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金-银和铂-银双金属纳米颗粒@埃洛石纳米管:形态调控、热稳定性改善及催化性能提升

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

作者信息

Li Siyu, Tang Feng, Wang Huixin, Feng Junran, Jin Zhaoxia

机构信息

Department of Chemistry, Renmin University of China Beijing 100872 P. R. China

出版信息

RSC Adv. 2018 Mar 14;8(19):10237-10245. doi: 10.1039/c8ra00423d. eCollection 2018 Mar 13.

Abstract

In this study, Au-Ag and Pt-Ag bimetallic nanocages were loaded on natural halloysite nanotubes (HNTs) 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 -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.

摘要

在本研究中,基于Ag@HNT通过电置换将金 - 银和铂 - 银双金属纳米笼负载在天然埃洛石纳米管(HNTs)上。通过在置换过程中改变金与银或铂与银的比例,生成了具有不同纳米结构的Au - Ag@HNT和Pt - Ag@HNT。与单金属Au@HNT和Pt@HNT相比,Au - Ag@HNT和Pt - Ag@HNT体系在氧化对苯二胺时作为过氧化物酶样催化剂表现出显著提高的效率,尽管在Au - Ag和Pt - Ag纳米笼的组成中惰性银占主导。另一方面,负载在HNTs上提高了每个体系的热稳定性,无论是单金属银纳米颗粒、双金属Au - Ag还是Pt - Ag纳米笼。Ag@HNT在氮气中400℃进行热处理后催化性能提高,而Au - Ag@HNT和Pt - Ag@HNT在氮气中200℃热处理后保持甚至略微提高了催化效率。本研究表明天然埃洛石纳米管是各种金属纳米颗粒的良好载体,可提高其催化效率和热稳定性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/296a/9078928/d0ce48aed3f4/c8ra00423d-s1.jpg

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