Femtosecond excitonic bleaching recovery in the optical Stark effect of GaAs/AlxGa1−xAs multiple quantum wells and directional couplers

1991 ◽  
Vol 43 (2) ◽  
pp. 1719-1725 ◽  
Author(s):  
S. G. Lee ◽  
P. A. Harten ◽  
J. P. Sokoloff ◽  
R. Jin ◽  
B. Fluegel ◽  
...  
1998 ◽  
Vol 184-185 ◽  
pp. 732-736 ◽  
Author(s):  
Takeshi Nagano ◽  
Ichirou Nomura ◽  
Masaru Haraguchi ◽  
Masayuki Arai ◽  
Hiroshi Hattori ◽  
...  

2016 ◽  
Vol 2 (6) ◽  
pp. e1600477 ◽  
Author(s):  
David Giovanni ◽  
Wee Kiang Chong ◽  
Herlina Arianita Dewi ◽  
Krishnamoorthy Thirumal ◽  
Ishita Neogi ◽  
...  

Ultrafast spin manipulation for opto–spin logic applications requires material systems that have strong spin-selective light-matter interaction. Conventional inorganic semiconductor nanostructures [for example, epitaxial II to VI quantum dots and III to V multiple quantum wells (MQWs)] are considered forerunners but encounter challenges such as lattice matching and cryogenic cooling requirements. Two-dimensional halide perovskite semiconductors, combining intrinsic tunable MQW structures and large oscillator strengths with facile solution processability, can offer breakthroughs in this area. We demonstrate novel room-temperature, strong ultrafast spin-selective optical Stark effect in solution-processed (C6H4FC2H4NH3)2PbI4 perovskite thin films. Exciton spin states are selectively tuned by ~6.3 meV using circularly polarized optical pulses without any external photonic cavity (that is, corresponding to a Rabi energy of ~55 meV and equivalent to applying a 70 T magnetic field), which is much larger than any conventional system. The facile halide and organic replacement in these perovskites affords control of the dielectric confinement and thus presents a straightforward strategy for tuning light-matter coupling strength.


1996 ◽  
Vol 53 (23) ◽  
pp. 15469-15472 ◽  
Author(s):  
J. L. Sánchez-Rojas ◽  
A. Sacedón ◽  
E. Calleja ◽  
E. Muñoz ◽  
A. Sanz-Hervás ◽  
...  

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