Hybrid Structure Research Articles

Helical Hybrid Nanostructure Based on Chiral M13 Bacteriophage via Evaporation-Induced Three-Dimensional Process

The use of naturally sourced organic materials with chirality, such as the M13 bacteriophage, holds intriguing implications, especially in the field of nanotechnology. The chirality properties of bacteriophages have been demonstrated through numerous studies, particularly in the analysis of liquid crystal phase transitions, developing specific applications. However, exploring the utilization of the M13 bacteriophage as a template for creating chiral nanostructures for optics and sensor applications comes with significant challenges. In this study, the chirality of the M13 bacteriophage was leveraged as a valuable tool for generating helical hybrid structures by combining it with nanoparticles through an evaporation-induced three-dimensional (3D) printing process. Utilizing on the self-assembly property of the M13 bacteriophage, metal nanoparticles were organized into a helical chain under the influence of the M13 bacteriophage at the meniscus interface. External parameters, including nanoparticle shape, the ratio between the bacteriophage and nanoparticles, and pulling speed, were demonstrated as crucial factors affecting the fabrication of helical nanostructures. This study aimed to explore the potential of chiral nanostructure fabrication by utilizing the chirality of the M13 bacteriophage and manipulating external parameters to control the properties of the resulting hybrid structures.

Syntheses and Applications of Coumarin-Derived Fluorescent Probes for Real-Time Monitoring of NAD(P)H Dynamics in Living Cells across Diverse Chemical Environments.

Fluorescent probes play a crucial role in elucidating cellular processes, with NAD(P)H sensing being pivotal in understanding cellular metabolism and redox biology. Here, the development and characterization of three fluorescent probes, A, B, and C, based on the coumarin platform for monitoring of NAD(P)H levels in living cells are described. Probes A and B incorporate a coumarin-cyanine hybrid structure with vinyl and thiophene connection bridges to 3-quinolinium acceptors, respectively, while probe C introduces a dicyano moiety for replacement of the lactone carbonyl group of probe A which increases the reaction rate of the probe with NAD(P)H. Initially, all probes exhibit subdued fluorescence due to intramolecular charge transfer (ICT) quenching. However, upon hydride transfer by NAD(P)H, fluorescence activation is triggered through enhanced ICT. Theoretical calculations confirm that the electronic absorption changes upon the addition of hydride to originate from the quinoline moiety instead of the coumarin section and end up in the middle section, illustrating how the addition of hydride affects the nature of this absorption. Control and dose-response experiments provide conclusive evidence of probe C's specificity and reliability in identifying intracellular NAD(P)H levels within HeLa cells. Furthermore, colocalization studies indicate probe C's selective targeting of mitochondria. Investigation into metabolic substrates reveals the influence of glucose, maltose, pyruvate, lactate, acesulfame potassium, and aspartame on NAD(P)H levels, shedding light on cellular responses to nutrient availability and artificial sweeteners. Additionally, we explore the consequence of oxaliplatin on cellular NAD(P)H levels, revealing complex interplays between DNA damage repair, metabolic reprogramming, and enzyme activities. In vivo studies utilizing starved fruit fly larvae underscore probe C's efficacy in monitoring NAD(P)H dynamics in response to external compounds. These findings highlight probe C's utility as a versatile tool for investigating NAD(P)H signaling pathways in biomedical research contexts, offering insights into cellular metabolism, stress responses, and disease mechanisms.

Residual squeeze-and-excitation convolutional auto-encoder for fault detection and diagnosis in complex industrial processes

Recently, deep learning has attracted increasing attention in process monitoring. However, it is still a big challenge to extract effective features of process data for fault detection and diagnosis (FDD) by using deep learning-based methods. In this study, a novel deep learning-based model, residual squeeze-and-excitation convolutional auto-encoder (RSECAE) is proposed for FDD in complex industrial processes. A hybrid structure that integrates convolution calculation and auto-encoder is proposed to construct multiple convolution layers and deconvolution layers in the encoder and decoder respectively. Thus, RSECAE can learn effective features from the process signals in an unsupervised manner. At the same time, multiple residual squeeze-and-excitation networks (RSENets) are embedded in the deep network, which effectively preserves the critical feature representations of the convolution layer and transmits them to the decoder in the form of residuals. Finally, maximum mean discrepancy (MMD) term is utilized in RSECAE to reduce the distribution difference between the process signals and the learned features. This enables RSECAE to extract effective features with prior distribution information. RSECAE provides a new solution for process FDD for complicated industrial processes. Two industrial cases are adopted to validate the effectiveness of the RSECAE in process FDD. The experimental results demonstrate the effectiveness and superiority of RSECAE in process fault detection and fault diagnosis.

Boosting Microfluidic Enzymatic Cascade Reactions with pH-Responsive Polymersomes by Spatio-Chemical Activity Control.

Microfluidic flow reactors permit the implementation of sensitive biocatalysts in polymeric environments (e.g., hydrogel dots), mimicking nature through the use of diverse microstructures within defined confinements. However, establishing complex hybrid structures to mimic biological processes and functions under continuous flow with optimal utilization of all components involved in the reaction process represents a significant scientific challenge. To achieve spatial, chemical, and temporal control for any microfluidic application, compartmentalization is required, as well as the unification of different sensitive compartments in the reaction chamber for the microfluidic flow design. This study presents a self-regulating microfluidic system fabricated by a sequential photostructuring process with an intermediate chemical process step to realize pH-sensitive hybrid structures for the fabrication of a microfluidic double chamber reactor for controlled enzymatic cascade reaction (ECR). The key point is the adaptation and retention of the function of pH-responsive horseradish peroxidase-loaded polymersomes in a microfluidic chip under continuous flow. ECR is successfully triggered and controlled by an interplay between glucose oxidase-converted glucose, the membrane state of pH-responsive polymersomes, and other parameters (e.g., flow rate and fluid composition). This study establishes a promising noninvasive regulatory platform for extended spatio-chemical control of current and future ECR and other cascade reaction systems.

Effect of soil conditioners based on geomimetic materials on plant growth in degraded soils: Poly(acrylic acid)/bentonite

Geomimetic materials (GEOMI) are composite materials based on polymer and clays, able to imitate structural and functional properties of soils, including their structure, cationic exchange capability (CEC), water uptake capability (WUC), pH buffering ability, immobilizing of substances, among other. Because they can be used to develop of fertilizer slow-release systems, they have been identified as a novel approach to advance toward a most sustainable agriculture. The aim of this work was to study the effect of GEOMI on the plant growth in degraded soils. For this, GEOMI-1.0 was synthesized using poly(acrylic acid) as model of humic substances and bentonite modified with trichlorovinylsilane as mineral fraction model. Materials were characterized by different techniques. GEOMI-1.0 showed a hybrid, homogeneous, and amorphous structure. In addition, it was thermally stable at below ⁓200 °C with a Tg about 49.3 °C, showed a high WUC (⁓1384 g of water per 100 g of material). Likewise, it was verified that GEOMI-1.0 can decreases the pH values and increases the CEC of degraded soils depending on the added amount of geomaterial; but also, the electric conductivity values showed no dependence on the added amount of GEOMI-1.0. By correlation analysis, an exponential dependence of CEC was observed respect to pH changes, the relative amount added of GEOMI-1.0 and the initial CEC. Finally, using Brachiaria Brizantha cv. Marandú as plant model, the increase in the biomass content of roots and leaves, and the number of germinated seeds, were observed when GEOMI-1.0 was used for restoration of in-lab degraded soils.

Synthesis of biocompatible Ti-6Al-4V composite reinforced with ZrO2 and bioceramic produced by powder metallurgy: Morphological, structural, and biocompatibility analysis.

In this experimental study, the initial phase involved preparing composite structures with various mix ratios using the Ti-6Al-4V alloy, widely used in clinical applications, in conjunction with ZrO2 and hydroxyapatite (HA) synthesized via the precipitation method, employing powder metallurgy techniques. Subsequently, the microstructures of the resultant hybrid composite materials were imaged, and x-ray diffraction (XRD) phase analyses were conducted. In the final phase of the experimental work, tests were performed to determine the biocompatibility properties of the hybrid composites. For this purpose, cytotoxicity and genotoxicity assays were carried out. The tests and examinations revealed that structures compatible both morphologically and elementally were obtained with no phase transformations that could disrupt the structure. The incorporation of ZrO2 into the Ti-6Al-4V alloy was observed to enhance cell viability values. The value of 98.25 ± 0.42 obtained by adding 20% ZrO2 gave the highest cell viability result. The addition of HA into the hybrid structures further increased the cell viability values by approximately 10%. All viability values for both HA-added and HA-free groups were obtained above the 70% viability level defined in the standard. According to the genotoxicity test results, the highest cytokinesis-block proliferation index values were obtained as 1.666 and 0.620 in structures containing 20% ZrO2 and 10% ZrO2 + 10% HA, respectively. Remarkably, all fabricated composite and hybrid composite materials surpassed established biocompatibility standards and exhibited nontoxic and nongenotoxic properties. This comprehensive study contributes vital insights for future biomechanical and other in vitro and in vivo experiments, as it meticulously addresses fundamental characterization parameters crucial for medical device development. RESEARCH HIGHLIGHTS: Support of optimum doping rates ions on hybrid composites and concentrations. Development of uniform surface appearance and distributions/orientations of microcrystals on ceramic compounds Improvement of cell viability and desired increase in biocompatibility with the doping of HA.

Dual band high tuning range frequency reconfigurable dielectric resonator antenna for sub-6 GHz applications

ABSTRACT A high-tuning range frequency reconfigurable dual-band compact cylindrical Dielectric Resonator Antenna (DRA) for 5 G Sub 6 GHz applications is presented in the proposed work. The work presented here provides compactness, frequency reconfigurability (FR), and dual-band. FR is obtained through two PIN diode switches, which operate in ON-ON, ON-OFF, OFF-ON, and OFF-OFF configurations and offer a maximum wide tuning range and a total spectrum of 44.44% and 71.49%, respectively. In the cylindrical DRA, the HE M 11 δ and HE M 12 δ modes create dual-band, while the hybrid structure and higher order mode excitation yield compactness.

Dual band high tuning range frequency reconfigurable dielectric resonator antenna for sub-6 GHz applications

ABSTRACT A high-tuning range frequency reconfigurable dual-band compact cylindrical Dielectric Resonator Antenna (DRA) for 5 G Sub 6 GHz applications is presented in the proposed work. The work presented here provides compactness, frequency reconfigurability (FR), and dual-band. FR is obtained through two PIN diode switches, which operate in ON-ON, ON-OFF, OFF-ON, and OFF-OFF configurations and offer a maximum wide tuning range and a total spectrum of 44.44% and 71.49%, respectively. In the cylindrical DRA, the HE M 11 δ and HE M 12 δ modes create dual-band, while the hybrid structure and higher order mode excitation yield compactness.

Harnessing Persistent Photocurrent in a 2D Semiconductor-Polymer Hybrid Structure: Electron Trapping and Fermi Level Modulation for Optoelectronic Memory.

Recently, 2D semiconductor-based optoelectronic memory has been explored to overcome the limitations of conventional von Neumann architectures by integrating optical sensing and data storage into one device. Persistent photocurrent (PPC), essential for optoelectronic memory, originates from charge carrier trapping according to the Shockley-Read-Hall (SRH) model in 2D semiconductors. The quasi-Fermi level position influences the activation of charge-trapping sites. However, the correlation between quasi-Fermi level modulations and PPC in 2D semiconductors has not been extensively studied. In this study, we demonstrate optoelectronic memory based on a 2D semiconductor-polymer hybrid structure and confirm that the underlying mechanism is charge trapping, as the SRH model explains. Under light illumination, electrons transfer from polyvinylpyrrolidone to p-type tungsten diselenide, resulting in high-level injection and majority carrier-type transitions. The quasi-Fermi level shifts upward with increasing temperature, improving PPC and enabling optoelectronic memory at 433 K. Our findings offer valuable insights into optimizing 2D semiconductor-based optoelectronic memory.

Fabricating Spinel-Type High-Entropy Oxides of (Co, Fe, Mn, Ni, Cr)3O4 for Efficient Oxygen Evolution Reaction

Fabricating efficient oxygen evolution reaction (OER) electrocatalysts is crucial for water electrocatalysis. Herein, the spinel-type high-entropy oxides of (Co, Fe, Mn, Ni, Cr)3O4 were synthesized through the high-temperature calcination approach. The influences of calcination temperatures on structures and electrochemical properties were investigated. The optimized catalyst of HEO-900 contains the hybrid structure of regular polyhedrons and irregular nanoparticles, which is beneficial for the exposure of electrochemically active sites. It was identified that the abundant high-valence metal species of Ni3+, Co3+, Fe3+, Mn4+, and Cr3+ are formed during the OER process, which is generally regarded as the electrochemically active sites for OER. Because of the synergistic effect of multi-metal active sites, the optimized HEO-900 catalyst indicates excellent OER activity, which needs the overpotential of 366 mV to reach the current density of 10 mA cm−2. Moreover, HEO-900 reveals the prominent durability of running for 24 h at the current density of 10 mA cm−2 without clear delay. Therefore, this work supplies a promising route for preparing high-performance multi-metal OER electrocatalysts for water electrocatalysis application.

Harnessing Persistent Photocurrent in a 2D Semiconductor-Polymer Hybrid Structure: Electron Trapping and Fermi Level Modulation for Optoelectronic Memory.

Recently, 2D semiconductor-based optoelectronic memory has been explored to overcome the limitations of conventional von Neumann architectures by integrating optical sensing and data storage into one device. Persistent photocurrent (PPC), essential for optoelectronic memory, originates from charge carrier trapping according to the Shockley-Read-Hall (SRH) model in 2D semiconductors. The quasi-Fermi level position influences the activation of charge-trapping sites. However, the correlation between quasi-Fermi level modulations and PPC in 2D semiconductors has not been extensively studied. In this study, we demonstrate optoelectronic memory based on a 2D semiconductor-polymer hybrid structure and confirm that the underlying mechanism is charge trapping, as the SRH model explains. Under light illumination, electrons transfer from polyvinylpyrrolidone to p-type tungsten diselenide, resulting in high-level injection and majority carrier-type transitions. The quasi-Fermi level shifts upward with increasing temperature, improving PPC and enabling optoelectronic memory at 433 K. Our findings offer valuable insights into optimizing 2D semiconductor-based optoelectronic memory.

Interfacial characteristics of Nickel-based hybrid structures fabricated using directed energy deposition

The wire-arc directed energy deposition technique was used to develop nickel-based hybrid structures or to repair conventional structures of nickel-718 superalloy. Three different cases were investigated: deposited IN718 and IN625, separately, over the conventional IN718 substrate and deposited IN718 over the previously deposited IN625 substrate. The interfacial characteristics with respect to the microstructural features, residual stresses, compositional changes, etc., were studied using a finite element computational framework and a Monte-Carlo grain growth model. The numerical results were successfully validated with the experimental results. All the hybrid structures revealed excellent interfacial bonding with no defects, as evidenced by the failures outside the interface during their tensile tests. However, the interfacial characteristics differed for each material condition. The results discussed in this study will improve the understanding of developing nickel-based hybrid structures using additive methods and can potentially be beneficial in repairing industrial components.

Tunable Radiation Patterns on Temperature-Dependent Materials

The utilization of optical antennas for active control of far-field radiation at the subwavelength scale is crucial in various scientific and technological applications. We propose a thermally tunable disk design of indium tin oxide (ITO) and aluminum gallium nitride (Al0.18Ga0.82As), enabling a switch between absorption and scattering. Furthermore, the control of far-field radiation pattern can be easily realized by combining ITO and Al0.18Ga0.82As to enhance or suppress emission. Our results demonstrate that hybrid structures can be dynamically tuned with temperature variations. In the proposed design, a frequency is achieved at the wavelength of 1240 nm. The thermal tunability of hybrid structures introduces new multifunctional possibilities for light manipulation, thereby enhancing the potential applications of new devices in the near-infrared range.

Metal-organic framework-derived base catalyst for conversion of dimethyl carbonate to glycerol carbonate

Glycerol carbonate (GLC) offers a range of benefits including biodegradability, versatility, and its potential for carbon capture and utilization. Base catalysts play a crucial role for GLC synthesis by facilitating the activation of reactants, enhancing nucleophilicity, accelerating reaction kinetics, and enabling catalyst regeneration. In this study, metal–organic framework (MOF) derived hybrid structure, CaO-MgO@Al2O3, was developed as a base catalyst to promote transesterification of glycerol with dimethyl carbonate (DMC) to form GLC. The results show that hydrothermal plus wet-impregnation routes formed the hybrid nanostructure with homogenously dispersed Ca, Mg and Al elements. Further, the synthesized catalysts showed significantly high specific surface area and basicity (2.656 mmol g−1). High selectivity (>99 %) and high GLC yield (96.2 %; 208.9 mmol g-cat−1) were achievable. This study demonstrated the rational design concept of MOF-derived hybrid structures used in the enhancement of base catalysis for transesterification of DMC to GLC, offering an effective solution with mild reaction conditions and high conversion.

Experimental and finite element analysis of ballistic properties of composite armor made of alumina, carbon and UHMWPE

AbstractThe performance of multi‐layer ceramic/composite ballistic armor consisting of Alumina, Carbon fiber, and Ultra High Molecular Weight Polyethylene (UHMWPE) under the impact of 7.62 × 51 M61 caliber armor‐piercing (AP) bullets was examined by experimental and finite element methods. The alumina ceramic thickness used in the experiments is 12 mm. The composite structure thickness used in all samples is 10 mm. Explicit dynamic analyses were also conducted using the Ls‐Dyna to verify the experimental studies. The analysis results were compared with experimental studies and evaluated by considering the damage status of the bullet and armor. According to ballistic test results, partial penetration was observed in all armor produced. The front ceramic layer caused corrosion of the bullet, and a mushrooming effect occurred on it. The carbon fiber layer has dramatically helped as an alternative or support to UHMWPE. Since the results obtained with the carbon fiber ratios used remain within the standards, it will not pose a problem regarding usage. On the contrary, using carbon fiber, which is relatively easier to produce and supply than UHMWPE and more economically suitable, will provide more significant benefits. Experimental and numerical studies have revealed consistent results for all armors.Highlights The effect of a 7.62 × 51 armor‐piercing bullet on ceramic/composite armor was examined. Carbon fiber and UHMWPE hybrid structure was created in different thicknesses. The carbon fiber layer has dramatically helped as an alternative or support to UHMWPE. Using carbon fiber, which is relatively easier to produce and supply than UHMWPE and is more economically suitable. Experimental and numerical studies have revealed consistent results for all armors.

Experimental and finite element analysis of ballistic properties of composite armor made of alumina, carbon and UHMWPE

AbstractThe performance of multi‐layer ceramic/composite ballistic armor consisting of Alumina, Carbon fiber, and Ultra High Molecular Weight Polyethylene (UHMWPE) under the impact of 7.62 × 51 M61 caliber armor‐piercing (AP) bullets was examined by experimental and finite element methods. The alumina ceramic thickness used in the experiments is 12 mm. The composite structure thickness used in all samples is 10 mm. Explicit dynamic analyses were also conducted using the Ls‐Dyna to verify the experimental studies. The analysis results were compared with experimental studies and evaluated by considering the damage status of the bullet and armor. According to ballistic test results, partial penetration was observed in all armor produced. The front ceramic layer caused corrosion of the bullet, and a mushrooming effect occurred on it. The carbon fiber layer has dramatically helped as an alternative or support to UHMWPE. Since the results obtained with the carbon fiber ratios used remain within the standards, it will not pose a problem regarding usage. On the contrary, using carbon fiber, which is relatively easier to produce and supply than UHMWPE and more economically suitable, will provide more significant benefits. Experimental and numerical studies have revealed consistent results for all armors.Highlights The effect of a 7.62 × 51 armor‐piercing bullet on ceramic/composite armor was examined. Carbon fiber and UHMWPE hybrid structure was created in different thicknesses. The carbon fiber layer has dramatically helped as an alternative or support to UHMWPE. Using carbon fiber, which is relatively easier to produce and supply than UHMWPE and is more economically suitable. Experimental and numerical studies have revealed consistent results for all armors.

Lamellar Ti3C2 MXene composite decorated with platinum-doped MoS2 nanosheets as electrochemical sensing functional platform for highly sensitive analysis of organophosphorus pesticides

Precisely detecting organophosphorus pesticides (OPs) is paramount in upholding human safety and environmental preservation, especially in food safety. Herein, an electrochemical acetylcholinesterase (AChE) sensing platform entrapped in chitosan (Chit) on the glassy carbon electrodes (GCEs) decorated with Pt/MoS2/Ti3C2 MXene (Pt/MoS2/TM) was constructed for the detection of chlorpyrifos. It is worth noting that Pt/MoS2/TM possesses good biocompatibility, remarkable electrical conductivity, environmental stability and large specific surface area. Besides, the heterostructure formed by the composite of TM and MoS2 improves the conductivity and maintains the original structure, which is conducive to improving the electrochemical property. The coordination effect between the individual components enables the even distribution of functional components and enhances the electrochemical performance of the biosensor (AChE-Chit/Pt/MoS2/TM). Under optimal efficiency and sensitivity, the AChE-Chit/Pt/MoS2/TM/GCE sensing platform exerts comparable analytical performance and a wide concentration range of chlorpyrifos from 10−12 to 10−6 M as well as a low limit of detection (4.71 × 10−13 M). Furthermore, the biosensor is utilized to detect OPs concerning three kinds of fruits and vegetables with good feasibility and recoveries (94.81% to 104.0%). This work would provide a new scheme to develop high-sensitivity sensors based on the two-dimensional nanosheet/laminar hybrid structure for practical applications in environmental monitoring and agricultural product detection.

Electrochemical Jet Machining of Surface Texture: Improving the Strength of Hot-Pressure-Welded AA6061-CF/PA66 Joints

Diverse industries are witnessing an increase in demand for hybrid structures of metals and carbon-fiber-reinforced thermoplastic composites (CFRTPs). Welding is an essential technique in the manufacture of metal–CFRTP hybrid structures. However, achieving high-strength metal–CFRTP welded joints faces serious challenges due to the considerable disparities in material characteristics. As an effective method to strengthen metal–CFRTP joints, surface texturing on metal is gaining significant attention. This study introduces an emerging surface texturing approach, electrochemical jet machining (EJM) using a film electrolyte jet, for enhancing the performance of AA6061-CF/PA66 hot-pressure-welded (HPW) joints. Parametric effects on surface morphology and roughness in the EJM of AA6061 are investigated. The results show that a rough surface with multiscale pores can be generated on AA6061 by EJM, and that surface morphology can be modulated by adjusting the applied current density and jet translational speed. Subsequently, the effects of different EJM-textured surface morphologies on the performance of HPW joints are examined. Surface textures created by EJM are demonstrated to significantly enhance the mechanical interlocking effect at the bonding interface between AA6061 and CF/PA66, resulting in a substantial increase in joint strength. The maximum joint strength attained in the present work with EJM texturing is raised by 45.29% compared to the joints without surface texturing. Additionally, the joint strength slightly improves as the roughness of EJM-textured surfaces rises, with the exception of rough surfaces that are textured with a combination of low current density and rapid translational speed. Overall, these findings suggest that EJM texturing using a film jet prior to welding is a potential approach for the manufacture of high-performance metal–CFRTP hybrid structures.

A tunable versatile metasurface in terahertz frequency based on graphene–metal hybrid structures

The increasing demands for device integration and reusability have led to the development of freely switchable and dynamically tunable diverse functions in both modern optics and wireless communications. This study proposes a versatile metasurface that integrates with four tunable functions in the terahertz region based on graphene patch and metal split-ring hybrid structures. By adjusting the Fermi level of the graphene patches through electrostatic gating, the proposed metasurface can effectively achieve free switching among four different functions and dynamic tuning of each function's characteristics over a broad frequency band. Moreover, the metasurface operates smoothly in reflection mode for x-polarization, y-polarization, and left-hand and right-hand circular polarization illuminations. All expected performances, including resonant absorption with tunable frequency (relative bandwidth is about 20 %) and regulable absorbance (from 10 % to 100 %), arbitrary interconversion of four polarization states (relative bandwidth is over 48 %), regulation of cross-polarization conversion rate (from 0 % to 100 %), tunable spatial power division (three-way outputs), and dual-channel high-efficiency signal modulation (modulation depth is over 81 %), are demonstrated through full-wave simulation experiments. This study opens up a new avenue for exploring tunable multifunctional integrated devices with graphene materials, with potential applications in various domains, such as wireless communication, terahertz sensing, and imaging.

Biogenic Bovine Serum Albumin/Zn3(PO4)2/Cr2O3 hybrid electrocatalyst for improved oxygen evolution reaction

The fabrication of nanostructured protein-inorganic hybrid materials is crucial for the development of advanced multifunctional materials. Protein-inorganic mesoporous composites are gaining attention due to their remarkable properties, including large surface areas and active surface functional groups. We have successfully synthesized mesoporous BSA/Zn3(PO4)2/Cr2O3 catalysts to improve the kinetics of the oxygen evolution reaction (OER) in electrocatalytic water splitting for sustainable energy generation. This approach utilizes BSA in the synthesis process and is environmentally friendly. By adjusting the BSA quantity, we could control the yield of BSA/Zn3(PO4)2/Cr2O3 mesoporous. We employed various techniques, including FE-SEM, XRD, and FTIR, to analyze the morphology and structural characteristics of the biogenic BSA/Zn3(PO4)2/Cr2O3 electrocatalyst. Our comprehensive evaluation of the electrocatalytic OER activity of the BSA/Zn3(PO4)2/Cr2O3 hybrid structure demonstrated its remarkable performance. The biologically synthesized catalyst exhibited exceptional OER efficiency, maintaining a high current density of 10 mA cm−2 at very low overpotentials (only 216 mV) under alkaline conditions. The elongated peptide backbone of BSA significantly facilitated ion and electron transport, contributing to improved OER activity. The synergistic interaction between various amino acids from BSA and the metal ions within Zn3(PO4)2/Cr2O3 can be attributed to this enhancement, highlighting the potential of this hybrid structure in electrocatalytic OER applications.