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Electrical detection schemes using nanoscale devices offer fast and label-free alternatives to biosensing techniques based on chemical and optical interactions. Here we report on the design, fabrication, and operation of oxide-on-graphene ion-sensitive field effect sensor arrays using large-area graphene sheets synthesized by chemical vapor deposition. In this scheme, HfO2 and SiO2 thin films are deposited atop the graphene sheet and play the dual role of the sensing interface, as well as the passivation layer protecting the channel and electrodes underneath from direct contact with the electrolyte. We further demonstrate the functionalization of the SiO2 surface with 3-aminopropyltrimethoxysilane (APTMS). The oxide-on-graphene sensors operate in solution with high stability and a high average mobility of 5, 000 cm2/(V·s). As a proof of principle, we demonstrate pH sensing using the bare or the APTMS-functionalized SiO2 as the sensing surface. The measured sensitivities, 46 mV/pH and 43 mV/pH, respectively, agree well with existing studies. We further show that by applying the solution gate voltage in pulse, the hysteresis in the transfer curve of the graphene transducer can be eliminated, greatly improving the ionic potential resolution of the sensor. These experiments demonstrate the potential of oxide-on-graphene ion-sensitive field effect sensors in on-chip, label-free and real-time biosensing applications.

Publication history
Copyright
Acknowledgements

Publication history

Received: 23 December 2013
Revised: 07 April 2014
Accepted: 02 May 2014
Published: 25 August 2014
Issue date: September 2014

Copyright

© Tsinghua University Press and Springer‐Verlag Berlin Heidelberg 2014

Acknowledgements

Acknowledgements

We thank Xiahua Zhong and Wenchong Hu for helpful discussions on experimental setup. The synthesis of graphene, device preparation and electrical measurements are supported by the US National Science Foundation Nanoscale Interdisciplinary Research Team (NSF NIRT) (grant No. ECS-0609243), Materials Research Science and Engineering Centers (MRSEC) (grant No. DMR-0820404), and CAREER grant No. DMR-0748604. Wet chemistry and chemical functionalization work was supported by the MSD Focus Center, one of six research centers funded under the Focus Center Research Program (FCRP), a Semiconductor Research Corporation entity. The authors acknowledge use of facilities at the Penn State (PSU) site of the US National Science Foundation National Nanotechnology Infrastructure Network (NSF NNIN).

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