Non-purified commercial multiwalled carbon nanotubes supported on electrospun polyacrylonitrile@polypyrrole nanofibers as photocatalysts for water decontamination

We present a photoactive composite material for water decontamination consisting of non-purified commercial multiwalled carbon nanotubes (CNT(NP)s) supported on an electrospun polymeric mat made of core–sheath polyacrylonitrile–polypyrrole nanofibers. This is the first system that specifically exploits the superior photocatalytic activity of CNT(NP)s compared with the purified carbon nanotubes usually employed. A CNT(NP) still contains the catalytic metal oxide nanoparticles (NPs) used for its synthesis, embedded in the nanotube structure. Under UV-visible irradiation, these NPs generate highly reactive ˙OH radicals capable of degrading the organic molecules adsorbed on the nanotube. Photocatalytic tests on the composite material show that CNT(NP)s act mostly as a source of photogenerated charge carriers. The adsorption of target substrates occurs preferentially onto the polypyrrole sheath, which shuttles the reactive carriers from CNT(NP)s to the substrates. In addition, UV-visible irradiation of semiconducting polypyrrole generates radical species that directly react with the adsorbed substrates. All synthetic procedures reported are scalable and sustainable. This mechanically resistant and flexible composite overcomes one of the weakest aspects of water treatments that employ suspended nanocatalysts, namely the expensive and poorly scalable recovery of the catalyst through nanofiltration. All these features are required for large-scale photocatalytic treatments of polluted water.

Under UV-Vis irradiation, the metallic impurities embedded in non-purified commercial carbon nanotubes generate radicals suitable for advanced oxidation processes. Semiconducting PPY membranes enhance the photo activity of a supported catalyst.     

Photocatalytic hydrogen production and storage in carbon nanotubes: a first-principles study

As it is a promising clean energy source, the production and storage of hydrogen are crucial techniques. Here, based on first-principles calculations, we proposed an integral strategy for the production and storage of hydrogen in carbon nanotubes via photocatalytic processes. We considered a core–shell structure formed by placing a carbon nitride nanowire inside a carbon nanotube to achieve this goal. Photo-generated holes on the carbon nanotube surface promote water splitting. Driven by intrinsic electrostatic field in the core–shell structures, protons produced by water splitting penetrate the carbon nanotube and react with photo-generated electrons on the carbon nitride nanowire to produce hydrogen molecules in the carbon nanotube. Because carbon nanotubes have high hydrogen storage capacity, this core–shell structure can serve as a candidate system for photocatalytic water splitting and safe hydrogen storage.

The production and storage of hydrogen in CNNW/CNT core–shell structures via photocatalytic processes.     

CNT–TiO2 core–shell structure: synthesis and photoelectrochemical characterization

Porous composite coatings, made of a carbon nanotube (CNT)–TiO₂ core–shell structure, were synthesized by the hybrid CVD-ALD process. The resulting TiO₂ shell features an anatase crystalline structure that covers uniformly the surface of the CNTs. These composite coatings were investigated as photoanodes for the photo-electrochemical (PEC) water splitting reaction. The CNT–TiO₂ core–shell configuration outperforms the bare TiO₂ films obtained using the same process regardless of the deposited anatase thickness. The improvement factor, exceeding 400% in photocurrent featuring a core–shell structure, was attributed to the enhancement of the interface area with the electrolyte and the electrons fast withdrawal. The estimation of the photo-electrochemically effective surface area reveals that the strong absorption properties of CNT severely limit the light penetration depth in the CNT–TiO₂ system.

CNT–TiO₂ core–shell nanostructured coatings were made using a hybrid CVD/ALD process. The evaluation of these films as photoanodes for the photoelectrochemical water splitting reaction reveals a clear benefit from the involvement of CNTs.     

Facile synthesis of silver nanocatalyst decorated Fe3O4@PDA core–shell nanoparticles with enhanced catalytic properties and selectivity

In this work, we have successfully prepared core–shell nanoparticles (Fe₃O₄@PDA) wrapped with Ag using a simple and green synthesis method. Without an external reducing agent, silver nanoparticles (Ag NPs) with good dispersibility were directly reduced and deposited on a polydopamine (PDA) layer. Fe₃O₄@PDA@Ag showed excellent catalytic activity and recyclability for 4-nitrophenol, and also exhibited good catalytic selectivity for organic dyes (MO and MB). This simple and green synthesis method will provide a platform for other catalytic applications.

In this work, we have successfully prepared core–shell nanoparticles (Fe₃O₄@PDA) wrapped with Ag using a simple and green synthesis method.     

A low-temperature technique and new strategy for the dual growth of carbon nanotubes and nanorods through the confinement of explosive materials inside a porous structure

In this paper, we report a low temperature technique and new strategy for the dual growth of carbon nanotubes (CNTs) and nanorods (CNRs) with alumina nanoparticles to avoid the high temperature required for CNT and CNR production and their assembling behaviour. In this trend, X-ray diffraction and thermal analysis indicated that the porous system of aluminium species was prepared and saturated with the crystalline structure of ammonium nitrate to act as a solid explosive composite and caused alcohol decomposition inside a pressurized vessel at 250 °C. TEM images and the Raman results confirmed that the CNTs had grown at 250 °C through the decomposition of methanol inside the boehmite structure. Also, the TEM images revealed that the growth of CNTs depended on the ratio between the methanol and the solid explosive. By calcination at 600 °C, the Raman results indicated that the CNTs became more ordered and had fewer defects. In the case of changing methanol to ethanol, the results indicated that methanol was more favorable than ethanol for growing CNTs by this technique. Also, it indicated that ethanol was a good source for producing carbon nanorods. Finally, we concluded that this was probably the first time that carbon nanotubes or nanorods had been prepared at 250 °C and their aggregations prevented through their dual growth with alumina nanoparticles. This dual growth approach is a very promising strategy for building homogeneous nanocomposites based on carbon nanotubes and nanorods.

In this paper, we report a low temperature technique and new strategy for the dual growth of carbon nanotubes (CNTs) and nanorods (CNRs) with alumina nanoparticles to avoid the high temperature required for CNT and CNR production.     

Coarse-grained molecular dynamics simulations of nanoplastics interacting with a hydrophobic environment in aqueous solution

Nanoplastics (NPs) are emerging threats for marine and terrestrial ecosystems, but little is known about their fate in the environment at the molecular scale. In this work, coarse-grained molecular dynamics simulations were performed to investigate nature and strength of the interaction between NPs and hydrophobic environments. Specifically, NPs were simulated with different hydrophobic and hydrophilic polymers while carbon nanotubes (CNTs) were used to mimic surface and confinement effects of hydrophobic building blocks occurring in a soil environment. The hydrophobicity of CNTs was modified by introducing different hydrophobic and hydrophilic functional groups at their inner surfaces. The results show that hydrophobic polymers have a strong affinity to adsorb at the outer surface and to be captured inside the CNT. The accumulation within the CNT is even increased in presence of hydrophobic functional groups. This contribution is a first step towards a mechanistic understanding of a variety of processes connected to interaction of nanoscale material with environmental systems. Regarding the fate of NPs in soil, the results point to the critical role of the hydrophobicity of NPs and soil organic matter (SOM) as well as of the chemical nature of functionalized SOM cavities/voids in controlling the accumulation of NPs in soil. Moreover, the results can be related to water treatment technologies as it is shown that the hydrophobicity of CNTs and functionalization of their surfaces may play a crucial role in enhancing the adsorption capacity of CNTs with respect to organic compounds and thus their removal efficiency from wastewater.

The binding mechanisms of nanoplastics (NPs) to carbon nanotubes as hydrophobic environmental systems have been explored by coarse-grained MD simulations. The results could be closely connected to fate of NPs in soil and water treatment technologies.     

Palladium/graphene oxide nanocomposites with carbon nanotubes and/or magnetite for the reduction of nitrophenolic compounds

Graphene oxide (GO) was synthesised via the oxidation of graphite and was characterised using ATR FTIR, PXRD, SEM, TEM and TGA. These techniques confirmed the presence of characteristic oxygen-containing functional groups and the resulting increase in interlayer spacing in the nanostructure. GO is used as the support to form nanocomposites composed of combinations of the following: iron oxide nanoparticles (Fe₃O₄), carbon nanotubes (CNT) and palladium nanoparticles (Pd). The four final nanocomposites formed are: Pd/GO, Pd/Fe₃O₄/GO, Pd/CNT/GO, and Pd/CNT/Fe₃O₄/GO. Key intermediates were analysed using ATR FTIR for the confirmation of the modification. Additionally, all composites and their precursors underwent electron microscopic analysis to visually assess composite morphologies and the size distribution of deposited nanoparticles. The Fe₃O₄ and Pd nanoparticles were indistinguishable from each other in their spherical shape and particle diameters, which were no bigger than 32 nm. From the TGA, incorporation of Fe₃O₄, CNT and finally Pd into the nanocomposites increased total thermal stability in terms of mass percentage lost over the temperature programme. GO showed significant decomposition, with all nanocomposites remaining relatively stable up to 120 °C. ICP OES results showed total Pd content by mass percentage for each final composite, varied from 7.9% to 9.1% mass Pd/collective mass. XPS confirmed the expected elemental compositions of composites according to their structures and the Pd⁰ : Pd^II ratios are obtained. The nanocomposites were tested for the catalytic reduction of nitrophenols. Pd/CNT/Fe₃O₄/GO gave the highest TOF′ for the reduction of 4-NP and 2-NP. For the reduction of 3-NP, Pd/GO showed the highest TOF′. Nitrophenol''s pK_a and catalyst TOF′ correlated in a direct proportional relationship for Pd/GO and Pd/Fe₃O₄/GO. It was found that Pd⁰ surpassed Pd^II in catalytic activity. Reduction of Pd^II to Pd⁰ took place during the first catalytic cycle.

Comparison of the catalytic activity for the reduction of nitrophenol over palladium-supported graphene oxide nanocomposites modified with iron oxide nanoparticles and/or carbon nanotubes.     

Characterization of contact resistances in ceramic-coated vertically aligned carbon nanotube arrays

Despite the technological significance of carbon nanotube (CNT) arrays and metal-oxide coated CNTs for electronic and electrochemical devices such as supercapacitors, lithium-ion batteries, and solar-chemical cells, sub-optimal device performance often results due to large contact resistance between the CNTs and the metallic current collectors or between the CNTs and their ceramic coatings. While contact resistance measurements are regularly carried out on individually contacted CNTs, contact resistance measurements on vertically aligned (VA) CNT arrays are not routine. Here, we demonstrate that two-probe electrical current–voltage measurements and electrochemical impedance spectroscopy can be used to probe the end contact resistance and side contact resistances of coated and uncoated VACNT arrays in order to optimize material deposition and selection.

End- and side-contact resistances between carbon nanotubes and contacts are easily probed in vertically aligned arrays.     

Core–shell Pd–P@Pt–Ni nanoparticles with enhanced activity and durability as anode electrocatalyst for methanol oxidation reaction

Pd–P@Pt–Ni core–shell nanoparticles, which consisted of a Pd–P alloy as a core and Pt–Ni thin layer as a shell, were explored as electrocatalysts for methanol oxidation reaction. The crystallographic information and the electronic properties were fully investigated by X-ray diffraction and X-ray photoelectron spectroscopy. In the methanol electrooxidation reaction, the particles showed high catalytic activity and strong resistance to the poisoning carbonaceous species in comparison with those of commercial Pt/C and the as-prepared Pt/C catalysts. The excellent durability was demonstrated by electrochemically active surface area loss and chronoamperometric measurements. These results would be due to the enhanced catalytic properties of Pt by the double synergistic effects from the core part and the nickel species in the shell part.

The Pd–P@Pt–Ni core–shell nanoparticles consist of an amorphous core and a low-crystalline shell. They exhibit the excellent catalytic properties in MOR owing to the double synergistic effects from the core and the nickel species in the shell.     

One-pot one-step synthesis of Au@SiO2 core–shell nanoparticles and their shell-thickness-dependent fluorescent properties

Herein, we report a one-pot one-step method for the preparation of Au@SiO₂ core–shell nanoparticles (NPs) via a facile heating treatment of an alcoholic-aqueous solution of chloroauric acid (HAuCl₄), 2-methylaminoethanol (2-MAE), cetyltrimethylammonimum bromide (CTAB), and tetraethylorthosilicate (TEOS). The size of the Au core and the thickness of the silica shell can be easily controlled by simply adjusting the volume of HAuCl₄ and TEOS, respectively, which can hardly be achieved by other approaches. The as-prepared Au@SiO₂ core–shell NPs exhibited shell-thickness-dependent fluorescent properties. The optimum fluorescence enhancement of fluorescein isothiocyanate (FITC) was found to occur at a silica shell thickness of 34 nm with an enhancement factor of 5.0. This work provides a new approach for the preparation of Au@SiO₂ core–shell NPs and promotes their potential applications in ultrasensitive analyte detection, theranostics, catalysts and thin-film solar cells.

Au@SiO₂ core–shell nanoparticles with tunable Au core size and silica shell thickness were prepared by a facile one-pot one-step method.     

Direct laser-patterned ultra-wideband antennae with carbon nanotubes

Ultra-wideband (UWB), a radio transmission technology with wide bandwidth exceeding the minimum of 500 MHz or at least 20% of the center frequency, is a revolutionary approach for short-range high-bandwidth wireless communication. In this study, carbon nanotube (CNT) UWB antennas by direct laser-patterning technology have been successfully designed, fabricated and characterized. In contrast with traditional fabrication methods, the direct laser-patterning technology offers an exceptional potential for custom-designed, high-complexity and accuracy device fabrication. The “engraving” process on CNTs exposed to laser can be attributed to the bond breaking of C–C, evaporation of carbon atoms, and oxidation of CNTs by the oxygen molecules. Numerical analysis and experimental studies provide characteristics of CNT slot antennas with a wide impedance bandwidth (from 3.4 GHz to 14 GHz for S₁₁ ≤ −10 dB), high average radiation efficiency (76%) and fractional bandwidth (121%) with small size of 30 × 30 mm². The results indicate the advantages of laser-patterned UWB antennas based on carbon nanotubes, which paves the way for industrial applications, particularly in the world of consumer electronics.

We report a novel one-step laser-patterning technology for CNT ultra-wideband antennas.     

The transport of a charged peptide through carbon nanotubes under an external electric field: a molecular dynamics simulation

The study of interactions between biomolecules and carbon nanotubes (CNTs) is of great importance in CNT-based drug delivery systems and biomedical devices. In this work, the transport of polyarginine (R8) peptide through CNTs under an external electric field was investigated via all-atom molecular dynamics (AAMD) simulation. It was found that the electric field can assist the R8 peptide to overcome the resistance and make the transport smooth. Moreover, the efficiency of transport was improved with the increasing intensity of the electric field in a suitable range. In addition, we also investigated the effects of different types of CNTs on the transport of the R8 peptide and found that the single-walled carbon nanotube (SWCNT) was more suitable for transporting the R8 peptide than the double-walled carbon nanotube (DWCNT) due to its lower energy barrier to the R8 peptide. All these findings shed light on the role of the electric field on the transport of the R8 peptide through CNTs and also gave some valuable insights into the effects of CNT types on the transport process of the peptide.

The role of electric field and types of carbon nanotube influencing the delivery process of peptide through CNTs were studied via all-atom molecular dynamics simulation.     

Modeling the effect of interfacial conductivity between polymer matrix and carbon nanotubes on the electrical conductivity of nanocomposites

This article presents the role of interfacial conductivity between the polymer matrix and nanoparticles in the electrical conductivity of polymer carbon nanotube (CNT) nanocomposites (PCNT) by simple equations. In this methodology, CNT size, CNT conductivity, CNT waviness and interfacial conductivity express the effective length and effective concentration of CNT in PCNT. Additionally, the percolation threshold and the percentages of CNT in the conductive networks are defined by the above mentioned terms. Finally, a simple model is developed to suggest the electrical conductivity of PCNT by CNT dimensions, CNT conductivity, CNT waviness, interphase thickness, interfacial conductivity and tunneling distance. The developed model is applied to show the roles of all parameters in the conductivity. Also, the experimental levels of percolation threshold and conductivity for several samples are compared to the predictions to validate the developed equations. The interfacial conductivity directly controls the electrical conductivity of nanocomposites. In addition, thick interphase, low waviness and short tunneling distance increase the conductivity. Moreover, the predictions show good agreement with the experimental measurements, providing evidence in support of the developed equations.

This article presents the role of interfacial conductivity between the polymer matrix and nanoparticles in the electrical conductivity of polymer carbon nanotube (CNT) nanocomposites (PCNT) by simple equations.     

Counterion coupled (COCO) gemini surfactant capped Ag/Au alloy and Ag@Au core–shell nanoparticles for cancer therapy

Hybrid silver (Ag)–gold (Au) nanoparticles (NPs) with different sizes and compositions were synthesized. Ag/Au alloy and Ag@Au core–shell type NPs were prepared from Ag and Au with various ratios using the COCO gemini surfactant, 1,6-bis (N,N-hexadecyldimethylammonium) adipate (COCOGS), 16-6-16 as a stabilizer. The formation of the Ag/Au alloy and Ag@Au core–shell was confirmed by UV-visible absorption spectroscopy, high-resolution transmission electron microscopy (HRTEM), energy-dispersive X-ray spectroscopy (EDX) and selected area electron diffraction (SAED) patterns. Depending on the composition of the Ag/Au alloy NPs, the λ_max values varied from 408 nm to 525 nm. FTIR measurements were used to evaluate the adsorption of the COCO gemini surfactant (16-6-16) on the Ag/Au alloy and Ag@Au core–shell surface. In this present work, we study how to achieve the stability and activity of the COCO gemini surfactant (16-6-16) capped Ag/Au alloy and Ag@Au core–shell NPs for developing novel anti-cancer agents by evaluating their potentials in the Hep-2 cell line model. Thus the developed core–shell NPs were possibly involved in inducing cytotoxicity followed by inhibition of cell proliferation to the cancer cells with apoptosis induction. The developed core–shell NPs might serve as highly applicable agents in the development of next-generation cancer chemotherapeutic agents.

In this work hybrid silver (Ag)–gold (Au) nanoparticles (NPs) with different sizes and compositions were synthesized and applied for anticancer evaluations and which is effectively involved in cancer cell apoptosis through DNA damage.     

Enhanced oxygen reduction activity of Pt shells on PdCu truncated octahedra with different compositions

Pd@Pt core–shell nanocrystals with ultrathin Pt layers have received great attention as active and low Pt loading catalysts for oxygen reduction reaction (ORR). However, the reduction of Pd loading without compromising the catalytic performance is also highly desired since Pd is an expensive and scarce noble-metal. Here we report the epitaxial growth of ultrathin Pt shells on Pd_xCu truncated octahedra by a seed-mediated approach. The Pd/Cu atomic ratio (x) of the truncated octahedral seeds was tuned from 2, 1 to 0.5 by varying the feeding molar ratio of Pd to Cu precursors. When used as catalysts for ORR, these three Pd_xCu@Pt core–shell truncated octahedra exhibited substantially enhanced catalytic activities compared to commercial Pt/C. Specifically, Pd₂Cu@Pt catalysts achieved the highest area-specific activity (0.46 mA cm⁻²) and mass activity (0.59 mA μg_Pt⁻¹) at 0.9 V, which were 2.7 and 4.5 times higher than those of the commercial Pt/C. In addition, these Pd_xCu@Pt core–shell catalysts showed a similar durability with the commercial Pt/C after 10 000 cycles due to the dissolution of active Cu and Pd in the cores.

Pd_xCu@Pt core–shell truncated octahedra were synthesized and exhibited substantially enhanced catalytic properties for oxygen reduction reaction relative to Pt/C.     

In situ synthesis of copper nanoparticles encapsulated by nitrogen-doped graphene at room temperature via solution plasma

Metal–carbon core–shell nanostructures have gained research interest due to their better performances in not only stability but also other properties, such as catalytic, optical, and electrical properties. However, they are limited by complicated synthesis approaches. Therefore, the development of a simple method for the synthesis of metal–carbon core–shell nanostructures is of great significance. In this work, a novel Cu–core encapsulated by a N-doped few-layer graphene shell was successfully synthesized in a one-pot in-liquid plasma discharge, so-called solution plasma (SP), to our knowledge for the first time. The synthesis was conducted at room temperature and atmospheric pressure by using a pair of copper electrodes submerged in a DMF solution as the precursor. The core–shell structure of the obtained products was confirmed by HR-TEM, while further insight information was explained from the results of XRD, Raman, and XPS measurements. The obtained Cu-core encapsulated by the N-doped few-layer graphene shell demonstrated relatively high stability in acid media, compared to the commercial bare Cu particles. Moreover, the stability was found to depend on the thickness of the N-doped few-layer graphene shell which can be tuned by adjusting the SP operating conditions.

An excellent corrosion protection for copper nanoparticles by nitrogen-doped few-layer graphene via solution plasma process.     

Liquid crystallinity of carbon nanotubes

In this review, we first briefly recapitulate the orientation characteristics of liquid crystalline carbon nanotubes (CNTs), emphasizing their inherent properties. Both the high Young''s modulus and the strong attractive interaction between them make the liquid crystallinity apt to show splay deformations (splay defects). It is these defects that often produce apparent low-order structures for long and deformed nanotubes. However, the application of doping, shearing, magnetic or electric fields will be efficient routes toward highly ordered CNT assemblies from such defects. Then, we describe the electrical behavior of CNTs in the electric field, which combines desirable features of the CNTS with those of classical liquid crystals (LCs). An electric field will generate an induced dipole moment on CNTs and align them in the field direction, minimizing the dipolar energy. Finally, we review the potential application of CNTs in the area of liquid crystal displays (LCD). In the LC cell unit, CNTs as dopants in LC layers can have compatible stability with LCs, with the orientation consistent and with surprising complementary advantages. And also CNT films as nanostructured electrodes can substitute ITO electrodes in the LC cell unit, exhibiting a strong electrical anisotropy due to their excellent axial conductivity. Furthermore, CNT films as an alignment layer have the potential to replace the traditional PI film, aligning LC molecules effectively along the direction of the nanotubes. Besides, CNTs acting as polarizers can absorb or transmit incident light when the electric vector propagates parallel or perpendicular to the nanotube axis. All of these applications demonstrate that CNTs in LC ordering will effectively improve the performance of materials and their related devices. Thus, we should improve the ordering of CNT assemblies as far as possible, which is critical to make full use of their exceptional axial properties and further to develop novel materials and applications successfully.

In this review, we first briefly recapitulate the orientation characteristics of liquid crystalline carbon nanotubes (CNTs), emphasizing their inherent properties.     

Non-photochemical catalytic hydrolysis of methyl parathion using core–shell Ag@TiO2 nanoparticles

Highly water-dispersible core–shell Ag@TiO₂ nanoparticles were prepared and shown to be catalytically active for the rapid degradation of the organothiophosphate pesticide methyl parathion (MeP). Formation of the hydrolysis product, p-nitrophenolate was monitored at pH 7.5 and 8.0, using UV-Vis spectroscopy. ³¹P NMR spectroscopy confirmed that hydrolysis is the predominant pathway for substrate breakdown under non-photocatalytic conditions. We have demonstrated that the unique combination of TiO₂ with silver nanoparticles is required for catalytic hydrolysis with good recyclability. This work represents the first example of MeP degradation using TiO₂ doped with AgNPs under mild and ambient conditions. Analysis of catalytic data and a proposed dark mechanism for MeP hydrolysis using core–shell Ag@TiO₂ nanoparticles are described.

Ag@TiO₂ non-photochemical catalyzed degradation of organophosphosphates.     

Melamine as a single source for fabrication of mesoscopic 3D composites of N-doped carbon nanotubes on graphene

Integration of two-dimensional graphene and one-dimensional carbon nanotubes (CNTs) to create potentially useful 3D mesoscopic carbon structures with enhanced properties relative to the original materials is very desirable. Here, we report a novel and simple route using chemical vapor deposition (CVD) methods to fabricate bead-like nitrogen-doped CNT/graphene composites (NCNT/G) via a simple pyrolysis of the N-rich melamine in the presence of graphene oxide (GO) as a substrate using a Mn–Ni–Co ternary catalyst. We have characterized these structures by field-emission scanning electron microscopy, transmission electron microscopy, X-ray diffraction, Raman spectra, isothermal analyses, and X-ray photoelectron spectroscopy. The three dimensional NCNT/G hybrids have unique network structures, moderate graphitization, high specific surface area, good mesoporosity, and N doping, which makes them promising materials for applications in energy storage and conversion.

Integration of two-dimensional graphene and one-dimensional carbon nanotubes (CNTs) to create potentially useful 3D mesoscopic carbon structures with enhanced properties relative to the original materials is very desirable.     

One-step chemical vapor deposition fabrication of Ni@NiO@graphite nanoparticles for the oxygen evolution reaction of water splitting

NiO combined with conductive materials is a practicable way to improve its catalytic property for the oxygen evolution reaction (OER) by enhancing its electrical conductivity. Herein, Ni@NiO@graphite nanoparticles less than 20 nm in average diameter were synthesized by a one-step chemical vapor deposition process. Due to the deliberately controlled lack of oxygen, Ni particles and carbon clusters decomposed from NiCp₂ precursors were oxidized incompletely and formed Ni@NiO core–shell nanoparticles coated by a graphite layer. The thickness of the graphite layer and the content of Ni were controlled by varying deposition temperature. The electrochemical activity towards the oxygen evolution reaction was assessed within alkaline media. Compared with commercial NiO powder, the Ni@NiO@graphite nanoparticles with the unique core–shell microstructure exhibit excellent OER performance, i.e., an overpotential of 330 mV (vs. RHE) at 10 mA cm⁻² and a Tafel slope of 49 mV dec⁻¹, due to the improved electrical conductivity and more active sites. This work provides a facile and rapid strategy to produce nanoparticles with unique microstructures as highly active electrocatalysts for the OER.

Ni@NiO@graphite nanoparticles with excellent OER performance were synthesized by a one-step chemical vapor deposition process.