutants, greenhouse gases, and other ground and water contaminants; also, these fuels are depleting; the world is facing an energy crisis in the years to come if no preventive actions are done. Renewable energies are arising as promising technologies that will complement and even replace conventional fuels shifting the global energy matrix to a cleaner and eco-friendly future. Microalgal biohydrogen is one of those emerging technologies that is showing positive results. This work provides an overview of the key parameters to produce hydrogen from microalgae especially from the genus Chlorella. Current status of chemical and biological hydrogen producing technologies is presented, along with the main metabolic processes for this purpose in microalgae, their characteristic enzymes, several strategies to induce hydrogen production, the key operation parameters and finally providing some remarks about scaling-up and industrial-scale applications.     

Current challenges and future technology in photofermentation-driven biohydrogen production by utilizing algae and bacteria

Biohydrogen is perceived as the versatile fuel of the future, having the ability to replace fossil fuels in many industrial and commercial sectors and offering the promise of fulfilling future renewable energy demands. Among various options available for the generation of biohydrogen, photofermentation with the help of microbes and algae is one of the most eye-catching approaches due to its relative efficiency, cost economics, and reduced environmental impacts. Generation of biohydrogen by dark fermentation, microbial electrolysis cell as well as photofermentation, along with their bioprocesses, already have been discussed in earlier literature. Photofermentation offers advantages of both biophotolysis (utilization of light energy) and dark fermentation (utilization of organic waste materials as substrate). Many researchers have been reported successful biohydrogen production from photofermentation-based techniques, however not much information is available regarding the considerable gap in industrial and economic challenges in the production of biohydrogen at the commercial level through photofermentation. Efforts have been made in this review to provide updated information on various new technologies being used in this sector, such as the integration of photofermentation with dark fermentation, the use of recombinant DNA technology, and the use of bionanotechnology to improve biohydrogen production through the utilization of various waste. Various challenges in this sector, as well as future perspectives, have been meticulously addressed in order to explore the future of green biohydrogen production for a sustainable future.     

A review on alloyed quantum dots and their applications as photocatalysts

Semiconductor driven artificial photocatalysis is the most sustainable technology towards addressing the growing energy and environmental pollution issues. In this context, alloyed quantum dots (QDs) are an emerging class of promising nanomaterials gathering tremendous attention in this area due to several beneficial features. Compared to other bulk semiconductors, alloyed QDs are cost-effective, stable, less-toxic with superior optoelectronic features, which significantly enhances their solar energy conversion efficiency. Herein, the present review summarizes the fundamentals of alloyed QDs, various synthesis techniques, and discusses optical as well as structural properties from data interpretation point of view taking suitably reported literature. Moreover, we have provided a comprehensive summary of recent state of art metal chalcogenides based alloyed QD systems towards H₂ evolution, CO₂ reduction, and pollutant degradation. Finally, the review discusses the associated challenges and future prospects of alloyed QDs with a special focus on preparation, property engineering, theoretical aspect, stability and other field application. Additionally, the overarching aim is to provide researchers an in-depth understanding in the field of alloyed QDs relating to synthesis, characterisation, and promotes their photocatalytic applications, and can foster as a manual to future researchers.     

Multi-state techno-economic model for optimal dispatch of grid connected hydrogen electrolysis systems operating under dynamic conditions

The production of hydrogen through water electrolysis is a promising pathway to decarbonize the energy sector. This paper presents a techno-economic model of electrolysis plants based on multiple states of operation: production, hot standby and idle. The model enables the calculation of the optimal hourly dispatch of electrolyzers to produce hydrogen for different end uses. This model has been tested with real data from an existing installation and compared with a simpler electrolyzer model that is based on two states. The results indicate that an operational strategy that considers the multi-state model leads to a decrease in final hydrogen production costs. These reduced costs will benefit businesses, especially while electrolysis plants grow in size to accommodate further increases in demand.     

Hydrogen production from phototrophic microorganisms: Reality and perspectives

Hydrogen is a promising alternative to fossil fuel for a source of clean energy due to its high energy content. Some strains of phototrophic microorganisms are known as important object of scientific research and they are being explored to raise biohydrogen (BioH₂) yield. BioH₂ is still not commonly used in industrial area because of the low biomass yield and valuable down streaming process. This article deals with the methods of the hydrogen production with the help of two large groups of phototrophic microorganisms – microalgae and cyanobacteria. Microalgal hydrogen is environmentally friendly alternative to conventional fossil fuels. Algal biomass has been considered as an attractive raw source for hydrogen production. Genetic modified strains of cyanobacteria are used as a perspective object for obtaining hydrogen. The modern photobioreactors and outdoor air systems have been used to obtain the biomass used for hydrogen production. At present time a variety of immobilization matrices and methods are being examined for their suitability to make immobilized H₂ producers.     

Corrosion-resistant non-noble metal electrodes for PEM-type water electrolyzer

Developing cheap and highly durable non-noble metal catalysts for water electrolysis to sustainably produce hydrogen as alternatives to platinum-based catalysts is essential. Herein, we report graphene-encapsulated NiMo alloys as acid-stable non-noble metal catalyst electrodes. The graphene-encapsulated NiMo cathode showed a highly stable performance in the potential cycling test (10,000 cycles) from 0 to 5.0 A cm⁻² and 100 h of durability at a 2.2 V constant cell voltage. A balance between catalytic activity and corrosion in acidic environments was achieved by tuning the number of N-doped graphene layers. Through their application in a full-cell PEM-type water electrolyzer, we verify that noble metal catalysts can be replaced by non-noble metal catalysts. Such cheap acid-stable non-noble metal electrodes have promising practical applications in PEM-type water electrolysis.     

Hydrogen-rich syngas production by gasification of Urea-formaldehyde plastics in supercritical water

Supercritical water is a promising medium to convert plastics into hydrogen and other recyclable products efficiently. In previous research, supercritical water gasification characteristics investigations focus on thermoplastics instead of thermoset plastics due to its chemical, thermal and mechanical stability. Urea-formaldehyde (UF) plastics were selected as a typical kind of thermoset plastics for investigation in this paper and quartz tubes were used as the reactor in order to avoid the potential catalytic effect of metal reactor wall. Conversion characteristic were studied and the influence of different operating parameters such as temperature, reaction time, feedstock mass fraction and pressure were investigated respectively. The molar fraction of hydrogen could reach about 70% in 700 °C. Products in gas phase and solid phase were analyzed, and properties, chemical structures and inhibition mechanism of thermoset plastics was analyzed after comparing with polystyrene (PS) plastics. The result showed that increase of high temperature and long reaction time could promote gasification process, meanwhile the increase in the feedstock mass fraction would result in suppression of the gasification process. Finally, kinetic study of UF was carried out and the activation energy and pre-exponential factor of the Arrhenius equation were calculated as 30.09 ± 1.62 kJ/mol and 0.1199 ± 0.0049 min⁻¹, respectively.     

Catalyst modification strategies to enhance the catalyst activity and stability during steam reforming of acetic acid for hydrogen production

A high energy content (∼122 MJ/kg H₂) and presence of hydrogen-bearing compounds abundance in nature make hydrogen forth runner candidate to fulfill future energy requirements. Biomass being abundant and carbon neutral is one of the promising source of hydrogen production. In addition, it also addresses agricultural waste disposal problems and will bring down our dependency on fossil fuel for energy requirements. Biomass-derived bio-oil can be an efficient way for hydrogen production. Acetic acid is the major component of bio-oil and has been extensively studied by the researchers round the globe as a test component of bio-oil for hydrogen generation. Hydrogen can be generated from acetic acid via catalytic steam reforming process which is thermodynamically feasible. A number of nickel-based catalysts have been reported. However, the coke deposition during reforming remains a major challenge. In this review, we have investigated all possible reactions during acetic acid steam reforming (AASR), which can cause coke deposition over the catalyst surface. Different operating parameters such as temperature and steam to carbon feed ratio affect not only the product distribution but also the carbon formation during the reaction. Present review elaborates effects of preparation methods, active metal catalyst including bimetallic catalysts, type of support and microstructure of catalysts on coke resistance behavior and catalyst stability during reforming reactions. The present study also focuses on the effects of a combination of a variety of alkali and alkaline earth metals (AAEM) promoters on coke deposition. Effect of specially designed reactors and the addition of oxygen on carbon deposition during AASR have also been analyzed. This review based on the available literature focuses mainly on the catalyst deactivation because of coke deposition, and possible strategies to minimize catalyst deactivation during AASR.     

Valorisation of lignocellulosic biomass investigating different pyrolysis temperatures

Presently, sugarcane bagasse (SB) and oat hulls (OH) have a distinctive potential as a renewable source of biomass, due to its global availability, which is advantageous for producing liquid and gaseous fuels by thermochemical processes. Thermo-Catalytic Reforming (TCR) is a pyrolysis based technology for generating energy vectors (char, bio-oil and syngas) from biomass wastes. This work aims to study the conversion of SB and OH into fuels, using TCR in a 2 kg/h continuous pilot-scale reactor at different pyrolysis temperatures. The pyrolysis temperatures were studied at 400, 450 and 500 °C, while the subsequent reforming temperature remained constant at 500 °C. The bio-oil contained the highest calorific value of 33.4 and 33.5 MJ/kg for SB and OH, respectively at 500 °C pyrolysis temperature, which represented a notable increase compared to the raw material calorific value of SB and OH (16.4 and 16.0 MJ/kg, respectively), this was the result of deoxygenation reactions occurring. Furthermore, the increment of the pyrolysis temperature improved the water content, total acid number (TAN), viscosity and density of the bio-oil. The syngas and the biochar properties did not change significantly with the increase of the pyrolysis temperature. In order to use TCR bio-oil as an engine fuel, it is necessary to carry out some upgrading treatments; or blend it with fossil fuels if it is to be used as a transportation fuel. Overall, TCR is a promising future route for the valorisation of lignocellulosic residues to produce energy vectors.     

Semi-analytical modeling of productivity analysis for five-spot well pattern scheme in methane hydrocarbon reservoirs

Five-spot well pattern (FSWP) scheme has shown appealing potentialities to enhance the recovery of coal-bed methane (CBM) from methane hydrocarbon reservoirs (MHR). In this paper, a new framework aimed at systematically investigating productivity performance of FSWP scheme with inter-well pressure interference (IWPI) is presented. First, mathematical models which are used to characterize the fluid flow within MHR and hydraulic fractures (HFs) are separately derived. Second, Laplace transformation and Stehfest numerical algorithm are utilized to couple those two flow systems and obtain the pressure-transient solutions of FSWP scheme. Finally, pressure characteristics are discerned and sensitivity analysis of key parameters is implemented as well. This semi-analytical approach outperforms numerical simulation from the point of computational efficiency. Several common flow regimes, e.g., linear and bi-linear flow regimes, are essentially deformed induced by IWPI. Several significant parameters, including gas rate, fracture half-length, and well spacing on the occurrence of IWPI are systematically analyzed. This work gains some new knowledge about the productivity performance of FSWP scheme with the existence of IWPI when extracting CBM from methane hydrate reservoirs (MHR), which provides energy engineers considerable instructions on optimizing the development of methane hydrate reservoirs.     

TiO2 photocatalyst with single and dual noble metal co-catalysts for efficient water splitting and organic compound removal

Photocatalysts can be used both for air cleaning and solar energy harvesting through water splitting. However, pure TiO₂ photocatalysts are often inefficient and therefore co-catalysts are needed to improve the yield. To achieve this goal, we prepared TiO₂ and deposited Pt, Ir and Ru co-catalysts on its surface. Two base TiO₂ nanoparticles were used: P25 and rutile TiO₂ synthesized via hydrothermal method. Co-catalysts were deposited by wet impregnation technique using single element and a combination of two elements (Pt and Ir or Pt and Ru), followed by annealing in either air or H₂/Ar. Annealing in reducing atmosphere increased the photocatalytic activity of oxidation of isopropanol compared to annealing in air. We demonstrated a clear influence of the co-catalysts on the photocatalytic degradation of isopropanol and on electrochemical water-splitting reaction. The platinum-containing samples showed the best HER activity.     

Electrocatalytic studies of siloxene sheets encrusted with cobalt chalcogenides (S,Se) for water splitting

Two-dimensional siloxene sheets were superficially coated with cobalt chalcogenides to optimize interfacial properties for broad applications in the field of catalysis. These catalytic composites were investigated for electrochemical water splitting in an alkaline electrolyte medium. The synthesis of siloxene sheet-cobalt chalcogenides composites was confirmed by X-ray diffraction, field emission scanning electron microscopy, high-resolution transmission electron microscopy, adsorption studies, and X-ray photoelectron spectroscopy analyses. Potentiometric and impedimetric experiments were performed to understand the inherent electrocatalytic activity of the developed catalysts. Variations in the onset potential and overpotential at a constant current density of ±10 mA/cm² for hydrogen and oxygen evolution reactions—HER and OER, respectively—were evaluated with respect to a reversible hydrogen electrode (RHE). The catalysts exhibit superior current and catalytic activity due to interfacial kinetics, retaining lower Tafel slopes of ～30 mV/dec for the OER and HER; they also exhibited improved, long-term stability for 12 h, indicating potential utility in commercial applications.     

Assessment of ammonia as energy carrier in the use with reversible solid oxide cells

Ammonia represents one of the most promising potential solutions as energy vector and hydrogen carrier, having a higher potential to transport energy than hydrogen itself in a pressurized form. Furthermore, solid oxide fuel cells (SOFCs) can directly be fed with ammonia, thus allowing for immediate electrical power and heat generation. This paper deals with the analysis of the dynamic behavior of commercial SOFCs when fueled with ammonia. Several measurements at different temperatures have been performed and performances are compared with hydrogen and a stoichiometrically equivalent mixture of H₂ and N₂ (3:1 M ratio). Higher temperature led to smaller drops in voltage for both fuels, thus providing higher efficiencies. Ammonia resulted slightly more performant (48% at 760 °C) than hydrogen (45% at 760 °C), in short stack tests. Moreover, different ammonia-to-air ratios have been investigated and the stack area-specific resistance has been studied in detail by comparing numerical modeling predictions and experimental values.     

Review of hydrogen economy in Malaysia and its way forward

Heavy fossil fuels consumption has raised concerns over the energy security and climate change while hydrogen is regarded as the fuel of future to decarbonize global energy use. Hydrogen is commonly used as feedstocks in chemical industries and has a wide range of energy applications such as vehicle fuel, boiler fuel, and energy storage. However, the development of hydrogen energy in Malaysia is sluggish despite the predefined targets in hydrogen roadmap. This paper aims to study the future directions of hydrogen economy in Malaysia considering a variety of hydrogen applications. The potential approaches for hydrogen production, storage, distribution and application in Malaysia have been reviewed and the challenges of hydrogen economy are discussed. A conceptual framework for the accomplishment of hydrogen economy has been proposed where renewable hydrogen could penetrate Malaysia market in three phases. In the first phase, the market should aim to utilize the hydrogen as feedstock for chemical industries. Once the hydrogen production side is matured in the second phase, hydrogen should be used as fuel in internal combustion engines or burners. In the final phase hydrogen should be used as fuel for automobiles (using fuel cell), fuel-cell combined heat and power (CHP) and as energy storage.     

Effect of B-site Al substitution on hydrogen production of La0.4Sr0.6Mn1-xAlx (x=0.4, 0.5 and 0.6) perovskite oxides

Thermochemical water splitting using perovskite oxides as redox materials is one of the important way to use solar energy to produce green hydrogen. Thus, it is hence important to discover new materials that can be used for this purpose. In this regard, we focused on Al-substituted La_0.4Sr_0.6Mn_1-xAl_xO₃ (x = 0.4, 0.5 and 0.6) perovskite oxides, namely as La_0.4Sr_0.6Mn_0.6Al_0.4 (LSMA4664), La_0.4Sr_0.6Mn_0.5Al_0.5 (LSMA4655), and La_0.4Sr_0.6Mn_0.4Al_0.6 (LSMA4646) which have been successfully synthesized. Herein, synthesized LSMA4664, LSMA4655, and LSMA4646 were subjected to three consecutive thermochemical cycles in order to determine their oxygen capacity, hydrogen capacity, re-oxidation capability and structural stability following three cycles. Thermochemical cycles were carried out at 1400 °C for reduction and 800 °C for the oxidation reaction. LSMA4646 exhibited the highest O₂ production capacity with 275 μmol/g among the other perovskites employed in the study. Moreover, LSMA4646 has also the highest H₂ production, 144 μmol/g, with 90% of re-oxidation capability by the end of three thermochemical water splitting cycles. On the other hand, LSMA4664 has the lowest H₂ production and only kept approximately one-third of its hydrogen production capacity by the end of cycles. Thus, the current study provides insight that the increase in the Al-substitution enhances both oxygen and hydrogen production capacity. Besides, increasing the Al amount increases the structural stability during the redox reactions, the re-oxidation capability was also increased from 38% to 89% after thermochemical cycles.