Rice husk-SiO2 supported bimetallic Fe–Ni nanoparticles: as a new,powerful magnetic nanocomposite for the aqueous reduction of nitro compounds to amines

This paper reports a novel green procedure for immobilization of bimetallic Fe/Ni on amorphous silica nanoparticles extracted from rice husk (RH-SiO₂). The heterogeneous nanocomposite (Fe/Ni@RH-SiO₂) was identified using SEM, EDX, TEM, BET, H₂-TPR, TGA, XRD, VSM, ICP-OES, and FT-IR analyses. The Fe/Ni@RH-SiO₂ nanocomposite was applied as a powerful catalyst for the reduction of structurally diverse nitro compounds with sodium borohydride (NaBH₄) in green conditions. This procedure suggests some benefits such as green chemistry-based properties, short reaction times, non-explosive materials, easy to handle, fast separation and simple work-up method. The catalyst was separated by an external magnet from the reaction mixture and was reused for 9 successive cycles with no detectable changes of its catalytic efficiency.

This paper reports a novel green procedure for immobilization of bimetallic Fe/Ni on amorphous silica nanoparticles extracted from rice husk (RH-SiO₂).     

Effect of thermal treatment of Pd decorated Fe/C nanocatalysts on their catalytic performance for formic acid oxidation

The thermal treatment of bimetallic nanocatalysts plays an important role in determining their catalytic performance. Here tuning the surface oxidized metal species of bimetallic Pd–Fe electrocatalysts for the formic acid (FA) oxidation reaction is reported and a correlation between the surface oxidized metal species of the Pd–Fe nanoparticles and their catalytic activities is proposed. The structural details of the Pd–Fe/C catalysts are characterized by X-ray diffraction, X-ray photoelectron spectroscopy and high-sensitivity low-energy ion scattering (HS-LEIS). Cyclic voltammetry measurements demonstrated that the mass activity of the Pd–Fe nanoparticles with a molar ratio of Pd/Fe = 1/15 is about 7.4 times higher than that of Pd/C. This enhancement could be attributed to the synergistic effect between Pd(0) and Pd oxidized species on the surface of the Pd–Fe/C treated sample and electronic effects. This finding demonstrates the importance of surface oxidized metal species at the nanoscale in harnessing the true electrocatalytic potential of bimetallic nanoparticles and opens up strategies for the development of highly active bimetallic nanoparticles for electrochemical energy conversion.

The thermal treatment of bimetallic nanocatalysts plays an important role in determining their catalytic performance.     

Re-dispersion of Pd-based bimetallic catalysts by hydrothermal treatment for CO oxidation

The Pd/CeO₂ catalyst, which is highly active catalyst in automobile emission control especially for CO oxidation, often suffers from severe sintering under harsh condition, specifically hydrothermal treatment. Here, we report re-dispersion of Pd-based bimetallic (Pd–Fe, Pd–Ni, and Pd–Co) catalysts deposited on ceria by hydrothermal treatment at 750 °C using 10% H₂O. The re-dispersion was confirmed by various characterization techniques of transmission electron microscopy, CO chemisorption, CO-diffuse reflectance infrared Fourier transform, CO-temperature programmed desorption, and X-ray absorption spectroscopy. The dispersion of Pd increased significantly after hydrothermal treatment, resulting in improved CO oxidation activity. The presence of secondary transition metals enhanced the CO oxidation activity further, especially hydrothermally treated Pd–Fe bimetallic catalyst showed the highest activity for CO oxidation.

PdM (M: Fe, Co, Ni) catalysts deposited on ceria were hydrothermally treated, resulting in re-dispersion of the metal species. They showed enhanced activity for CO oxidation.     

Pyroelectric synthesis of Au/Pt bimetallic nanoparticles–BaTiO3 hybrid nanomaterials

This paper introduces an approach to synthesize bimetallic nanoparticles under an alternating temperature field in aqueous solution. During the synthesis, pyro-catalytic barium titanate is used as the substrate to reduce the metallic ions dispersed in the solution due to the generated charges at the surface of pyro-materials under temperature oscillation. Chloroauric acid and potassium tetrachloroplatinate are used as precursors to produce gold/platinum bimetallic nanoparticles through a pyro-catalytic process. Transmission electron microscopy characterization, in combination with energy dispersive X-ray spectroscopy mapping, demonstrates that the bimetallic nanoparticle is composed of an Au core and Au/Pt alloy shell structure. Compared to the conventional approaches, the pyroelectric synthesis approach demonstrated in this work requires no toxic reducing agents and waste heat can be used as a thermal energy source in the synthesis. Hence, it offers a potential “green” synthetic method for bimetallic nanoparticles.

A “green” synthetic approach to Au/Pt bimetallic nanoparticles under an alternating temperature field.     

The promoted catalytic hydrogenation performance of bimetallic Ni–Co–B noncrystalline alloy nanotubes

A noncrystalline Ni–B alloy in the shape of nanotubes has demonstrated its superior catalytic performance for some hydrogenation reactions. Remarkable synergistic effects have been observed in many reactions when bimetallic catalysts were used; however, bimetallic noncrystalline alloy nanotubes are far less investigated. Here, we report a simple acetone-assisted lamellar liquid crystal approach for synthesizing a series of bimetallic Ni–Co–B nanotubes and investigate their catalytic performances. The dilution effect of acetone on liquid crystals was characterized by small-angle X-ray diffraction (SAXRD) and scanning electron microscopy (SEM). The Ni/Co molar ratio of the catalyst was varied to study the composition, porous structure, electronic interaction, and catalytic efficiency. In the liquid-phase hydrogenation of p-chloronitrobenzene, the as-prepared noncrystalline alloy Ni–Co–B nanotubes exhibited higher catalytic activity and increased stability as compared to Ni–B and Co–B alloy nanotubes due to electronic interactions between the nickel and cobalt. The excellent hydrogenation performance of the Ni–Co–B nanotubes was attributed to their high specific surface area and the characteristic confinement effects, compared with Ni–Co–B nanoparticles.

Ni–Co–B noncrystalline alloy nanotubes exhibited higher catalytic activity and better stability due to the synergistic interactions between nickel and cobalt.     

Green synthesis of a Cu/MgO nanocomposite by Cassytha filiformis L. extract and investigation of its catalytic activity in the reduction of methylene blue,congo red and nitro compounds in aqueous media

This work reports the green synthesis of a Cu/MgO nanocomposite using Cassytha filiformis L. extract as a reducing agent without stabilizers or surfactants. The immobilization of Cu NPs was confirmed by Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), transmission electron microscopy (TEM), field emission scanning electron microscopy (FESEM) and energy dispersive X-ray spectroscopy (EDS). The Cu/MgO nanocomposite acts as a heterogeneous and recyclable catalyst for the reduction of 4-nitrophenol (4-NP), 2,4-dinitrophenylhydrazine (2,4-DNPH), methylene blue (MB) and congo red (CR) using sodium borohydride in aqueous media at room temperature. The catalyst was recycled multiple times without any significant loss of its catalytic activity.

This work reports the green synthesis of a Cu/MgO nanocomposite using Cassytha filiformis L. extract as a reducing agent without stabilizers or surfactants.     

A nanostructured SnO2/Ni/CNT composite as an anode for Li ion batteries

A SnO₂/Ni/CNT nanocomposite was synthesized using a simple one-step hydrothermal method followed by calcination. A structural study via XRD shows that the tetragonal rutile structure of SnO₂ is maintained. Further, X-ray photoelectron spectroscopy (XPS) and Raman studies confirm the existence of SnO₂ along with CNTs and Ni nanoparticles. The electrochemical performance was investigated via cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and galvanostatic charge–discharge measurements. The nanocomposite has been used as an anode material for lithium-ion batteries. The SnO₂/Ni/CNT nanocomposite exhibited an initial discharge capacity of 5312 mA h g⁻¹ and a corresponding charge capacity of 2267 mA h g⁻¹ during the first cycle at 50 mA g⁻¹. Pristine SnO₂ showed a discharge/charge capacity of 1445/636 mA h g⁻¹ during the first cycle at 50 mA g⁻¹. This clearly shows the effects of the optimum concentrations of CNTs and Ni. Further, the nanocomposite (SnNiCn) shows a discharge capacity as high as 919 mA h g⁻¹ after 210 cycles at a current density of 400 mA g⁻¹ in a Li-ion battery set-up. Thus, the obtained capacity from the nanocomposite is much higher compared to pristine SnO₂. The higher capacity in the nanoheterostructure is due to the well-dispersed nanosized Ni-decorated stabilized SnO₂ along with the CNTs, avoiding pulverization as a result of the volumetric change of the nanoparticles being minimized. The material accommodates huge volume expansion and avoids the agglomeration of nanoparticles during the lithiation and delithiation processes. The Ni nanoparticles can successfully inhibit Sn coarsening during cycling, resulting in the enhancement of stability during reversible conversion reactions. They ultimately enhance the capacity, giving stability to the nanocomposite and improving performance. Additionally, the material exhibits a lower Warburg coefficient and higher Li ion diffusion coefficient, which in turn accelerate the interfacial charge transfer process; this is also responsible for the enhanced stable electrochemical performance. A detailed mechanism is expressed and elaborated on to provide a better understanding of the enhanced electrochemical performance.

SnO₂/Ni/CNT nanocomposite approach has been demonstrated which confers shielding against volume expansion due to the use of optimum % of Ni & CNT exhibiting superior cycling stability and rate capabilities of the stable electrode structure.     

Synergistic effect of Co–Ni co-bridging with MoS2 nanosheets for enhanced electrocatalytic hydrogen evolution reactions

The depletion of fossil fuels and associated environmental problems have drawn our attention to renewable energy resources in order to meet the global energy demand. Electrocatalytic hydrogen evolution has been considered a potential energy solution due of its high energy density and environment friendly technology. Herein, we have successfully synthesized a noble-metal-free Co–Ni/MoS₂ nanocomposite for enhanced electrocatalytic hydrogen evolution. The nanocomposite has been well characterized using HRTEM, elemental mapping, XRD, and XPS analysis. The as-synthesized nanocomposite exhibits a much smaller onset potential and better current density than those of Co–MoS₂, Ni–MoS₂ and MoS₂, with a Tafel value of 49 mV dec⁻¹, which is comparable to that of a commercial Pt/C catalyst. The synergistic effect and interfacial interaction of Co–Ni bimetallic nanoparticles enhances the intrinsic modulation in the electronic structure resulting in an improved HER performance. Moreover, the electrochemical impedance spectroscopic results suggest smaller resistance values for the Co–Ni/MoS₂ nanocomposite, compared to those for the charge transfer of bare nanosheets, which increase the faradaic process and in turn enhance the HER kinetics for a better performance. Our as-synthesized Co–Ni/MoS₂ nanocomposite holds great potential for the future synthesis of noble-metal-free catalysts.

A noble-metal-free Co–Ni/MoS₂ nanocomposite was synthesized, which showed enhanced electrocatalytic hydrogen evolution performance.     

Preparation and characterization of Ag–Pd bimetallic nano-catalysts in thermosensitive microgel nano-reactor

Thermosensitive microgels consisting of a solid core of polystyrene and a shell of cross-linked poly(N-isopropylacrylamide) (PNIPA) were synthesized as nano-reactors, in which Ag–Pd bimetallic nanoparticles were prepared through simultaneous in situ reduction reaction. The spatial distribution of metallic nanoparticles in the microgels was analyzed by small angle X-ray scattering (SAXS) and the results indicated that metal nanoparticles were mainly located in the inner layer of microgels. The catalytic activity of Ag–Pd bimetallic nanoparticles was investigated using the reduction of p-nitrophenol to p-aminophenol by NaBH₄ as model reaction. The data demonstrated that Ag–Pd bimetallic nanoparticles showed enhanced catalytic activity compared to each monometallic nanoparticle alone and their catalytic activity was controllable by temperature due to the volume transition of PNIPA microgels.

Thermosensitive microgels with PS core and cross-linked PNIPA shell were synthesized as nano-reactor to prepare Ag–Pd bimetallic nanoparticles.     

Influence of electrochemical co-deposition of bimetallic Pt–Pd nanoclusters on polypyrrole modified ITO for enhanced oxidation of 4-(hydroxymethyl) pyridine

Bimetallic Pt–Pd nanoparticles were dispersed on polypyrrole coated indium-tin oxide coated polyethylene terephthalate sheets (ITO-PET sheets). The excellent filming property of pyrrole gives a high porous uniform active area for the proper adsorption of bimetallic transition metal nanoparticles. Electrochemical behavior of the modified electrodes was determined using cyclic voltammetry and impedance studies. The physicochemical properties of the modified electrodes were analyzed by scanning electron microscopy, X-ray diffraction spectroscopy, X-ray photoelectron spectroscopy and Fourier transform infrared spectroscopy. To study the electrochemical oxidation of 4-(hydroxymethyl) pyridine in the presence of sodium nitrate in aqueous acidic medium, the modified electrode was used. It is evident from the study that the modified electrode shows better electrochemical activity towards the oxidation of 4-(hydroxymethyl) pyridine.

Bimetallic Pt–Pd nanoparticles were dispersed on polypyrrole coated indium–tin oxide coated polyethylene terephthalate sheets (ITO-PET sheets).     

Synthesis and characterization of graphene oxide sheets integrated with gold nanoparticles and their applications to adsorptive removal and catalytic reduction of water contaminants

Here, we report the facile synthesis of graphene oxide–gold (GO–Au) nanocomposites and their use as adsorbents for the removal of toxic industrial dyes from water and as catalysts for the individual and simultaneous reduction of a dye and a nitro compound in aqueous medium. GO sheets were prepared using a modified Hummers method while Au nanoparticles were integrated on GO sheets by reducing Au(iii) ions on the surfaces of GO sheets using sodium citrate as a reducing agent. The prepared composite was characterized with field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), elemental dispersive X-ray analysis (EDX), X-ray diffraction (XRD), Fourier transform infra-red (FT-IR) spectroscopy and thermal gravimetric analysis (TGA). The GO–Au nanocomposite demonstrated efficient adsorption capacities and recyclability for malachite green (MG) and ethyl violet (EV) dyes. The effects of various experimental parameters including temperature, pH, contact time, and adsorbent dose were studied. From the simulation of experimental data with different adsorption isotherms and kinetic models it was found that the adsorption of both the dyes followed the Freundlich adsorption model and a pseudo-second order kinetic model, respectively. Moreover, the adsorbent showed better recyclability for both dyes without any compromise on the removal efficiency. Similarly, the catalytic performance for the reduction of 2-nitroaniline (2-NA) has been investigated in detail by using the prepared nanocomposite as a catalyst. Most importantly, we reported the simultaneous adsorption of cationic and anionic dyes from water using the prepared nanocomposite as well as the simultaneous catalytic reduction of a mixture of EV and 2-NA. So, considering the facile synthesis process and the efficient removal of a variety of dyes and the catalytic performance this work opens up a tremendous opportunity to bring GO based nanocomposites from experimental research to practically applied materials for wastewater treatment.

Preparation of graphene oxide–gold (GO–Au) nanocomposites as adsorbents and catalysts for decontamination of water.     

Diatomite/Cu/Al layered double hydroxide hybrid composites for polyethylene degradation

A diatomite/Cu/Al layered double hydroxide hybrid composite (DI-LDH) was synthesized using the hydrothermal method. The synthesized DI-LDH composites were characterized via X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM) and the Brunauer–Emmett–Teller (BET) method. Polyethylene degradation over DI-LDH was studied in a batch reactor. DI-LDH showed layered structures, indicating that the diatomite/Cu/Al double hydroxide hybrid was successfully synthesized. A significant decrease in the degradation temperature and the released amounts of CO and CO₂ was observed in the DI-LDH catalytic degradation reaction, which indicated that DI-LDH was helpful for the polyethylene degradation reaction. The X-ray photoelectron spectroscopy (XPS) results suggested that the reaction of Cu²⁺ → Cu⁺ occurred in polyethylene catalytic pyrolysis, which resulted in the decrease in the released CO amount. DI-LDH may be a potential environmental catalyst that can be applied to treat LDPE waste.

DI-LDH that can reduce the pyrolysis temperature of LDPE and the release of carbon monoxide (CO) and carbon dioxide (CO₂).     

Mussel-inspired immobilization of Au on bare and graphene-wrapped Ni nanoparticles toward highly efficient and easily recyclable catalysts

Bimetallic nanocatalysts have been gaining huge research attention in the heterogeneous catalysis community recently owing to their tunable properties and multifunctional characteristics. In this work, we fabricated a bimetallic core–shell nanocomposite catalyst by employing a mussel-inspired strategy for immobilizing gold nanoparticles (AuNP) on the surface of nickel nanoparticles (NiNP). NiNPs obtained from the reduction of Ni(ii) were first coated with polydopamine to provide the anchoring sites towards the robust immobilization of AuNPs. The as-synthesized nanocomposite (Ni–PD–Au) exhibited outstanding catalytic activity while reducing methylene blue (MB) and 4-nitrophenol (4-NP) yielding rate constants 13.11 min⁻¹ and 4.21 min⁻¹, respectively, outperforming the catalytic efficiency of its monometallic counterparts and other similar reported catalysts by large margins. The superior catalytic efficiency of the Ni–PD–Au was attributed to the well-known synergistic effect, which was experimentally investigated and compared with prior reports. Similar bio-inspired immobilization of AuNPs was also applied on graphene-wrapped NiNPs (Ni-G) instead of bare NiNPs to synthesize another composite catalyst (Ni-G–PD–Au), which yet again exhibited synergistic catalytic activity. A comparative study between the two nanocomposites suggested that Ni–PD–Au excelled in catalytic activity but Ni-G–PD–Au provided noteworthy stability showing ∼100% efficiency over 17 repeated cycles. However, along with excellent synergistic performance, both nanocomposites demonstrated high magnetization and thermal stability up to 350 °C ascertaining their easy separation and sustainability for high-temperature applications, respectively.

Employing a bio-inspired strategy we combine Ni and Au nanoparticles into a single scaffold to achieve excellent synergistic catalysis along with high recyclability.     

Controlling crystal growth of MIL-100(Fe) on Ag nanowire surface for optimizing catalytic performance

Ag/MIL-100(Fe) core/sheath nanowire with controllable thickness of the MIL-100(Fe) sheath was prepared by controlling the crystal growth of MIL-100(Fe) on the Ag nanowire surface. The evolution of the MIL-100(Fe) sheath monitored by transmission electron microscopy (TEM), scanning electron microscopy (SEM), powder X-ray diffraction (XRD), thermogravimetric analyses (TGA), X-ray photoelectron spectroscopy (XPS), fourier transform infrared spectroscopy (FT-IR), and N₂ adsorption–desorption analysis indicates that the thickness of the MIL-100(Fe) sheath increases with the increasing number of crystal growth cycles of MIL-100(Fe) on the Ag nanowire surface. Catalytic reaction over Ag/MIL-100(Fe) core/sheath nanowire suggests that the thickness of the MIL-100(Fe) sheath largely influences the catalytic performance and it is quite important to control the crystal growth of MIL-100(Fe) on the Ag nanowire surface for optimizing catalytic performance.

Ag/MIL-100(Fe) core/sheath nanowire with controlled crystal growth of MIL-100(Fe) on the Ag nanowire surface was prepared for optimizing catalytic performance.     

Synthesis of plasmonic Fe/Al nanoparticles in ionic liquids

Bottom-up and top-down approaches are described for the challenging synthesis of Fe/Al nanoparticles (NPs) in ionic liquids (ILs) under mild conditions. The crystalline phase and morphology of the metal nanoparticles synthesized in three different ionic liquids were identified by powder X-ray diffractometry (PXRD), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), selected-area electron diffraction (SAED) and fast Fourier transform (FFT) of high-resolution TEM images. Characterization was completed by scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM-EDX) for the analysis of the element composition of the whole sample consisting of the NPs and the amorphous background. The bottom-up approaches resulted in crystalline FeAl NPs on an amorphous background. The top-down approach revealed small NPs and could be identified as Fe₄Al₁₃ NPs which in the IL [OPy][NTf₂] yield two absorption bands in the green-blue to green spectral region at 475 and 520 nm which give rise to a complementary red color, akin to appropriate Au NPs.

Fe/Al NPs of the right size mimic with their red color the electronic surface structure of Au NPs.     

Microbial synthesis of hollow porous Prussian blue@yeast microspheres and their synergistic enhancement of organic pollutant removal performance

In this work, Prussian blue nanoparticles (PB NPs) were in situ grown on S. cerevisiae cells via one-step hydrothermal synthesis and the as-prepared Prussian blue@yeast (PB@yeast) hybrids exhibited synergistic adsorption and Fenton catalytic activities. FE-SEM, XRD and BET analysis of the prepared samples confirmed the successful formation of hollow porous structured PB@yeast microspheres, while FT-IR and XPS spectra indicated the fine structures were occupied by both functional adsorptive and catalytic sites. The experimental results of adsorption coupled Fenton reaction of PB@yeast hybrid microspheres revealed that the functional groups on the cell wall and the active iron sites in PB framework were fully utilized due to the triple synergistic effects of adsorption–Fenton catalysis–adsorption sites regeneration, thus endowing synergistically enhanced performance in removal of the selected cationic methylene blue (MB), anionic Methyl Orange (MO) and fluorescent brightener 71 (CXT) in aqueous solution. The high Fenton catalytic efficiency was related to the improvement of adsorption, in which the enrichment of contaminant molecules on the outer and inner surface of the hollow porous microspheres could lower mass transfer resistance and shorten charge transport pathways, thereby introducing more efficient Fenton catalytic activity than PB NPs.

Prussian blue was in situ grown on S. cerevisiae cells to obtain PB@yeast, which exhibited synergistically enhanced activity in dye wastewater treatment.     

Chemoselective reduction of nitro and nitrile compounds using an Fe3O4-MWCNTs@PEI-Ag nanocomposite as a reusable catalyst

Multi-walled carbon nanotubes (MWNTs) were modified with carboxylic acid functional groups (MWCNTs-(COOH)_n) prior to decoration with Fe₃O₄ nanoparticles. A further modification step by polyethyleneimine (PEI) resulted in Fe₃O₄-MWCNTs@PEI which provided a suitable platform for coordination and in situ reduction of silver ions to obtain an Fe₃O₄-MWCNTs@PEI-Ag nanocomposite with highly dispersed Ag nanoparticles. The Fe₃O₄-MWCNTs@PEI-Ag hybrid material was characterized by various techniques such as Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), transmission electron microscopy (TEM), vibrating sample magnetometry (VSM), X-ray photoelectron spectroscopy (XPS) and thermogravimetric analysis (TGA), and was used as an efficient catalyst for chemoselective reduction of nitroaromatic and nitrile compounds to their corresponding amines in aqueous solution at ambient temperature. Nitrofurazone, a cytotoxic antibiotic, as a non-aromatic example was also reduced selectively at the nitro group without reduction of the other functionalities in the presence of Fe₃O₄-MWCNTs@PEI-Ag. The catalyst was magnetically recoverable and maintained its activity for at least six cycles without considerable loss of efficiency.

Chemoselective reductions by an Fe₃O₄-MWCNTs@PEI-Ag nanocomposite.     

NiCo alloy nanoparticles electrodeposited on an electrochemically reduced nitrogen-doped graphene oxide/carbon-ceramic electrode: a low cost electrocatalyst towards methanol and ethanol oxidation

In this work, nickel–cobalt alloy nanoparticles were electrodeposited on/in an electrochemically reduced nitrogen-doped graphene oxide (ErN-GO)/carbon-ceramic electrode (CCE) and the resulting nanocomposite (NiCo/ErN-GO/CCE) was evaluated as a low cost electrocatalyst for methanol and ethanol electrooxidation. Field-emission scanning electron microscopy coupled with energy dispersive X-ray spectroscopy, X-ray diffraction, and Fourier-transform infrared spectroscopy were used for the physical characterization of the electrocatalyst. To study the electrochemical behavior and electrocatalytic activity of the prepared electrocatalyst towards the oxidation of methanol and ethanol in alkaline media, cyclic voltammetry, chronoamperometry and electrochemical impedance spectroscopy were utilized. Electrochemical investigation of the introduced electrocatalysts (NiCo alloy and Ni nanoparticles alone electrodeposited on/in different substrates) indicated that NiCo/ErN-GO/CCE has highest activity and stability towards methanol (J_p = 88.04 mA cm⁻²) and ethanol (J_p = 64.23 mA cm⁻²) electrooxidation, which highlights its potential use as an anodic material in direct alcohol fuel cells.

NiCo alloy nanoparticles on the electrochemically reduced nitrogen-doped graphene oxide/carbon-ceramic electrode: a low cost electrocatalyst towards methanol and ethanol oxidation.     

Gold,silver and nickel nanoparticle anchored cellulose nanofiber composites as highly active catalysts for the rapid and selective reduction of nitrophenols in water

Highly active metal nanoparticle (MNP) supported cellulose nanofiber (CNF) composites (Au/CNF, Ni/CNF and Ag/CNF) were prepared for the reduction of 4- and 2-nitrophenols (4-NP and 2-NP) in water. Transmission electron microscopy (TEM) images showed that the ultrafine nanoparticles (Au, Ni and Ag NPs) were uniformly deposited on CNFs surface. The content of Au (9.7 wt%), Ni (21.5 wt%) and Ag (22.6 wt%) in Au/CNF, Ni/CNF and Ag/CNF respectively was determined by energy dispersive spectroscopy (EDS) and inductive coupled plasma-mass spectroscopy (ICP-MS) analysis. The chemical state of the MNPs in Au/CNF, Ni/CNF and Ag/CNF was determined by X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD). The significant metal-support interaction was studied by means of XPS. The Au/CNF, Ni/CNF and Ag/CNF demonstrated excellent catalytic activity towards the reduction of nitrophenols to aminophenols in water. To our delight, even a very low amount of catalyst was also found to be good enough to achieve 100% reduction of 4- and 2-NP with a higher reaction rate (within 5 min). The best rate constant (k_app) values were determined for the cellulose nanocomposites. To the best our knowledge, Au/CNF, Ni/CNF and Ag/CNF are the most efficient nanocatalysts for the reduction of 4- and 2-NP reported to date. The catalytic performance of Au/CNF, Ni/CNF and Ag/CNF was compared with previously reported results. A possible mechanism has been proposed for these catalytic systems.

Metal nanoparticles supported cellulose nanofiber composites (Au/CNF, Ni/CNF and Ag/CNF) were found to be highly efficient nanocatalysts for the rapid and selective reduction of nitrophenols in water.     

Investigation on the enhanced catalytic activity of a Ni-promoted Pd/C catalyst for formic acid dehydrogenation: effects of preparation methods and Ni/Pd ratios

In this present work, we studied the effects of preparation methods and Ni/Pd ratios on the catalytic activity of a Ni-promoted Pd/C catalyst for the formic acid dehydrogenation (FAD) reaction. Two catalysts prepared by co-impregnation and sequential impregnation methods showed completely different Pd states and catalytic activities. As the sequentially impregnated catalyst showed better activity than the co-impregnated catalyst, the sequentially impregnated catalyst was investigated further to optimize the ratio of Ni/Pd. The highest catalytic activity for the FAD reaction was obtained over the seq-impregnated catalyst having a 1 : 1.3 molar ratio of Pd : Ni. The results of X-ray diffraction (XRD) and transmission electron microscopy (TEM) showed that small particle size is one factor improving the catalytic activity, while those of X-ray photoelectron spectroscopy (XPS) and X-ray adsorption near edge structure (XANES) indicate that the electronic modification of Pd to a positively charged ion is another factor. Thus, it can be concluded that the enhanced catalytic activity of the Ni-promoted Pd/C catalyst is attributed to the role of pre-impregnated Ni in facilitating the activity of Pd by constraining the particle growth and withdrawing an electron from Pd.

In this present work, we studied the effects of preparation methods and Ni/Pd ratios on the catalytic activity of a Ni-promoted Pd/C catalyst for the formic acid dehydrogenation (FAD) reaction.