Evidence map›Paper›PMID 36431477›Full record

ArticleMaterials (Basel, Switzerland)2022

D-π-A-Type Pyrazolo[1,5-

Fatiha Bouihi, Bruno Schmaltz, Fabrice Mathevet, David Kreher, Jérôme Faure-Vincent, Ceren Yildirim, Ahmed Elhakmaoui, Johann Bouclé, Mohamed Akssira, François Tran-Van and 1 more

Abstract read
In one paragraph

Article in Materials (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Fatiha BouihiLaboratoire de Physico-Chimie des Matériaux et des Electrolytes pour l'Energie (EA 6299), Université de Tours, Parc de Grandmont, 37200 Tours, France.ORCID 0000-0001-7057-565X
Bruno SchmaltzLaboratoire de Physico-Chimie des Matériaux et des Electrolytes pour l'Energie (EA 6299), Université de Tours, Parc de Grandmont, 37200 Tours, France.
Fabrice MathevetCenter for Organic Photonics and Electronics Research (OPERA), Kyushu University, 744 Motooka, Nishi-ku, Fukuoka 819-0395, Japan.
David KreherCNRS, Institut Parisien de Chimie Moléculaire, IPCM, Sorbonne Université, 4 Place Jussieu, 75005 Paris, France.ORCID 0000-0002-0968-5224
Jérôme Faure-VincentCEA, CNRS, IRIG-SyMMES, Université Grenoble-Alpes, 38000 Grenoble, France.
Ceren YildirimCNRS, XLIM, UMR 7252, Université de Limoges, 87000 Limoges, France.
Ahmed ElhakmaouiLaboratoire de Chimie Physique et Biotechnologies des Biomolécules et des Matériaux (LCP2BM), Faculté des Sciences et Techniques de Mohammedia, Université Hassan II de Casablanca, BP 146, Mohammedia 28800, Morocco.
Johann BoucléCNRS, XLIM, UMR 7252, Université de Limoges, 87000 Limoges, France.ORCID 0000-0002-7851-1842
Mohamed AkssiraLaboratoire de Chimie Physique et Biotechnologies des Biomolécules et des Matériaux (LCP2BM), Faculté des Sciences et Techniques de Mohammedia, Université Hassan II de Casablanca, BP 146, Mohammedia 28800, Morocco.ORCID 0000-0001-8867-2837
François Tran-VanLaboratoire de Physico-Chimie des Matériaux et des Electrolytes pour l'Energie (EA 6299), Université de Tours, Parc de Grandmont, 37200 Tours, France.
Mohamed AbarbriLaboratoire de Physico-Chimie des Matériaux et des Electrolytes pour l'Energie (EA 6299), Université de Tours, Parc de Grandmont, 37200 Tours, France.ORCID 0000-0002-6742-1075

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Donor−acceptor (D−A) small molecules are regarded as promising hole-transporting materials for perovskite solar cells (PSCs) due to their tunable optoelectronic properties. This paper reports the design, synthesis and characterization of three novel isomeric D-π-A small molecules PY1, PY2 and PY3. The chemical structures of the molecules consist of a pyrazolo[1,5-a]pyrimidine acceptor core functionalized with one 3,6-bis(4,4′-dimethoxydiphenylamino)carbazole (3,6-CzDMPA) donor moiety via a phenyl π-spacer at the 3, 5 and 7 positions, respectively. The isolated compounds possess suitable energy levels, sufficient thermal stability (Td > 400 °C), molecular glass behavior with Tg values in the range of 127−136 °C slightly higher than that of the reference material Spiro-OMeTAD (126 °C) and acceptable hydrophobicity. Undoped PY1 demonstrates the highest hole mobility (3 × 10−6 cm2 V−1 s−1) compared to PY2 and PY3 (1.3 × 10−6 cm2 V−1 s−1). The whole isomers were incorporated as doped HTMs in planar n-i-p PSCs based on double cation perovskite FA0.85Cs0.15Pb(I0.85Br0.15)3. The non-optimized device fabricated using PY1 exhibited a power conversion efficiency (PCE) of 12.41%, similar to that obtained using the reference, Spiro-OMeTAD, which demonstrated a maximum PCE of 12.58% under the same conditions. The PY2 and PY3 materials demonstrated slightly lower performance in device configuration, with relatively moderate PCEs of 10.21% and 10.82%, respectively, and slight hysteresis behavior (−0.01 and 0.02). The preliminary stability testing of PSCs is also described. The PY1-based device exhibited better stability than the device using Spiro-OMeTAD, which could be related to its slightly superior hydrophobic character preventing water diffusion into the perovskite layer.

Indexed as

3,6-CzDMPAD-π-Ahole-transporting materialsperovskite solar cellspyrazolo[1,5-a]pyrimidine

Identifiers

PMID36431477
PMCPMC9697137

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.