scholarly journals Comparison of the Effect of Polypyrimidine on Catalytic Performance of Polypyrimidine/CNT as Fuel Cell Catalyst Carrier

2019 ◽  
Author(s):  
Naziermu Dongmulati ◽  
Caijin Shi ◽  
Xieraili Maimaitiyiming

A new type π-conjugated poly(2,5-didodecyloxy-1,4-diethynyl-phenylene-alt-2-methyl-4,6-pyrimidine) was prepared by Sonogashira polycondensation. A fuel cell catalyst is prepared by depositing platinum particles on carbon nanotubes which was modified with poly(2,5-didodecyloxy-1,4-diethynyl-phenylene-alt-2-methyl-4,6-pyrimidine) and the previously reported poly(2,5-didodecyloxy-1,4-diethynyl-phenylene-alt-2-amino-4,6-pyrimidine). After comparing the two catalysts, it is found that active sites and catalytic performance of catalysts are significantly influenced by the copolymer on the carbon nanotubes which was the catalysis carrier. The electrochemically active surface area (ECSA) of catalysts containing poly(2,5-didodecyloxy-1,4-diethynyl-phenylene-alt-2-methyl-4,6-pyrimidine) was calculated to be 25.5 m2 g-1, which is higher than the ECSA of the poly(2,5-didodecyloxy-1,4-diethynyl-phenylene-alt-2-amino-4,6-pyrimidine) containing catalyst (18.2 m2 g-1). And the first polymer provides better methanol oxidizability and durability than second polymer for catalyst.

2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
Qiao Xia Li ◽  
Ming Shuang Liu ◽  
Qun Jie Xu ◽  
Hong Min Mao

Two kinds of carbon-support 20% Pd/C catalysts for use in direct ethanol fuel cell (DEFC) have been prepared by an impregnation reduction method using NaBH4and NaH2PO2as reductants, respectively, in this study. The catalysts were characterized by XRD and TEM. The results show that the catalysts had been completely reduced, and the catalysts are spherical and homogeneously dispersed on carbon. The electrocatalytic activity of the catalysts was investigated by electrochemical measurements. The results indicate that the catalysts had an average particle size of 3.3 nm and showed the better catalytic performance, when NaBH4was used as the reducing agent. The electrochemical active surface area of Pd/C (NaBH4) was 56.4 m2·g−1. The electrochemical activity of the Pd/C (NaBH4) was much higher than that of Pd/C (NaH2PO2).


2020 ◽  
Vol 4 (4) ◽  
pp. 1747-1753 ◽  
Author(s):  
Yuanyuan Ma ◽  
Wenjie Zang ◽  
Afriyanti Sumboja ◽  
Lu Mao ◽  
Ximeng Liu ◽  
...  

Hollow structuring of active components is an effective strategy to improve the kinetics of oxygen electrode catalysts, arising from the increased the active surface area, the defects on the exposed surface, and the accessible active sites.


2012 ◽  
Vol 124 (28) ◽  
pp. 7104-7107 ◽  
Author(s):  
Patraporn Luksirikul ◽  
Karaked Tedsree ◽  
Mark G. Moloney ◽  
Malcolm L. H. Green ◽  
Shik Chi Edman Tsang

2019 ◽  
Vol 7 (2) ◽  
pp. 764-774 ◽  
Author(s):  
Xuncai Chen ◽  
Zixun Yu ◽  
Li Wei ◽  
Zheng Zhou ◽  
Shengli Zhai ◽  
...  

Carbon nanotubes increase electrochemically active surface area and reduce charge transfer resistance of transition metal borides.


2012 ◽  
Vol 1 (1) ◽  
pp. 31-56 ◽  
Author(s):  
Rongchao Jin

AbstractThis review article focuses on the impacts of recent advances in solution phase precious metal nanoparticles on heterogeneous catalysis. Conventional nanometal catalysts suffer from size polydispersity. The advent of nanotechnology has significantly advanced the techniques for preparing uniform nanoparticles, especially in solution phase synthesis of precious metal nanoparticles with excellent control over size, shape, composition and morphology, which have opened up new opportunities for catalysis. This review summarizes some recent catalytic research by using well-defined nanoparticles, including shape-controlled nanoparticles, high index-faceted polyhedral nanocrystals, nanostructures of different morphology (e.g., core-shell, hollow, etc.), bi- and multi-metallic nanoparticles, as well as atomically precise nanoclusters. Such well-defined nanocatalysts provide many exciting opportunities, such as identifying the types of active surface atoms (e.g., corner and edge atoms) in catalysis, the effect of surface facets on catalytic performance, and obtaining insight into the effects of size-induced electron energy quantization in ultra-small metal nanoparticles on catalysis. With well-defined metal nanocatalysts, many fundamentally important issues are expected to be understood much deeper in future research, such as the nature of the catalytic active sites, the metal-support interactions, the effect of surface atom arrangement, and the atomic origins of the structure-activity and the structure-selectivity relationships.


2018 ◽  
Vol 913 ◽  
pp. 831-837
Author(s):  
Ju Gang Ma ◽  
Jun Mei Wang ◽  
Shuai Li ◽  
Yu Jun Song

The ternary FePtSn alloy nanoparticles (NPs) were synthesized via a simple programmed microfluidic process, showing a great electrochemical performance in methanol oxidation reaction (MOR). The synthesis process exhibited convenient and spatial-temporal kinetics control of the NPs formation for a narrow size distribution, ultra-small (~2nm) and good dispersion features. The morphology, crystal structure and composition of FePtSn NPs were characterized by transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDS), powder X-ray diffraction (XRD). FePtSn/C nanocatalyst ink could be further prepared by mixing the as-synthesized or annealed FePtSn NPs with carbon black powder and nafion. Their electrocatalytic performances were tested by the electrochemical work station. By contrast, the annealing treatment made more active sites exposed and facilitated the catalytic performance of FePtSn/C NPs. The electrochemical active surface areas (ECSAs, 42.8m2/g), catalytic activity (If: 588.1 mA/mg-Pt) and electrochemical durability of FePtSn/C nanocatalysts after annealing were greatly improved, comparing with as-synthesized samples and commercial Pt/C nanocatalysts for MOR. In addition, the onset potential of annealed FePtSn/C nanocatalysts was improved, much better than the commercial Pt/C nanocatalysts.


The Analyst ◽  
2020 ◽  
Vol 145 (2) ◽  
pp. 402-414 ◽  
Author(s):  
Vuslat B. Juska ◽  
Martyn E. Pemble

We report the development of a dual-enzyme electrochemical biosensor based on microfabricated gold band array electrodes which were first modified by gold foam (Au-foam) in order to dramatically increase the active surface area.


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