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Covalently Linked Pigment@TiO2 Hybrid Materials by One‐Pot Solvothermal Synthesis.

Authors :
Sailer, Frank
Moura, Hipassia M.
Purkait, Taniya
Vogelsang, Lars
Sauer, Markus
Foelske, Annette
Winter, Rainer F.
Ponrouch, Alexandre
Unterlass, Miriam M.
Source :
Small Structures. Sep2024, Vol. 5 Issue 9, p1-12. 12p.
Publication Year :
2024

Abstract

Hybrid materials (HMs) combine the high diversity of functionalities of organic compounds with properties typical for inorganic materials, such as high mechanical strength or high thermal stability. Herein, HMs combining organic pigment molecules and TiO2 as inorganic component, with covalently linked components, i.e., so‐called class II HMs, are reported. The synthesis of such HMs is intrinsically challenging, as the apolar organic pigment component and the inorganic polar TiO2 component require different conditions for their respective formation. Herein, we circumvent this issue by employing solvothermal synthesis in superheated isopropanol, which through temperature tunability of the solvent properties allows for both generating and linking both components in one‐pot. First, it is shown that an organic benzimidazole‐based pigment molecule designed for readily binding to Ti can be synthesized solvothermally. Second, new class II titanium‐based HMs are generated from Ti(OiPr)4 and pigment precursors in a solvothermal reaction. The pigment@TiO2 HMs feature significant porosity and are structurally identified as layered structures of lepidocrocite‐like TiO2 linked via pigment molecules. These layered HMs assemble into hierarchical nanoflowers, and depending on the pigment segments, different interlayer spacings in between inorganic layers are observed. Third, the pigment@TiO2 materials are shown to be usable as electrode materials in lithium‐ion batteries. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
26884062
Volume :
5
Issue :
9
Database :
Academic Search Index
Journal :
Small Structures
Publication Type :
Academic Journal
Accession number :
180229139
Full Text :
https://doi.org/10.1002/sstr.202400074