ArticleAngewandte Chemie (International ed. in English)2026
An Energy-Dense Aqueous All-Polymer Battery Enabled by Unique Cross-Conjugated Dual-Active-Center Design in Organic Redox Chemistry.
Article in Angewandte Chemie (International ed. in English), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
Abstract
The emergence of aqueous all-organic batteries (AAOBs) has attracted surging attention, yet their progress is hindered by the limited energy density due to the scarcity of large-capacity and high-potential positive electrode materials. Herein, we develop a cross-conjugated dual-active-center design strategy to modulate the electron distribution and frontier orbitals of 2D redox polymers (2DRPs) for attaining energy-dense AAOBs. Theoretical studies reveal that simply embedding more pyrazine units in the polymer skeleton can elevate capacity and potential but at the expense of reduced activity, while introducing quinone units can form a cross-conjugated donor-acceptor (D-A) structure that improves all above metrics. Accordingly, we synthesized 2DRP with alternating pyrazine-quinone units (PQ) and its analogues with pure pyrazine units (P1 and P3). All predicted advantages over its analogues are realized by PQ in acidic electrolytes, presenting fast Grotthuss-type proton transport, a larger capacity (251 mAh g
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.