Evidence map›Paper›PMID 27436175›Full record

ArticleDalton transactions (Cambridge, England : 2003)2016

Design and synthesis of novel organometallic dyes for NiO sensitization and photo-electrochemical applications.

Julien Massin, Siliu Lyu, Michele Pavone, Ana B Muñoz-García, Brice Kauffmann, Thierry Toupance, Murielle Chavarot-Kerlidou, Vincent Artero, Céline Olivier

Abstract read
In one paragraph

Article in Dalton transactions (Cambridge, England : 2003), 2016. 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. Dye-sensitized solar cells strike back.Chemical Society reviews · 2021
    Review
  3. Review
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

9 authors.

Julien MassinLaboratoire de Chimie Biologie des Métaux, Université Grenoble Alpes, CNRS UMR 5249, CEA Fundamental Research Division, Grenoble, France. vincent.artero@cea.fr.
Siliu LyuInstitut des Sciences Moléculaires, Université de Bordeaux, CNRS UMR 5255, Talence, France. celine.olivier@u-bordeaux.fr.
Michele PavoneDepartment of Chemical Sciences, University of Naples Federico II, Napoli, Campania, Italy.
Ana B Muñoz-GarcíaDepartment of Chemical Sciences, University of Naples Federico II, Napoli, Campania, Italy.
Brice KauffmannInstitut Européen de Chimie et Biologie, Université de Bordeaux, UMS CNRS-INSERM 3033, Pessac, France.
Thierry ToupanceInstitut des Sciences Moléculaires, Université de Bordeaux, CNRS UMR 5255, Talence, France. celine.olivier@u-bordeaux.fr.
Murielle Chavarot-KerlidouLaboratoire de Chimie Biologie des Métaux, Université Grenoble Alpes, CNRS UMR 5249, CEA Fundamental Research Division, Grenoble, France. vincent.artero@cea.fr.
Vincent ArteroLaboratoire de Chimie Biologie des Métaux, Université Grenoble Alpes, CNRS UMR 5249, CEA Fundamental Research Division, Grenoble, France. vincent.artero@cea.fr.
Céline OlivierInstitut des Sciences Moléculaires, Université de Bordeaux, CNRS UMR 5255, Talence, France. celine.olivier@u-bordeaux.fr.

Funding

European Research Council 306398
6 · The paper itself

Abstract

Two metallo-organic dyes were synthesized and used for NiO sensitization in view of their photoelectrochemical applications. The new dyes present an original π-conjugated structure containing the [Ru(dppe)2] metal fragment with a highly delocalized allenylidene ligand on one side and a σ-alkynyl ligand bearing an electron-rich group, i.e. a thiophene or triphenylamine unit, and one or two anchoring functions on the other side. The optoelectronic, electrochemical and photoelectrochemical properties of the dyes were systematically investigated. A broad photoresponse was observed with the absorption maximum at 600 nm. The X-ray crystal structure of one precursor was obtained to elucidate the structural conformation of the organometallic complexes and theoretical calculations were performed in order to address the photophysical properties of the new dyes. These photosensitizers were further implemented in NiO-based photocathodes and tested as photocurrent generators under pertinent aqueous conditions in association with [Co(NH3)5Cl]Cl2 as an irreversible electron acceptor. The dye-sensitized photocathodes provided good photocurrent densities (40 to 60 μA cm(-2)) at neutral pH in phosphate buffer and a high stability was observed for the two dyes.

Identifiers

PMID27436175
PMCPMC5495160

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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.