Evidence map›Paper›PMID 42323280›Full record

ArticleNature communications2026

Hydroxyl chemistry regulation of cellulose biopolymers for aqueous zinc battery binders.

Rongfu Xu, Ningxin Chen, Zichan Yuan, Zihan Guo, Jie Deng, En Chen, Yinglin Yan, Xianhui Wang, Chaoji Chen, Zhaohui Wang

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Rongfu Xu *State Key Laboratory of Water Engineering Ecology and Environment in Arid Area, School of Eco-environmental and Chemical Engineering, Xi'an University of Technology, Xi'an, PR China.
Ningxin Chen *Department of Materials Science and Engineering, Hunan University, Changsha, PR China.
Zichan YuanDepartment of Materials Science and Engineering, Hunan University, Changsha, PR China.
Zihan GuoDepartment of Materials Science and Engineering, Hunan University, Changsha, PR China.
Jie DengDepartment of Materials Science and Engineering, Hunan University, Changsha, PR China.
En ChenDepartment of Materials Science and Engineering, Hunan University, Changsha, PR China.
Yinglin YanState Key Laboratory of Water Engineering Ecology and Environment in Arid Area, School of Eco-environmental and Chemical Engineering, Xi'an University of Technology, Xi'an, PR China. yyl3550@xaut.edu.cn.ORCID http://orcid.org/0000-0002-9953-2933
Xianhui WangSchool of Materials Science and Engineering, Xi'an University of Technology, Xi'an, PR China.
Chaoji ChenHubei Biomass-Resource Chemistry and Environmental Biotechnology Key Laboratory, School of Resource and Environmental Sciences, Wuhan University, Wuhan, PR China. chenchaojili@whu.edu.cn.ORCID http://orcid.org/0000-0001-9553-554X
Zhaohui WangDepartment of Materials Science and Engineering, Hunan University, Changsha, PR China. sunnywang@hnu.edu.cn.ORCID http://orcid.org/0000-0003-4623-5609

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aqueous batteries offer inherent safety and low cost, but the inherently fixed physicochemical functionality and poor interfacial compatibility of existing binders limit their ability to boost positive electrode performance. Here we present a hydroxyl-chemistry regulation strategy that transforms cellulose, an abundant biopolymer on Earth, into a high-affinity, interfacially compatible binder that stabilizes high-capacity, shuttling-prone positive electrodes. By selectively opening the rigid cellulose ring structure within its molecular chains, we enhance dipole polarity, chain flexibility, and intermolecular hydrogen-bond density, thereby increasing functional-group accessibility and interfacial adhesion. These molecular-level modifications drive the formation of a dense nanofibrous network that conformally encapsulates active particles and anchors polyiodides, accelerating redox kinetics and reinforcing electrode stability. Iodine positive electrode incorporating the engineered binder deliver a reversible capacity of 150.9 mAh g

Identifiers

PMID42323280
PMCPMC13454342

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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.