Evidence map›Paper›PMID 41190139›Full record

ArticleRSC advances2025

Theoretical design and analysis of D-π-A-A' organic dyes for enhanced efficiency in DSSCs by modifying donor (D) and acceptor (A) moieties.

Smiti Rani Bora, Banashmita Barman, Dhruba Jyoti Kalita

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Article in RSC advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

3 authors.

Smiti Rani BoraDepartment of Chemistry, Gauhati University Guwahati-781014 India dhrubajyoti.kalita@gauhati.ac.in.
Banashmita BarmanDepartment of Chemistry, Gauhati University Guwahati-781014 India dhrubajyoti.kalita@gauhati.ac.in.
Dhruba Jyoti KalitaDepartment of Chemistry, Gauhati University Guwahati-781014 India dhrubajyoti.kalita@gauhati.ac.in.ORCID https://orcid.org/0000-0001-5434-0682

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study presents a comprehensive investigation of ten different dyes using DFT and TD-DFT calculations. The dyes feature a D-π-A-A' architecture with a thiophene π-bridge, cyanoacrylic acid serving as both an electron-acceptor and anchoring group, and a selection of electron-donor and electron-acceptor moieties. The electron-donor moieties explored include coumarin (COU), triphenylamine (TPA), indoline (IN), carbazole (CAR), diphenylamine (DPA), tetrahydroquinoline (THQ), triazatruxene (TAT), azulene (AZ), and julolidine (JUD). Besides, the electron-acceptor moieties consist of quinoline (QN), [1,2,5]thiadiazole[3,4-

Identifiers

PMID41190139
PMCPMC12580974

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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.