Commodity Thermoplastic Elastomer-Enabled Templated Synthesis of Large-Pore Ordered Mesoporous Materials

被引:0
|
作者
Griffin, Anthony [1 ]
Frame, Parker [1 ]
Xiang, Yizhi [2 ]
Qiang, Zhe [1 ]
机构
[1] Univ Southern Mississippi, Sch Polymer Sci & Engn, Hattiesburg, MS 39406 USA
[2] Univ Missouri, Dept Chem & Biomed Engn, Columbia, MO 65211 USA
来源
ACS OMEGA | 2025年 / 10卷 / 11期
基金
美国国家科学基金会;
关键词
ATOMIC LAYER DEPOSITION; METAL-OXIDES; SIZE; CARBONS; SILICA;
D O I
10.1021/acsomega.5c00553
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Fabrication of ordered mesoporous materials (OMMs) has predominantly relied on templating-based methods. However, these methods are constrained by several limitations, especially the limited pore sizes attainable with commercially available surfactants used as structure-directing agents. To unlock the full potential of the OMMs, it is essential to develop synthetic strategies that facilitate the production of large-pore OMMs using scalable processes and cost-effective precursors. This work demonstrates the use of thermoplastic elastomer (TPE)-derived carbon replicas for synthesizing ordered mesoporous silica (OMS) and metal oxides (OMMOs) via precursor infiltration and template removal. The nanostructural evolution of the resulting inorganic materials was systematically investigated. Specifically, using tetraethyl orthosilicate (TEOS) as a silica precursor, this method can produce an OMS with relatively large pores. To establish the generalizability of this process, the fabrication approach was extended to other commercially available TPEs with varied chemical compositions and molecular weights while consistently resulting in ordered structures. Additionally, this synthetic strategy can be successfully applied to the production of OMMOs, including tin and titanium oxide matrix chemistries, yielding pore sizes of 16.0 and 19.2 nm, respectively. By developing a general method and using low-cost precursors, this work presents a scalable approach for fabricating large-pore OMMs with tunable pore textures and matrix chemistries.
引用
收藏
页码:11554 / 11561
页数:8
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