Journal
MATERIALS CHEMISTRY FRONTIERS
Volume 2, Issue 3, Pages 475-482Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c7qm00620a
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Funding
- Materials Research Science and Engineering Centers (MRSEC) program at Northwestern University [NSF DMR-1121262]
- Office of Naval Research [N000141310556, N000141612838]
- U.S. Department of Defense (DOD) [N000141612838] Funding Source: U.S. Department of Defense (DOD)
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Exfoliated thin sheets of layered materials can readily reassemble to form a macroscopic lamellar film containing a massive array of parallel two-dimensional (2D) nanochannels. These 2D nanofluidic channels exhibit enhanced unipolar ionic conductivity with the counterions as the majority charge carriers, thus conceptually become an ionic analogue of extrinsically doped semiconductor wafers. Here we demonstrate kirigami nanofluidics'', where ionic transport can be manipulated by tailor-cutting the shape of the film. Shapes with an asymmetric source and drain exhibit rectifying ionic currents, which is attributed to the asymmetric concentration polarization zones developed in the two reservoirs. Therefore, the rectification ratio can be continuously tuned simply by adjusting the relative edge sizes of the shape, or even programmed by selecting the number of source and drain branches in multi-armed shapes. Kirigami-made ionic rectifiers and resistors can be conveniently connected together to demonstrate simple AND and OR logic functions. These results demonstrate nanoscale ionic transport can be manipulated by patterning materials at the macroscopic length scale.
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