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Peer-reviewedCC BYRSC advances

Spatial halide exchange reactions for sculpting light in hybrid perovskites.

  1. 1Department of Chemistry, College of Arts and Sciences, IUBAT-International University of Business Agriculture and Technology Uttara Model Town Dhaka 1230 Bangladesh [email protected].
  2. 2Department of General Medicine, Saveetha Medical College and Hospitals, Saveetha Institute of Medical and Technical Sciences Chennai India [email protected].

Abstract

Hybrid perovskites have emerged as transformative materials in optoelectronics because their halide composition enables wide and controllable changes in bandgap and photoluminescence. Yet, translating this compositional tunability into spatially programmed optical functionality remains challenging. This review focuses specifically on spatially controlled halide exchange in hybrid and related lead-halide perovskites, emphasizing how the location, kinetics, and confinement of ion exchange determine the resulting optical landscape. We critically compare light-mediated/photocatalytic, laser-assisted, lithographic, solution-solid, solid-solid, and vapor-phase strategies in terms of localization mechanism, processing time, spatial resolution, compositional stability, scalability, and demonstrated functionality. Particular attention is given to vacancy-assisted ion migration, concentration gradients, interfacial diffusion, and optically driven precursor accumulation as the mechanistic basis of spatial control. We distinguish experimentally demonstrated outcomes-such as localized multicolor emission, compositionally graded nanowires, and single-crystal heterojunctions-from applications that remain prospective, including fully integrated micro-LED arrays and complex photonic circuits. The review identifies a central trade-off between spatial precision and throughput/stability and proposes standardized reporting of feature size, exchange time, compositional fidelity, and post-exchange stability as priorities for moving spatial halide exchange toward practical devices.

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BibTeX
@article{islam2026spatial,
  title = {{Spatial halide exchange reactions for sculpting light in hybrid perovskites.}},
  author = {Md Jahidul Islam and Ajoy Kumer},
  journal = {RSC advances},
  year = {2026},
  month = oct,
  doi = {10.1039/d6ra06645c},
  url = {https://europepmc.org/article/MED/42847092},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - Spatial halide exchange reactions for sculpting light in hybrid perovskites.
AU  - Md Jahidul Islam
AU  - Ajoy Kumer
PY  - 2026
DA  - 2026/10/07
JO  - RSC advances
DO  - 10.1039/d6ra06645c
UR  - https://europepmc.org/article/MED/42847092
AB  - Hybrid perovskites have emerged as transformative materials in optoelectronics because their halide composition enables wide and controllable changes in bandgap and photoluminescence. Yet, translating this compositional tunability into spatially programmed optical functionality remains challenging. This review focuses specifically on spatially controlled halide exchange in hybrid and related lead-halide perovskites, emphasizing how the location, kinetics, and confinement of ion exchange determine the resulting optical landscape. We critically compare light-mediated/photocatalytic, laser-assisted, lithographic, solution-solid, solid-solid, and vapor-phase strategies in terms of localization mechanism, processing time, spatial resolution, compositional stability, scalability, and demonstrated functionality. Particular attention is given to vacancy-assisted ion migration, concentration gradients, interfacial diffusion, and optically driven precursor accumulation as the mechanistic basis of spatial control. We distinguish experimentally demonstrated outcomes-such as localized multicolor emission, compositionally graded nanowires, and single-crystal heterojunctions-from applications that remain prospective, including fully integrated micro-LED arrays and complex photonic circuits. The review identifies a central trade-off between spatial precision and throughput/stability and proposes standardized reporting of feature size, exchange time, compositional fidelity, and post-exchange stability as priorities for moving spatial halide exchange toward practical devices.
SN  - 2046-2069
ER  -