Synergistic interface engineering in n-p-n type heterojunction Co3O4/MIL/Mn-STO with dual S-scheme multi-charge migration to enhance visible-light photocatalytic degradation of antibiotics.

Constructing an effective multi-heterojunction photocatalyst with maximum charge carrier separation remains challenging. Herein, a high-efficient Co3O4/MIL-88A/Mn-SrTiO3 (Co3O4/MIL/Mn-STO) n-p-n heterojunction photocatalyst was successfully prepared by a simple hydrothermal method for the photodegradation of sulfamethoxazole (SMX). The combination of MIL and Co3O4/Mn-STO established an internal electric field and heterojunction, accelerating the separation of carriers, and thus improved photocatalytic performance. In the Co3O4/MIL/Mn-STO photocatalytic system, 95.5 % of SMX was degraded in 90 min. The photocatalytic kinetic removal rate of Co3O4/MIL/Mn-STO reached 0.0337 min-1, 8 times of Co3O4 (0.0041 min-1), 5.2 times of Mn-STO (0.0062 min-1), 4.6 times of MIL (0.0078 min-1), and 3.6 times of MIL/Mn-STO (0.0095 min-1). Remarkably, superoxide radicals (•O2-) and holes (h+) have been recognized as the main active species in the degradation process through reactive species elimination experiments and electron spin resonance (ESR) tests. The experimental and theoretical proved the in-built interfacial contact and synergistic effect between the photocatalyst accomplished with low bandgaps, high specific surface area, more reaction sites, high electron-hole pair separation, and maximum solar-light utilization. The molecular structure and possible degradation routes with intermediate products in the photocatalytic system were investigated using a liquid chromatography-mass spectrometer (LC-MS) and DFT calculations. This work provided new insight into the guidelines of rational design/growth of new multicomponent photocatalysts to remove antibiotics and other emerging contaminants in wastewater.

Recent advances in Metal Organic Framework (MOF)-based hierarchical composites for water treatment by adsorptional photocatalysis: A review.

Architecting a desirable and highly efficient nanocomposite for applications like adsorption, catalysis, etc. has always been a challenge. Metal Organic Framework (MOF)-based hierarchical composite has perceived popularity as an advanced adsorbent and catalyst. Hierarchically structured MOF material can be modulated to allow the surface interaction (external or internal) of MOF with the molecules of interest. They are well endowed with tunable functionality, high porosity, and increased surface area epitomizing mass transfer and mechanical stability of the fabricated nanostructure. Additionally, the anticipated optimization of nanocomposite can only be acquired by a thorough understanding of the synthesis techniques. This review starts with a brief introduction to MOF and the requirement for advanced nanocomposites after the setback faced by conventional MOF structures. Further, we discussed the background of MOF-based hierarchical composites followed by synthetic techniques including chemical and thermal treatment. It is important to rationally validate the successful nanocomposite fabrication by characterization techniques, an overview of challenges, and future perspectives associated with MOF-based hierarchically structured nanocomposite.

Covalent organic frameworks (COFs) core@shell nanohybrids: Novel nanomaterial support towards environmental sustainability applications.

Covalent organic frameworks (COFs) based on core@shell nanohybrids have recently received significant attention and have become one of the most promising strategies for improving the stability and catalytic activity of COFs. Compared with traditional core@shell, COF-based core@shell hybrids own remarkable advantages, including size-selective reactions, bifunctional catalysis, and integration of multiple functions. These properties could enhance the stability and recyclability, resistance to sintering, and maximize the electronic interaction between the core and the shell. The activity and selectivity of COF-based core@shell could be simultaneously improved by taking benefit of the existing synergy between the functional encapsulating shell and the covered core material. Considering that, we have highlighted various topological diagrams and the role of COFs in COF-based core@shell hybrid for activity and selectivity enhancement. This concept article provides all-inclusive advances in the design and catalytic applications of COF-based core@shell hybrids. Various synthetic techniques have been developed for the facile tailoring of functional core@shell hybrids, including novel seed growth, in-situ, layer-by-layer, and one-pot method. Importantly, charge dynamics and structure-performance relationships are investigated through different characterization techniques. Different COF-based core@shell hybrids with established synergistic interactions have been detailed, and their influence on stability and catalytic efficiency for various applications is explained and discussed in this contribution. A comprehensive discussion on the remaining challenges associated with COF-based core@shell nanoparticles and research directions has also been provided to deliver insightful ideas for additional future developments.

White LED active α-Fe2O3/rGO photocatalytic nanocomposite for an effective degradation of tetracycline and ibuprofen molecules.

The formation of phase pure magnetically separable α-Fe2O3 and α-Fe2O3/rGO nanostructures were achieved through a simple hydrothermal technique. The properties of synthesized materials were investigated through different analytical techniques. The formation of phase pure FO and FO/rGO nanostructures were confirmed by XRD analysis with crystallite size of about ∼42 nm and ∼65 nm, respectively. The morphological analysis reveals the formation of sphere-like nanoparticles with high agglomeration. The UV-DRS analysis clearly shows the enhanced visible-light activity of FO/rGO nanoparticles. The BET analysis revealed the mesoporous property of FO/rGO nanocomposite. The enhancement in the photoinduced charge transfer process is observed after including rGO nanoparticles with FO. The photocatalytic efficiency of nanomaterials was analyzed using tetracycline and ibuprofen as model organic pollutants under white LED irradiation. The enhanced photocatalytic degradation ability of FO/rGO nanocomposite is studied against both tetracycline and ibuprofen molecules.

Low carbon footprint preparation of MXene incorporated lignocellulosic fibers for high thermal conductivity applications.

New wood-based composite materials with thermal conductivity are greatly desired in the fields of packaging materials for electronic components. In this study, a new multifunctional composite material (M@FC) is prepared by simply blending clay-like Ti3C2Tx MXene and delignified wood fibers together, and then followed by an infusing epoxy resin with environmentally friendly vacuum assisted resin transfer molding (VARTM) process. The resulting M@FC (0.92 W m-1 K-1) possesses superior thermal conductivity as compared to natural wood (0.099 W m-1 K-1) and most polymers. Furthermore, after the VARTM process, the structure of the M@FC is tighter, and thus showing excellent mechanical properties (tensile strength of 93.0 MPa and flexural strength of 172.7 MPa). In addition, good water resistance and excellent flame retardant property are observed for M@FC. The improvement of thermal conductivity provides the possibility for its application for packaging materials in electronic components. This study using waste wood as the important component provides a new idea for carbon cycling and recycling of natural resources.

Boosting light-driven CO2 reduction into solar fuels: Mainstream avenues for engineering ZnO-based photocatalysts.

The realization of artificial photosynthesis in the photocatalytic CO2 transformation into valuable chemicals or solar fuels, such as CO, CH4, HCOOH, and CH3OH, by solar-light harvesting is a promising solution to both global-warming and energy-supply issues. Recently, zinc oxide (ZnO) has emerged as an excellent oxidative photocatalyst among non-titanium metal oxides due to its availability, outstanding semiconducting and optical properties, non-toxicity, affordability, and ease of synthesis. However, ZnO wide bandgap and inability to absorb in the visible region has demanded particular modification for its practical use as a sustainable photocatalyst. This review provides a panorama of the latest advancement on ZnO photocatalysis for CO2 reduction with an overview of fundamental aspects. Various modification strategies such as transition metal and non-metal doping, loading of plasmonic metals, and surface vacancy engineering for tunning the properties and improving the performance of ZnO are elaborated. Composites or hetero-structuralization-based Z-scheme formation is also presented along with a detailed photocatalytic reduction mechanism. Moreover, a new novel Step-scheme (S-scheme) heterostructure modification with a charge transfer pathway mechanism is also highlighted. Finally, the key challenges and new directions in this field are proposed to provide a new vision for further improvement for ZnO-based photocatalytic CO2 conversion.

Multi-walled carbon nanotube-based nanobiosensor for the detection of cadmium in water.

Industrial and agricultural processes have led to the prevalence of cadmium in the ecosystem. A successive build-up of cadmium in food and drinking water can result in inadvertent consumption of hazardous concentrations. Such environmental contamination of cadmium can pose a substantial threat to human and animal life. In humans, it is known to cause hypertension, cardiovascular diseases, DNA lesions, inhibition of DNA repair protein or disturb the functioning of lung, liver, prostate and kidney. The development of a reliable method for Cd (II) ions detection would reduce the exposure and complement existing conventional methods. In this study, a DNA based electrochemical method is employed for the detection of Cd (II) ions using ethyl green (EG) and multi-walled carbon nanotube (MWCNT). Glassy carbon electrode (GCE)/MWCNT forms the working electrode for differential pulse voltammetry (DPV) analysis for the detection of Cd (II) ions. The dsDNA is immobilized onto the working electrode. The indicator dye EG, preferably binds to ssDNA and its reduction peak current is noticeably less in the presence of dsDNA. The Cd (II) ions after interacting with dsDNA, unwinds the dsDNA to ssDNA, upon which the EG molecules bind to ssDNAs, giving a higher reduction peak current. The difference in the reduction peak currents in the presence and absence of Cd (II) ions is proportional to its concentration. The linear detection range achieved in this method is 2 nM-10.0 nM with a sensitivity of around 5 nA nM-1 and the limit of detection is 2 nM, which is less than the permissible limit of WHO for human exposure. This study considerably broadens the possible application of multi-walled carbon nanotube modified electrodes as biosensors and holds prospects for the detection of other heavy metals in environmental samples.

NH2-MIL-125(Ti) doped CdS/Graphene composite as electro and photo catalyst in basic medium under light irradiation.

The development of active electrocatalysts and photocatalysts for hydrogen evolution reaction (HER) and for environmental remediation is a huge challenge. Research is still underway on the development of low-cost catalytic materials with appreciable efficiency for HER. In the present study, a composite of metal organic framework (MOF) with CdS and graphene (NH2-MIL-125(Ti)/CdS-graphene) composites were developed with different loadings of graphene material via solvothermal technique. Further the electrocatalytic activity of the synthesized catalysts were investigated for HER and photocatalytic degradation of dye. Results show that the synthesized catalyst with a less amount of graphene was more active. HER results showed a less Tafel slope of 70.8 and 61.9 mVdec-1 with 15.6 mA/cm2 and 15.46 mA/cm2 current densities under light on and off conditions. Further the dye degradation activity of the synthesized catalysts was tested with Rhodamine B dye and results showed that the catalyst showed excellent activity for low weight loading of graphene with a degradation efficiency of 95 % and followed pseudo first order kinetic model. Overall results showed that the synthesized composites are promising for HER and photocatalytic applications.

Metal salt-modified biochars derived from agro-waste for effective congo red dye removal.

Anionic Congo red dye (CR) is not effectively removed by conventional adsorbents. Three novel biochars derived from agro-waste (Acacia auriculiformis), modified with metal salts of FeCl3, AlCl3, and CaCl2 at 500 °C pyrolysis have been developed to enhance CR treatment. These biochars revealed significant differences in effluents compared to BC, which satisfied initial research expectations (P < 0.05). The salt concentration of 2 M realized optimal biochars with the highest CR removal of 96.8%, for AlCl3-biochar and FeCl3-biochar and 70.8% for CaCl2-biochar. The modified biochars were low in the specific surface area (137.25-380.78 m2 g-1) compared normal biochar (393.15 m2 g-1), had more heterogeneous particles and successfully integrated metal oxides on the surface. The CR removal increased with a decrease in pH and increase in biochar dosage, which established an optimal point at an initial loading of 25 mg g-1. Maximum adsorption capacity achieved 130.0, 44.86, and 30.80 mg g-1 for BFe, BCa, and BAl, respectively. As magnetic biochar, which is easily separated from the solution and achieves a high adsorption capacity, FeCl3-biochar is the preferred biochar for CR treatment application.

Recent advances in cellulose supported photocatalysis for pollutant mitigation: A review.

In recent times, green chemistry or "green world" is a new and effective approach for sustainable environmental remediation. Among all biomaterials, cellulose is a vital material in research and green chemistry. Cellulose is the most commonly used natural biopolymer because of its distinctive and exceptional properties such as reproducibility, cost-effectiveness, biocompatibility, biodegradability, and universality. Generally, coupling cellulose with other nanocomposite materials enhances the properties like porosity and specific surface area. The polymer is environment-friendly, bioresorbable, and sustainable which not only justifies the requirements of a good photocatalyst but boosts the adsorption ability and degradation efficiency of the nanocomposite. Hence, knowing the role of cellulose to enhance photocatalytic activity, the present review is focused on the properties of cellulose and its application in antibiotics, textile dyes, phenol and Cr(VI) reduction, and degradation. The work also highlighted the degradation mechanism of cellulose-based photocatalysts, confirming cellulose's role as a support material to act as a sink and electron mediator, suppressing the charge carrier's recombination rate and enhancing the charge migration ability. The review also covers the latest progressions, leanings, and challenges of cellulose biomaterials-based nanocomposites in the photocatalysis field.

Constructing α-Fe2O3/g-C3N4/SiO2 S-scheme-based heterostructure for photo-Fenton like degradation of rhodamine B dye in aqueous solution.

This work successfully fabricated graphitic carbon nitride and magnetically recoverable α-Fe2O3/g-C3N4/SiO2 photo-Fenton catalysts using thermal polycondensation and in situ-simple precursor drying-calcination process, respectively, was examined for model synthetic rhodamine B (RhB) dye in the presence of H2O2 and acidic pH under simulated visible light irradiation. An aqueous suspension of the reaction mixture of dye-containing wastewater was fully degraded and reached 97% of photo-Fenton degradation efficiency within 120 min followed by the production of hydroxyl radical (•OH). The dominant hydroxyl radical position generated surface charge, electrostatic potential distribution, and average local ionization potential, which contributed to the complete mineralization of RhB dye, according to the density functional theory (DFT) calculations. HPLC and GCMS experiments were performed to examine the degradation fragments of RhB and draw a plausible mechanistic pathway which showed that RhB degradation generated a series of N-deethylated products, followed by a one-time ring-opening, which indicated that photosensitization induced a photocatalysis reaction mechanism.

Advances in gum-based hydrogels and their environmental applications.

Gum-based hydrogels (GBHs) have been widely employed in diverse water purification processes due to their environmental properties, and high absorption capacity. More desired properties of GBHs such as biodegradability, biocompatibility, material cost, simplicity of manufacture, and wide range of uses have converted them into promising materials in water treatment processes. In this review, we explored the application of GBHs to remove pollutants from contaminated waters. Water resources are constantly being contaminated by a variety of harmful effluents such as heavy metals, dyes, and other dangerous substances. A practical way to remove chemical waste from water as a vital component is surface adsorption. Currently, hydrogels, three-dimensional polymeric networks, are quite popular for adsorption. They have more extensive uses in several industries, including biomedicine, water purification, agriculture, sanitary products, and biosensors. This review will help the researcher to understand the research gaps and drawbacks in this field, which will lead to further developments in the future.

Integrating K and P co-doped g-C3N4 with ZnFe2O4 and graphene oxide for S-scheme-based enhanced adsorption coupled photocatalytic real wastewater treatment.

Recently, there has been a significant increase in the interest of using photocatalysis for environmental clean-up applications. In this research, potassium, and phosphorus co-doped graphitic carbon nitride (KPCN) photocatalyst modified with graphene oxide (GO) and heterostructured with ZnFe2O4 was synthesized via the hydrothermal method (KPCN/GO/ZnFe2O4). The photoactivity of KPCN/GO/ZnFe2O4 photocatalyst was examined for the photocatalytic degradation of target pollutants such as methylene blue (MB) dye, rhodamine B (RhB) dye, and tetracycline (TC) antibiotic. Furthermore, the chemical oxygen demand (COD) removal efficiency for real wastewater was determined to explore the practical application of KPCN/GO/ZnFe2O4 photocatalyst. The degradation efficiencies of bare graphitic carbon nitride, KPCN, KPCN/GO, and KPCN/GO/ZnFe2O4 photocatalysts for tetracycline antibiotics were 30%, 42%, 57%, and 87% within 60 min, respectively. Moreover, KPCN/GO/ZnFe2O4 photocatalyst showed 71% COD removal efficiency within 240 min. The •OH and •O2- were the major reactive species in the photocatalytic process. Results showed that the degradation efficiencies of graphitic carbon nitride were greatly enhanced upon doping and further improved with the addition of GO and ZnFe2O4. Doping improved light harvesting, GO enhanced the adsorption ability and heterojunction with ZnFe2O4 enhanced the charge separation as well as the reusability of synthesized KPCN/GO/ZnFe2O4 photocatalyst.

O and S co-doping induced N-vacancy in graphitic carbon nitride towards photocatalytic peroxymonosulfate activation for sulfamethoxazole degradation.

Doping-induced vacancy engineering of graphitic carbon nitride (GCN) is beneficial for bandgap modulation, efficient electronic excitation, and facilitated charge carrier migration. In this study, synthesis of oxygen and sulphur co-doped induced N vacancies (OSGCN) by the hydrothermal method was performed to activate peroxymonosulfate (PMS) for sulfamethoxazole (SMX) antibiotic degradation and H2 production. The results from experimental and DFT simulation studies validate the synergistic effects of co-dopants and N-vacancies, i.e., bandgap lowering, electron-hole pairs separation, and high solar energy utilization. The substitution of sp2 N atom by O and S co-dopants causes strong delocalization of HOMO-LUMO distribution, enhancing carrier mobility, increasing reactive sites, and facilitating charge-carrier separation. Remarkably, OSGCN/PMS photocatalytic system achieved 99.4% SMX degradation efficiency and a high H2 generation rate of 548.23 µ mol g-1 h-1 within 60 min and 36 h, respectively under visible light irradiations. The SMX degradation kinetics was pseudo-first-order with retained recycling efficiency up to 4 catalytic cycles. The results of EPR and chemical scavenging experiments revealed the redox action of reactive oxidative species, wherein 1O2 was the dominant reactive species in SMX degradation. The identification of formed intermediates and the SMX stepwise degradation pathway was investigated via LC-MS analysis and DFT studies, respectively. The results from this work anticipated deepening the understanding of PMS activation by substitutional co-doping favoring N-vacancy formation in GCN lattice for improved photocatalytic activity.

Nanostructure and nanoindentation study of pulse electric-current sintered TiB2-SiC-Cf composite.

A carbon-fiber (Cf) doped TiB2-SiC composite was prepared and investigated to determine its densification behavior, micro/nanostructural properties, and mechanical characteristics. TiB2-25 vol% SiC-2 wt% Cf was prepared at 40 MPa and 1800 °C for 7 min using the pulsed electric-current sintering technique, and a relative density of 98.5% was realized. The as-sintered composite was characterized using advanced techniques, e.g., X-ray diffractometry, energy-dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy, field-emission scanning electron microscopy, high-resolution transmission electron microscopy, field-emission electron probe micro-analysis, and nanoindentation. The Cf additive could remove the surface oxide layers from the TiB2 and SiC domains, thus transforming them into TiB2 and SiC. According to micro/nanostructural studies, Cf could not retain its initial structure and was eventually converted into graphite nanosheets. In addition, the prepared composite was examined using the nanoindentation technique, and the following results were obtained for the calculated hardness, elastic modulus, and stiffness values: TiB2 > SiC > TiB2/SiC interface.

An overview on ZnO-based sonophotocatalytic mitigation of aqueous phase pollutants.

Over the past several decades, the increase in industrialization provoked the discharge of harmful pollutants into the environment, affecting human beings and ecosystems. ZnO-based photocatalysts seem to be the most promising photocatalysts for treating harmful pollutants. However, fast charge carrier recombination, photo corrosion, and long reaction time are the significant factors that reduce the photoactivity of ZnO-based photocatalysts. In order to enhance the photoactivity of such photocatalysts, a combined process i.e., sonocatalysis + photocatalysis = sonophotocatalysis was used. Sonophotocatalysis is one of several different AOP methods that have recently drawn considerable interest, as it produces high reactive oxygen species (ROS) which helps in the oxidation of pollutants by acoustic cavitation. This combined technique enhanced the overall efficiency of the individual method by overcoming its limiting factors. The current review aims to present the theoretical and fundamental aspects of sonocatalysis and photocatalysis along with a detailed discussion on the benefits that can be obtained by the combined process i.e., US + UV (sonophotocatalysis). Also, we have provided a comparison of the excellent performance of ZnO to that of the other metal oxides. The purpose of this study is to discuss the literature concerning the potential applications of ZnO-based sonophotocatalysts for the degradation of pollutants i.e., dyes, antibiotics, pesticides, phenols, etc. That are carried out for future developments. The role of the produced ROS under light and ultrasound stimulation and the degradation mechanisms that are based on published literature are also discussed. In the end, future perspectives are suggested, that are helpful in the development of the sonophotocatalysis process for the remediation of wastewater containing various pollutants.

Potential of novel dual Z-scheme carbon quantum dots decorated MnIn2S4/CdS/Bi2S3 heterojunction for environmental applications.

In this work, CQDs decorated MnIn2S4/CdS/Bi2S3 heterojunction was prepared successfully by hydrothermal technique for photocatalytic disinfection of Escherichia coli (E. coli) and mineralization of methyl orange (MO) dye. The charge transferal route and mineralization process in CQDs-MnIn2S4/CdS/Bi2S3 heterojunction were comprehensively investigated by advanced spectroscopic techniques. The improved visible-light activity and enhanced photo-generated charge transferal efficacy caused dual Z-scheme CQDs-MnIn2S4/CdS/Bi2S3 heterojunction to achieve boosted photodegradation ability. The catalytic degradation trend was followed as CQDs-MnIn2S4/CdS/Bi2S3 > MnIn2S4 > CdS > Bi2S3. The dye was mineralized within 180 min under visible light irradiation. The effect of reaction parameters, pH effect, catalyst dosage, and H2O2 addition on MO degradation was also investigated. The degradation rate was maximal at pH 4 with a pseudo-first-order rate constant, 0.0438 min-1. The assessment of antibacterial properties revealed that CQDs-MnIn2S4/CdS/Bi2S3 composite effectively inactivated E. coli under visible light. Scavenging experiments, transient photocurrent response, and electron spin resonance spectroscopy suggested that •[Formula: see text] and holes were the dominant reactive species. The Z-scheme heterojunction is recyclable up to ten photocatalytic cycles according to recycling experiments. This research indicates the importance of dual Z-scheme CQDs decorated MnIn2S4/CdS/Bi2S3 heterojunction in wastewater remediation.

Visible-light photocatalysis of Ag-doped graphitic carbon nitride for photodegradation of micropollutants in wastewater.

This work reports on graphitic carbon nitride (C3N4) modified with silver to investigate its visible-light-driven photocatalysis for decomposition of micropollutants in wastewater. Various characterization methods were conducted to examine the physico-chemical properties of Ag-doped C3N4 (Ag-C3N4) photocatalyst. The results from structural, morphological, and surface chemical analysis indicated that C3N4 was successfully doped with Ag. Photoluminescence and transient photocurrent density studies revealed that the recombination rate of electron-hole pairs was reduced, leading to the enhancement of photocatalytic activities of the photocatalyst. Ag-C3N4 showed high photocatalytic performance for photodegradation of our target micropollutant, bisphenol A (BA). It could completely remove BA in 1 h with kinetic constant 6.2 times higher than that of the undoped C3N4 photocatalyst. Recycling test and the assessment of the photocatalyst in wastewater further confirmed the excellent stability and applicability of the Ag-C3N4 photocatalyst. This work could provide a new solution to the practical application of photocatalyts for the degradation of micropollutants in wastewater.

Phyto-mediated synthesis of nanoparticles and their applications on hydrogen generation on NaBH4, biological activities and photodegradation on azo dyes: Development of machine learning model.

This work reports the synthesis of the silver-platinum bimetallic nanoparticles (N@Pt-Ag BNPs) reduced by an ethanolic extract of black seed (Nigella sativa, N) using the green synthesis method, these nanoparticles show a great antibacterial, anticancer, and catalytic activity. The characterization of physicochemical properties of Ag-Pt BNP was carried out using UV-visible spectroscopy (Uv-vis), Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and Transmission electron microscope (TEM) analysis. The structural morphology shows that the N@Pt-Ag BNPs are spherical particles with a diameter of 5.6 nm. The cytotoxic effects of N@Pt-Ag BNPs were examined by MTT test in human breast cancer, human colon cancer, human pancreatic cancer, L929-Murine fibroblast cells. N@Pt-Ag BNPs have been observed to be much more effective in breast cancer cell lines. The cytotoxic effect of N@Pt-Ag BNPs against healthy L929-murine fibroblast cell lines was not observed. Also, high antibacterial activity on each of the bacteria Escherichia coli (E. coli), Bacillus subtilis (B. subtilis), Methicillin-resistant Staphylococcus aureus (MRSA), Staphylococcus aureus (S. aureus), where we note that most strains of E. coli and S. aureus were damaged with a 73% percentage, 67% bacterial inhibition respectively. The results of the catalytic activities of N@Pt-Ag BNPs were obtained by performing the hydrolysis experiments of sodium borohydride (NaBH4). According to the results obtained, TOF, enthalpy, entropy, and activation energy, values were found to be 2497.14 h-1, 13.52 kJ/mol, -137.47 J/mol.K, 16.02 kJ/mol, respectively. N@Pt-Ag BNPs were found to be highly effective catalysts for hydrogen production which this was also confirmed by the machine learning model. The photocatalytic activity of N@Pt-Ag BNPs was tested against methylene blue (MB) dye and the highest activity was found as 80%.