Selectively Sized Graphene-Based Nanopores for in Situ Single Molecule Sensing

被引:25
作者
Crick, Colin R. [1 ]
Sze, Jasmine Y. Y. [1 ]
Rosillo-Lopez, Martin [2 ]
Salzmann, Christoph G. [2 ]
Edel, Joshua B. [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Chem, London SW7 2AZ, England
[2] Univ London Univ Coll, Dept Chem, London WC1H 0AJ, England
基金
英国生物技术与生命科学研究理事会; 英国工程与自然科学研究理事会;
关键词
nanopore; graphene; DNA; translocation; graphene nanoflake; size tuning; DNA-MOLECULES; CURRENT RECTIFICATION; STRANDED-DNA; TRANSPORT; BIOSENSORS; LAYER; ELECTROCHEMISTRY; TRANSLOCATION; NANOPIPETTES; FABRICATION;
D O I
10.1021/acsami.5b06212
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The use of nanopore biosensors is set to be extremely important in developing precise single molecule detectors and providing highly sensitive advanced analysis of biological molecules. The precise tailoring of nanopore size is a significant step toward achieving this, as it would allow for a nanopore to be tuned to a corresponding analyte. The work presented here details a methodology for selectively opening nanopores in real-time. The tunable nanopores on a quartz nanopipette platform are fabricated using the electroetching of a graphene-based membrane constructed from individual graphene nanoflakes (empty set similar to 30 nm). The device design allows for in situ opening of the graphene membrane, from fully closed to fully opened (empty set similar to 25 nm), a feature that has yet to be reported in the literature. The translocation of DNA is studied as the pore size is varied, allowing for subfeatures of DNA to be detected with slower DNA translocations at smaller-pore sizes, and the ability to observe trends as the pore is opened. This approach opens the door to creating a device that can be target to detect specific analytes.
引用
收藏
页码:18188 / 18194
页数:7
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