Investigation of Borohydride Oxidation on Graphene Supported Gold-Copper Nanocomposites

2014 ◽  
Vol 61 (29) ◽  
pp. 19-30
Author(s):  
E. Norkus ◽  
A. Baronaite ◽  
I. Stankevi iene ◽  
J. Vaiciuniene ◽  
R. Kondrotas ◽  
...  

2014 ◽  
Vol 161 (12) ◽  
pp. F1237-F1242 ◽  
Author(s):  
L. Tamašauskaitė-Tamašiūnaitė ◽  
A. Baronaitė ◽  
I. Stankevičienė ◽  
J. Vaičiūnienė ◽  
R. Kondrotas ◽  
...  

2013 ◽  
Vol 25 (46) ◽  
pp. 6724-6729 ◽  
Author(s):  
Jaewon Hwang ◽  
Taeshik Yoon ◽  
Sung Hwan Jin ◽  
Jinsup Lee ◽  
Taek-Soo Kim ◽  
...  

Nanomaterials ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 366
Author(s):  
Margarita Gabrovska ◽  
Ivan Ivanov ◽  
Dimitrinka Nikolova ◽  
Jugoslav Krstić ◽  
Anna Maria Venezia ◽  
...  

Supported gold on co-precipitated nanosized NiAl layered double hydroxides (LDHs) was studied as an effective catalyst for medium-temperature water–gas shift (WGS) reaction, an industrial catalytic process traditionally applied for the reduction in the amount of CO in the synthesis gas and production of pure hydrogen. The motivation of the present study was to improve the performance of the Au/NiAl catalyst via modification by CeO2. An innovative approach for the direct deposition of ceria (1, 3 or 5 wt.%) on NiAl-LDH, based on the precipitation of Ce3+ ions with 1M NaOH, was developed. The proposed method allows us to obtain the CeO2 phase and to preserve the NiAl layered structure by avoiding the calcination treatment. The synthesis of Au-containing samples was performed through the deposition–precipitation method. The as-prepared and WGS-tested samples were characterized by X-ray powder diffraction, N2-physisorption and X-ray photoelectron spectroscopy in order to clarify the effects of Au and CeO2 loading on the structure, phase composition, textural and electronic properties and activity of the catalysts. The reduction behavior of the studied samples was evaluated by temperature-programmed reduction. The WGS performance of Au/NiAl catalysts was significantly affected by the addition of CeO2. A favorable role of ceria was revealed by comparison of CO conversion degree at 220 °C reached by 3 wt.% CeO2-modified and ceria-free Au/NiAl samples (98.8 and 83.4%, respectively). It can be stated that tuning the properties of Au/NiAl LDH via CeO2 addition offers catalysts with possibilities for practical application owing to innovative synthesis and improved WGS performance.


2021 ◽  
Author(s):  
Jingjing Yu ◽  
Bihao Hu ◽  
Chuanlan Xu ◽  
Jiazhi Meng ◽  
Shu Yang ◽  
...  

Nickel is widely researched in the electrooxidation of borohydride due to its low cost and abundant reserves, but it’s catalytic activity and stability need to be improved for practical application....


2021 ◽  
Vol 3 (6) ◽  
Author(s):  
Santanu Dey ◽  
Pradipta Chakraborty ◽  
Dhiraj Kumar Rana ◽  
Subhamay Pramanik ◽  
Soumen Basu

AbstractWe have synthesized carbon-supported silver (Ag/C) nanobars by a simple surfactant-free hydrothermal method using glucose as the reducing reagent as well as the source of carbon in Ag/C nanobars. Physicochemical characterization of the materials was performed by X-ray Diffraction (XRD), field emission scanning electron microscopy, and energy-dispersive X-ray spectroscopy. The XRD pattern confirmed the presence of a pure metallic silver phase. No carbon phase was detected, which indicates that the carbon exists mainly in the amorphous form. The electrocatalytic activity of Ag/C in different electrolyte solutions such as 0.5 M NaOH, 0.5 M NaOH + 1 M ethanol (EtOH), 0.5 M NaOH + 1 M ethylene glycol (EG), and 0.5 M NaOH + 0.01 M NaBH4 (sodium borohydride) was studied by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and chronoamperometry (CA) study. Alcohol tolerance of the catalysts was also established in the presence of ethanol and ethylene glycol. The forward-to-backward current ratio from cyclic voltammetry (CV) study of Ag/C-20 (20 h) in 0.5 M NaOH + 1 M ethanol solution at 100 mV s−1 scan rate is 4.13 times higher compared to that of Ag/C-5 (5 h). Hence, Ag/C-20 is a better candidate for the tolerance of ethanol. In the presence of ethylene glycol (1 M) in 0.5 M NaOH solution, it is obtained that the forward-to-backward current ratio at the same scan rate for Ag/C-20 is lower than that in the presence of ethanol. The durability of the catalyst was studied by chronoamperometry measurement. We studied the electrochemical kinetics of Ag/C catalysts for borohydride oxidation in an alkaline medium. The basic electrochemical results for borohydride oxidation show that Ag/C has very well strength and activity for direct borohydride oxidation in an alkaline medium. The reaction of borohydride oxidation with the contemporaneous BH4−. hydrolysis was noticed at the oxidized silver surface. Among all the synthesized Ag/C catalysts, Ag/C-20 exhibited the best electrocatalytic performance for borohydride oxidation in an alkaline medium. The activation energy and the number of exchange electrons at Ag/C-20 electrode surface for borohydride electro-oxidation were estimated as 57.2 kJ mol−1 and 2.27, respectively.


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