nitrophenols and ceric-oxide

The catalytic performance of gold (Au) decorated cerium oxide nanoparticles (nanoceria) can be potentially crucial because such a defined arrangement of multiple materials may provide improved chemical and biological catalytic activities. In this work, we have utilized a highly localized approach to reduce Au nanoparticles (AuNPs) on the nanoceria-phosphotungstate composite's surface. Phosphotungstic acid (PTA) bound on nanoceria's surface acts as a UV-light dependent redox molecule that specifically reduces AuNPs. The mechanistic study demonstrates that PTA* molecules outstanding electron transfer ability leads to an excellent improvement in the catalytic performance of nanoceria-PTA*-AuNPs composite. Nanoceria-PTA*-AuNPs showed better and faster degradation of 4-nitrophenol than either nanoceria or PTA*-AuNPs. The developed nanoceria-PTA*-AuNPs exhibited efficient (>80 % in 5 min) conversion of 4-NP into 4-AP at room temperature and neutral pH. Additionally, the nanoceria-PTA*-AuNPs also showed improved peroxidase enzyme-like activity than the corresponding control samples. The observed catalytic activity could be due to the rapid electron transfer from nanoceria to AuNPs, where the metal nanoparticle acts as an electron sink, mediated by PTA*. Nanoceria-PTA*-AuNPs showed ∼ 2-fold better catalytic oxidation of peroxidase substrate than PTA*-AuNPs. The reported nanoceria-PTA*-AuNPs nanocomposites are expected to display improved biological enzyme-like activities, photocatalysis, and other biomedical applications.

Topics: Cerium; Gold; Metal Nanoparticles; Nanoparticles; Nitrophenols; Oxidation-Reduction; Peroxidase; Peroxidases

Nanoceria with phosphatase-like behavior shows its great potential for many important biological applications through a catalytic dephosphorylation process. Herein, we synthesize a series of porous nanorods of ceria (PN-CeO

Topics: 4-Nitrophenylphosphatase; Catalysis; Cerium; Hot Temperature; Hydrogen-Ion Concentration; Nanotubes; Nitrophenols; Organophosphorus Compounds; Porosity

A novel dual-mode analytical method by employing nanozyme was developed for the detection of organophosphorus pesticides (OPP) for the first time. The detection principle is that the pesticide could be hydrolyzed to para-nitrophenol (p-NP) in the presence of nanoceria as nanozyme. p-NP exhibits the bright yellow color, and its color intensity has a positive correlation with the pesticide concentration. Meanwhile, the characteristic absorption peak at 400 nm of p-NP increases gradually with the raised concentration of pesticide. Therefore, a dual-mode method including smartphone-based colorimetric and spectroscopic strategies was rationally developed. Herein, methyl-paraoxon was selected as the representative compound. Under the optimum conditions, the detection limits of both two strategies were calculated to be 0.42 μmol L

Topics: Cerium; Colorimetry; Environmental Pollutants; Limit of Detection; Nanoparticles; Nitrophenols; Organophosphorus Compounds; Paraoxon; Pesticides; Plants, Medicinal; Spectrophotometry

Ce2O3 nanoparticle decorated CNT nanocomposites (Ce2O3.CNT NCs) were prepared by a wet-chemical method in basic medium. The Ce2O3.CNT NCs were examined using FTIR, UV/Vis, Field-Emission Scanning Electron Microscopy (FESEM), X-ray electron dispersive spectroscopy (XEDS), X-ray photoelectron spectroscopy (XPS), and powder X-ray diffraction (XRD). A selective 2-nitrophenol (2-NP) sensor was developed by fabricating a thin-layer of NCs onto a flat glassy carbon electrode (GCE, surface area = 0.0316 cm2). Higher sensitivity including linear dynamic range (LDR), long-term stability, and enhanced electrochemical performances towards 2-NP were achieved by a reliable current-voltage (I-V) method. The calibration curve was found linear (R2 = 0.9030) over a wide range of 2-NP concentration (100 pM ~ 100.0 mM). Limit of detection (LOD) and sensor sensitivity were calculated based on noise to signal ratio (~3N/S) as 60 ± 0.02 pM and 1.6×10-3 μAμM-1cm-2 respectively. The Ce2O3.CNT NCs synthesized by a wet-chemical process is an excellent way of establishing nanomaterial decorated carbon materials for chemical sensor development in favor of detecting hazardous compounds in health-care and environmental fields at broad-scales. Finally, the efficiency of the proposed chemical sensors can be applied and utilized in effectively for the selective detection of toxic 2-NP component in environmental real samples with acceptable and reasonable results.

Topics: Carbon; Cerium; Electrochemical Techniques; Electrodes; Environment; Limit of Detection; Metal Nanoparticles; Microscopy, Electron, Scanning; Nanocomposites; Nanotubes, Carbon; Nitrophenols; Photoelectron Spectroscopy; Spectrophotometry, Ultraviolet; Spectroscopy, Fourier Transform Infrared; X-Ray Diffraction

To enhance the catalytic activity of gold nanoparticles (AuNPs) for the hydrogenation of nitro-aromatic chemicals, Pt was introduced into AuNPs to form "bare" PtAu alloy NPs using a physical approach, pulsed laser ablation in liquid (PLAL), on single metal-mixture targets. These PLAL-NPs are deemed to favor catalysis due to the absence of any surfactant molecules on their unique "bare and clean" surface. The PLAL-NPs were facilely assembled onto CeO2 nanotubes (NTs) by simply mixing them without conducting any surface functionalization, representing another advantage of these NPs. Their catalytic activity was assessed in 4-nitrophenol (4-NP) hydrogenation. The reaction catalyzed by alloy-NP/CeO2-NT catalysts demonstrates a remarkably higher reaction rate in comparison with that catalyzed by pure Au and Pt NPs, and other similar Au and Pt containing catalysts reported recently. A "volcano-like" catalytic activity dependence of the alloy NPs on their chemical composition suggests a strong synergistic effect between Au and Pt in the 4-NP reduction, far beyond the simple sum of their individual contributions. It leads to the significantly enhanced catalytic activity of Pt30Au70 and Pt50Au50 alloy NPs, outperforming not only each single constituent, but also their physical mixtures and most recently reported AuNP based nanocatalysts. The favorable d-band center shift of Pt after alloying, and co-operative actions between Pt clusters and nearby Au (or mixed PtAu) sites were proposed as possible mechanisms to explain such a strong synergistic effect on catalysis.

Topics: Alloys; Catalysis; Cerium; Gold; Metal Nanoparticles; Nitrophenols; Oxidation-Reduction; Platinum

We report a simple biogenic-route to narrow the band gap of TiO2 nanocrystals for visible light application by offering a greener method. When an electrochemically active biofilm (EAB) was challenged with a solution of Degussa-TiO2 using sodium acetate as the electron donor, greyish blue-colored TiO2 nanocrystals were obtained. A band gap study showed that the band gap of the modified TiO2 nanocrystals was significantly reduced (E(g) = 2.85 eV) compared to the unmodified white Degussa TiO2 (E(g) = 3.10 eV).

Topics: Bioelectric Energy Sources; Catalysis; Cerium; Electrochemical Techniques; Light; Methylene Blue; Nanoparticles; Nitrophenols; Titanium

Platinum-cerium oxide hybrid nanocatalysts (CeO(2)-Pt) were for the first time designed as bionanolabels for highly efficient electrochemical immunosensing of low-abundance proteins coupling nanocatalyst-based redox cycling with in situ signal amplification strategy.

Topics: Carcinoembryonic Antigen; Catalysis; Cerium; Electrochemical Techniques; Immunoassay; Metal Nanoparticles; Nitrophenols; Oxidation-Reduction; Oxides; Platinum; Polymers; Proteins

Direct fabrication of core-shell or yolk-shell functional nanomaterials via a facile template-free method remains a challenge. In this work, we present a novel approach that involves straightforward chemical transformation and thermal treatment of the infinite coordination polymer particles to obtain composition-tunable CeO(2) yolk-shell structures. Uniform CeO(2) yolk-shell hollow spheres with a high surface area are promising support materials for tiny gold nanoparticles (ca. 4 nm), forming Au-CeO(2) nanocomposites which exhibit a remarkable catalytic activity and high stability for the reduction of p-nitrophenol. A possible mechanism for the formation of CeO(2) yolk-shell microspheres is also proposed.

Topics: Catalysis; Cerium; Gold; Metal Nanoparticles; Nanocomposites; Nitrophenols; Oxidation-Reduction; Polymers; Surface Properties

In an effort to characterize the interaction of cerium oxide nanoparticles (CNPs) in biological systems, we explored the reactivity of CNPs with the phosphate ester bonds of p-nitrophenylphosphate (pNPP), ATP, o-phospho-l-tyrosine, and DNA. The activity of the bond cleavage for pNPP at pH 7 is calculated to be 0.860 ± 0.010 nmol p-nitrophenol/min/μg CNPs. Interestingly, when CNPs bind to plasmid DNA, no cleavage products are detected. While cerium(IV) complexes generally exhibit the ability to break phosphorus-oxygen bonds, the reactions we report appear to be dependent on the availability of cerium(III) sites, not cerium(IV) sites. We investigated the dephosphorylation mechanism from the first principles and find the reaction proceeds through inversion of the phosphate group similar to an S(N)2 mechanism. The ability of CNPs to interact with phosphate ester bonds of biologically relevant molecules has important implications for their use as potential therapeutics.

Topics: Adenosine Triphosphate; Cerium; DNA; Hydrolysis; Nanoparticles; Nitrophenols; Organophosphates; Organophosphorus Compounds; Phosphotyrosine