4.3 Article

Electroless plating of silver nanoparticles on porous silicon for laser desorption/ionization mass spectrometry

Journal

INTERNATIONAL JOURNAL OF MASS SPECTROMETRY
Volume 281, Issue 1-2, Pages 1-7

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.ijms.2008.10.026

Keywords

Silver nanoparticles; 4-Aminothiophenol; Self-assembled monolayer; Laser desorption/ionization mass spectrometry

Funding

  1. National Basic Research Program of China [2007CB925101]
  2. NSFC [20721002, 20571042]

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An improved DIOS (desorption ionization on porous silicon) method for laser desorption/ionization mass spectrometry (LDI MS) by electroless plating of silver nanoparticles (AgNPs) on porous silicon (PSi) was developed. By addition of 4-aminothiophenol (4-ATP) into the AgNO3 plating solution, the plating speed can be slowed down and Simultaneously 4-ATP self-assembled monolayers (SAMs) on AgNPs (4-ATP/AgNPs) were formed. Both AgNPs and 4-ATP/AgNPs coated PSi Substrates present much higher stability, sensitivity and reproducibility for LDI MS than the un-treated porous silicon ones. Their shelf life in air was tested for several weeks to a month and their mass spectra still displayed the same high quality and sensitivity as the freshly prepared ones. And more 4-ATP SAMs partly play a role of matrix to increase the ionization efficiency. A small organic molecule of tetrapyridinporphyrin (TPyP), oligomers of polyethylene glycol (PEG 400 and 2300), and a peptide of oxytocin were used as examples to demonstrate the feasibility of the silver-plated PSi as a matrix-free-like method for LDI MS. This approach can obtain limits of detection to femtomoles for TPyP, subpicomoles for oxytocin, and picomoles for PEG 400 and 2300, comparable to the traditional matrix method and much better than the DIOS method. It simplifies the sample preparation as a matrix-free-like method without addition of matrix molecules and homogenizes the sample spread over the spot for better and more even mass signals. (C) 2008 Elsevier B.V. All rights reserved.

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