| Literature DB >> 26709716 |
Girish S Kulkarni1, Karthik Reddy1,2, Wenzhe Zang1, Kyunghoon Lee1, Xudong Fan2, Zhaohui Zhong1.
Abstract
The ability to tune the molecular interaction electronically can have profound impact on wide-ranging scientific frontiers in catalysis, chemical and biological sensor development, and the understanding of key biological processes. Despite that electrochemistry is routinely used to probe redox reactions involving loss or gain of electrons, electrical probing and tuning of the weaker noncovalent interactions, such as molecular physisorption, have been challenging, primarily due to the inability to change the work function of conventional metal electrodes. To this end, we report electrical probing and tuning of the noncovalent physisorption of polar molecules on graphene surface by using graphene nanoelectronic heterodyne sensors. Temperature-dependent molecular desorptions for six different polar molecules were measured in real-time to study the desorption kinetics and extract the binding affinities. More importantly, we demonstrate electrical tuning of molecule-graphene binding kinetics through electrostatic gating of graphene; the molecular desorption can be slowed down nearly three times within a gate voltage range of 15 V. Our results provide insight into small molecule-nanomaterial interaction dynamics and signify the ability to electrically tailor interactions, which can lead to rational designs of complex chemical processes for catalysis and drug discovery.Entities:
Keywords: Noncovalent interaction; binding energy; electrical tuning; graphene; heterodyne sensor; physisorption
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Year: 2015 PMID: 26709716 DOI: 10.1021/acs.nanolett.5b04500
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 11.189