Fe <sup>3+</sup> -Coordination-Directed Assembly of Robust Fe-Incorporated Polymethylsilsesquioxane Xerogels with Branched Networks

Polymethylsilsesquioxane (PMSQ) xerogels represent a compelling alternative to conventional silica aerogels for ambient pressure drying, owing to their pendant methyl groups that confer low skeletal density (∼1.40 g/cm<sup>3</sup>), mechanical flexibility, and intrinsic hydrophobicity. However, their practical application has been limited by insufficient mechanical strength. Here, we address this limitation by developing Fe-incorporated PMSQ (Fe-PMSQ) xerogels via a synergistic acid-base catalytic route using FeCl<sub>3</sub> and NH<sub>3</sub>·H<sub>2</sub>O. The total base molarity (<i>c</i><sub>base</sub>) governs the sol pH, which in turn regulates Fe<sup>3+</sup> hydrolysis speciation and the condensation kinetics of methyltriethoxysilane. Within an optimal pH range of 7.0-7.5, Fe(OH)<sub>3</sub> dominates the speciation and coordinates with cetyltrimethylammonium bromide (CTAB) micelles via Fe<sup>3+</sup>-directed assembly. This process templates a branched architecture that diverges from the conventional spherical or coral-like PMSQ networks. The resulting structure features Fe<sup>3+</sup> nanoclusters acting as densely cross-linked nodes that form multiple Si-O-Fe linkages and restrict Si-OH condensation into rigid branches, while CTAB promotes local Fe<sup>3+</sup> enrichment at network junctions. Gelation completes within 2 h with only about 10% linear shrinkage, surpassing the performance of both pristine PMSQ and Al-incorporated PMSQ benchmarks. Deviations from this optimal pH range hinder gelation: at pH ∼6.5, gelation is either delayed beyond 60 h or leads to macroscopic stratification, whereas above 7.5, rapid sol-precipitate phase separation occurs. The hierarchically branched structure endows the Fe-PMSQ xerogels with exceptional mechanical robustness, enabling them to withstand up to 80% compression strain without fracture and exhibit exponential strain stiffening between 80% and 90% strain. Moreover, the materials endure 400 compression cycles at 60% strain without failure and show stress recovery after rest periods of over 4 days. These properties collectively ensure structural integrity under demanding loading conditions, positioning Fe-PMSQ xerogels as viable candidates for industrial applications.

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Publication Details

Journal
Langmuir
Published
2025-11-20
DOI
https://doi.org/10.1021/acs.langmuir.5c04426
Primary Topic
Aerogels and thermal insulation
Type
article
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article

Fe 3+ -Coordination-Directed Assembly of Robust Fe-Incorporated Polymethylsilsesquioxane Xerogels with Branched Networks

Hanqing Zhao, Yuanhang Wang, Chengdong Li
Langmuir
Aerogels and thermal insulation
article

Fe 3+ -Coordination-Directed Assembly of Robust Fe-Incorporated Polymethylsilsesquioxane Xerogels with Branched Networks

Hanqing Zhao, Yuanhang Wang, Chengdong Li
article en

Abstract

Polymethylsilsesquioxane (PMSQ) xerogels represent a compelling alternative to conventional silica aerogels for ambient pressure drying, owing to their pendant methyl groups that confer low skeletal density (∼1.40 g/cm<sup>3</sup>), mechanical flexibility, and intrinsic hydrophobicity. However, their practical application has been limited by insufficient mechanical strength. Here, we address this limitation by developing Fe-incorporated PMSQ (Fe-PMSQ) xerogels via a synergistic acid-base catalytic route using FeCl<sub>3</sub> and NH<sub>3</sub>·H<sub>2</sub>O. The total base molarity (<i>c</i><sub>base</sub>) governs the sol pH, which in turn regulates Fe<sup>3+</sup> hydrolysis speciation and the condensation kinetics of methyltriethoxysilane. Within an optimal pH range of 7.0-7.5, Fe(OH)<sub>3</sub> dominates the speciation and coordinates with cetyltrimethylammonium bromide (CTAB) micelles via Fe<sup>3+</sup>-directed assembly. This process templates a branched architecture that diverges from the conventional spherical or coral-like PMSQ networks. The resulting structure features Fe<sup>3+</sup> nanoclusters acting as densely cross-linked nodes that form multiple Si-O-Fe linkages and restrict Si-OH condensation into rigid branches, while CTAB promotes local Fe<sup>3+</sup> enrichment at network junctions. Gelation completes within 2 h with only about 10% linear shrinkage, surpassing the performance of both pristine PMSQ and Al-incorporated PMSQ benchmarks. Deviations from this optimal pH range hinder gelation: at pH ∼6.5, gelation is either delayed beyond 60 h or leads to macroscopic stratification, whereas above 7.5, rapid sol-precipitate phase separation occurs. The hierarchically branched structure endows the Fe-PMSQ xerogels with exceptional mechanical robustness, enabling them to withstand up to 80% compression strain without fracture and exhibit exponential strain stiffening between 80% and 90% strain. Moreover, the materials endure 400 compression cycles at 60% strain without failure and show stress recovery after rest periods of over 4 days. These properties collectively ensure structural integrity under demanding loading conditions, positioning Fe-PMSQ xerogels as viable candidates for industrial applications.

LangmuirVol. 41(47)
Jiangnan University (CN), Ministry of Education of the People's Republic of China (CN)
Openalex Percentile: Top 68%
Aerogels and thermal insulation
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