Rational design of porous binary Pt-based nanodendrites as efficient catalysts for direct glucose fuel cells over a wide pH range

2017 ◽  
Vol 7 (13) ◽  
pp. 2819-2827 ◽  
Author(s):  
Kamel Eid ◽  
Yahia H. Ahmad ◽  
Siham Y. AlQaradawi ◽  
Nageh K. Allam

Porous binary PtPd, AuPt, PtCu, and PtNi nanodendrites prepared by a facile one-step reduction under ultrasonic irradiation at room temperature, exhibited a substantial catalytic activity towards glucose oxidation reaction at different pH values relative to a commercial Pt/C catalyst.

Catalysts ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 101
Author(s):  
Siyong Gu ◽  
Chien-Te Hsieh ◽  
Chih-Peng Kao ◽  
Chun-Chieh Fu ◽  
Yasser Ashraf Gandomi ◽  
...  

A novel solvothermal technique has been developed in the presence of C/N/B precursor for synthesizing B-N-coped graphene quantum dots (GQDs) as non-metal electrocatalysts towards the catalytic glucose oxidation reaction (GOR). Both N-doped GQD and B-N-codoped GQD particles (~4.0 nm) possess a similar oxidation and amidation level. The B-N-codoped GQD contains a B/C ratio of 3.16 at.%, where the B dopants were formed through different bonding types (i.e., N‒B, C‒B, BC2O, and BCO2) inserted into or decorated on the GQDs. The cyclic voltammetry measurement revealed that the catalytic activity of B-N-codoped GQD catalyst is significantly higher compared to the N-doped GQDs (~20% increase). It was also shown that the GOR activity was substantially enhanced due to the synergistic effect of B and N dopants within the GQD catalysts. Based on the analysis of Tafel plots, the B-N-codoped-GQD catalyst electrode displays an ultra-high exchange current density along with a reduced Tafel slope. The application of B-N-codoped GQD electrodes significantly enhances the catalytic activity and results in facile reaction kinetics towards the glucose oxidation reaction. Accordingly, the novel design of GQD catalyst demonstrated in this work sets the stage for designing inexpensive GQD-based catalysts as an alternative for precious metal catalysts commonly used in bio-sensors, fuel cells, and other electrochemical devices.


2020 ◽  
Vol 45 (38) ◽  
pp. 19163-19173
Author(s):  
Yahia H. Ahmad ◽  
Assem T. Mohamed ◽  
Ahmed El-Shafei ◽  
Siham Y. Al-Qaradawi ◽  
Amina S. Aljaber

Author(s):  
Francisco G. Cirujano ◽  
Nuria Martin ◽  
Neyvis Almora-Barrios ◽  
Carlos Martí-Gastaldo

Room temperature one-step synthesis of the peptide-based porous material with a periodic distribution of pockets decorated with lysine side chain active sites behaves as a heterogeneous organocatalyst. The pockets are...


2014 ◽  
Vol 58 (43) ◽  
pp. 11-28
Author(s):  
E. Norkus ◽  
I. Stankevi iene ◽  
L. Tamaauskaite-Tamai naite ◽  
G. Stalnionis ◽  
K. Pruinskas ◽  
...  

2017 ◽  
Vol 5 (21) ◽  
pp. 10510-10516 ◽  
Author(s):  
Jing Wang ◽  
Zhongzhe Wei ◽  
Haiyan Wang ◽  
Yiqing Chen ◽  
Yong Wang

CoOx–CNT–CC electrodes not only displayed outstanding performance over a wide pH range, but also showed superb catalytic activity at low temperature.


2014 ◽  
Vol 2014 ◽  
pp. 1-11 ◽  
Author(s):  
Shuang Zhang ◽  
Ying Guan ◽  
Gen-Que Fu ◽  
Bo-Yang Chen ◽  
Feng Peng ◽  
...  

The unique organic/inorganic superabsorbent hydrogels based on xylan and inorganic clay montmorillonite (MMT) were prepared via grafting copolymerization of acrylic acid (AA) and 2-acrylamido-2-methylpropanesulfonic acid (AMPS) withN,N-methylenebisacrylamide (MBA) as a cross-linking agent and potassium persulfate (KPS) as an initiator. The effect of variables on the swelling capacity of the hydrogels, such as the weight ratios of MMT/xylan, MBA/xylan, and AMPS/AA, was systematically optimized. The results indicated that the superabsorbent hydrogels comprised a porous cross-linking structure of MMT and xylan with side chains that carry carboxylate, carboxamide, and sulfate. The hydrogels exhibit the high compressive modulus (E), about 35–55 KPa, and the compression strength of the hydrogels increased with an increment of the MMT content. The effect of various cationic salt solutions (LiCl, CaCl2, and FeCl3) on the swelling has the following order: Li+> Ca2+> Fe3+. Furthermore, the influence of pH values on swelling behaviors showed that the superabsorbent composites retained around 1000 g g−1over a wide pH range of 6.0–10.0. The xylan-based hydrogels with the high mechanical and swelling properties are promising for the applications in the biomaterials area.


1993 ◽  
Vol 48 (12) ◽  
pp. 1845-1847 ◽  
Author(s):  
P. A. M. Williams ◽  
S. B. Etcheverry ◽  
E. J. Baran

The interaction of VO2+ with the nucleic bases adenine, guanine, cytosine, thymine and uracil has been investigated spectrophotometrically in a wide pH-range and with metal to base ratios 1:1 and 1:10. Adenine, guanine and uracil interact with the cation at pH-values >5, but whereas adenine apparently coordinates through Natoms, the other two bases seem to be coordinated through oxygen donors.


2019 ◽  
Vol 104 (3) ◽  
pp. 1055-1062 ◽  
Author(s):  
Ngoc T. N. Ngo ◽  
Carl Grey ◽  
Patrick Adlercreutz

AbstractMethodology was developed to expand the range of benign alkyl glycoside surfactants to include also anionic types. This was demonstrated possible through conversion of the glycoside to its carboxyl derivative. Specifically, octyl β-D-glucopyranoside (OG) was oxidised to the corresponding uronic acid (octyl β-D-glucopyranoside uronic acid, OG-COOH) using the catalyst system T. versicolor laccase/2,2,6,6-tetramethylpiperidinyloxy (TEMPO) and oxygen from air as oxidant. The effects of oxygen supply methodology, concentrations of laccase, TEMPO and OG as well as reaction temperature were evaluated. At 10 mM substrate concentration, the substrate was almost quantitatively converted into product, and even at a substrate concentration of 60 mM, 85% conversion was reached within 24 h. The surfactant properties of OG-COOH were markedly dependent on pH. Foaming was only observed at low pH, while no foam was formed at pH values above 5.0. Thus, OG-COOH can be an attractive low-foaming surfactant, for example for cleaning applications and emulsification, in a wide pH range (pH 1.5–10.0).


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