journal article·2025-10-01

Encapsulation of Monolayer 2D Materials Using Kinetic Energy-Controlled Pulsed Laser Deposition

Daniel T. Yimam, Sumner B. Harris, Austin C. Houston, Ivan V. Vlassiouk, Alexander A. Puretzky, Sujoy Ghosh, Kyungnam Kang, Christopher Rouleau, Gerd Duscher, Gyula Eres, David B. Geohegan, Kai Xiao

ACS Applied Materials & Interfaces· Volume 17· Issue 39
Publisher page

Abstract

The integration of monolayer (ML) two-dimensional (2D) materials into next-generation microelectronics, optoelectronics, and sensors is hindered by their sensitivity to environmental exposure. Deposition of additional layers for encapsulation or growth on ML 2D materials by versatile but energetic plasma techniques such as pulsed laser deposition (PLD) has not been considered at the monolayer level because of potential damage caused by hyperthermal species with kinetic energies (KEs) exceeding the threshold displacement energy (TDE) of the ML. Here, we describe a general strategy to understand and mitigate damage during PLD by reducing the incident KE of ablated species below the TDE of the 2D monolayer using background gas collisions. Ion flux diagnostics, combined with in situ Raman spectroscopy of monolayer graphene during PLD of amorphous boron nitride (a-BN) as a dielectric encapsulation layer, show that damage is primarily correlated with fast ions that penetrate the background gas in accordance with Beer’s Law and are often overlooked in ICCD imaging due to the dominance of the bright, delayed plasma luminescence. Significantly, if fast ions are eliminated and a ∼2 nm-thick a-BN layer is “soft landed”, the monolayer graphene is effectively protected from damage by high KE species in the boron nitride plasma plume. Deposited a-BN films display a characteristic dielectric constant of 3.6 at 100 kHz and tunable charge injection properties. Our results enable PLD as a viable option for encapsulation and thin film growth onto ML 2D materials, with implications for both fundamental research and device integration.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Graphene research and applications · Diamond and Carbon-based Materials Research · Semiconductor materials and devices

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

Affiliations

Center for Nanophase Materials Sciences

Oak Ridge National Laboratory

Department of Materials Science and Engineering

University of Tennessee

Materials Science and Technology Division

Funding

Basic Energy Sciences

References (51)

Show source-provided references
1. 10.1088/2053-1583/ab20d610.1088/2053-1583/ab20d6 ↗
2. 10.1021/acs.nanolett.4c0011710.1021/acs.nanolett.4c00117 ↗
3. 10.1016/j.cclet.2021.08.08610.1016/j.cclet.2021.08.086 ↗
4. 10.1021/acsami.2c1870610.1021/acsami.2c18706 ↗
5. 10.1038/s41467-024-48429-410.1038/s41467-024-48429-4 ↗
6. 10.1002/adfm.20150545510.1002/adfm.201505455 ↗
7. 10.1021/acsami.2c0280310.1021/acsami.2c02803 ↗
8. 10.1038/s44287-025-00141-110.1038/s44287-025-00141-1 ↗
9. 10.1109/TED.2023.325840310.1109/TED.2023.3258403 ↗
10. 10.1002/admt.20220002210.1002/admt.202200022 ↗
11. 10.1016/S0169-4332(97)00670-310.1016/S0169-4332(97)00670-3 ↗
12. 10.1063/1.35987110.1063/1.359871 ↗
13. 10.1016/j.apsusc.2020.14857310.1016/j.apsusc.2020.148573 ↗
14. 10.1016/S0925-9635(01)00386-710.1016/S0925-9635(01)00386-7 ↗
15. 10.1063/1.35749110.1063/1.357491 ↗
16. 10.1117/12.35270810.1117/12.352708 ↗
17. 10.1103/PhysRevB.107.09411210.1103/PhysRevB.107.094112 ↗
18. 10.1063/1.494558710.1063/1.4945587 ↗
19. 10.1016/j.carbon.2015.11.04010.1016/j.carbon.2015.11.040 ↗
20. 10.1016/j.tsf.2014.07.05910.1016/j.tsf.2014.07.059 ↗
21. 10.1063/1.491906810.1063/1.4919068 ↗
22. 10.1021/acsnano.2c0995210.1021/acsnano.2c09952 ↗
23. 10.1021/acsnano.9b1019610.1021/acsnano.9b10196 ↗
24. 10.1021/acsomega.7b0034110.1021/acsomega.7b00341 ↗
25. 10.1021/acs.nanolett.7b0104710.1021/acs.nanolett.7b01047 ↗
26. Geohegan D. · 1994 · 59
27. 10.1103/PhysRevLett.79.157110.1103/PhysRevLett.79.1571 ↗
28. 10.1103/PhysRevB.58.153310.1103/PhysRevB.58.1533 ↗
29. 10.1016/0169-4332(95)00421-110.1016/0169-4332(95)00421-1 ↗
30. 10.1063/1.10685910.1063/1.106859 ↗
31. 10.1063/1.359265110.1063/1.3592651 ↗
32. 10.1088/0953-8984/27/8/08300210.1088/0953-8984/27/8/083002 ↗
33. 10.1021/nl300901a10.1021/nl300901a ↗
34. 10.1016/j.nimb.2017.04.05410.1016/j.nimb.2017.04.054 ↗
35. 10.1063/1.306285110.1063/1.3062851 ↗
36. 10.1016/j.apsusc.2024.16060410.1016/j.apsusc.2024.160604 ↗
37. 10.1038/nnano.2013.4610.1038/nnano.2013.46 ↗
38. 10.1088/0957-4484/21/46/46570510.1088/0957-4484/21/46/465705 ↗
39. 10.1021/nl901073g10.1021/nl901073g ↗
40. 10.1038/srep0033710.1038/srep00337 ↗
41. 10.1088/1367-2630/13/2/02500810.1088/1367-2630/13/2/025008 ↗
42. 10.1103/PhysRevB.88.08541910.1103/PhysRevB.88.085419 ↗
43. 10.1103/PhysRevLett.98.16680210.1103/PhysRevLett.98.166802 ↗
44. 10.1038/s41598-017-16969-z10.1038/s41598-017-16969-z ↗
45. 10.1021/nn800459e10.1021/nn800459e ↗
46. 10.1038/s41586-020-2375-910.1038/s41586-020-2375-9 ↗
47. 10.1088/2053-1583/aa9ea310.1088/2053-1583/aa9ea3 ↗
48. 10.1016/j.jcis.2019.10.02010.1016/j.jcis.2019.10.020 ↗
49. 10.1016/j.vacuum.2021.11021110.1016/j.vacuum.2021.110211 ↗
50. 10.1016/j.solidstatesciences.2010.05.02910.1016/j.solidstatesciences.2010.05.029 ↗
51. 10.1016/0925-8388(95)01532-910.1016/0925-8388(95)01532-9 ↗