Title: Surface Chemically Switchable Ultraviolet Luminescence from Interfacial Two-Dimensional Electron Gas

Journal Article · · Nano Letters
 [1];  [2];  [3];  [2];  [4];  [5];  [6];  [3];  [5];  [6];  [2];  [3]
  1. Drexel Univ., Philadelphia, PA (United States); University of Pennsylvania
  2. Univ. of Pennsylvania, Philadelphia, PA (United States)
  3. Drexel Univ., Philadelphia, PA (United States)
  4. Univ. of Illinois at Urbana-Champaign, IL (United States)
  5. Temple Univ., Philadelphia, PA (United States)
  6. 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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Tunable 2D electron gas at the LaAlO 3 / SrTiO 3 ( 001 ) interface journal July 2019
Physics of SrTiO$_3$-based heterostructures and nanostructures: a review text January 2017