Band structure engineering via piezoelectric fields in strained anisotropic CdSe/CdS nanocrystals

Strain in colloidal heteronanocrystals with non-centrosymmetric lattices presents a unique opportunity for controlling optoelectronic properties and adds a new degree of freedom to existing wavefunction engineering and doping paradigms. We synthesized wurtzite CdSe nanorods embedded in a thick CdS shell, hereby exploiting the large lattice mismatch between the two domains to generate a compressive strain of the CdSe core and a strong piezoelectric potential along its c-axis. Efficient charge separation results in an indirect ground-state transition with a lifetime of several microseconds, almost one order of magnitude longer than any other CdSe/CdS nanocrystal. Higher excited states recombine radiatively in the nanosecond time range, due to increasingly overlapping excited-state orbitals. k˙p calculations confirm the importance of the anisotropic shape and crystal structure in the buildup of the piezoelectric potential. Strain engineering thus presents an efficient approach to highly tunable single- and multiexciton interactions, driven by a dedicated core/shell nanocrystal design.F.R., J.I.C. and J.P. acknowledge financial support from MINECO project CTQ2011-27324 and UJI-Bancaixa P1-1B2011-01. S.B. and F.M. acknowledge support from the Cariplo Foundation (2012-0844). S.B. thanks the European Community’s Seventh Framework Programme (FP7/2007-2013) under grant agreement no. 324603 for financial support (EDONHIST). The present publication is further realized with the support of the Ministero degli Affari Esteri e della Cooperazione Internazionale (IONX-NC4SOL, I.M.). K. Miszta (IIT, Italy) is acknowledged for initial discussions on the RIR samples, and W. Langbein (Cardiff University, UK) for enlightening conversations on strain and the Stark effect in CdSe/CdS superlattices