ArticleSmall (Weinheim an der Bergstrasse, Germany)2026
Molecular Engineering of Fluorinated Nitriles as Self-Passivating Electrolyte for High Voltage Lithium Metal Batteries.
Article in Small (Weinheim an der Bergstrasse, Germany), 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
11 authors.
Funding
Abstract
Electrolyte engineering is essential for developing high-voltage lithium metal batteries (HV-LMBs). Nitrile-based compounds are one of the most promising electrolyte solvents with high chemical and oxidative stability, but their low stability against lithium metal anode is a notorious problem that hinders its practical applications. Herein, through molecular engineering of modulating the fluorination degree, partially fluorinated nitrile compounds were first reported, enabling self-passivation toward lithium metal anodes. Both theoretical calculation and experimental results revealed that the mono-fluorinated nitrile (F1EON) based solvent not only exhibits a horizontal adsorption configuration on the lithium metal surface, resulting in the spontaneous formation of a dense LiF passivation layer, but also forms a unique tridentate solvation structure, thereby inducing a LiF-rich cathode electrolyte interphase. Consequently, the 4.6 V high-voltage Li||LiCoO
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.