Hydrogen Production Technologies Research Articles

Exploiting the Ocean Thermal Energy Conversion (OTEC) technology for green hydrogen production and storage: Exergo-economic analysis

This study presents and analyses three plant configurations of the Ocean Thermal Energy Conversion (OTEC) technology. All the solutions are based on using the OTEC system to obtain hydrogen through an electrolyzer. The hydrogen is then compressed and stored. In the first and second layouts, a Rankine cycle with ammonia and a mixture of water and ethanol is utilised respectively; in the third layout, a Kalina cycle is considered. In each configuration, the OTEC cycle is coupled with a polymer electrolyte membrane (PEM) electrolyzer and the compression and storage system. The water entering the electrolyzer is pre-heated to 80 °C by a solar collector. Energy, exergy, and exergo-economic studies were conducted to evaluate the cost of producing, compressing, and storing hydrogen. A parametric analysis examining the main design constraints was performed based on the temperature range of the condenser, the mass flow ratio of hot and cold resource flows, and the mass fraction. The maximum value of the overall exergy efficiency calculated is equal to 93.5% for the Kalina cycle, and 0.524 €/kWh is the minimum cost of hydrogen production achieved. The results were compared with typical data from other hydrogen production systems.

Membrane reformer technology for sustainable hydrogen production from hydrocarbon feedstocks

Hydrogen (H2) is receiving growing interest as a clean energy carrier as the world’s energy system transitions towards net zero. Today, H2 is primarily produced from hydrocarbons using the steam methane reforming (SMR) process. This well-established method converts methane-rich gas into syngas, which is further treated with steam to increase H2 yield via the water-gas-shift (WGS) process. However, this conventional route results in high carbon intensity of 10 tons CO2/ton of H2. Therefore, there is a growing need for sustainable H2 production technologies that utilize existing fossil energy sources and infrastructure while minimizing carbon emissions and costs.Membrane reactors (MR) are a promising technology for sustainable H2 production from hydrocarbons. A H2-selective palladium-alloy (Pd–Au) membrane is integrated within the catalyst bed, creating a system where H2 production and separation occur simultaneously in a single unit. This integration offers several advantages over the conventional system; process intensification allows thermodynamic equilibrium conversion limitations to be overcome while producing high purity (>99%) H2 at milder operating temperatures of ∼550 °C compared to 800–1000 °C in conventional packed bed reactors. Downstream processes such as WGS reactors and pressure swing adsorption are eliminated, resulting in reduced capital and operating costs. Moreover, the by-product stream remains pressurized at 25–40 bar and contains CO2 at concentrations above 60%, enabling CO2 capture at reduced cost.

Graphitic carbon nitride nanosheets decorated with HAp@Bi2S3 core–shell nanorods: Dual S-scheme 1D/2D heterojunction for environmental and hydrogen production solutions

By combining different semiconductors, scientists have developed innovative materials capable of converting solar energy into useful forms of energy or driving chemical reactions that clean up pollutants. These materials offer a promising path to combat global environmental and energy challenges. In this study, HAp@Bi2S3 core–shell structures were synthesized using a facile microemulsion technique, and then loaded onto graphitic carbon nitride via a hydrothermal method to create an advanced HAp@Bi2S3/g-C3N4 dual S-scheme heterojunction. The engineered heterojunction exhibited enhanced hydrogen production and visible light photocatalytic oxidation of metronidazole. The improved photocatalytic efficiency was attributed to the core–shell structure of HAp@Bi2S3 along with the formation of a dual S-scheme heterojunction in HAp@Bi2S3/g-C3N4. As a result, the novel dual S-scheme HAp@Bi2S3/g-C3N4 heterojunction demonstrated a significantly higher hydrogen production rate, ca. 20 times higher than that of hydroxyapatite (HAp), 11 times higher than Bi2S3, and 5 times higher than the HAp@Bi2S3. This research introduces a novel approach to crafting dual S-scheme heterojunctions based on Bi2S3, which enables swift electron transfer across heterojunction interfaces, thereby enlarged possibility windows to sustainable hydrogen production and wastewater remediation technologies.

The influence of operating parameters on the performance of PEMWE electrolytic cell

Proton exchange membrane (PEM) is considered the most promising green hydrogen production technology in the future. The proton exchange membrane electrolysis cell (PEMEC) involves a complex process of multiple physical fields, including charge transfer, gas transfer, and heat transfer, during operation. Increasing the inlet water flow rate within a certain range is beneficial for increasing the output performance of the electrolysis cell and can also reduce the average temperature of the proton exchange membrane. But when the inlet flow rate increases to a certain amount, it has no effect. As the electrolysis voltage increases, the electrochemical performance of the electrolysis cell also increases, and the temperature of the proton exchange membrane and the current density of the catalytic layer also increase with the increase of voltage.

Optimization of Hydrogen Production System Performance Using Photovoltaic/Thermal-Coupled PEM

A proton exchange membrane electrolyzer can effectively utilize the electricity generated by intermittent solar power. Different methods of generating electricity may have different efficiencies and hydrogen production rates. Two coupled systems, namely, PV/T- and CPV/T-coupling PEMEC, respectively, are presented and compared in this study. A maximum power point tracking algorithm for the photovoltaic system is employed, and simulations are conducted based on the solar irradiation intensity and ambient temperature of a specific location on a particular day. The simulation results indicate that the hydrogen production is relatively high between 11:00 and 16:00, with a peak between 12:00 and 13:00. The maximum hydrogen production rate is 99.11 g/s and 29.02 g/s for the CPV/T-PEM and PV/T-PEM systems. The maximum energy efficiency of hydrogen production in CPV/T-PEM and PV/T-PEM systems is 66.7% and 70.6%. Under conditions of high solar irradiation intensity and ambient temperature, the system demonstrates higher total efficiency and greater hydrogen production. The CPV/T-PEM system achieves a maximum hydrogen production rate of 2240.41 kg/d, with a standard coal saving rate of 15.5 tons/day and a CO2 reduction rate of 38.0 tons/day. Compared to the PV/T-PEM system, the CPV/T-PEM system exhibits a higher hydrogen production rate. These findings provide valuable insights into the engineering application of photovoltaic/thermal-coupled hydrogen production technology and contribute to the advancement of this field.

Evaluation of sustainable hydrogen production technologies by fuzzy AHP analysis with bootstrapping

The concept of a hydrogen economy has received increasing attention worldwide. Hydrogen is a promising energy carrier that contributes to the development of a sustainable and reliable energy sector. Selection of the most sustainable hydrogen production technology (HPT) plays a significant role in promoting a hydrogen economy. However, it is regarded as a multi-criteria decision-making (MCDM) problem with several incompatible evaluation criteria. In this study, we develop an MCDM approach based on Fuzzy Analytic Hierarchy Process (FAHP) for prioritizing HPT alternatives, focusing on Egypt as a case study. Our contributions are twofold. First, to combat the issue of a small number of subject matter experts, a bootstrap method is employed to validate the main criteria weights in FAHP. Second, we conduct a comparative FAHP analysis from a broad perspective of the national experts from a developing country and the international experts from developed countries. Our results show that PV electrolysis is the most preferable technology option from the perspectives of both the national and international experts. Since the FAHP approach proposed is a flexible framework that can be applied to countries other than Egypt, it will support global policymakers and industry stakeholders in their decision making toward a sustainable and efficient hydrogen economy strategy.

Progress on Si‐based photoelectrodes for industrial production of green hydrogen by solar‐driven water splitting

AbstractSolar power has been regarded as the ultimate green‐energy source because of its inexhaustibility and eco‐friendliness. The solar‐driven water‐splitting technology for green hydrogen production is considered to be one of effective ways for solar energy harvesting and storage, which may provide solutions for the energy crisis and environmental issues. In the past decades, great progress has been achieved in this area. Photoelectrochemical (PEC) water splitting is especially promising for the production of solar fuels because of expected large‐scale industrial application. Silicon (Si), as an ideal candidate for the photoelectrode, is the most suitable material for the PEC device in industrial photocatalytic water splitting because of its abundance, mature fabrication technology, and suitable band gap. Here, we give a systematic review on the recent progress for Si‐based photoelectrodes for water splitting with a focus on the industrial application. Particularly, the strategies, such as band‐alignment control, morphology design, and surface engineering, are summarized to enhance the PEC performance and durability for practical application. Furthermore, the perspective for the design of commercial Si‐based PEC devices with high PEC performance, long‐term stability, large‐size, and low cost are given at the end, which shall guide the development of PEC water splitting for industrial application.

Control Structures for Combined H2/Electricity from Offshore Wind Turbines

Wind energy proves to be a highly favourable choice for electricity generation due to its clean and renewable nature, and is playing a significant role in reducing global greenhouse gas emissions. Offshore wind turbine systems have gained widespread popularity as they can capitalise on elevated and consistent wind speeds surpassing those found in onshore locations, resulting in increased energy efficiency. Furthermore, offshore wind power possesses the potential to emerge as a significant electricity source for the production of green hydrogen. As water electrolysis technology for hydrogen production continues to advance, utilizing offshore wind power for hydrogen generation is becoming more economically viable and practical. Offshore wind power with higher wind speeds in combination with efficient control structures presents an attractive option for electricity generation and hydrogen co-production. This paper aims to present and evaluate four different production structures for combined H2/energy generation from offshore wind turbines. Previous research studies in this area often overlook control structures and lack information on power converter operations. In contrast, this article studies control structures that enable proper functionality and ensure adequate interoperability, enhancing the reliability of renewable energy integration. Each structure, including both wind turbines and electrolyser, is described in detail, along with the corresponding controllers. Simulation results are presented for each structure and controller to demonstrate their effective operation.

Proton exchange membrane‐based electrocatalytic systems for hydrogen production

AbstractHydrogen energy from electrocatalysis driven by sustainable energy has emerged as a solution against the background of carbon neutrality. Proton exchange membrane (PEM)‐based electrocatalytic systems represent a promising technology for hydrogen production, which is equipped to combine efficiently with intermittent electricity from renewable energy sources. In this review, PEM‐based electrocatalytic systems for H2 production are summarized systematically from low to high operating temperature systems. When the operating temperature is below 130°C, the representative device is a PEM water electrolyzer; its core components and respective functions, research status, and design strategies of key materials especially in electrocatalysts are presented and discussed. However, strong acidity, highly oxidative operating conditions, and the sluggish kinetics of the anode reaction of PEM water electrolyzers have limited their further development and shifted our attention to higher operating temperature PEM systems. Increasing the temperature of PEM‐based electrocatalytic systems can cause an increase in current density, accelerate reaction kinetics and gas transport and reduce the ohmic value, activation losses, ΔGH*, and power consumption. Moreover, further increasing the operating temperature (120–300°C) of PEM‐based devices endows various hydrogen carriers (e.g., methanol, ethanol, and ammonia) with electrolysis, offering a new opportunity to produce hydrogen using PEM‐based electrocatalytic systems. Finally, several future directions and prospects for developing PEM‐based electrocatalytic systems for H2 production are proposed through devoting more efforts to the key components of devices and reduction of costs.

Current Status of Green Hydrogen Production Technology: A Review

As a clean energy source, hydrogen not only helps to reduce the use of fossil fuels but also promotes the transformation of energy structure and sustainable development. This paper firstly introduces the development status of green hydrogen at home and abroad and then focuses on several advanced green hydrogen production technologies. Then, the advantages and shortcomings of different green hydrogen production technologies are compared. Among them, the future source of hydrogen tends to be electrolysis water hydrogen production. Finally, the challenges and application prospects of the development process of green hydrogen technology are discussed, and green hydrogen is expected to become an important part of realizing sustainable global energy development.

Predictive modeling of membrane reactor efficiency using advanced artificial neural networks for green hydrogen production

The imperative to decarbonize the energy sector has prompted substantial advancements in clean electricity generation, with hydrogen emerging as a promising low-carbon energy carrier. While hydrogen synthesis from renewable sources is crucial, challenges persist, necessitating innovative approaches for efficient and sustainable production. This study leverages diverse artificial neural network (ANN) models to assess and predict system efficiency based on key operational variables in membrane reactor systems. The multilayered perceptron (MLP) and radial basis function (RBF) methodologies are employed, with the MLP models optimized across twelve training algorithms and eight activation functions, exploring up to three hidden layers with variable neuron counts. The MLP model, utilizing the Levenberg-Marquard training algorithm and Tangent-Sigmoid activation function, achieved a high correlation coefficient (R2) of 0.9975 for training and 0.9962 for testing, and a mean squared error (MSE) of 0.00425 for training and 0.23951 for testing, indicating precise and accurate efficiency predictions. The Log-Sigmoid activation function also performed well, with R² values of 0.9971 (training) and 0.9961 (testing), and MSE values of 0.004086 (training) and 0.17694 (testing). Optimization of the RBF network identified the best performance with a spread parameter of 1 and 35 neurons, although the MLP model demonstrated superior accuracy and reduced computational time. Statistical analysis, encompassing correlation coefficient, mean squared error, Root Mean Squared error, absolute average deviation, absolute average relative deviation, and runtime, confirms the network’s consistent and accurate estimation of system efficiency across various input variables. The study highlights that applying tansig and logsig activation functions, configured with neuron counts of 20, 17, 6 and 23, 20, 2 at the first, second and third hidden layers, respectively, offers enhanced accuracy and reliability. The MLP model’s high performance underscores its potential to identify optimal conditions for H2 generation based on system efficiency, thereby advancing membrane reactor technology for hydrogen production.

Techno economic analysis of electrolytic hydrogen production by alkaline and PEM electrolysers using MCDM methods

Hydrogen, a crucial clean and renewable energy source, addresses pressing challenges of energy security and environmental pollution. Water electrolysis for hydrogen production is a promising approach to satisfy the growing demand for sustainable energy. This study uniquely performs a comprehensive techno-economic analysis of hydrogen production using both Alkaline and Proton Exchange Membrane (PEM) electrolyzers, a first in the field to evaluate their performance comprehensively with advanced Multi-Criteria Decision-Making (MCDM) techniques. Leveraging TOPSIS, WASPAS interval methods, and the Best Worst Method (BWM) with fuzzy logic, this research introduces a novel evaluation framework that incorporates a wide-ranging set of factors, including environmental, technical, technological, economic, and social aspects, divided into 30 sub-criteria. These insights offer a comprehensive understanding of each electrolyser's strengths and weaknesses, helping stakeholders make informed decisions about cost reduction in hydrogen production technologies. This has not been done before. Although cost results favour Alkaline electrolysers, PEM electrolysers are attractive for specific applications where their benefits justify the higher initial cost, choosing between Alkaline and PEM electrolysers dependent on a given hydrogen production project's requirements.

Comparative assessment of the scientific structure of biomass-based hydrogen from a cross-domain perspective

Biomass-based hydrogen production is an innovative approach for realizing carbon-neutral energy solutions. Despite their promise, both structures differ in terms of the biomass energy domain, which is at the entry point of the technology, and the hydrogen energy domain, which is at the exit point of the technology. In this study, we conducted structural and predictive analyses via cross-domain bibliometric analysis to clarify the differences in the structures and perspectives of researchers across domains and to suggest ways to strengthen collaboration to promote innovation. Our study revealed that the hydrogen energy domain has a balanced impact on realizing a hydrogen society using biomass-based hydrogen production technology, while the biomass energy domain has a strong interest in the process of processing biomass. The results reveal that different communities have different ideas about research, resulting in a divide in the areas to be achieved. This comparative analysis reveals the importance of synergistic progress through interdisciplinary efforts. By filling these gaps, our findings can lead to the development of a roadmap for future research and policy development in renewable energy and highlight the importance of a unified approach to sustainable hydrogen production. The contribution of this study is to provide evidence for the importance of cross-disciplinary cooperation for R&D directors and policy makers.

Regulating Ru-O Bond and Oxygen Vacancies of RuO2 by Ta Doping for Electrocatalytic Oxygen Evolution in Acid Media.

Proton exchange membrane water electrolysis (PEMWE) is considered an ideal green hydrogen production technology with promising application prospects. However, the development of efficient and stable acid electroanalytic oxygen electrocatalysts is still a challenging bottleneck. This progress is achieved by adopting a strategic approach with the introduction of the high valence metal Ta to regulate the electronic configuration of RuO2 by manipulating its local microenvironment to optimize the stability and activity of the electrocatalysts. The Ta-RuO2 catalysts are notable for their excellent electrocatalytic activity, as evidenced by an overpotential of only 202 mV at 10 mA cm-2, which significantly exceeds that of homemade RuO2 and commercial RuO2. Furthermore, the Ta-RuO2 catalyst exhibits exceptional stability with negligible potential reduction observed after 50 h of electrolysis. Theoretical calculations show that the asymmetric configuration of Ru-O-Ta breaks the thermodynamic activity limitations usually associated with adsorption evolution, weakening the energy barrier for the formation of the OOH* formation. The strategic approach presented in this study provides an important reference for the development of a stable active center for acid water splitting.

Improved morphological stability of NiFe2O4 via Sr doping for chemical looping hydrogen production

As a new hydrogen production technology, chemical looping hydrogen production has the advantage of internal CO2 separation. NiFe2O4 is considered as promising oxygen carrier material for chemical looping hydrogen production due to the high oxygen carrying capacity and low cost. However, rapid redox performance fading caused by structure degradation and interface instability in successive redox reactions that led fto poor stability, and seriously limited the practical application of NiFe2O4 in chemical looping hydrogen production. Herein, we reported a method for improving the morphological stability of NiFe2O4 through Sr doping. NiFe2O4 samples containing different SrO contents (2 wt%, 5 wt% and 8 wt%) were prepared by a simple mechanical mixing method. A series of characterization analysis results showed that adding an appropriate amount of Sr could significantly improve the microstructure, increase the oxygen vacancy concentration and inhibit the phase segregation of NiFe2O4. The NiFe-5Sr presented the largest BET surface area (24.63 m2/g) and highest concentration of oxygen vacancies (77.49 %). NiFe-0Sr and NiFe-2Sr experienced severe phase segregation during continuous cyclic reactions, resulting in significant surface sintering and deactivation. During 20 redox cycles, NiFe-5Sr presented the highest hydrogen yield (around 10 mmol/g) and stable surface morphology. The research results indicated that the optimal doping amount for SrO was 5 %.

Interfacial Acid‐Like Microenvironment and Orbital Modulating Strategy toward Efficient Hydrogen Evolution in Neutral High‐Salinity Wastewater/Seawater

Electrochemical high‐salinity wastewater splitting is a promising technology for green hydrogen (H2) production. However, the kinetics of hydrogen evolution reaction (HER) in neutral media is slow, and the high theoretical potential of oxygen evolution reaction leads to large energy losses. Herein, an iron‐based electrocoagulation‐coupled hydrogen production integrated system (IEHPS) is constructed, which is realized by coupling low‐potential anodic iron oxidation reaction with cathodic HER. The non‐noble metal HxWO3‐Ni catalyst is synthesized by fabricating a proton sponge HxWO3 to achieve an interfacial acid‐like microenvironment and doping it with Ni heteroatom to modulate the 4d orbital of W, thereby weakening the adsorption strength of the W site toward hydrogen. Consequently, the HxWO3 Ni demonstrates remarkable performance characteristics, boasting a mere 131 mV overpotential at 10 mA cm−2 and Tafel slope of 44 mV dec− in neutral media. Operating at an applied voltage of 1.5 V, the IEHPS exhibits a high hydrogen production rate of 235 mL g−1 min−1 in seawater. It achieves nearly complete removal of contaminants like rhodamine B and heavy metal ions within a rapid 8–20 min, with an energy consumption of only 3.7 kWh Nm−3. This study provides a promising pathway for efficient and energy‐saving production of high‐purity hydrogen and effective treatment of high‐salinity wastewater.

DEVELOPMENT OF PLASMA RESEARCH AND TECHNOLOGIES AT THE GAS INSTITUTE OF THE NATIONAL ACADEMY OF SCIENCES OF UKRAINE AND THE GLOBAL SITUATION

A multi-faceted analysis of the development of the subject of plasma research and technologies was performed, the center of which is the production of hydrogen from hydrocarbon-containing raw materials. The competitive selection of scientific and technical (experimental) developments under the state order, the implementation of which will begin in 2024 at the expense of the state budget, objectively proved the relevance of the subject matter of the department of plasma processes and technologies. Indeed, immediately two of the total number of 25 competitive works are directly based on plasma technologies in the field of competence of the department. The in-depth history of the initiation at the world level of plasma research or the “fourth state of matter”, as it was called in the 19th century, is analyzed; the outstanding role of the Ukrainian scientist Ivan Pulyuy is shown in it (in addition to his already well-known X-ray research, which is similar in terms of experimental technique). Peculiarities of the early formation of the problem of gasification of hydrocarbon-containing raw materials (as the basis of modern plasma technologies of hydrogen production) are also analyzed on the basis of a comparison of publications from the early period of the existence of the former USSR and Germany. In order to return to historical justice, the most prominent role of the former director of the Gas Institute of the National Academy of Sciences of Ukraine, Academician V.F. Kopytov in the establishment of the institute as a powerful scientific organization and a scientist who also actively supported the development of research into high-temperature processes and plasma technologies. Individual scientific achievements of employees of the department of plasma processes and technologies at various stages of its formation and development are analyzed. The directions of development of plasma technologies are classified according to the physical state of the plasma and areas of application; the developments of the institute are briefly presented according to the directions where they are carried out. Bibl. 77, Fig. 6.

Integrating Pt single atoms and Mo into PtNi/C through Mo doping-displacement synchronisation strategy for enhanced HER at all pH values

This paper proposes a Mo doping-displacement synchronization strategy to integrate Pt SAs and Mo atoms into PtNi/C, synthesizing Pt SAs/Mo-doped PtNi octahedra/carbon support catalyst (Pt SAs/Mo-PtNi/C). In this approach, Mo atoms are doped into PtNi alloy octahedra and displace some Pt atoms, forming Mo-PtNi octahedra. Importantly, the substituted Pt atoms can adhere to carbon substrate, creating Pt SAs. Pt SAs/Mo-PtNi/C exhibits lower overpotentials (38, 59, and 110 mV at 10 mA cm−2) and smaller Tafel slopes (44, 51, and 139 mV dec-1) in acidic, alkaline, and neutral environments. Additionally, the electron pathway of Mo-PtNi → Pt SAs/C has been confirmed, and Pt SAs/Mo-PtNi/C exhibits an optimized hydrogen adsorption energy (ΔGH*=-0.29 eV). Furthermore, catalyzed by Pt SAs/Mo-PtNi/C, the H-O bond length of H2O extends to 1.11 Å and the bond angle reduces to 102.741°, directly confirming that the Pt SAs and doped Mo could facilitate H-O bond breaking. The proposed Mo doping-displacement synchronization strategy not only simplifies the fabrication process of Pt SAs catalyst, but also improves its durability and activity across a wide pH range, thereby potentially advancing hydrogen production technologies.

Research Progress in Structure Evolution and Durability Modulation of Ir- and Ru-Based OER Catalysts under Acidic Conditions.

Green hydrogen energy, as one of the most promising energy carriers, plays a crucial role in addressing energy and environmental issues. Oxygen evolution reaction catalysts, as the key to water electrolysis hydrogen production technology, have been subject to durability constraints, preventing large-scale commercial development. Under the high current density and harsh acid-base electrolyte conditions of the water electrolysis reaction, the active metals in the catalysts are easily converted into high-valent soluble species to dissolve, leading to poor structural durability of the catalysts. There is an urgent need to overcome the durability challenges under acidic conditions and develop electrocatalysts with both high catalytic activity and high durability. In this review, the latest research results are analyzed in depth from both thermodynamic and kinetic perspectives. First, a comprehensive summary of the structural deactivation state process of noble metal oxide catalysts is presented. Second, the evolution of the structure of catalysts possessing high durability is discussed. Finally, four new strategies for the preparation of stable catalysts, "electron buffer (ECB) strategy", combination strength control, strain control, and surface coating, are summarized. The challenges and prospects are also elaborated for the future synthesis of more effective Ru/Ir-based catalysts and boost their future application.

Flexible design of renewable hydrogen production systems through identifying bottlenecks under uncertainty

Renewable hydrogen production technology within the energy sector stands as a vital avenue towards decarbonization in process industries. However, for systems characterized by high penetration of renewable energy, the challenges posed by uncertain parameters impacting stable production present significant obstacles to the large-scale application of hydrogen production from renewable energy. To address the issues, this work proposed a comprehensive four-step strategy for the bottleneck identification and optimization of the renewable hydrogen production systems (RHPS), which encompasses four models including system configuration optimization, flexibility analysis, bottleneck identification, and debottlenecking models. The effectiveness of the proposed strategy is substantiated through a case study. The results indicate that positive fluctuations on supply side and negative fluctuations on demand side contribute to bolstering the flexibility of RHPS. When the RHPS possesses sufficient flexibility, the critical fluctuation amplitude for photovoltaic power is −36 %, whereas for wind turbine power, it stands at −32 %. It highlights that when the photovoltaic power fluctuates, the ability of RHPS to maintain its own stability is stronger than when the wind turbine power fluctuates. Furthermore, when the fluctuations of supply side are positive, the rate of change in critical fluctuation amplitudes on the supply side is 4.63 times than that of the demand side. This underscores that the power decline in the supply side has a more pronounced detrimental effect on the stability of RHPS than an increase in the demand side. The proposed strategy for optimizing RHPS offers valuable theoretical insights for the system design and retrofitting under uncertainty.