Nanometer-Thick MgxZn(1–x)O Ternary Films for Photovoltaics
Source abstract
Abstract
Owing to their tunable bandgap with the concentration of the Mg dopant, magnesium–zinc oxide (MgxZn(1–x)O) ternary nanometer-thick thin films have been widely studied for applications in the fields of microelectronics and optoelectronics. There are a few reports about the promise of using atomic layer deposition (ALD) to synthesize MgxZn(1–x)O for applications in photovoltaics. The synthesis–structure–property relationship of MgxZn(1–x)O ALD thin films is not yet clear. In this work, we present a systematic study about the growth behavior of MgxZn(1–x)O nanometer thin films by ALD by using in-situ quartz crystal microbalance analysis and a set of ex-situ analyses. We employed diethylzinc (DEZ), biscyclopentadienyl-magnesium (MgCp2), and H2O as the precursors for ZnO and MgO ALD chemistries in our study. We find that the nucleation of ZnO on the MgO-doped ZnO surface can be accelerated at 200 °C but be delayed at 120 °C in the growth of MgxZn(1–x)O. The crystal structure and optical properties of MgxZn(1–x)O ALD films are also different at growth temperatures of 200 and 120 °C. Such understanding can help rationally choose the deposition conditions for ALD MgxZn(1–x)O nanoscale thin films in various applications.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: ZnO doping and properties · Ga2O3 and related materials · Semiconductor materials and devices
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Energy Systems Division, Argonne National Laboratory, 9700 South Cass Ave., Argonne, Illinois 60439, United States
Chemical and Biological Engineering Department, University of Alabama, Tuscaloosa, Alabama 35401, United States
Funding
U.S. Department of Energy · American Chemical Society · University of Alabama
References (30)
Show source-provided references
1. 10.1063/1.221881310.1063/1.2218813 ↗
2. 10.1063/1.242972910.1063/1.2429729 ↗
3. 10.1063/1.140581110.1063/1.1405811 ↗
4. 10.1021/jp500605t10.1021/jp500605t ↗
5. 10.1021/jp803129e10.1021/jp803129e ↗
6. 10.1063/1.199266610.1063/1.1992666 ↗
7. 10.1063/1.145626610.1063/1.1456266 ↗
8. 10.1063/1.160925010.1063/1.1609250 ↗
9. 10.1016/S0038-1098(01)00431-810.1016/S0038-1098(01)00431-8 ↗
10. 10.1063/1.12138410.1063/1.121384 ↗
11. 10.1002/pip.85910.1002/pip.859 ↗
12. 10.1002/pip.73310.1002/pip.733 ↗
13. 10.1063/1.307385810.1063/1.3073858 ↗
14. 10.1021/cm903197810.1021/cm9031978 ↗
15. 10.1063/1.149041010.1063/1.1490410 ↗
16. 10.1021/cr900056b10.1021/cr900056b ↗
17. 10.1002/anie.20030165210.1002/anie.200301652 ↗
18. 10.1021/nl062948i10.1021/nl062948i ↗
19. 10.1063/1.194072710.1063/1.1940727 ↗
20. 10.1021/jp709731210.1021/jp7097312 ↗
21. 10.1021/cm020607+10.1021/cm020607+ ↗
22. 10.1149/1.156948110.1149/1.1569481 ↗
23. 10.1039/C0JM02786C10.1039/C0JM02786C ↗
24. 10.1063/1.490238910.1063/1.4902389 ↗
25. 10.1116/1.492241010.1116/1.4922410 ↗
26. 10.1116/1.501595810.1116/1.5015958 ↗
27. 10.1021/jp806088m10.1021/jp806088m ↗
28. 10.1016/j.mseb.2005.08.11210.1016/j.mseb.2005.08.112 ↗
29. 10.1007/s11664-007-0201-x10.1007/s11664-007-0201-x ↗
30. 10.1016/j.jcrysgro.2010.01.01810.1016/j.jcrysgro.2010.01.018 ↗