纳米颗粒
合金
化学
化学工程
介孔材料
X射线光电子能谱
粒径
催化作用
粒子(生态学)
材料科学
纳米技术
物理化学
有机化学
海洋学
地质学
工程类
作者
Takumi Moriyama,Satoshi Muratsugu,Mitsuhiko Sato,Kimitaka Higuchi,Yasumasa Takagi,Mizuki Tada
摘要
Pt2Gd alloy nanoparticles supported in hollow mesoporous carbon spheres (HMCS; Pt2Gd/HMCS) were successfully prepared by the thermal reduction of organometallic Pt and Gd complexes without oxygen atoms supported in the pores of HMCS. The structures of Pt2Gd alloy nanoparticles were fully characterized by TEM, HAADF-STEM-EDS, XRD, XAFS, and XPS, suggesting the formation of uniform Pt2Gd alloy nanoparticles with an average particle size of 5.9 nm. Pt2Gd/HMCS showed superior oxygen reduction reaction activity (2.4 times higher mass-specific activity to Pt nanoparticles on HMCS (Pt/HMCS)) and remarkable durability even after the 100,000 cycles of accelerated degradation tests compared to Pt/HMCS and a commercial Pt/C catalyst. The structure of the Pt2Gd alloy nanoparticles after initial aging and the durability tests suggested that the Pt2Gd core–Pt shell structure with a particle size similar to the pore size of HMCS was stably formed inside the porous structure of HMCS and maintained under the oxygen-reduction working conditions.
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