Conventional Co-precipitation Method Research Articles

Soft chemistry-derived Al-substituted hydrated nickel hydroxide electrodes for rechargeable aqueous batteries.

Hydrated nickel hydroxides with partial aluminum substitution were synthesized using the conventional coprecipitation and soft chemistry methods. The soft chemistry derived sample showed better reversibility owing to the low activity for oxygen evolution during charging. Operando X-ray diffraction indicated the increased interlayer distance and decreased crystallinity during discharging caused by water accommodation.

Resources, energy consumption and economic analysis for flame synthesis of ternary cathode materials

Cathode materials account for around one third of the manufacturing cost of lithium-ion battery, which are the major factor preventing the wider applications of power battery packs. Flame synthesis (FS) is a new manufacturing technology of nanostructured materials with few equipment and high efficiency, which potentially can substantially bring down the manufacturing cost of cathode materials. The primary objective of the present study was to quantitatively evaluate the resources, energy consumption and economic feasibility of large-scale production of cathode materials though FS. In the analysis process, the mass flow of reactants and resultants as well as the minimum cathode material selling price (MCSP) of ternary cathode material LiNixCoyMn(1-x-y)O2 (x + y + z = 1) produced by FS were calculated, and compared with that of the conventional hydroxide co-precipitation method. Results show that the production of ternary cathode material through FS can reduce CO2 emissions by ∼60% and water consumption by ∼30%. MCSP of LiNi0.5Co0.2Mn0.3O2 (NCM523), LiNi0.6Co0.2Mn0.2O2 (NCM622), and LiNi0.8Co0.1Mn0.1O2 (NCM811) produced by FS are 224.8 k¥/t, 235.1 k¥/t, 240.0 k¥/t, which respectively are about 2%, 10% and 14% lower than the average selling prices in Chinese market, indicating that FS is economically feasible for producing ternary cathode materials. Particularly, for the production of high-nickel cathode materials, FS has notable potential in simplifying the production process and manufacturing costs. Sensitivity analysis of NCM811 produced by FS shows that when raw material price, fuel and power costs are reduced by 25%, MCSP can be as low as 186.4 k¥/t. When the metal cation concentration of the solution increases to 3.2 mol/L, it enables FS to meet the most rigorous energy consumption limitation standards in China. When the lithium excess is reduced from 10% to 5%, MCSP of NCM811 can be further reduced by 5.6 k¥/t, indicating that lithium loss due to high temperatures in FS is a moderate factor for reducing the manufacturing cost. Finally, this work presents a life cycle assessment (LCA) of NCM materials produced by FS in China. Comparison to the global warming potential (GWP) of the co-precipitation method in the literature indicated that GWP of FS is lower.

Revisiting hydrotalcite synthesis: Efficient combined mechanochemical/coprecipitation synthesis to design advanced tunable basic catalysts

Abstract Hydrotalcite materials (HTs) were synthesized by a facile and swift combined mechanochemistry/coprecipitation approach, and their catalytic activity was evaluated and compared with conventionally synthesized hydrotalcites (co-precipitation method) in the Knoevenagel condensation between furfural and ethyl cyanoacetate/malononitrile. Characterization and catalytic activity results clearly demonstrate that the proposed combined mechanochemical/coprecipitation approach provides an improvement in crystallinity, morphology, tunable basicity, and textural properties (higher surface area and enhanced surface properties) as compared to HTs obtained via conventional coprecipitation methods. In addition, mechanochemically synthesized HTs largely improve catalytic activities, including conversion and product selectivity to Knoevenagel condensation products under solventless conditions, short reaction times, or reaction at room temperature as compared to conventional counterparts (e.g., 30–40 vs > 99% product yields).

Hydrothermally Synthesized ZnCr- and NiCr-Layered Double Hydroxides as Hydrogen Evolution Photocatalysts.

The layered double hydroxides (LDHs) of transition metals are of great interest as building blocks for the creation of composite photocatalytic materials for hydrogen production, environmental remediation and other applications. However, the synthesis of most LDHs is reported only by the conventional coprecipitation method, which makes it difficult to control the catalyst's crystallinity. In the present study, ZnCr- and NiCr-LDHs have been successfully prepared using a facile hydrothermal approach. Varying the hydrothermal synthesis conditions allowed us to obtain target products with a controllable crystallite size in the range of 2-26 nm and a specific surface area of 45-83 m2∙g-1. The LDHs synthesized were investigated as photocatalysts of hydrogen generation from aqueous methanol. It was revealed that the photocatalytic activity of ZnCr-LDH samples grows monotonically with the increase in their average crystallite size, while that of NiCr-LDH ones reaches a maximum with intermediate-sized crystallites and then decreases due to the specific surface area reduction. The concentration dependence of the hydrogen evolution activity is generally consistent with the standard Langmuir-Hinshelwood model for heterogeneous catalysis. At a methanol content of 50 mol. %, the rate of hydrogen generation over ZnCr- and NiCr-LDHs reaches 88 and 41 μmol∙h-1∙g-1, respectively. The hydrothermally synthesized LDHs with enhanced crystallinity may be of interest for further fabrication of their nanosheets being promising components of new composite photocatalysts.

Enhancing Oxygen Evolution Reaction through In Situ Electrochemical Oxidation for the Structural Control of Co-Fe Prussian Blue Analogue

The development of exceptionally efficient catalysts for the oxygen evolution reaction (OER) and gaining a deep understanding of their activity is essential for advancing electrochemical conversion technologies. Prussian blue analogues (PBAs) serve as promising pre-catalysts for the OER. However, PBAs, typically prepared through the conventional co-precipitation method, exhibit a lower active site density and limited electrical transport, making them suitable precursors for the derivation of PBA derivatives. In this research, we identified a significant enhancement in the electrocatalytic performance of Co-Fe Prussian blue analogue (CoFe PBA) through electrochemical oxidation. The cubic CoFe PBA was synthesized by one-step co-precipitation method using adjusting the amount of sodium citrate and potassium ferricyanide. After the electrochemical treatment, CoFe PBA demonstrates remarkable attributes, including a low overpotential of 331mV at a current density of 10mA·cm-2, a small Tafel slope of 50.4mV·dec-1, and excellent long-term stability during electrolysis in a 1M KOH alkaline medium for over 37h. Moreover, the electrochemical oxidation of CoFe PBA was comprehensive, employing techniques such as Transmission electron microscope, Powder X-ray diffraction, and X-ray photoelectron spectroscopy. These analyses confirmed the presence of real active substances, including CoOOH and a part of FeOOH species, further supporting the observed improvements in electrocatalytic activity.

Hydrolysis Precipitation Method for the Preparation of Cu‐ZnO@Al2O3 Catalyst in Methanol Steam Reforming

AbstractA hydrolysis precipitation method was developed to prepare Cu based catalyst for methanol steam reforming. A comparison of the hydrolysis precipitation and the conventional coprecipitation method was conducted. The test results present that Cu‐ZnO@Al2O3 prepared by hydrolysis precipitation exhibits better catalytic activity and stability in MSR reaction. XRD, XRF, EDS, SEM, TPR, XPS and N2 adsorption/desorption reveal that the high catalytic performance of Cu based catalyst from hydrolysis precipitation could be attributed to developed pore organization, surface enrichment of active components and higher reducibility.

Effect of PVP Molecular Weights on the Synthesis of Ultrasmall Cus Nanoflakes: Synthesis, Properties, and Potential Application for Phototheranostics.

Copper sulfide nanoparticles (CuS) hold tremendous potential for applications in photothermal therapy (PTT) and photoacoustic imaging (PAI). However, the conventional chemical coprecipitation method often leads to particle agglomeration issues. To overcome this challenge, we utilized polyvinylpyrrolidone (PVP) as a stabilizing agent, resulting in the synthesis of small PVP-CuS nanoparticles named PC10, PCK30, and PC40. Our study aimed to investigate how different molecular weights of PVP influence the nanoparticles' crystalline characteristics and essential properties, especially their photoacoustic and photothermal responses. While prior research on PVP-assisted CuS nanoparticles has been conducted, our study delves deeper into this area, providing insights into optical properties. Remarkably, all synthesized nanoparticles exhibited a crystalline structure, were smaller than 10 nm, and featured an absorbance peak at 1020 nm, indicating their robust photoacoustic and photothermal capabilities. Among these nanoparticles, PC10 emerged as the standout performer, displaying superior photoacoustic properties. Our photothermal experiments demonstrated significant temperature increases in all cases, with PC10 achieving an impressive efficiency of 51%. Moreover, cytotoxicity assays revealed the nanoparticles' compatibility with cells, coupled with an enhanced incidence of apoptosis compared to necrosis. These findings underscore the promising potential of PVP-stabilized CuS nanoparticles for advanced cancer theranostics.

Elucidating the Bioinspired Synthesis Process of Magnetosomes-Like Fe3O4 Nanoparticles.

Iron oxide nanoparticles are a kind of important biomedical nanomaterials. Although their industrial-scale production can be realized by the conventional coprecipitation method, the controllability of their size and morphology remains a huge challenge. In this study, a kind of synthetic polypeptide Mms6-28 which mimics the magnetosome protein Mms6 is used for the bioinspired synthesis of Fe3O4 nanoparticles (NPs). Magnetosomes-like Fe3O4 NPs with uniform size, cubooctahedral shape, and smooth crystal surfaces are synthesized via a partial oxidation process. The Mms6-28 polypeptides play an important role by binding with iron ions and forming nucleation templates and are also preferably attached to the [100] and [111] crystal planes to induce the formation of uniform cubooctahedral Fe3O4 NPs. The continuous release and oxidation of Fe2+ from pre-formed Fe2+-rich precursors within the Mms6-28-based template make the reaction much controllable. The study affords new insights into the bioinspired- and bio-synthesis mechanism of magnetosomes.

Removal of direct blue FFRL by layered double hydroxides: Thermodynamics and kinetics

In this paper, MgAl layered double hydroxides (LDH) with molar ratio of nMg:nAl = 2:1 was successfully synthesized by conventional co-precipitation method to remove direct blue FFRL (FFRL). In order to study the influence of calcined temperature to FFRL removal, a series of calcined layered double hydroxides (CLDH) samples was obtained by calcination at 200, 450, 600, 800 °C for 6 h, respectively. BET, XRD and SEM were used to analyze the structure of MgAl-CLDH calcined at different temperature. The MgAl-CLDH calcined at 450 °C exhibits the most considerable removal efficiency, which is corresponding to the results of BET. The equilibrium isotherm of FFRL removal by MgAl-CLDH can be better described by Langmuir model. The process of FFRL removal by MgAl-CLDH is spontaneous and exothermic with an increasing in molecular order. Removal of FFRL by MgAl-CLDH also conforms to the pseudo-first-order model with activating energy of 129.6 kJ/mol, which proves that the removal of FFRL by MgAl-CLDH is controlled by a chemical reaction between FFRL and MgAl-CLDH.

Investigations of the structure and tunable magnetic properties of Cu doped cobalt chromite nanoparticles

This article reports the synthesis, microstructural, magnetic and optical properties of copper ions substituted cobalt chromite nanoparticles. We have prepared four nanosized chromite samples with a general composition of CuxCo1-xCr2O4 (x = 0.0, 0.1, 0.2 and 0.3) using conventional wet chemical co-precipitation method. The x-ray diffraction profiles verified the presence of pure spinel crystal structure of the samples. Using the Williamson-Hall (W-H) method, the average crystallite size of all the samples were calculated to be between 11 nm and 16 nm. A tensile microstrain in all the samples was noticed. Surface morphology and average particle size of doped cobalt chromite nanocrystals was examined using HRTEM images. A moderate increment in the optical band gap was detected with increasing Cu ions in cobalt chromite nanoparticles which is attributed to the nanosize effect of the samples. The presence of all five distinctive Raman active modes in the chromite samples ensured phase purity and a decrease in crystal symmetry was also observed as the amount of Cu dopants was increased. Due to low magnetic moment of Cu2+ ions when compared with Co2+ ions, incorporation of copper ions reduces the coercive field of the host chromite system. With increasing Cu percentage in chromite especially for 30 % Cu doped sample, the spin-spiral transition TS vanishes which indicates TS is affected by the dopant concentrations.

Lindgrenite as an efficient heterogeneous catalyst to obtain biodiesel

Lindgrenite, Cu3MoO42OH2, presents considerable potential to be used as a catalyst for obtaining biodiesel from soybean oil and methanol. Lindgrenite samples were obtained using conventional coprecipitation and ultrasound-assisted coprecipitation methods. Several catalytic tests were performed to reach the optimal conditions (methanol/oil molar ratio: 45/1, catalyst mass: 1%, reaction time: 4 h, reaction temperature: 180 °C) for obtaining biodiesel, with a 96% yield in the first catalytic cycle and 85% yield in its tenth catalytic cycle. Inductively Coupled Plasma Mass Spectrometry (ICP-MS) of the biodiesel obtained by catalytic method revealed negligible amount of leached metal ions (less than 1 ppm of Cu2+ and less than 3 ppm of Mo6+) with the catalyst obtained by ultrasound-assisted coprecipitation method. The similarity between the FTIR spectra of industrial biodiesel and that obtained in this work confirms the effectiveness of using lindgrenite as an efficient catalyst for the transesterification reaction. Biodiesel synthesis was also confirmed by Nuclear Magnetic Resonance (1H and 13C NMR). The results obtained from Gas Chromatography-Mass Spectrometry (GC-MS) indicate methyl linoleate is the main component of the biodiesel, corresponding to approximately 50.50%. In addition to being easily obtained, lindgrenite is thermally stable and efficient under the applied conditions. The 96% yield after the fifth catalytic cycle is above the catalytic performance commonly observed in the literature. These characteristics indicate that lindgrenite has enormous potential to be used as a new heterogeneous catalyst to obtain biodiesel.

Synthesis of Ca-Mg-Al layered double hydroxide from dolomite with ultrasound-assisted method. Application in phosphate removal

The aim of this work was to obtain a Layered Double Hydroxide (LDH) from natural dolomite and to apply the synthetized solid (CaMgAl-LDH) for phosphate removal by adsorption. Both the conventional coprecipitation method and ultrasound-assisted method were used to obtain CaMgAl-LDH. The obtained solids were characterized by N2 adsorption/desorption, size of pores, X-ray diffraction, and FTIR. Batch scale experiments were carried out to evaluate the phosphate adsorption capacity on CaMgAl-LDH using design of experiments (DOE). The studied parameters were pH, solid dosage, contact time and phosphate removal percentage, which was selected as the response function. Experimental data were fitted to kinetics and isotherms mathematical models. The process thermodynamics was also studied. Results showed that the ultrasound-assisted method was more efficient to obtain LDH even in a short period of sonication. The solids presented good crystallization, structure between layers, and high purity. Besides, LDH obtained by ultrasound exhibited a surface area of ​​about 40% greater than the LDH obtained by the conventional method. The results of LDH application for phosphate removal showed high adsorption capacity (>94%) in several conditions of contact time and pH, even in low solid dosage. The kinetics of the process followed the pseudo-second-order model and Redlich-Peterson was the isotherm model that presented the best adjust. The thermodynamic parameters suggested a spontaneous, endothermic, and randomness process at the solid/solution interface, confirming an adsorption system favorable. The results exhibited that the ultrasound-assisted method is promissory to obtain LDH from mineral sources such as dolomite due to decrease energy expenditure and short synthesis time. It was found the ultrasound-assisted method also improve the solid physicochemical characteristics for its use in the adsorption process, enhancing the phosphate removal.

Synthesis of a homogeneous CeO2–ZrO2-Al2O3 composite material by a novel hydrothermal assisted precipitation method

CeO2-ZrO2-Al2O3(CZA) composites, combining the advantages of CeO2-ZrO2 (CZ) and Al2O3, are widely used in three-way catalyst as an indispensable support material. However, due to the adverse Zr-Al interaction and the different precipitation conditions for Ce3+/Ce4+ and Zr4+, the CZA prepared by conventional co-precipitation method has poor compositional homogeneity, resulting in degradation of redox properties. In this study, a homogeneous CZA composite is synthesized by a novel hydrothermal assisted precipitation method, in which the CZ-precipitates and Al-precipitates will be controlled separately. A quantitative EDX points analysis reveals that the Ce/Zr ratio in the resulting CZA material exhibits slight fluctuations between 0.72 and 0.91, which is much narrow than that from conventional precipitation method (0.38∼0.83). As a result, the resulting CZA material exhibits the better redox property, higher specific surface area, and more importantly, its supported Pd/CZA catalyst exhibit superior three-way catalytic activity, the T50 (temperature for 50% conversion) for CO, NO, C3H6 and C3H8 over which is 41 ℃, 26 ℃, 28 ℃ and 12 ℃, respectively, lower than that from conventional method.

Enhancing quantum efficiency of Mn4+-doped fluoride phosphors through reverse doping strategy toward potential biological detection

Mn4+-doped fluoride red-emitting materials are renowned for their distinct characteristics, including fixed emission peaks and narrow spectral emission, rendering them highly favored in photoluminescent light-emitting diodes (LEDs). However, achieving ultra-high-concentration Mn4+ doping in fluoride phosphors is imperative to enhance quantum efficiency. Nevertheless, attaining such doping levels in metastable compound systems poses considerable challenges. In this study, we introduce an innovative reverse doping strategy, leading to the synthesis of Mn4+-doped cubic K2SiF6 phosphor (11.38 mol %) from hexagonal K2MnF6. Remarkably, this approach significantly improves the external quantum efficiency (EQE) to 66.7 % upon 450 nm excitation. Through systematic comparisons with conventional co-precipitation and ion exchange methods, our findings unequivocally demonstrate the superior efficacy of this approach in achieving high-concentration Mn4+ ion doping within relatively insoluble matrices. The successful application of our optimized phosphor enabled the fabrication of a red light-emitting diode (LED) that exhibits an exceptional photoelectric efficiency of 31.67 % at 350 mA, surpassing the performance of a commercial red LED chip. Furthermore, the stable red-light emission from the phosphor-converted LED (pc-LED) proves instrumental in rapid-response vascular imaging, showcasing the potential of our findings in advancing light sources for biological detection applications. This research provides valuable insights into enhancing red emission efficiency in slightly-soluble fluoride phosphors via novel synthetic strategy, unlocking possibilities for the development of highly efficient light sources in biological detection and imaging applications.

Microwave absorption and hyperthermia properties of titanium dioxide–nickel zinc copper ferrite nanocomposite

Ni0.5Zn0.4Cu0.1Fe2O4 ferrite nanoparticles (NZCUFO) were prepared using a conventional co-precipitation method. The NZCUFO nanoparticles were then combined with titanium dioxide matrix to make the nanocomposite of [TiO2]0.2[Ni0.5Zn0.4Cu0.1Fe2O4]0.8 (TNZCUFO). The formation of the appropriate crystallographic phase was confirmed by analyzing the X-ray diffraction pattern of the samples. Investigations extracted from the X-ray fluorescence spectroscopy, high-resolution transmission electron microscopy, and Raman spectroscopy imply the successful association of ferrite nanoparticles into the TiO2 matrix. At 300 K, the saturation magnetization of NZCUFO and TNZCUFO reaches 34.6 and 23.4 emu/g, respectively. Mössbauer spectra recorded at 77 and 300 K indicate the presence of superparamagnetic behavior. These results were in agreement with the data obtained from magnetic hysteresis loop, zero field cooled, and field-cooled magnetization measurements. Both the samples were exposed to alternating current inductive heating and the extracted results successfully satisfy the condition of hyperthermia therapy for cancer treatment. The electromagnetic wave absorption capabilities of the samples were measured in the microwave region (8–18 GHz). The microwave reflection loss reaches −13.6 dB at 11.6 GHz and −29.7 dB at 11 GHz for the 2 mm thick samples of NZCUFO and TNZCUFO, respectively. The balanced matching of magnetic and dielectric loss, high magnetization, and specific absorption rate of the samples would be extremely useful for diverse soft magnetic applications.

Temperature sensing based on upconversion properties of Yb3+/Ho3+/Tm3+ tri-doped Y2O3 micro particles phosphors obtained by conventional precipitation method

Upconverter materials based on Y0.983-xYb0.012Ho0.005TmxO3, x = 0.000 – 0.012, were synthesized by conventional coprecipitation method followed by calcination process at different temperatures: 900, 1000, and 1100 °C for 4 h under air atmosphere. The materials were characterized by XRD, SEM, and PL. The effects of the dopant concentration and calcination temperature on the upconversion emission quantum yield were investigated upon excitation with CW laser diode at 980 nm, with tunable laser power pump. Predominant emission narrow bands arising from Ho3+ transitions (5F4,5S2→5I8) in the green region and Tm3+ (1G4→3H6) in the blue spectral region, and (3H4 → 4H6) in the infrared region, were observed. The material containing Yb3+, Ho3+ presented values of relative sensitivity (SR) from 1.3 K−1 (13 K) to 0.00119 K−1 (450 K) while the presence of the Yb3+, Ho3+, and Tm3+ in material exhibited 1.2 K−1 (13 K) to 0.00097 K−1 (450 K). The system showed emission via upconversion mechanism, even suspended in aqueous medium. Furthermore, the concentration of Tm3+ showed to be crucial for the change in the upconversion intensity of the present materials. These outcomes strongly suggest that the tri-doped Ho3+, Yb3+, and Tm3+ materials discussed here may be suitable for optical temperature sensing and PDT.

A Liquid and Waste-free Method for Preparing Single Crystal Positive Electrode Materials for Li-ion Batteries

Nickel-rich layered positive electrode materials are normally made by a “co-precipitation-sintering” method. Mixed transition metal hydroxides called “precursors” are prepared by co-precipitation to ensure homogeneous cation mixing at the atomic level and to create spherical particles which ensure high-performance poly-crystalline materials. Single crystal materials, which show better capacity retention in long-term cycling can be made from the same mixed transition metal hydroxide precursors by sintering at a higher temperature which inevitably destroys the spherical morphology present in the initial precursors. Here we describe a method for single crystal positive electrode material production which we call “all-dry synthesis” since it does not require the use of any liquid and creates no waste unlike the co-precipitation method. The exemplary reaction between Ni, MnCO3, and LiOH·H2O was studied in situ by synchrotron XRD in order to define a proper heating scheme for the all-dry process. The crystal structure, particle morphology, surface residual impurities, and electrochemical performance of materials prepared by the “all-dry synthesis” method are equivalent to or even better than those of materials made using a conventional co-precipitation method.

Homogeneous CoCeOx nanocomposites with rich oxygen vacancies for effective catalytic oxidation of toluene

A CoCeOx nanocomposite catalyst was obtained by a template sacrificing method, with hydrothermally prepared carbon spheres as the template. The existence of plenty of functional groups on the surface of carbon spheres led to the uniform dispersion of the Co and Ce metal oxides, with an average crystal size of 6.1 nm. Compared with the conventional coprecipitation method, the catalyst prepared by template sacrificing exhibits better catalytic activity and stability, lower activation energy, and higher turnover frequency in the catalytic oxidation of toluene. The small crystal size, larger pore size, enhanced low-temperature reducibility and abundant oxygen vacancies are responsible for the superior activity. Using in situ FTIR, the oxidation intermediates and reaction pathways were proposed over the Co-Ce oxide nanocomposite catalyst. This work provides an effective method for the synthesis of uniform bimetallic nanocomposites with ultrasmall crystal size, which opens an avenue for new catalyst design methods for the oxidation of volatile organic compounds.

Upconversion properties of Er, Yb co-doped KBi(MoO4)2 nanomaterials for optical thermometry

Rare earth ions doped upconversion materials have an extensive range of utilizations because of their exceptional luminescence properties. Here, scheelite type Yb3+, Er3+ co-doped KBi(MoO4)2 nanomaterials were produced by means of a conventional co-precipitation method at room temperature with a typical crystallite size of 13 nm. 980 nm excitation aided in the investigation of the concentration and power-dependent upconversion emission. The optimum upconversion emission is obtained with Er and Yb concentrations of 0.035 and 0.125 mol%, respectively in KBi(MoO4)2 nanomaterials. The intensity ratio of upconversion emission bands based on 529 and 551 nm is investigated in the temperature range of 200–550 K and the theoretical function is used for fitting the exploratory information. The absolute sensitivity is found to be of maximum value of 0.0123 K-1, indicating that this double molybdate can be utilized as a potential probe for luminescence-based temperature sensing.

Magnetic bentonite decorated with Pd nanoparticles and cross-linked polyvinyl pyridine as an efficient nanocatalyst for Suzuki coupling and 4-Nitrophenol reduction reactions

This study reports the preparation of a novel type of support based on magnetically recyclable bentonite functionalized with divinylbenzene-polyvinyl pyridine (PVP-DVB) for Pd (II) nanocatalyst by a simple cost-effective method. Firstly, the conventional co-precipitation method synthesized Fe3O4 nanoparticles (NPs) onto bentonite sheets. Then the prepared magnetic support surface was functionalized by divinylbenzene-polyvinyl pyridine (PVP-DVB) to create a cross-linked polymer with a high coordination ability with palladium. Repeated nitrogen units in the PVP-DVB polymer chain increase the number of Pd bonds and thus lead to higher performance of the nanocatalyst. Finally, the palladium NPs were simultaneously synthesized and immobilized under mild conditions. The synthesized nanocatalyst was characterized by several methods such as scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy, X-ray diffraction, Fourier-transform infrared spectroscopy, vibrating sample magnetometer, inductively coupled plasma mass spectrometry and thermogravimetric analysis. The efficiency of synthesized heterogeneous nanocatalyst was investigated in Suzuki–Miyaura cross-coupling reactions between a range of aryl halides (X = Cl, Br, I) with phenylboronic acid and in the reduction of 4-nitrophenol (4-NP). Moreover, the synthesized nanocatalyst could be easily recovered and reused several times with an efficiency greater than 90%.