posted on 2020-12-04, 15:35authored byParth Vashishtha, Benjamin E. Griffith, Alasdair A.M. Brown, Thomas J.N. Hooper, Yanan Fang, Mohammed S. Ansari, Annalisa Bruno, Suan Hui Pu, Subodh G. Mhaisalkar, Tim White, John V. Hanna
Inorganic
cesium lead halide perovskite nanocrystals are promising
materials for optoelectronic applications as they exhibit high thermal
stability alongside precise color tunability and high color purity;
however, their optical properties are degraded by surface defects.
This work demonstrates a room temperature synthesis of CsPbBr3 nanocrystals facilitating in situ surface
passivation via the incorporation of Zn2+ cations. The
facile incorporation ZnBr2 into the precursor solution
facilitates Zn2+ and Br− substitution
into the nanocrystal surface/subsurface layers to induce passivation
of existing Pb2+ and Br– vacancies and
increase the photoluminescence quantum yield from ∼48 to 86%.
The XPS and solid-state 1H MAS NMR techniques show that
the key modification is a reduction of the octylamine:oleic acid ratio
leading to a near-neutral surface charge; this is accompanied by the
appearance of larger nanosheets and nanowires observed by quantitative
powder XRD and HR-TEM. The suitability of these perovskite nanocrystals
for electrically driven applications was confirmed by the fabrication
of light-emitting diodes, which demonstrate that the in situ Zn2+ passivation strategy enhanced the external quantum
efficiency by ∼60%.