In
this work, compared with the corresponding pure CsPbCl3 nanocrystals (NCs) and Mn2+-doped CsPbCl3 NCs,
Mn2+/Cu2+-codoped CsPbCl3 NCs exhibited
improved photoluminescence (PL) and photoluminescence quantum yields
(PL QYs) (57.6%), prolonged PL lifetimes (1.78 ms), and enhanced thermal
endurance (523 K) as a result of efficient Mn2+ doping
(3.66%) induced by the addition of CuCl2. Furthermore,
we applied pressure on Mn2+/Cu2+-codoped CsPbCl3 NCs to reveal that a red shift of photoluminescence followed
by a blue shift was caused by band gap evolution and related to the
structural phase transition from cubic to orthorhombic. Moreover,
we also found that under the preheating condition of 523 K, such phase
transition exhibited obvious morphological invariance, accompanied
by significantly enhanced conductivity. The pressure applied to the
products treated with high temperature enlarged the electrical difference
and easily intensified the interface by closer packaging. Interestingly,
defect-triggered mixed ionic and electronic conducting (MIEC) was
observed in annealed NCs when the applied pressure was 2.9 GPa. The
pressure-dependent ionic conduction was closely related to local nanocrystal
amorphization and increased deviatoric stress, as clearly described
by in situ impedance spectra. Finally, retrieved
products exhibited better conductivity (improved by 5–6 times)
and enhanced photoelectric response than those when pressure was not
applied. Our findings not only reveal the pressure-tuned optical and
electrical properties via structural progression
but also open up the promising exploration of more amorphous all-inorganic
CsPbX3-based photoelectric applications.
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