Conversion Applications Research Articles

Unidirectional freezing robust PPy@GO-SA aerogel for stable and efficient solar desalination

Solar interfacial evaporation technology is an effective and sustainable method for seawater desalination. It is crucial to achieve high photothermal conversion efficiency, rapid evaporation rate, and long-term stability. In this study, a vertically aligned porous aerogel evaporator is prepared using sodium alginate as the substrate material and graphene oxide (GO) and polypyrrole (PPy) as the photothermal materials through a directional freezing technology. The polypyrrole@graphene oxide-sodium alginate evaporator exhibits a high solar photothermal conversion efficiency as high as 98.6 % and an evaporation rate of up to 4.66 kg·m−2·h−1 under 1 sun. During the 144-hour desalination, the evaporator transports brine for evaporation in the daytime and removes salt residue from the evaporator surface at night. It has demonstrated a self-cleaning behavior and restored its desalination stability. Thus, this aerogel evaporator with a high evaporation rate and stable salt resistance shows great potential for practical applications in solar thermal conversion and seawater desalination.

Conversion of atmospheric CO2 catalyzed by thiolate-based ionic liquids under mild conditions: efficient synthesis of 2-oxazolidinones.

Thiolate-based ionic liquids, specifically the catalyst [TBP][2-Tp], have demonstrated their efficiency in catalyzing the reaction of CO2 with propargylic amine. This novel synthetic method can be used to synthesize various 2-oxazolidinone derivatives with high yields. The catalyst can be easily regenerated and reused without any decline in its catalytic activity. Experimental and spectroscopic investigations have confirmed that the high activity of [TBP][2-Tp] is attributed to the synergistic effect of its S and N sites in activating CO2, rather than depending solely on basicity to activate the amino group of propargylic amine. These findings highlight the significant potential of thiolate-based ionic liquids for applications in CO2 activation and conversion.

Visible Light Active 0.95KNbO3‐0.05Ba(Nb1/2Sc1/2)O3 Ferroelectric for Enhanced Photocatalytic Activity

AbstractThis study reports a visible light active Ba/Sc co‐doped potassium niobate (KNbO3) ferroelectric material for enhanced photocatalytic applications. Through 5% Ba and Sc co‐doping in KNbO3 (i.e., 0.95KNbO3‐0.05Ba(Nb1/2Sc1/2)O3), the electronic band gap (Eg) is narrowed down to the visible range of the solar spectrum. The prepared samples are systematically examined by using X‐ray diffraction and Raman spectroscopy, which confirms the successful incorporation of Ba and Sc ions into the KNbO3 lattice. Scanning electron microscopy (SEM) and energy dispersive spectroscopy (EDS) analysis reveal particle morphology and chemical homogeneity of prepared samples. The UV–vis spectroscopy and ferroelectric PE‐loop demonstrate enhanced optical absorption compared to host KNbO3 while retaining ferroelectric behavior. The photoelectrochemical (PEC) measurements under visible light irradiation demonstrate a notable enhancement in the photocurrent for 0.95KNbO3‐0.05Ba(Nb1/2Sc1/2)O3 (hereafter denoted by 5KBSNO) compared to undoped KNbO3. Additionally, the 5KBSNO sample displays enhanced RhB dye degradation efficiency, reaching ≈50% compared to parent KNbO3 (≈30%) under light irradiation. First‐principles density functional theory (DFT) calculations are employed to understand the mechanism responsible for the reduced band gap. This study presents a promising material for developing advanced ferroelectric photocatalysts with tailored band structures for efficient solar energy harvesting for energy conversion and contamination remediation applications.

Unlocking Unexpected Charge Transfer Pathways in Interconnected Nanostructures.

Accurate control of charge transfer pathways is critical to unlocking the full potential of charge transfer plasmons (CTPs) and exploring their diverse applications. We show that the intentional manipulation of junctions in Al nanocrosses on graphene induces asymmetry, unlocking unexpected charge transfer pathways and facilitating the generation of coupled resonators. The junction asymmetry, which is induced by nanotrench formation facilitated by focused electron beam irradiation, provides a versatile means to achieve precise and controlled interconnect manipulation. We find that tuning the nanotrench dimensions in nanocrosses allows for the tailored modulation of the charge transfer speed and the energies of CTPs. Furthermore, CTPs excited in our experimental nanocrosses, featuring nanotrenches, exhibit weak coupling. This crucial insight underscores the importance of controlled trench formation in unlocking various functionalities of CTPs for use in sensing, catalysis, and energy conversion applications. The controlled manipulation of interconnects in Al nanocrosses thus emerges as a promising avenue for advancing the device performance in these fields.

NiMOF-Derived MoSe2/NiSe Hollow Nanoflower Structures as Electrocatalysts for Hydrogen Evolution Reaction in Alkaline Medium.

Metal-organic frameworks (MOFs) are crystalline porous materials for storage and energy conversion applications with three-dimensional pore structure, high porosity, and specific surface area, which are widely utilized in electrocatalysis. Herein, MoSe2/NiSe composites were synthesized by selenization reaction using NiMOF as the precursor. The composites were hollow nanoflower structures with a synergistic effect between MoSe2 and NiSe to promote rapid electron transfer, which exhibited good hydrogen evolution reaction performance in an alkaline medium. At a current density of 10 mA/cm2, the HER overpotential reaches 80 mV, the Tafel slope is 33.86 mV/dec, and the material has good stability, with polarization curves remaining essentially unchanged after 3000 cycles. These results indicate that the method has a promising application in the preparation of efficient and sustainable catalysts for hydrogen production in alkaline medium.

Revealing Intrinsic Functionalization, Structure, and Photo-Thermal Oxidation in Hexagonal Antimonene.

Antimonene is one of the more exciting members of the post-graphene family with promising applications in optoelectronics, energy storage and conversion, catalysis, sensing or biomedicine. Efforts have been focused on developing a large-scale production route, and indeed, through a colloidal approach, high-quality few-layers antimonene (FLA) hexagons have been recently obtained. However, their oxidation behavior remains unexplored, as well as their interface, inner structure, and photothermal properties. Herein, it is revealed that the hexagons have an intrinsic surface functionalization with alkyl thiols that protects the core of the hexagonal flake against oxidation, and displayed inner defects related to the crystal formation during synthesis, as confirmed by cross-sectional scanning transmission electron microscopy energy dispersive X-ray spectroscopy (STEM-EDX) and temperature-dependent X-ray photoelectron spectroscopy (XPS) and selected area electron diffraction (SAED) analysis. A comprehensive study of temperature and laser power-dependent Raman spectroscopy on varying FLA hexagon thicknesses is carried out. Thinner flakes (<20nm) exhibited a blueshift and intensity decrease, contrasting with thicker ones resembling typical exfoliated flakes with a redshift. This work addresses a literature gap, providing insights into hexagonal FLA structure and characterization, and highlighting the influence of surface functional groups on oxidation behavior. Additionally, it emphasizes the potential of antimonene hexagons as building blocks for 2D heterostructures, including combinations with antimonene oxides and other 2D materials.

Design and Analysis of a Novel Bidirectional DC‐DC Converter With Ultra‐Conversion Ratio and Reduced Current Stress

ABSTRACTConventional nonisolated bidirectional DC‐DC converters are limited because of their low conversion voltage ratio. To overcome the limitation, this paper proposed a new bidirectional DC‐DC converter to introduce the novel regenerative configuration merged with the switched inductor technique for high voltage conversion applications. This design enables extreme DC‐voltage conversion with a minimal number of semiconductors and passive components. As a result, the converter's cost is reduced, and it can attain a high voltage gain with less duty ratio. In general, ultra‐gain converters suffer from high current stress across the input and output side switches in the step‐up and step‐down modes. To reduce high current stress, an active network configuration is imposed in the proposed converter. This paper describes the operating principle, steady‐state analysis of the voltage gain, and presents the performance matrices of the proposed converter. Furthermore, a comparative analysis is made with conventional and recent literature converters. Finally, a 350‐V, 500‐W, and 20‐kHz experimental prototype has been fabricated to validate the operation and corroborate the theoretical waveforms with experimental results.

Novel 2D Material of MBenes: Structures, Synthesis, Properties, and Applications in Energy Conversion and Storage.

2D transition metal borides (MBenes) have garnered significant attention from researchers due to their exceptional electrical conductivity, strong mechanical rigidity, excellent dynamic and thermodynamic stability, which stimulates the enthusiasm of researchers for the study of MBenes. Over the past few years, extensive research efforts have been dedicated to the study of MBenes, resulting in a growing number of synthesis methods being developed. However, there remains a scarcity of comprehensive reviews on MBenes, particularly in relation to the synthesis techniques employed. To address this gap, this review aims to provide a comprehensive summary of the latest research findings on MBenes. An exhaustive exploration of the crystal structure types of MBenes is presented, highlighting the greater structural diversity compared to MXenes. Furthermore, a comprehensive review of the recent advancements in MBenes synthesis methodologies is provided. The review also delves into the physical and chemical properties of MBenes, while elucidating their applications in the realms of energy conversion and energy storage. Lastly, this review concludes by summarizing and offering insights on MBenes from three angles: synthesis, structure-property relationships, and application prospects.

Unlocking the Electrocatalytic Behavior of Cu2MnS2 Nanoflake-Anchored rGO for the Oxygen Evolution Reaction in an Alkaline Medium.

A catalyst of the oxygen evolution reaction (OER) that is viable, affordable, and active for effective water-splitting applications is critical. A variety of electrocatalysts have been discovered to replace noble metal-based catalysts. Of these, transition metal-based sulfides are essential for incorporating carbonaceous materials to improve electrical conductivity, resulting in better electrocatalytic performance. Our study illustrates the synthesis of Cu2MnS2 (CMS) nanoflakes and their different rGO composites (10 to 40 wt %) via a hydrothermal technique for an effective water oxidation reaction. The X-ray diffraction pattern reveals that the prepared Cu2MnS2 nanoflakes exhibit a cubic crystal structure. The high-resolution scanning electron microscopy and the high resolution transmission electron microscopy images corroborate the formation of the nanoflake-like morphology of Cu2MnS2 with the strong interaction of rGO. The selected area electron diffraction analysis pattern reveals a polycrystalline nature. The Fourier transform infrared spectrum shows the existence of a metal sulfur vibrational band at 590 cm-1, and Raman analysis infers the presence of rGO. The X-ray photoelectron spectroscopy spectra reveal the oxidation states of the elements present in the samples. Using Brunauer-Emmett-Teller analysis, the surface area of CMS-20 is found to be 117.04 m2/g. The measured OER overpotentials using linear sweep volammetry and the values are 380, 370, 340, 376, and 400 mV at 10 mA/cm2 for CMS, CMS-10, CMS-20, CMS-30, and CMS-40, respectively, and the corresponding Tafel slope values are 179, 158, 149, 206, and 240 mV/decade, respectively. The electrochemical active surface area is estimated using cyclic voltammetry for all of the catalysts, where CMS-20 showed a larger surface area. Also, the same catalyst exhibits good stability for ∼24 h at a constant potential, which is confirmed via chronoamperometry. Thus, combining transition metal-based sulfides with carbonaceous materials indicates improved catalytic behavior for the preparation of high-performance OER electrocatalysts. Overall, the prepared CMS-20 performed as an efficient OER electrocatalyst and can be utilized for practical applications in energy conversion.

Regulating Composition and Structure of Coal-based Graphene and Its Electrochemical Characteristics

Abstract Coal, a carbon-rich mineral with plentiful reserves, serves not only as a fuel but also as a raw material, presenting lower pollution emissions in the latter use. From a materials chemistry standpoint, coal is a viable raw material for graphene production. This study develops a promising and sustainable method to convert coal into graphene, leveraging its unique macromolecular aromatic structure and high carbon content. The investigation includes an analysis of the lateral size, morphology, and chemical composition of coal-derived graphene using techniques such as X-ray diffraction, Raman spectroscopy, X-ray photoelectron spectroscopy, and optical microscopy. Results confirm that coal can effectively replace natural graphite flakes in graphene production, with the derived graphene featuring 3-6 exfoliated layers and an oxygen content below 5.5%. While the graphene from coal shares a similar morphology to that derived from graphite, it exhibits more structural defects. Interestingly, the macroscopic size of the coal does not influence the microscopic composition and structure of the graphene. However, the thermal reduction method for oxidized graphene proves more effective at repairing structural defects than chemical reduction. Employing coal-derived graphene as a supercapacitor electrode demonstrates excellent cycling stability and ultra-high capacitance storage capacity. The H-CG-325 shows the highest discharge area-specific capacitance across various current densities. At an increased current density of 10 A/g, the H-CG-325 maintains 80.6% of its initial capacitance of 79 F/g observed at 1 A/g. Electrochemical tests reveal that coal-based graphene holds significant potential as a supercapacitor material, indicating promising applications in energy storage and conversion.

Copper-catalyzed plastic waste synthesized graphene nanosheets/polypyrrole nanocomposites for efficient thermoelectric applications

Presently, various catalysts have been reported for the synthesis of carbon nanomaterials from a variety of plastic waste, which needs to be removed at the end of the synthesis process by using chemical techniques and hence make the process more typical from the aspect of cost-benefit and circular economic aspects. Herewith, we report copper turnings as the cost-effective and greener catalytic templates for synthesizing highly conducting graphene nanosheets (GNs). The synthesis of the GNs from plastic waste was done as we previously reported in the steps of the pyrolytic process, where the copper turnings are used as catalytic templates in the present study. Because of the excellent catalytic efficiency towards breaking old carbon-carbon bonds and forming new carbon-carbon bonds, the copper turnings act as an excellent degradation catalyst and promote the growth of graphitic skeletons and, consequently, graphene nanosheets. The synthesized GNs showed a high conductivity of ∼ 1730 S/m. GNs thus synthesized is implemented for synthesizing GNs/polypyrrole nanocomposites, which is later investigated for the TE applications. The values of the Seebeck coefficient showed that the composite of GNs/polypyrrole performs as a p-type semiconductor. The TE figure of merit (ZT) for GNs/polypyrrole demonstrated good thermoelectric characteristics and showed a value of 3.75 × 10−6 at the temperature. Thus, the present method of synthesis of GNs showed a more convenient, industrial friendly technique for the production of plastic waste derived graphene nanosheets and its application for thermal energy conversion applications.

Online DMD-based Kalman filter for current sensor fault-tolerant control of MMC-HVDC transmission systems

With the growing application of modular multilevel converter based high-voltage direct current transmission (MMC-HVDC), the sensor fault-tolerant capability in modular multilevel converters has become critical. This paper aims to boost the sensor fault-tolerant performance of the MMC-HVDC systems using advanced data-driven techniques. A novel online dynamic mode decomposition based Kalman filter (ODMDKF) is designed for fault detection and control reconfiguration. Besides, a modified dual-check fault detection module based on local outlier factor algorithm is proposed to reduce false alarm rate. Simulation studies are conducted on a modified IEEE 9-bus system with MMC-HVDC transmission lines. The results indicate that the proposed sensor fault-tolerant control method can ensure the continuous operation of the MMC-HVDC systems under the condition of three types of current sensor faults and its fault-tolerant capability is better than that of extended Kalman filter-based fault-tolerant control method.

Enhanced oxygen evolution reaction in alkaline water electrolysis using bimetallic NiFe metal-organic frameworks integrated with carbon nanotubes

Hydrogen is considered a very clean and highly available renewable energy resource for the future. Water electrolysis (WE) is a conspicuous promising technology to produce hydrogen on a large scale, without generating carbon dioxide. In this study, we prepared bimetallic NiFe-based metal–organic frameworks (MOFs) integrated with CNTs (NiFe–BTC@CNTs) as highly efficient electrocatalysts for the oxygen evolution reaction (OER) in alkaline water electrolysis. Combining NiFe MOFs and CNTs significantly enhanced the electrochemical performance and structural integrity of the catalyst. The NiFe–BTC@CNT (30 wt% CNTs) demonstrates a significant low overpotential of 230 mV at 10 mA·cm⁻2, superior catalytic activity with a Tafel slope of 36 mV·dec⁻1, and excellent stability under both constant and dynamic operating conditions. These unique characteristics are attributed to the high surface area and abundant active sites provided by the bimetallic MOF structure, combined with the exceptional electrical conductivity and mechanical strength of CNTs. Furthermore, the integration of CNTs improves the dispersion while preventing the agglomeration of MOF particles, ensuring a more uniform and accessible active surface area. This research highlights the potential of the NiFe–BTC@CNT catalysts as high-performance durable electrocatalysts for sustainable hydrogen production, offering a significant advance in the development of advanced materials for energy conversion and storage applications.

DEVELOPMENT PROCESS OF A FREQUENCY CONVERTER FOR INDUCTION HEATING OF OIL PIPELINE

The article provides a detailed overview of the history, development and applications of frequency converters, with particular emphasis on their use in the oil and gas industry. It traces the evolution of frequency converters from their inception in the late 19th and early 20th centuries to their modern applications, which use microprocessors and digital signal processing to precisely control the output frequency. In the oil and gas industry, frequency converters are critical to efficient and accurate induction heating of pipelines. They convert a fixed frequency and voltage power supply into a variable frequency and variable voltage output, controlling the speed of the induction motors used in the heating process. The article also covers the design and modeling of frequency converters, discussing the process of characterizing them, creating mathematical models, and using modeling software tools such as MatLab. It presents equations for inductive energy, capacitor energy, resonance conditions and power factor, which are necessary in the mathematical modeling of frequency converters. The article concludes by highlighting the impact of frequency converters on the efficiency and economics of induction heating systems. It emphasizes the need for careful design and modeling to ensure optimal performance and safety.

Enhancing electromechanical conversion and motion-monitoring application of pore-oriented cellulose nanocrystal/agarose aerogel modified with flexible heterojunction structures

Oriented-porous cellulose nanocrystal (CNC)-based aerogels excel in directional energy conversion but face reduced toughness, and triboelectric performance bottlenecks owing to the absence of electron acceptors. In this work, we crosslinked quaternary ammonium CNC with another flexible carboxymethyl agarose (AG-), via borate dynamic bonds, exploiting the electron-accepting traits of boron and electrophilic modifications to boost the mechanical and triboelectric performance of aerogels. These results demonstrate that the compressive resilience and modulus of CNC/AG aerogel are improved up to 70.79 % (after 10-cycle 20 % strain) and 18.77 kPa attributing to the borate cross-linking network and oriented structure. Furthermore, the electromechanical response sensitivity and output energy density of the CNC/AG aerogel increased by 6.06 times (to 7.51 V/Hz) and 28.3 times (to 1.87 W/m2), respectively. The structure characteristics of the CNC/AG aerogel reveal that the oriented structure and heterojunction of the CNC/AG aerogel with electron transfer pathways reduce dielectric losses. The COMSOL simulation also show that oriented pores increase the polarization and charge density of the CNC/AG aerogel, thereby improving the electromechanical conversion efficiency. This work offers a synergistic approach for toughening aerogels and generating heterojunctions via flexible modification, presenting significant potential for smart devices with energy-collection ability.

Advanced approach for active and durable proton exchange membrane fuel cells: Coupling synergistic effects of MNC nanocomposites

AbstractAtomically dispersed metal and nitrogen co‐doped carbon (MNC) is a promising oxygen reduction reaction (ORR) catalyst for electrochemical energy storage and conversion applications but typically suffers from low durability and activity under the acidic conditions of practical polymer electrolyte exchange membrane fuel cells (PEMFCs). Recently, the performance of MNC nanocomposites under acidic ORR conditions has been enhanced by exploiting the synergistic coupling effects of their constituents (single‐atom sites, nanoclusters, and nanoparticles). The unique geometric structures formed by the coupling of diverse sites in these nanocomposites provide optimal electronic structures and efficient reaction pathways, thus resulting in high activity and long‐term durability. This work provides an overview of MNC nanocomposites as ORR electrocatalysts under practical PEMFC conditions, focusing on activity and durability enhancement methods and highlighting the strategies used to prepare electrocatalytically efficient MNC nanocomposites containing no or low amounts of platinum group metals. Progress in the development of advanced MNC nanocomposites as acidic ORR catalysts is discussed, and the pivotal role of synergistic effects resulting from the coupling sites within the nanocomposites is explored together with the characterization methods used to elucidate these effects. Finally, the challenges and prospects of developing MNC nanocomposites as next‐generation electrocatalysts are presented.image

Improving of thermoelectric figure of merit in Sr0.925Dy0.075TiO3 ceramics

Rare earth doped SrTiO3 is one of the most promising oxide materials meeting the safety and stability requirements for potential applications in thermoelectric converters. This work aims to assess the feasibility of engineering SrTiO3-based materials to improve their thermoelectric performance. A comparative analysis of the thermoelectric properties of Sr0.925Dy0.075TiO3 ceramic samples obtained from preliminarily mechanically activated Sr0.925Dy0.075TiO3 nano-powder by two methods – solid-state reaction synthesis and spark plasma sintering – was carried out. Significant differences in the morphology of the samples lead to significant differences in the temperature dependences of electrical resistivity and the Seebeck coefficient. Ceramics obtained by solid-state reaction synthesis exhibit lower porosity and lower electrical resistivity. The thermoelectric power factor of such ceramics is 2–3 times higher than that of samples obtained by spark plasma sintering. The obtained value of thermoelectric figure of merit ZT = 0.41 at T = 673 K for Sr0.925Dy0.075TiO3 is the highest value among n-type oxide thermoelectric ceramics at a given temperature and maintains a tendency to increase with increasing temperature.

AI in higher education: unveiling academicians’ perspectives on teaching, research, and ethics in the age of ChatGPT

ABSTRACT This study examines the potentials and challenges of integrating conversational AI (Artificial Intelligence) tools in higher education. Specifically, the study delves into how ChatGPT is reshaping teaching, learning, research, and student evaluation while addressing ethical concerns such as academic integrity. We employ a qualitative research design based on semi-structured interviews with 12 highly accomplished academicians from North America, Asia, and Europe’s higher education institutions. Our analysis reveals ChatGPT’s potential to uplift educational productivity, learning outcomes, creativity, and idea generation but raises apprehensions about academic honesty, authenticity, and over-reliance. While ChatGPT can enhance educational practices such as brainstorming, analysis, and skills acquisition, its unchecked use may impede learning, critical thinking, and research quality. The study advocates for the responsible AI use in academia, underscoring educators and policymakers to establish policies guiding conversational AI ethical applications. Thus, training faculty and executing institutional policies are essential for effective and ethical integration of ChatGPT and other AI tools in higher education. Finally, this research contributes to ongoing research on AI in education by providing valuable insights that can harness potential of these transformative tools while upholding academic integrity and standards.

Semi-Ionic F Modified N-Doped Porous Carbon Implanted with Ruthenium Nanoclusters towardHighlyEfficient pH-Universal Hydrogen Generation.

Developing high electroactivity ruthenium (Ru)-based electrocatalysts for pH-universal hydrogen evolution reaction (HER) is challenging due to the strong bonding strengths of key Ru─H/Ru─OH intermediates and sluggish water dissociation rates on active Ru sites. Herein, a semi-ionic F-modified N-doped porous carbon implanted with ruthenium nanoclusters (Ru/FNPC) is introduced by a hydrogel sealing-pyrolying-etching strategy toward highly efficient pH-universal hydrogen generation. Benefiting from the synergistic effects between Ru nanoclusters (Ru NCs) and hierarchically F, N-codoped porous carbon support, such synthesized catalyst displays exceptional HER reactivity and durability at all pH levels. The optimal 8Ru/FNPC affords ultralow overpotentials of 17.8, 71.2, and 53.8mV at the current density of 10mA cm-2 in alkaline, neutral, and acidic media, respectively. Density functional theory (DFT) calculations elucidate that the F-doped substrate to support Ru NCs weakens the adsorption energies of H and OH on Ru sites and reduces the energy barriers of elementary steps for HER, thus enhancing the intrinsic activity of Ru sites and accelerating the HER kinetics. This work provides new perspectives for the design of advanced electrocatalysts by porous carbon substrate implanted with ultrafine metal NCs for energy conversion applications.

Enhancing Performance and Stability of Perovskite Solar Cells with a Novel Formamidine Group Additive.

Perovskite materials, particularly FAPbI3, have emerged as promising candidates for solar energy conversion applications. However, these materials are plagued by well-known defects and suboptimal film quality. Enhancing crystallinity and minimizing defect density are therefore essential steps in the development of high-performance perovskite solar cells. In this study, 1H-Pyrazole-1-carboximidamide hydrochloride (PCH) is introduced into FAPbI3 perovskite films. The molecular structure of PCH features a pyrazole ring bonded to formamidine (FA). The FA moiety of PCH facilitated the incorporation of this additive into the film lattice, while the negatively charged pyrazole ring effectively passivated positively charged iodine vacancies. The presence of PCH led to the fabrication of an FAPbI3 device with improved crystallinity, a smoother surface, and reduced defect density, resulting in enhanced Voc and fill factor. A record power conversion efficiency of 24.62% is achieved, along with exceptional stability under prolonged air exposure and thermal stress. The findings highlight the efficacy of PCH as a novel additive for the development of high-performance perovskite solar cells.