A facile strategy is proposed to synthesize monodispersed Pt3Ni nanoparticles. Such a kind of electrocatalyst shows a larger electrochemical surface area (98.9 m2 gpt−1) and double the mass activity of the oxygen reduction reaction activity compared to commercial Pt/C catalyst. The results show that the suitable addition of Ni and triethylamine in the reduction process plays an important role in controlling the size and dispersion of Pt3Ni nanoparticles. A further membrane electrode assembly test proves that as-prepared Pt3Ni nanoparticles can greatly enhance the electrochemical performance of a proton exchange membrane fuel cell, which exhibits a great potential of application in fuel cells.
A facile strategy is proposed to synthesize boron-doped ECP600 carbon black (B-ECP600), and the catalyst of Pt supported on boron-doped ECP600 (Pt/B-ECP600) shows smaller particle sizes and a higher electrochemical surface area (95.62 m2·gPt−1) and oxygen reduction reaction activity (0.286 A·mgPt−1 for mass activity; 0.299 mA·cm−2 for area specific activity) compared to the catalyst of Pt supported on ECP600 (Pt/ECP600). The results show that the boron doping of the carbon supports plays an important role in controlling the size and dispersion of Pt nanoparticles and the O2 adsorption/dissociation of the oxygen reduction reaction. A further accelerated durability test proves that boron doping can greatly enhance the stability of carbon support and thus improves the electrochemical performance of the catalyst during the long-time running. All these results suggest boron-doped carbon has great potential for application in fuel cells.
In order to achieve the commercialization of proton exchange membrane fuel cells (PEMFCs), it is necessary to synthesize electrocatalyst with higher electrochemical activity. In this study, PtCo nano-alloy electrocatalyst was prepared by liquid phase synthesis method with sodium borohydride as reducing agent, triethylamine as complexing agent, and by sequential heat-treatment. The physical properties of the catalyst were characterized by different analytical methods. We studied the effects of heat-treatment temperature, different amounts of sodium borohydride and triethylamine on electrochemical performance. The results show that heat-treatment can greatly improve the mass activity of the catalyst, and 500 ℃ is the optimal temperature for preparing the catalyst with the highest catalytic performance towards oxygen reduction reaction(ORR). Compared with commercial TKK-PtCo alloy catalyst under the same test system, the as-prepared catalysts exhibits advantages of more uniform particle size distribution, smaller particle size and higher electrochemical performance. In particular, the mass activity (MA) of the prepared catalyst is 133 mA/mg Pt , which is 3 times of TKK-PtCo alloy catalyst.
The pursuit of highly active and cost-effective catalysts toward oxygen evolution reaction (OER) is a crucial strategy to resolve the imminent energy crisis. NiFe layered double hydroxide (NiFe LDH) is acknowledged as one of the most promising OER electrocatalysts in alkaline electrolytes. Herein, we report a novel stepwise approach to synthesize NiFe LDHs materials merging with carbon black (CB) via trisodium citrate (TC), modifying toward OER. Benefiting from the inimitable wrapped structure, the decreased size of porous nanosheets and the superconductivity of CB substrate, NiFe LDHs/CB-TC presents excellent catalytic features with a comparative overpotential (236 mV at 10 mA cm−2) and an ultralow Tafel slope (31 mV dec−1), which are almost lower than those of advanced catalysts associated with expensive carbonaceous materials. Therefore, it is expected that such a high-activity and low-cost material can be a promising catalyst employed for the electrochemical energy storage and conversion systems.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.