Abstract
Palladium (Pd)-based catalysts, as an ideal alternative to platinum (Pt) for oxygen reduction reaction (ORR), have been the focus of recent research because of their comparable catalytic activities, low cost, and abundant resource. Unfortunately, Pd is easy to suffer from agglomeration because of the decrease of their excessive metal surface free energy at elevated temperature, dramatically reducing their catalytic activities for ORR. Herein, we report a facile in-situ self-assembly strategy coupled with the annealing method to synthesize the well-dispersed Pd nanoparticles on nitrogen-doped mesoporous carbon spheres (Pd-NMCS) catalysts, and analyze the catalytic activities for ORR. More importantly, the nitrogen atoms in the NMCS can expose more basic/catalytic sites that can coordinate with Pd nanoparticles to form the strong Pd-N interactions, which can not only tightly anchor Pd nanoparticles but also be advantageous to show outstanding stability and good resistance to methanol crossover. As expected, the obtained Pd-NMCS exhibit good ORR catalytic activities, desirable reaction kinetics, excellent stability, as well as better methanol tolerance, which may offer potential for the practical application of fuel cells. The existence of strong Pd-N interaction enables the Pd nanoparticles to uniformly disperse on the NMCS (Pd-NMCS), thus achieving good ORR catalytic activities, desirable reaction kinetics, outstanding stability as well as better tolerance to methanol crossover of the Pd-NMCS catalyst in the alkaline condition.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.