Evidence map›Paper›PMID 39519676›Full record

ReviewMolecules (Basel, Switzerland)2024

Advancements in Carbazole-Based Sensitizers and Hole-Transport Materials for Enhanced Photovoltaic Performance.

Ayagoz Ibrayeva, Urker Abibulla, Zulfiya Imanbekova, Bakhytzhan Baptayev, Robert J O'Reilly, Mannix P Balanay

Abstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 2-(N-Hexylcarbazole-3'-yl)-4-pyridinealdehyde: Cyanide Detection via Benzoin Condensation.Luminescence : the journal of biological and chemical luminescence · 2025
    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

6 authors.

Ayagoz IbrayevaNational Laboratory Astana, Nazarbayev University, 53 Kabanbay Batyr Ave., Astana 010000, Kazakhstan.
Urker AbibullaChemistry Department, Nazarbayev University, 53 Kabanbay Batyr Ave., Astana 010000, Kazakhstan.
Zulfiya ImanbekovaChemistry Department, Nazarbayev University, 53 Kabanbay Batyr Ave., Astana 010000, Kazakhstan.ORCID 0009-0005-1432-7391
Bakhytzhan BaptayevNational Laboratory Astana, Nazarbayev University, 53 Kabanbay Batyr Ave., Astana 010000, Kazakhstan.ORCID 0000-0001-5970-5660
Robert J O'ReillySchool of Science and Technology, University of New England, Armidale, NSW 2351, Australia.ORCID 0000-0002-5000-1920
Mannix P BalanayNational Laboratory Astana, Nazarbayev University, 53 Kabanbay Batyr Ave., Astana 010000, Kazakhstan.ORCID 0000-0003-2479-8582

Funding

Ministry of Science and Higher Education of the Republic of Kazakhstan AP14870560Nazarbayev University under the Faculty Development Competitive Research Grants Program 20122022FD4122
6 · The paper itself

Abstract

Carbazole-based molecules play a significant role in dye-sensitized solar cells (DSSCs) due to their advantageous properties. Carbazole derivatives are known for their thermal stability, high hole-transport capability, electron-rich (p-type) characteristics, elevated photoconductivity, excellent chemical stability, and commercial availability. This review focuses on DSSCs, including their structures, working principles, device characterization, and the photovoltaic performance of carbazole-based derivatives. Specifically, it covers compounds such as 2,7-carbazole and indolo[3,2-b]carbazole, which are combined with various acceptors like benzothiadiazole, thiazolothiazole, diketopyrrolopyrrole, and quinoxaline, as reported over the past decade. The review will also outline the relationship between molecular structure and power-conversion efficiencies. Its goal is to summarize recent research and advancements in carbazole-based dyes featuring a D-π-A architecture for DSSCs. Additionally, this review addresses the evolution of carbazole-based hole-transport materials (HTMs), which present a promising alternative to the costly spiro-OMeTAD. We explore the development of novel HTMs that leverage the unique properties of carbazole derivatives to enhance charge transport, stability, and overall device performance. By examining recent innovations and emerging trends in carbazole-based HTMs, we provide insights into their potential to reduce costs and improve the efficiency of DSSCs.

Indexed as

carbazole-based dyesdonor-pi-acceptorhole-transport materialsmetal-free organic sensitizer

Identifiers

PMID39519676
PMCPMC11547213

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.