ELECTROCATALYTIC OXYGEN REDUCTION PERFORMANCE OF SILVER NANOPARTICLE DECORATED ELECTROCHEMICALLY EXFOLIATED GRAPHENE (original) (raw)
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Metal nanoclusters exhibit unusually high catalytic activity toward oxygen reduction reaction (ORR) due to their small size and unique electronic structures. However, controllable synthesis of stable metal nanoclusters is a challenge, and the durability of metal clusters suffers from the deficiency of dissolution, aggregation, and sintering during catalysis reactions. Herein, silver nanoclusters (AgNCs) (diameter < 2 nm) were controllably electrochemically reduced on nitrogen-doped graphene (NG) using effective single-stranded oligonucleotide sequences (ssDNA) as the performed template in absence of any other reluctant. The ssDNA is significant for providing AgNCs with growth template and anchoring the cluster on graphene surface. The strong interaction between the AgNCs, ssDNA and NG renders the as-synthesized AgNCs/NG composite with high-performance onset potential, half-wave potential and mass activity for ORR approaching to commercial Pt/C catalyst, and remarkably superior ORR performance than NG and Ag nanoparticle/NG. Importantly, the AgNCs/NG composite shows excellent methanol tolerance and accelerated electrochemical stability (8000 cycles), which is vital in high performance fuel cells, batteries and nanodevices.
Nanomaterials
Copper-silver and cobalt-silver alloy nanoparticles deposited on reduced graphene oxide (CuAg/rGO and CoAg/rGO) were synthesized and examined as electrocatalysts for oxygen reduction reaction (ORR) and hydrogen peroxide reduction reaction (HPRR) in alkaline media. Characterization of the prepared samples was done by transmission electron microscopy (TEM), Fourier-transform infrared spectroscopy (FTIR), Raman spectroscopy, X-ray diffraction analysis (XRD), and scanning electron microscopy with integrated energy-dispersive X-ray spectroscopy (SEM-EDS). CuAg/rGO and CoAg/rGO nanoparticles diameter ranged from 0.4 to 9.2 nm. The Ag loading was ca. 40 wt.% for both electrocatalysts, with that for Cu and Co being 35 and 17 wt.%, respectively. CoAg/rGO electrocatalyst showed a Tafel slope of 109 mV dec−1, significantly lower than that for CuAg/rGO (184 mV dec−1), suggesting faster ORR kinetics. Additionally, a higher diffusion current density was obtained for CoAg/rGO (−2.63 mA cm−2) than ...
Electroreduction of oxygen on nitrogen-doped graphene oxide supported silver nanoparticles
Journal of Electroanalytical Chemistry, 2017
Nitrogen-doped graphene oxide supported silver nanoparticles (Ag/NGO) have been synthesised using three different methods. The prepared catalysts were studied by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and electrochemically tested for oxygen reduction reaction (ORR) in alkaline solution. The Ag/NGO catalysts prepared by borohydride reduction showed the least degree of nanoparticle agglomeration and the material which was prepared using ascorbic acid yielded the biggest Ag particles. XPS revealed that the nitrogen to carbon atomic ratio was about 0.07 and EDS mapping showed that it was uniformly distributed over the graphene. The ORR on all the Ag/NGO catalysts
Electrocatalysis, 2018
Silver-iron carbon nitride, which has been prepared by pyrolysis (under inert atmosphere) of silver hexacyanoferrate(II) deposited on graphene nanoplatelets, is considered here as electrocatalyst for oxygen reduction in alkaline medium (0.1 M potassium hydroxide electrolyte) in comparison to simple silver nanoparticles and iron carbon nitride (prepared separately in a similar manner on graphene nanoplatelets). The performance of catalytic materials has been examined using such electrochemical diagnostic techniques as cyclic voltammetry and rotating ring-disk electrode voltammetry. Upon application of the graphene nanoplatelet-supported mixed silver-iron carbon nitride catalyst, the reduction of oxygen proceeds at more positive potentials, as well as the amounts of hydrogen peroxide (generated during reduction of oxygen at potentials more positive than 0.3 V) are lower relative to those determined at pristine silver nanoparticles and iron carbon nitride (supported on graphene nanoplatelets), when they have been examined separately. The enhancement effect shall be attributed to high activity of silver toward the reduction/ decomposition of H 2 O 2 in basic medium. Additionally, it has been observed that the systems based on carbon nitrides show considerable stability due to strong fixation of metal complexes to CN shells.
Silver metal nanoparticles were decorated by electron beam evaporation on graphene foam (GF) grown by chemical vapour deposition. X-ray diffraction, Raman spectroscopy, scanning and transmission electron microscopy, and atomic force microscopy were used to investigate the structure and morphology of the graphene foam/silver nanoparticles (GF/Ag). Both samples were tested as electrodes for supercapacitors. The GF/Ag exhibited a significantly higher capacitive performance, including a specific capacitance value of ( $ 110 Fg À 1 ) and excellent cyclability in a three-electrode electrochemical cell. These results demonstrate that graphene foam could be an excellent platform for metal particles for investigating improved electrochemical performance.
Cornell University - arXiv, 2018
Silver-iron carbon nitride has been obtained by pyrolysis (under inert atmosphere) of silver hexacyanoferrate(II), precipitated on graphene nanoplatelets, and examined as electrocatalyst for oxygen reduction reaction in alkaline media in comparison to silver nanoparticles and iron carbon nitride (prepared separately in a similar manner on graphene nanoplatelets). The catalytic materials have been studied in 0.1 M potassium hydroxide electrolyte using such electrochemical diagnostic techniques as cyclic voltammetry and rotating ring-disk electrode voltammetry. Upon application of graphene nanoplateletssupported mixed silver-iron carbon nitride catalyst, the reduction of oxygen proceeds at more positive potentials and the amounts of hydrogen peroxide (generated during reduction of oxygen at potentials more positive than 0.3 V) are lower relative to silver nanoparticles and iron carbon nitride (supported on graphene nanoplatelets) examined separately. Promoting effect is ascribed to high activity of silver toward the reduction/decomposition of H2O2 in basic medium. Additionally, it has been observed that the systems based on carbon nitrides show considerable stability due to strong fixation of metal complexes to CN shells.
Graphene modified nanosized Ag electrocomposites
Materials Research Bulletin, 2017
Electrochemical oxygen reduction and methanol oxidation are two important reactions in the development of clean energy technology. Substantial progresses in the design of cheap, robust, and efficient catalysts are still required and remain a significant challenge. Here, we report a double pulse electrodeposition process, capable of controlling the density and the size of silver nanoparticle supported on graphene. We found that this catalyst afforded a current density of 5.5 mA cm À2 at a low potential for ORR, comparing favourably with the state-of-the-art Pt/C catalyst. Additionally, we demonstrate that size and distribution effects are critical parameters for more efficient ORR and MOR catalysis. Our results suggest possibility for the development of effective and robust ORR and MOR electrocatalysts based on cheap silver metal and graphene and as replacements for the commercially available but expensive Pt/C catalysts.
Oxygen reduction on silver catalysts electrodeposited on various nanocarbon supports
SN Applied Sciences, 2021
In this work, Ag particles were electrodeposited onto nitrogen-doped graphene oxide, graphene, multi-walled carbon nanotube (MWCNT), and Vulcan carbon XC-72R supports by varying the upper potential limit. The surface morphology of the resulting Ag-based catalysts was examined by scanning electron microscopy. The electrochemical oxygen reduction reaction (ORR) was tested in alkaline media employing the rotating disk electrode method. The variation of the upper potential limit influenced the size of silver nanoparticles and their number density on the substrate surface. All the Ag-based electrocatalysts studied in this work showed remarkable ORR activity in terms of half-wave potentials. The ORR results combined with hydrogen peroxide reduction results prove that all Ag catalysts tested are suitable for both reactions. Ag/NGO2 catalyst possesses the highest mass activity for ORR, which indicates a relationship between the Ag loading and electrocatalytic activity. The electroreduction ...