Surface Chemically Switchable Ultraviolet Luminescence from Interfacial Two-Dimensional Electron Gas
- Drexel Univ., Philadelphia, PA (United States); University of Pennsylvania
- Univ. of Pennsylvania, Philadelphia, PA (United States)
- Drexel Univ., Philadelphia, PA (United States)
- Univ. of Illinois at Urbana-Champaign, IL (United States)
- Temple Univ., Philadelphia, PA (United States)
- Univ. of California, Berkeley, CA (United States)
We report intense, narrow line-width, surface chemisorption-activated and reversible ultraviolet (UV) photoluminescence from radiative recombination of the two-dimensional electron gas (2DEG) with photoexcited holes at LaAlO3/SrTiO3. The switchable luminescence arises from an electron transfer-driven modification of the electronic structure via H-chemisorption onto the AlO2-terminated surface of LaAlO3, at least 2 nm away from the interface. The control of the onset of emission and its intensity are functionalities that go beyond the luminescence of compound semiconductor quantum wells. Connections between reversible chemisorption, fast electron transfer, and quantum-well luminescence suggest a new model for surface chemically reconfigurable solid-state UV optoelectronics and molecular sensing.
- Research Organization:
- Univ. of Pennsylvania, Philadelphia, PA (United States)
- Sponsoring Organization:
- National Science Foundation (NSF); USDOE Office of Science (SC)
- Grant/Contract Number:
- FG02-07ER15920; FG02-07ER46453; SC0004764
- OSTI ID:
- 1867857
- Journal Information:
- Nano Letters, Journal Name: Nano Letters Journal Issue: 1 Vol. 16; ISSN 1530-6984
- Publisher:
- American Chemical SocietyCopyright Statement
- Country of Publication:
- United States
- Language:
- English
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journal | December 2019 |
Tunable 2D electron gas at the LaAlO 3 / SrTiO 3 ( 001 ) interface
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journal | July 2019 |
| Physics of SrTiO$_3$-based heterostructures and nanostructures: a review | text | January 2017 |
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