Versatile Graphene-Based Platform for Robust Nanobiohybrid Interfaces
arXiv:1904.11806 · doi:10.1021/acsomega.8b03152
Abstract
Technologically useful and robust graphene-based interfaces for devices require the introduction of highly selective, stable, and covalently bonded functionalities on the graphene surface, whilst essentially retaining the electronic properties of the pristine layer. This work demonstrates that highly controlled, ultrahigh vacuum covalent chemical functionalization of graphene sheets with a thiol-terminated molecule provides a robust and tunable platform for the development of hybrid nanostructures in different environments. We employ this facile strategy to covalently couple two representative systems of broad interest: metal nanoparticles, via S-metal bonds, and thiol-modified DNA aptamers, via disulfide bridges. Both systems, which have been characterized by a multi-technique approach, remain firmly anchored to the graphene surface even after several washing cycles. Atomic force microscopy images demonstrate that the conjugated aptamer retains the functionality required to recognize a target protein. This methodology opens a new route to the integration of high-quality graphene layers into diverse technological platforms, including plasmonics, optoelectronics, or biosensing. With respect to the latter, the viability of a thiol-functionalized chemical vapor deposition graphene-based solution-gated field-effect transistor array was assessed.
References in corpus (8)
- Quantum ESPRESSO: a modular and open-source software project for quantum simulations of materials
- Experimental Observation of Quantum Hall Effect and Berry's Phase in Graphene
- Raman spectroscopy as a versatile tool for studying the properties of graphene
- The quasi-free-standing nature of graphene on H-saturated SiC(0001)
- Point defects on graphene on metals
- Double- and Single-Sided bis-Functionalization of Graphene
- All-carbon vertical van der Waals heterostructures: Non-destructive functionalization of graphene for electronic applications
- Disorder induced phase segregation in La2/3Ca1/3MnO3 manganites