Structural Tuning of Layered Perovskites for Enhanced Broadband Emission at Room Temperature

The versatile structure of organic–inorganic layered perovskites has enabled the fabrication of strongly luminescent material sources with narrow emission. However, although demonstrated to be beneficial for many applications, their structural tunability to achieve broadband emission and thus white light is often limited to changes in the organic cation. Herein, the role of solvent–organic cation interactions on the structural arrangement of the organic and inorganic building blocks in a room‐temperature synthesis is investigated. It is shown that changes in the solvent properties coupled with the molecular configuration of the organic cation can disrupt the conventional platelet‐like shape of layered perovskites, leading to disconnected corner‐sharing ribbons of octahedra, from which micrometer‐elongated crystals with nanoscale grooves are formed. With an 18% white light photoluminescence quantum efficiency, the crystal shape enables localized Mn doping at the groove interfaces. These findings highlight the crucial role of the interaction among solvent molecules and organic cations in shaping the assembly of the structural framework and their optical properties.

Authors

Institutions

Publication Details

Journal
Small Structures
Published
2025-09-12
DOI
https://doi.org/10.1002/sstr.202500311
Primary Topic
Perovskite Materials and Applications
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Structural Tuning of Layered Perovskites for Enhanced Broadband Emission at Room Temperature

Mauro Gemmi, Iryna Andrusenko, Liberato Manna, Simone Lauciello et al.
Small Structures
Perovskite Materials and Applications
article

Structural Tuning of Layered Perovskites for Enhanced Broadband Emission at Room Temperature

Mauro Gemmi, Iryna Andrusenko, Liberato Manna, Simone Lauciello, Giorgio Divitini, Quentin Evrard, Luca Goldoni, Serena De Negri, Pavlo Solokha, Aarya Prabhakaran, Balaji Dhanabalan, Luiz G. Bonato, Danilo Marchetti, Sirous Khabbaz Abkenar, Milena P. Arciniegas, Moussa D. Faye Diouf
article en

Abstract

The versatile structure of organic–inorganic layered perovskites has enabled the fabrication of strongly luminescent material sources with narrow emission. However, although demonstrated to be beneficial for many applications, their structural tunability to achieve broadband emission and thus white light is often limited to changes in the organic cation. Herein, the role of solvent–organic cation interactions on the structural arrangement of the organic and inorganic building blocks in a room‐temperature synthesis is investigated. It is shown that changes in the solvent properties coupled with the molecular configuration of the organic cation can disrupt the conventional platelet‐like shape of layered perovskites, leading to disconnected corner‐sharing ribbons of octahedra, from which micrometer‐elongated crystals with nanoscale grooves are formed. With an 18% white light photoluminescence quantum efficiency, the crystal shape enables localized Mn doping at the groove interfaces. These findings highlight the crucial role of the interaction among solvent molecules and organic cations in shaping the assembly of the structural framework and their optical properties.

Small StructuresVol. 6(11)
University of Parma (IT), Piaggio (Italy) (IT), Italian Institute of Technology (IT), Piaggio Aerospace (Italy) (IT), University of Genoa (IT)
Openalex Percentile: Top 76%
Perovskite Materials and Applications
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.