journal article·2017-09Open access

High Conduction Hopping Behavior Induced in Transition Metal Dichalcogenides by Percolating Defect Networks: Toward Atomically Thin Circuits

Michael G. Stanford, Pushpa R. Pudasaini, Elisabeth T. Gallmeier, Nicholas Cross, Liangbo Liang, Akinola Oyedele, Gerd Duscher, Masoud Mahjouri‐Samani, Kai Wang, Kai Xiao, David B. Geohegan, Alex Belianinov, Bobby G. Sumpter, Philip D. Rack

Advanced Functional Materials· Volume 27· Issue 36

Abstract

Atomically thin circuits have recently been explored for applications in next‐generation electronics and optoelectronics and have been demonstrated with 2D lateral heterojunctions. In order to form true 2D circuitry from a single material, electronic properties must be spatially tunable. Here, tunable transport behavior is reported which is introduced into single layer tungsten diselenide and tungsten disulfide by focused He+ irradiation. Pseudometallic behavior is induced by irradiating the materials with a dose of ≈1 × 1016 He+ cm−2 to introduce defect states, and subsequent temperature‐dependent transport measurements suggest a nearest neighbor hopping mechanism is operative. Scanning transmission electron microscopy and electron energy loss spectroscopy reveal that Se is sputtered preferentially, and extended percolating networks of edge states form within WSe2 at a critical dose of 1 × 1016 He+ cm−2. First‐principle calculations confirm the semiconductor‐to‐metallic transition of WSe2 after pore and edge defects are introduced by He+ irradiation. The hopping conduction is utilized to direct‐write resistor loaded logic circuits in WSe2 and WS2 with a voltage gain of greater than 5. Edge contacted thin film transistors are also fabricated with a high on/off ratio (>106), demonstrating potential for the formation of atomically thin circuits.
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Research context

OpenAlex topics: 2D Materials and Applications · Topological Materials and Phenomena · Graphene research and applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Materials Science and Engineering University of Tennessee Knoxville TN 37996 USA

Center for Nanophase Materials Sciences Oak Ridge National Laboratory Oak Ridge TN 37831 USA

Materials Science and Technology Division Oak Ridge National Laboratory Oak Ridge TN 37831 USA

Computational Sciences & Engineering Division Oak Ridge National Laboratory Oak Ridge TN 37831 USA

Funding

U.S. Department of Energy · National Science Foundation · Battelle

References (45)

Show source-provided references
1. 10.1016/0301-0104(91)80136-610.1016/0301-0104(91)80136-6 ↗
2. 10.1038/nnano.2010.27910.1038/nnano.2010.279 ↗
3. 10.1021/nl304777e10.1021/nl304777e ↗
4. 10.1039/C5NR04592D10.1039/C5NR04592D ↗
5. 10.1038/nnano.2014.2510.1038/nnano.2014.25 ↗
6. 10.1038/nnano.2014.2610.1038/nnano.2014.26 ↗
7. 10.1038/nnano.2012.19310.1038/nnano.2012.193 ↗
8. 10.1016/0167-577X(89)90128-610.1016/0167-577X(89)90128-6 ↗
9. 10.1038/ncomms364210.1038/ncomms3642 ↗
10. 10.1021/nn500044q10.1021/nn500044q ↗
11. 10.1021/nl400747910.1021/nl4007479 ↗
12. 10.1021/acs.nanolett.5b0095210.1021/acs.nanolett.5b00952 ↗
13. 10.1021/acs.nanolett.5b0451310.1021/acs.nanolett.5b04513 ↗
14. 10.1002/aelm.20160046810.1002/aelm.201600468 ↗
15. 10.1103/PhysRevLett.87.19680310.1103/PhysRevLett.87.196803 ↗
16. 10.1103/PhysRevB.67.08541010.1103/PhysRevB.67.085410 ↗
17. 10.1088/2053-1583/3/2/02200210.1088/2053-1583/3/2/022002 ↗
18. 10.1021/acs.nanolett.6b0226310.1021/acs.nanolett.6b02263 ↗
19. 10.1088/0953-8984/28/36/36400210.1088/0953-8984/28/36/364002 ↗
20. 10.1063/1.482420510.1063/1.4824205 ↗
21. 10.1021/acs.nanolett.6b0185310.1021/acs.nanolett.6b01853 ↗
22. 10.1021/acs.jpcc.6b0324710.1021/acs.jpcc.6b03247 ↗
23. 10.1103/PhysRevB.88.03530110.1103/PhysRevB.88.035301 ↗
24. 10.1103/PhysRevLett.109.03550310.1103/PhysRevLett.109.035503 ↗
25. 10.1038/srep3048110.1038/srep30481 ↗
26. 10.1021/acs.nanolett.5b0167310.1021/acs.nanolett.5b01673 ↗
27. 10.1038/srep2727610.1038/srep27276 ↗
28. 10.1088/2053-1583/aa6b1710.1088/2053-1583/aa6b17 ↗
29. 10.1039/C6NR00154H10.1039/C6NR00154H ↗
30. 10.1016/j.carbon.2014.01.07110.1016/j.carbon.2014.01.071 ↗
31. 10.1021/acsnano.6b0303610.1021/acsnano.6b03036 ↗
32. 10.1103/PhysRevB.91.12530410.1103/PhysRevB.91.125304 ↗
33. 10.1021/nn100343f10.1021/nn100343f ↗
34. 10.1103/PhysRevLett.104.05680110.1103/PhysRevLett.104.056801 ↗
35. 10.1143/JJAP.48.11120310.1143/JJAP.48.111203 ↗
36. 10.1038/ncomms880110.1038/ncomms8801 ↗
37. 10.1021/acsnano.5b0027110.1021/acsnano.5b00271 ↗
38. 10.1021/acsnano.6b0303610.1021/acsnano.6b03036 ↗
39. 10.1002/smtd.20160006010.1002/smtd.201600060 ↗
40. Zhao M. · Nat. Nanotechnol. · 2016
41. 10.1002/adma.20150507010.1002/adma.201505070 ↗
42. 10.1021/nn504812410.1021/nn5048124 ↗
43. 10.1021/acsnano.6b0148610.1021/acsnano.6b01486 ↗
44. 10.1016/0927-0256(96)00008-010.1016/0927-0256(96)00008-0 ↗
45. 10.1103/PhysRevLett.77.386510.1103/PhysRevLett.77.3865 ↗