Convenient modulation
of bandgap for the mixed halide perovskites
(MHPs) (e.g., CsPbBr
x
I1–x
) through varying the halide composition (i.e., the
ratio of bromide to iodide) allows for optimizing the light-harvesting
properties in perovskite solar cells (PSCs) and emission color in
perovskite light-emitting diodes (PeLEDs). Such MHPs, yet, severely
suffered from the instability under light irradiation and electrical
bias as a result of an intrinsic soft, ionic lattice and a high halide
ion mobility. Understanding the halide ion migration (mediated through
halide vacancies) and suppressing the halide ion segregation, thus,
remain a significant challenge both in the field of PSCs and PeLEDs
since it is directly linked to the long-term stability and performances
of the corresponding devices. In this Mini-Review, we discuss the
intrinsic instability of the MHPs arising from the ionic nature of
perovskites. The liquid crystalline properties with the low formation
energy of halide ion defects facilitate the defect-mediated halide
ion migration. Several different mechanistic models are provided to
explain the fundamental origin of the photo- or electric field-driven
halide ion segregation based upon thermodynamics and kinetics. These
reflect that lattice strains (internal or polaron-induced) and bandgap
energy differences between parent mixed halide and iodide-rich domain
serve as the thermodynamic driving forces for halide segregation.
On the basis of the deeper understanding of the underpinning segregation
mechanism mediated through hole trapping and accumulation at the iodide-rich
sites, we further discuss the strategies to mitigate the detrimental
halide segregation through composition-, defect-, dimension-, and
interface-engineering. Finally, we provide a fundamental insight into
designing perovskite-based photovoltaic and optoelectronic devices
for the long-term operational stability.
Two-dimensional transition metal dichalcogenide (2D TMD) crystals are versatile platforms for realizing emergent optoelectronic devices. However, the ability to produce large-area 2D TMDs with spatial homogeneity and to accomplish broadband photodetection by tuning the operating wavelengths in photodetectors are two paramount prerequisites for practical applications of 2D TMD-based photodetectors. Here, we demonstrated all-solution-processed broadband photodetectors based on the wafer-scale perovskite quantum dots (PQDs)/MoS2 through light management via the monochromatization effect of the PQDs. The photodetectors exhibited broadband photodetection behavior that retained high photocurrents over a wide spectral range (254, 365, and 532 nm) by enhancing the photoresponse in the UV region through light management via the monochromatization effect of the PQDs. This intriguing strategy was proven with (i) electrical isolation realized by inserting an Al2O3 insulator between the PQDs and MoS2 and (ii) alteration of the PQD density. The rational nanohybrid-based photodetectors also exhibited superb air stability and exceptional bending durability.
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