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Monocarboxylic Acid Structural Analogues Facilitate In Situ Composite of Functional Complexes for Aqueous Batteries
Author(s) -
Su Yichun,
Zhang Yanfei,
Feng Wanchang,
Zhang Guangxun,
Sun Yangyang,
Yin Chenhui,
Yuan Guoqiang,
Tang Yijian,
Zhou Wenfeng,
Chen HsiaoChien,
Pang Huan
Publication year - 2025
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.202502752
Subject(s) - microporous material , composite number , materials science , nanomaterials , in situ , intermolecular force , nanotechnology , aqueous solution , mesoporous material , hydrogen bond , chemical engineering , molecule , chemistry , composite material , catalysis , organic chemistry , engineering
Abstract In situ composite methods have aroused research interest in materials science and acted as a novel strategy to achieve structural tailoring of materials. However, the controllable preparation of composites containing functional groups remains a challenge. Herein, we report an approach based on competitive coordination between structural analogs, by which the functionally composite metal complex (NiSH@Ni‐FSA) was synthesized. The introduction of different functional groups allows precise control of the functionality of composites, ranging from NiSH@Ni‐ClSA‐D, NiSH@Ni‐BrSA to NiSH@Ni‐CF 3 SA. More interestingly, the synthesized material retained the microporous and mesoporous structure of the original complexes. The incorporation of hydrophobic functional groups effectively protects the electrode materials from degradation and corrosion. Meanwhile, the presence of intermolecular hydrogen bonding facilitates new composite nanomaterials with better performance for advanced energy storage applications.
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