| Literature DB >> 31194558 |
Negar Ashari-Astani1,2, Farzaneh Jahanbakhshi2, Marko Mladenović2,3, Anwar Q M Alanazi4, Iman Ahmadabadi1, Mohammad Reza Ejtehadi1, M Ibrahim Dar4, Michael Grätzel4, Ursula Rothlisberger2.
Abstract
5-Ammonium valeric acid (AVA) is a frequently used additive in the preparation of lead halide perovskites. However, its microscopic role as passivating, cross-linking, or templating agent is far from clear. In this work, we provide density functional theory-based structural models for the Ruddlesden-Popper (RP) phases of AVA2(CH3NH3) n-1Pb nI3 n+1 for n = 1, 2, and 3 and validate with experimental data on polycrystalline samples for n = 1. The structural and electronic properties of the AVA-based RP phases are compared to the ones of other linker families. In contrast to aromatic and aliphatic spacers without additional functional groups, the RP phases of AVA are characterized by the formation of a regular and stable H-bonding network between the carbonyl head groups of adjacent AVA molecules in opposite layers. Because of these additional interactions, the penetration depth of the organic layer into the perovskite sheet is reduced with direct consequences for its crystalline phase. The possibility of forming strong interlinker hydrogen bonds may lead to an enhanced thermal stability.Entities:
Year: 2019 PMID: 31194558 DOI: 10.1021/acs.jpclett.9b01111
Source DB: PubMed Journal: J Phys Chem Lett ISSN: 1948-7185 Impact factor: 6.475