Natural Layered Phlogopite Dielectric for Ultrathin Two-Dimensional Optoelectronics
Source abstract
Abstract
High Resolution Image Download MS PowerPoint Slide The integration of high-dielectric-constant (high-κ) materials with two-dimensional (2D) semiconductors is promising to overcome performance limitations and reach their full theoretical potential. Here, we show that naturally occurring phlogopite mica, exfoliated into ultrathin flakes, can serve as a robust high-κ dielectric layer for transition metal dichalcogenide-based 2D electronics and optoelectronics. The wide band gap (∼4.8 eV), high dielectric constant (∼11), and large breakdown field (>10 MV cm –1 ) of phlogopite enable transistors with subthreshold swings down to 100 mV dec –1, minimal hysteresis (∼30–60 mV), and interface trap densities comparable to those of state-of-the-art oxide dielectrics. Moreover, phototransistors built upon monolayer molybdenum disulfide (MoS 2 ) and phlogopite exhibit responsivities up to 3.3 × 10 4 AW –1 and detectivities close to 10 10 Jones, surpassing devices based on conventional gate insulators. We further demonstrate the versatility of this natural dielectric by integrating phlogopite/MoS 2 heterostructures into NMOS inverters, showcasing robust voltage gains and low-voltage operation. Our findings establish phlogopite as a promising, earth-abundant dielectric for next-generation 2D transistor technologies and high-performance photodetection.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: 2D Materials and Applications · Perovskite Materials and Applications · Advanced biosensing and bioanalysis techniques
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
2D Foundry Research Group
Instituto de Ciencia de Materiales de Madrid (ICMM-CSIC)
ESISNA Research Group
Funding
Comunidad de Madrid · Ministerio de Ciencia y Tecnolog?a
References (78)
Show source-provided references
1. 10.1038/nphoton.2015.28210.1038/nphoton.2015.282 ↗
2. 10.1038/s41928-021-00670-110.1038/s41928-021-00670-1 ↗
3. 10.1021/nl903868w10.1021/nl903868w ↗
4. 10.1038/nnano.2010.27910.1038/nnano.2010.279 ↗
5. 10.1021/nn500480u10.1021/nn500480u ↗
6. 10.1038/s41699-019-0096-410.1038/s41699-019-0096-4 ↗
7. 10.1038/nnano.2013.10010.1038/nnano.2013.100 ↗
8. 10.1038/s41467-023-40055-w10.1038/s41467-023-40055-w ↗
9. 10.1016/j.mattod.2019.04.01910.1016/j.mattod.2019.04.019 ↗
10. 10.1021/acs.nanolett.5b0255910.1021/acs.nanolett.5b02559 ↗
11. 10.1038/s41467-020-16640-810.1038/s41467-020-16640-8 ↗
12. 10.1038/s41586-022-04588-210.1038/s41586-022-04588-2 ↗
13. 10.1038/s41928-022-00753-710.1038/s41928-022-00753-7 ↗
14. 10.1021/acs.nanolett.2c0239510.1021/acs.nanolett.2c02395 ↗
15. 10.1038/s41467-023-40123-110.1038/s41467-023-40123-1 ↗
16. 10.1038/s41563-023-01502-710.1038/s41563-023-01502-7 ↗
17. 10.1038/s41563-023-01626-w10.1038/s41563-023-01626-w ↗
18. 10.1038/s41928-025-01353-x10.1038/s41928-025-01353-x ↗
19. 10.1038/s41928-024-01245-610.1038/s41928-024-01245-6 ↗
20. 10.1038/s41928-024-01129-910.1038/s41928-024-01129-9 ↗
21. 10.1038/s43246-020-00103-010.1038/s43246-020-00103-0 ↗
22. 10.1021/nl502339q10.1021/nl502339q ↗
23. 10.1088/1361-6528/ad7b3a10.1088/1361-6528/ad7b3a ↗
24. 10.1088/2053-1583/ac6cf410.1088/2053-1583/ac6cf4 ↗
25. 10.1038/s41598-022-18320-710.1038/s41598-022-18320-7 ↗
26. 10.1063/5.016173610.1063/5.0161736 ↗
27. Steinfink H. · Am. Mineral. · 1962 · 47 · 886
28. Deer W. A. · 201310.1180/DHZ ↗
29. Anthony J. W. · 1990
30. Hazen R. M. · Am. Mineral. · 1973 · 58 · 889
31. 10.1002/jrs.468010.1002/jrs.4680 ↗
32. 10.2138/am-2022-805110.2138/am-2022-8051 ↗
33. 10.1038/s41699-020-00172-210.1038/s41699-020-00172-2 ↗
34. 10.1088/2053-1583/1/1/01100210.1088/2053-1583/1/1/011002 ↗
35. 10.1023/B:COLL.0000030843.30563.c910.1023/B:COLL.0000030843.30563.c9 ↗
36. 10.1038/s41699-021-00276-310.1038/s41699-021-00276-3 ↗
37. 10.1002/adpr.20210022110.1002/adpr.202100221 ↗
38. 10.1021/nn404747410.1021/nn4047474 ↗
39. 10.1002/adpr.20200002510.1002/adpr.202000025 ↗
40. 10.1021/acsanm.4c0533810.1021/acsanm.4c05338 ↗
41. 10.1088/0022-3719/6/6/02210.1088/0022-3719/6/6/022 ↗
42. 10.1180/minmag.1989.053.370.0410.1180/minmag.1989.053.370.04 ↗
43. 10.1016/j.jmgm.2013.05.00510.1016/j.jmgm.2013.05.005 ↗
44. 10.1088/0022-3719/5/8/01410.1088/0022-3719/5/8/014 ↗
45. 10.1016/j.ceramint.2019.06.29410.1016/j.ceramint.2019.06.294 ↗
46. 10.1002/smll.20231183610.1002/smll.202311836 ↗
47. 10.1002/adma.20210608410.1002/adma.202106084 ↗
48. 10.1051/epjap:200420610.1051/epjap:2004206 ↗
49. 10.1063/1.141576610.1063/1.1415766 ↗
50. 10.1038/s41467-024-51322-910.1038/s41467-024-51322-9 ↗
51. 10.1155/2014/57816810.1155/2014/578168 ↗
52. 10.1126/science.aao424910.1126/science.aao4249 ↗
53. 10.1038/ncomms966210.1038/ncomms9662 ↗
54. 10.1038/s41928-022-00824-910.1038/s41928-022-00824-9 ↗
55. 2022
56. 10.1021/nn200026e10.1021/nn200026e ↗
57. 10.1038/s41563-024-02043-310.1038/s41563-024-02043-3 ↗
58. 10.1038/srep3044910.1038/srep30449 ↗
59. 10.1002/adfm.20240944710.1002/adfm.202409447 ↗
60. Sze S. M. · 200610.1002/0470068329 ↗
61. 10.1021/acsami.4c1933710.1021/acsami.4c19337 ↗
62. 10.1038/s41467-024-53907-w10.1038/s41467-024-53907-w ↗
63. 10.1007/s12274-022-5241-210.1007/s12274-022-5241-2 ↗
64. 10.1002/adma.20130124410.1002/adma.201301244 ↗
65. 10.1038/s41563-022-01398-910.1038/s41563-022-01398-9 ↗
66. 10.1021/acsami.9b0397110.1021/acsami.9b03971 ↗
67. 10.1002/adma.20140247110.1002/adma.201402471 ↗
68. 10.3390/s2108275810.3390/s21082758 ↗
69. 10.1039/C5NR01205H10.1039/C5NR01205H ↗
70. 10.1002/adma.20160355010.1002/adma.201603550 ↗
71. 10.1007/s12274-017-1941-410.1007/s12274-017-1941-4 ↗
72. 10.3390/nanomanufacturing101000510.3390/nanomanufacturing1010005 ↗
73. 10.3390/nano809072510.3390/nano8090725 ↗
74. 10.1038/s41598-018-25472-y10.1038/s41598-018-25472-y ↗
75. 10.5281/ZENODO.767763810.5281/ZENODO.7677638 ↗
76. 10.1088/1361-6528/ad77dc10.1088/1361-6528/ad77dc ↗
77. 10.1088/1361-6463/aa525610.1088/1361-6463/aa5256 ↗
78. 10.1088/1361-6463/adc27310.1088/1361-6463/adc273 ↗