Evidence map›Paper›PMID 42446228›Full record

ArticleAdvanced materials (Deerfield Beach, Fla.)2026

Self-Regulating Interfacial-Boosted Electrolytes for Fast-Charging and Long-Life Aqueous Batteries.

Huan Li, Liwei Jiang, Shaocheng Li, Yang Huang, Zhao Chen, Bowen Wang, Weiping Li, Xuefeng Wang, Yongsheng Hu, Junmei Zhao

Abstract read
In one paragraph

Article in Advanced materials (Deerfield Beach, Fla.), 2026. 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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0cells of the map it votes in
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

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.

Huan LiCAS Key Laboratory of Green Process and Engineering, Institute of Process Engineering, Chinese Academic of Sciences, Beijing, P. R. China.
Liwei JiangCAS Key Laboratory of Green Process and Engineering, Institute of Process Engineering, Chinese Academic of Sciences, Beijing, P. R. China.
Shaocheng LiCAS Key Laboratory of Green Process and Engineering, Institute of Process Engineering, Chinese Academic of Sciences, Beijing, P. R. China.
Yang HuangCAS Key Laboratory of Green Process and Engineering, Institute of Process Engineering, Chinese Academic of Sciences, Beijing, P. R. China.
Zhao ChenBeijing National Laboratory For Condensed Matter Physics, Institute of Physics, Chinese Academy of Sciences, Beijing, P. R. China.
Bowen WangBeijing National Laboratory For Condensed Matter Physics, Institute of Physics, Chinese Academy of Sciences, Beijing, P. R. China.ORCID https://orcid.org/0009-0002-5582-9046
Weiping LiBeijing National Laboratory For Condensed Matter Physics, Institute of Physics, Chinese Academy of Sciences, Beijing, P. R. China.
Xuefeng WangBeijing National Laboratory For Condensed Matter Physics, Institute of Physics, Chinese Academy of Sciences, Beijing, P. R. China.ORCID https://orcid.org/0000-0001-9666-8942
Yongsheng HuBeijing National Laboratory For Condensed Matter Physics, Institute of Physics, Chinese Academy of Sciences, Beijing, P. R. China.ORCID https://orcid.org/0000-0002-8430-6474
Junmei ZhaoCAS Key Laboratory of Green Process and Engineering, Institute of Process Engineering, Chinese Academic of Sciences, Beijing, P. R. China.ORCID https://orcid.org/0000-0001-6809-5032

Funding

Beijing Municipal Natural Science Foundation 26JL002International Cooperation and Exchange Program of the National Natural Science Foundation of China 52561160145National Natural Science Foundation of China 22579169National Natural Science Foundation of China 92472201
6 · The paper itself

Abstract

Aqueous batteries are promising for large-scale energy storage due to inherent safety and low cost; however, their long-term cycling stability is fundamentally limited by interfacial degradation. Although existing strategies such as "water-in-salt" and water-organic hybrid electrolytes can widen the electrochemical stability window (ESW), trace water electrolysis still occurs at the interface, leading to gradual pH drift, electrode dissolution, and eventual battery failure. Here, we propose a self-regulating interfacial-boosted electrolyte that effectively addresses these challenges. By introducing phosphate‑based components into wide‑ESW electrolytes, this design autonomously ensures pH stability via intrinsic buffering capability, spontaneously forms a protective cathode-electrolyte interphase in response to metal-ion dissolution, and reconfigures the ion solvation structure to widen the electrochemical stability window and lowers the interfacial impedance. Demonstrated in a Na

Indexed as

aqueous sodium‐ion batteriescathode‐electrolyte interphaseelectrolyte designphosphate buffertrace water electrolysis

Identifiers

PMID42446228
PMCPMC13496110

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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.