Journal of Materials Science

, Volume 50, Issue 9, pp 3399–3408 | Cite as

In situ assembly of dispersed Ag nanoparticles on hierarchically porous organosilica microspheres for controllable reduction of 4-nitrophenol

  • Yongju Gao
  • Songfang Zhao
  • Guoping Zhang
  • Libo Deng
  • Jinhui Li
  • Rong Sun
  • Liyi Li
  • Ching-Ping Wong
Original Paper


Hierarchically porous organosilica microspheres have been facilely synthesized by improved self-assembly of flexible-bridged organosilica precursor without templates and harsh conditions. Subsequently, monodispersed silver nanoparticles (Ag NPs) are in situ grown on the porous microspheres via silver mirror reaction. The as-prepared hybrid composites of Ag supported on porous microspheres are characterized by scanning electron microscopy, energy-dispersive spectroscopy, transmission electron microscopy, X-ray diffraction, thermal gravimetric analysis and nitrogen adsorption and desorption, respectively. These results indicate that not only Ag NPs (20–40 nm) are grown on the organosilica uniformly but also the content of Ag NPs immobilized in the hybrid materials can be well controlled by simply tuning the amount of the Ag(NH3)2OH. The resultant hybrid microspheres exhibit remarkable and durable performances for the reduction of 4-nitrophenol to 4-aminophenol by NaBH4 in aqueous solution. Moreover, the catalytic kinetic mode can be tuned by adjusting the parameter in catalytic reaction, and it can be recycled for seven successive cycles with excellent conversion of 100 % within 8 min. Therefore, the present structure design and scalable route for the synthesis of hierarchical catalyst can provide a highly efficient solution for the reduction of nitro-aromatic compounds in the view of environmentally friendly strategy.


NaBH4 Reactant Molecule Isocyanate Group Yellow Green Hexamethylene Diisocyanate 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.



This work was financially supported by the National Natural Science Foundation of China (Grant No. 21201175), Guangdong and Shenzhen Innovative Research Team Program (No.2011D052, KYPT20121228160843692) and R&D Funds for basic Research Program of Shenzhen (Grant No. JCYJ20120615140007998).

Supplementary material

10853_2015_8898_MOESM1_ESM.docx (1.5 mb)
Supplementary material 1 (DOCX 1504 kb)


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Copyright information

© Springer Science+Business Media New York 2015

Authors and Affiliations

  • Yongju Gao
    • 1
    • 2
  • Songfang Zhao
    • 1
  • Guoping Zhang
    • 1
    • 3
  • Libo Deng
    • 1
  • Jinhui Li
    • 1
  • Rong Sun
    • 1
  • Liyi Li
    • 3
  • Ching-Ping Wong
    • 3
  1. 1.Shenzhen Institutes of Advanced TechnologyUniversity of Chinese Academy of SciencesShenzhenChina
  2. 2.Nano Science and Technology InstituteUniversity of Science and Technology of China (USTC)SuzhouChina
  3. 3.School of Materials Science and EngineeringGeorgia Institute of TechnologyAtlantaUSA

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