PDDA induced step-pyramidal growth of nickel-platinum (Ni-Pt) nanoparticles for enhanced 4-nitrophenol reduction.

Herein, we report the synthesis of novel platinum-based nanoparticles with step-pyramidal growth induced by poly(diallyldimethylammonium chloride) (PDDA). The complex stepped pyramidal shape became the central point for outstanding catalytic reduction of 4-nitrophenol, overcoming the activity of bare Pt nanoparticles. These results are valuable for the catalytic degradation of reactive molecules.

Electrospun 1D-NiO hollow nanowires on glass support for the sunlight-driven photodegradation of methylene blue.

Sunlight-driven semiconductor photocatalysts have received substantial attention due to environmental degradation, but a simple and reusable photocatalyst design has been a challenging task. Herein, we report the fabrication of a one-dimensional hollow semiconducting nanowire structure by electrospun-mediated nickel oxide nanowires (NiO NWs) as a reusable photocatalyst by direct deposition on glass substrates. The effective control of the sunlight-driven hollow nanowires as the photocatalyst has a high surface area for multiple light-harvesting and interface redox reactions, a nanostructured thin shell for accelerated charge separation, transportation, and a large length-diameter ratio for easy recycling. The electrospun NiO NWs were nest-like hollow nanostructure fibers, crystalline, and with a high density, and the synthesis and parameters were thoroughly investigated to achieve the characteristic shape of the hollow NiO NWs. Further, the photocatalytic activity of the NiO NWs on glass substrates for the selective breakdown of methylene blue (MB) under sunlight irradiation to optimize the efficiency of the NiO NWs, such as degradation techniques, concentration, and pH of the MB solution. The stability and reusability of the NiO NWs were tested successfully in several reusable cycles, with only a 2% degradation difference. The reaction rate was found to be 0.054 min-1 for MB (5 µM) and 0.033 min-1 for MB (10 µM) at pH 11 for 60 min, and the higher activity parameter was calculated to be 3.3 × 10-3 min-1 mg-1 L-1 due to their hollow structure and effective area of the NiO NWs. They contain more superficially-entrapped holes that change with chemisorbed oxyhydroxyl OH or H2O to form OH- radicals. The specific active hollow surface area rises, whereas the rate of optical-electronic hole recombination drops. The photocatalytic degradation performance of the fabricated one-step electrospun hollow NiO NW-based photocatalyst on substrates showed speed, reusability, and promoted the formation of radicals capable of decomposing organic pollutants, which were shown to have application in photocatalysis.

Synthesis of cetyl trimethyl ammonium bromide (CTAB) capped copper oxide nanocubes for the remediation of organic pollutants using photocatalysis and catalysis.

The aim of this report is to synthesize copper oxide nanocubes (CuO NCs) at room temperature, using sodium borohydride as a reducing agent, and Cetyl Trimethyl Ammonium Bromide (CTAB) as a stabilizing agent. The crystallinity and morphology of the synthesized CuO NCs are investigated via X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscope (TEM). The optical properties were analyzed by means of UV-visible absorbance and Raman spectroscopy. The existence of specific functional groups and structural stability were established via FTIR spectroscopy and thermogravimetric analysis (TGA). Furthermore, the catalytic efficiency of the as-prepared CuO NCs was tested using catalytic and photocatalytic studies of para-nitrophenol (p-NP) reduction and methylene blue (MB) degradation, respectively. The catalytic results demonstrated the nanocubes' excellent catalytic and photocatalytic responses with respect to the abatement of p-NP and MB within 50 s and 240 min, with kinetic rate constants of 3.9 × 10-2 s-1 and 6.47 × 10-3 min-1, respectively.

Nitrogen-Doped Graphene Oxide Dots-Based "Turn-OFF" H2O2, Au(III), and "Turn-OFF-ON" Hg(II) Sensors as Logic Gates and Molecular Keypad Locks.

Fluorescent nitrogen-doped graphene oxide dots (NGODs) have been demonstrated as an on-off nanosensor for the detection of Hg2+, Au3+, and H2O2. As compared to l-cystine, where the luminescence signal recovery results from the detachment of Hg2+ from the NGODs, signal recovery through l-ascorbic acid (turn-off-on model) has been attributed to the reduction of Hg2+ to Hg0. The sustainable recovery of the photoluminescence signal is demonstrated using common citrus fruits containing vitamin C (l-AA), suggesting a promising practical usage of this sensing system. Additionally, the sensitivity of NGOD- and AA-originated signal recovery from the Hg(II)-NGODs mixture has been successfully tested in Hg2+ ion-spiked tap water from three different places. Mimic devices were executed and verified on the basis of characteristic spectral changes, and the possible utility of this system in electronic security and memory element devices has also been demonstrated. Considering an easy synthesis process and excellent performance of NGODs, this investigation opens up new opportunities for preparing high-quality fluorescent NGODs to meet the requirements of many applications.

Persea americana seed extract mediated gold nanoparticles for mercury(ii)/iron(iii) sensing, 4-nitrophenol reduction, and organic dye degradation.

In this work, Persea americana (Avocado) seed extract mediated systematically optimized synthesis has been employed for the formation of small sized gold nanoparticles (Av-AuNPs) at different pH values. The size, shape and crystallinity of the as-prepared AuNPs have been studied using transmission electron microscopy and X-ray diffraction. The nanoparticles were found to be selective towards mercury(ii) upon the prior or subsequent addition of iron(iii), revealing a blue shift and an enhancement of the characteristic surface plasmon resonance (at 519 nm). Similar absorbance based selectivity has been observed towards Fe(iii) in the presence of Hg(ii). The high sensitivity and selectivity of Av-AuNPs towards Hg(ii) and Fe(iii) has been attributed to the formation of core-shell structures. From the UV-visible spectroscopic measurements, the limits of detection for Hg(ii) and Fe(iii) are found to be 50 nM and 30 nM (around one order of magnitude less than the Environment Protection Agency limit of 0.7 µM for Fe(iii) in drinking water) respectively, with an excellent linear dependence over a wide range of concentrations. Additionally, as-prepared Av-AuNPs have been demonstrated to be efficient in the reduction of organic pollutant 4-nitrophenol to 4-aminophenol and degradation of some organic dyes, such as Methylene Blue, Direct blue, Rhodamine 6G, Bromophenol blue and methyl orange. The use of the proposed Av-AuNPs for sensing and green catalysis can form the basis of high-performance analytical assays, effective multiplexed intracellular sensors, and sophisticated and sustainable probes/catalysts.