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Intralayer bidentate diammoniums for stable two-dimensional perovskites

  • Chenjian Lin
  • , Yuanhao Tang
  • , Zhichen Nian
  • , Aidan H. Coffey
  • , Yunfei Wang
  • , Hanjun Yang
  • , Pengfei Wu
  • , Yu Ting Yang
  • , Syed Joy
  • , Kenneth R. Graham
  • , Wenzhan Xu
  • , Chenhui Zhu
  • , Brett M. Savoie
  • , Letian Dou

Research output: Contribution to journalArticlepeer-review

14 Scopus citations

Abstract

Two-dimensional (2D) metal halide perovskites have attracted considerable attention for optoelectronic applications. Conventional 2D perovskites include Ruddlesden–Popper (R-P), Dion–Jacobson (D-J) and alternating cation phases. Here we introduce a class of 2D perovskite incorporating intralayer bidentate ligands, termed B-D phase perovskites, designed to enhance structural diversity and stability. We synthesized bidentate ligands with a rigid core unit and two ipsilateral ammonium-terminated linker groups, and obtained single crystals incorporating these B-D ligands with intralayer bidentate coordination. Molecular dynamics simulations reveal that the B-D ligand exhibits stronger binding energies to the inorganic layer compared with its R-P and D-J phase counterparts. Polycrystalline thin films of B-D phase showed superior thermal resistance, outperforming R-P and D-J phase analogues by 1,600% and 140% respectively, based on absorption stability assessments. Photovoltaic devices incorporating the B-D ligand exhibited higher power conversion efficiency and extended stability. These findings establish B-D phase 2D perovskites as a promising platform for next-generation optoelectronic applications, advancing ligand engineering for metal halide perovskites and other hybrid materials. (Figure presented.)

Original languageEnglish
Pages (from-to)275-282
Number of pages8
JournalNature Chemistry
Volume18
Issue number2
DOIs
StatePublished - Feb 2026

Bibliographical note

Publisher Copyright:
© The Author(s), under exclusive licence to Springer Nature Limited 2026.

Funding

This work is primarily supported by US Department of Energy’s Office of Energy Efficiency and Renewable Energy (EERE) under the Solar Energy Technologies Office Award DE-EE0009519 (L.D. and B.M.S.). S.J. and K.R.G. acknowledge funding from the National Science Foundation through DMR-2102257 (K.R.G.). This work is supported in part by the Research Instrumentation Center in the Department of Chemistry at Purdue University. The views expressed herein do not necessarily represent the views of the US Department of Energy or the US government. The authors acknowledge M. Zeller for single-crystal data collection and refinement, and X. Li and W. Shao for helpful discussions.

FundersFunder number
Purdue Climate Change Research Center, Purdue University
Office of Energy Efficiency and Renewable Energy
U.S. Department of Energy
US Government or NYU
Solar Energy Technologies OfficeDE-EE0009519
National Science Foundation Arctic Social Science ProgramDMR-2102257

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 7 - Affordable and Clean Energy
      SDG 7 Affordable and Clean Energy

    ASJC Scopus subject areas

    • General Chemistry
    • General Chemical Engineering

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