Photoluminescence-Based Sensing With Porous Silicon Films, Microparticles, and Nanoparticles
Here, chemical sensors made from porous Si are reviewed, with an emphasis on systems that harness photoluminescence and related energy‐ and charge‐transfer mechanisms available to porous Si‐derived nanocrystallites. Quenching of luminescence by molecular adsorbates involves the harvesting of energy...
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Published in | Advanced functional materials Vol. 19; no. 20; pp. 3195 - 3208 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Weinheim
WILEY-VCH Verlag
23.10.2009
WILEY‐VCH Verlag |
Subjects | |
Online Access | Get full text |
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Summary: | Here, chemical sensors made from porous Si are reviewed, with an emphasis on systems that harness photoluminescence and related energy‐ and charge‐transfer mechanisms available to porous Si‐derived nanocrystallites. Quenching of luminescence by molecular adsorbates involves the harvesting of energy from a delocalized nanostructure that can be much larger than the molecule being sensed, providing a means to amplify the sensory event. The interaction of chemical species on the surface of porous Si can exert a pronounced influence on this process, and examples of some of the key chemical reactions that modify either the surface or the bulk properties of porous Si are presented. Sensors based on micron‐scale and smaller porous Si particles are also discussed. Miniaturization to this size regime enables new applications, including imaging of cancerous tissues, indirect detection of reactive oxygen species (ROS), and controlled drug release. Examples of environmental and in vivo sensing systems enabled by porous Si are provided.
The nanoscale features in porous silicon have interesting photoluminescence and related energy‐ and charge‐transfer properties that can be harnessed to sense chemicals in the gas or liquid phases. This review discusses macro‐, micro‐, and nanosensor devices derived from porous silicon, providing examples of environmental and in vivo applications. The influence of surface chemistry is particularly highlighted. |
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Bibliography: | U.S. National Science Foundation, Division of Materials Research - No. DMR-0806859 ark:/67375/WNG-GH6HQ4XK-D istex:62F8701D23AF0AE8F0F3BA37FD9DE3E4DFEEC9F1 ArticleID:ADFM200900535 ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 1616-301X 1616-3028 |
DOI: | 10.1002/adfm.200900535 |