Tailoring GaN Semiconductor Surfaces with Biomolecules - Université de Montpellier Accéder directement au contenu
Article Dans Une Revue Journal of Physical Chemistry B Année : 2008

Tailoring GaN Semiconductor Surfaces with Biomolecules

Frédéric Cuisinier
Zoltán Bálint
  • Fonction : Auteur
Csilla Gergely

Résumé

Functionalization of semiconductors constitutes a crucial step in using these materials for various electronic, photonic, biomedical, and sensing applications. Within the various possible approaches, selection of materialbinding biomolecules from a random biological library, based on the natural recognition of proteins or peptides toward specific material, offers many advantages, most notably biocompatibility. Here we report on the selective functionalization of GaN, an important semiconductor that has found broad uses in the past decade due to its efficient electroluminescence and pronounced chemical stability. A 12-mer peptide (“GaN_probe”) with specific recognition for GaN has evolved. The subtle interplay of mostly nonpolar hydrophobic and some polar amino acidic residues defines the high affinity adhesion properties of the peptide. The interaction forces between the peptide and GaN are quantified, and the hydrophobic domain of the GaN_probe is identified as primordial for the binding specificity. These nanosized binding blocks are further used for controlled placement of biotin-streptavidin complexes on the GaN surface. Thus, the controlled grow of a new, patterned inorganic-organic hybrid material is achieved. Tailoring of GaN by biological molecules can lead to a new class of nanostructured semiconductor-based devices.

Dates et versions

hal-01743324 , version 1 (26-03-2018)

Identifiants

Citer

Elias Estephan, Christian Larroque, Frédéric Cuisinier, Zoltán Bálint, Csilla Gergely. Tailoring GaN Semiconductor Surfaces with Biomolecules. Journal of Physical Chemistry B, 2008, 112 (29), pp.8799 - 8805. ⟨10.1021/jp804112y⟩. ⟨hal-01743324⟩
61 Consultations
0 Téléchargements

Altmetric

Partager

Gmail Facebook X LinkedIn More