Evidence map›Paper›PMID 39505870›Full record

ArticleNature communications2024

Enhancing photocatalytic performance of covalent organic frameworks via ionic polarization.

Jiahe Zhang, Xiaoning Li, Haijun Hu, Hongwei Huang, Hui Li, Xiaodong Sun, Tianyi Ma

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

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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

7 authors.

Jiahe Zhang *Institute of Clean Energy Chemistry, Key Laboratory for Green Synthesis and Preparative Chemistry of Advanced Materials, College of Chemistry, Liaoning University, Shenyang, People's Republic of China.
Xiaoning Li *Centre for Atomaterials and Nanomanufacturing (CAN), School of Science, RMIT University, Melbourne, Australia.ORCID http://orcid.org/0000-0001-5991-0955
Haijun HuInstitute of Clean Energy Chemistry, Key Laboratory for Green Synthesis and Preparative Chemistry of Advanced Materials, College of Chemistry, Liaoning University, Shenyang, People's Republic of China.
Hongwei HuangBeijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes, National Laboratory of Mineral Materials, School of Materials Science and Technology, China University of Geosciences, Beijing, China.ORCID http://orcid.org/0000-0003-0271-1079
Hui LiCentre for Atomaterials and Nanomanufacturing (CAN), School of Science, RMIT University, Melbourne, Australia.
Xiaodong SunInstitute of Clean Energy Chemistry, Key Laboratory for Green Synthesis and Preparative Chemistry of Advanced Materials, College of Chemistry, Liaoning University, Shenyang, People's Republic of China. sunxiaodong@lnu.edu.cn.ORCID http://orcid.org/0000-0003-2905-9826
Tianyi MaCentre for Atomaterials and Nanomanufacturing (CAN), School of Science, RMIT University, Melbourne, Australia. tianyi.ma@rmit.edu.au.ORCID http://orcid.org/0000-0002-1042-8700

Funding

National Natural Science Foundation of China (National Science Foundation of China) 22101105National Natural Science Foundation of China (National Science Foundation of China) 52071171
6 · The paper itself

Abstract

Covalent organic frameworks have emerged as a thriving family in the realm of photocatalysis recently, yet with concerns about their high exciton dissociation energy and sluggish charge transfer. Herein, a strategy to enhance the built-in electric field of series β-keto-enamine-based covalent organic frameworks by ionic polarization method is proposed. The ionic polarization is achieved through a distinctive post-synthetic quaternization reaction which can endow the covalent organic frameworks with separated charge centers comprising cationic skeleton and iodide counter-anions. The stronger built-in electric field generated between their cationic framework and iodide anions promotes charge transfer and exciton dissociation efficiency. Moreover, the introduced iodide anions not only serve as reaction centers with lowered H* formation energy barrier, but also act as electron extractant suppressing the recombination of electron-hole pairs. Therefore, the photocatalytic performance of the covalent organic frameworks shows notable improvement, among which the CH

Identifiers

PMID39505870
PMCPMC11541737

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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.