Au–Ag and Pt–Ag bimetallic nanoparticles@halloysite nanotubes: morphological modulation,improvement of thermal stability and catalytic performance

In this study, Au–Ag and Pt–Ag bimetallic nanocages were loaded on natural halloysite nanotubes (HNTs) via galvanic exchange based on Ag@HNT. By changing the ratio of Au to Ag or Pt to Ag in exchange processes, Au–Ag@HNT and Pt–Ag@HNT with different nanostructures were generated. Both Au–Ag@HNT and Pt–Ag@HNT systems showed significantly improved efficiency as peroxidase-like catalysts in the oxidation of o-phenylenediamine compared with monometallic Au@HNT and Pt@HNT, although inert Ag is dominant in the composition of both Au–Ag and Pt–Ag nanocages. On the other hand, loading on HNTs enhanced the thermal stability for every system, whether monometallic Ag nanoparticles, bimetallic Au–Ag or Pt–Ag nanocages. Ag@HNT sustained thermal treatment at 400 °C in nitrogen with improved catalytic performance, while Au–Ag@HNT and Pt–Ag@HNT maintained or even had slightly enhanced catalytic efficiency after thermal treatment at 200 °C in nitrogen. This study demonstrated that natural halloysite nanotubes are a good support for various metallic nanoparticles, improving their catalytic efficiency and thermal stability.

Bimetallic Au–Ag@HNT and Pt–Ag@HNT nanocages showed significantly improved efficiency in the oxidation of o-phenylenediamine as peroxidase-like catalyst compared with corresponding monometallic nanoparticles.