Directed emission of CdSe nanoplatelets originating from strongly anisotropic 2D electronic structure

abstract

Intrinsically directional light emitters are potentially important for applications in photonics including lasing and energyefficient display technology. Here, we propose a new route to overcome intrinsic efficiency limitations in light-emitting devices by studying a CdSe nanoplatelets monolayer that exhibits strongly anisotropic, directed photoluminescence. Analysis of the two-dimensional k-space distribution reveals the underlying internal transition dipole distribution. The observed directed emission is related to the anisotropy of the electronic Bloch states governing the exciton transition dipole moment and forming a bright plane. The strongly directed emission perpendicular to the platelet is further enhanced by the optical local density of states and local fields. In contrast to the emission directionality, the off-resonant absorption into the energetically higher 2D-continuum of states is isotropic. These contrasting optical properties make the oriented CdSe nanoplatelets, or superstructures of parallel-oriented platelets, an interesting and potentially useful class of semiconductor-based emitters.

keywords

LIGHT-EMITTING-DIODES; ORIENTATION; ABSORPTION; EFFICIENCY; ENERGY

subject category

Science & Technology - Other Topics; Materials Science

authors

Scott, R; Heckmann, J; Prudnikau, AV; Antanovich, A; Mikhailov, A; Owschimikow, N; Artemyev, M; Climente, JI; Woggon, U; Grosse, NB; Achtstein, AW

our authors

Groups

acknowledgements

R.S., U.W. and A.W. A acknowledge DFG grants WO477-1/32 and AC290-1/1 and 2/1. J.I.C. acknowledges support from MINECO project CTQ2014-60178-P and UJI project P1-1B2014-24, M.A. from the CHEMREAGENTS program and A.A. from BRFFI grant no. X16M-020.

Share this project:

Related Publications

We use cookies for marketing activities and to offer you a better experience. By clicking “Accept Cookies” you agree with our cookie policy. Read about how we use cookies by clicking "Privacy and Cookie Policy".