Su Qian, Yu Lei
College of Chemistry & Chemical and Environmental Engineering, Weifang University, Weifang 261061, China.
Molecules. 2024 Oct 13;29(20):4853. doi: 10.3390/molecules29204853.
By controlling the structure and composition of Pt-based nanoalloys, the ethanol oxidation reaction (EOR) performances of Pt alloy catalysts can be effectively improved. Herein, we successfully synthesis sub-10 nm PdNi@PtNi nanoparticles (PdNi@PtNi NPs) with a core-shell structure by a one-pot method. The sub 10 nm core-shell nanoparticles possess more effective atoms and exhibit a synergistic effect which can lead to a shift in the d-band center and alter binding energies toward adsorbates. Due to the synergistic effect and unique core-shell structure, the PdNi@PtNi NP catalysts exhibit excellent electrocatalytic performance for ethanol oxidation reactions in alkaline, achieving 9.30 times more mass activity and 7.05 times more specific activity that of the state-of-the-art Pt/C catalysts. Moreover, the stability of PdNi@PtNi NPs was also greatly improved over PtNi nanoparticles, PtPd nanoparticles, and commercial Pt/C. This strategy provides a new idea for improving the electrocatalytic performance of Pt-based catalysts for EORs.
通过控制铂基纳米合金的结构和组成,可以有效提高铂合金催化剂的乙醇氧化反应(EOR)性能。在此,我们通过一锅法成功合成了具有核壳结构的亚10纳米PdNi@PtNi纳米颗粒(PdNi@PtNi NPs)。亚10纳米核壳纳米颗粒拥有更有效的原子,并表现出协同效应,这会导致d带中心发生位移,并改变对吸附质的结合能。由于协同效应和独特的核壳结构,PdNi@PtNi NP催化剂在碱性条件下对乙醇氧化反应表现出优异的电催化性能,质量活性是最先进的Pt/C催化剂的9.30倍,比活性是其7.05倍。此外,与PtNi纳米颗粒、PtPd纳米颗粒和商业Pt/C相比,PdNi@PtNi NPs的稳定性也大大提高。该策略为提高用于EORs的铂基催化剂的电催化性能提供了新思路。