Compared
to zero-dimensional (0D) semiconductor quantum dots, 2D
semiconductor nanoplatelets (NPLs) offer a spectrally narrow luminescence
and superior absorption coefficients, which makes this geometry an
attractive candidate for optoelectronic applications. However, optical
devices based on NPLs still suffer from nonradiative Auger decay of
multiple excitons (MX), which limits the efficiency of the processes,
including MX luminescence, electroluminescence, and optical gain.
Here, we demonstrate that Auger recombination is strongly suppressed
in spherically shaped nanoplatelets, called quantum shells (QSs),
where a relaxed confinement of charges leads to diminished exciton–exciton
interactions. In particular, we use single photon counting and photon
correlation spectroscopy to show that two-dimensional CdS/CdSe/CdS
core/shell/shell spherical QSs reach near-unity biexciton emission
yield. The Auger suppression was found most prominent in QSs with
the largest shell diameter. A combination of ultralong (>15 ns)
biexciton
(BX) emission lifetimes and strong exciton–exciton repulsion
in these QS samples allowed demonstrating low-threshold amplified
spontaneous emission (ASE), large modal gain, and microcavity lasing
featuring sharp emission modes at the BX and MX transitions. Finally,
by introducing QSs within perovskite matrices, we achieved a strong
electroluminescence enhancement in light-emitting devices, yielding
devices as bright as 213 W/m2 and a 2.3-fold enhancement
of the maximum external quantum efficiency. These results represent
a major step toward realizing solution-processed colloidal lasers
and LEDs.