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 language | English |
|---|---|
| Pages (from-to) | 275-282 |
| Number of pages | 8 |
| Journal | Nature Chemistry |
| Volume | 18 |
| Issue number | 2 |
| DOIs | |
| State | Published - 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.
| Funders | Funder 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 Office | DE-EE0009519 |
| National Science Foundation Arctic Social Science Program | DMR-2102257 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
ASJC Scopus subject areas
- General Chemistry
- General Chemical Engineering
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