Ultrafast laser synthesis of zeolites

Fuente: arXiv
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Main Authors: Galioglu, Sezin, Hagverdiyev, Mehdi, Doğan, Meryem M., Yavuz, Özgün, Nizam, Ü. Seleme, Makey, Ghaith, Choura, Aladin, Laçin, Mesut, Kurç, Burcu Akata, Elahi, Parviz, Ilday, F. Ömer, Ilday, Serim
Format: Preprint
Published: 2025
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author Galioglu, Sezin
Hagverdiyev, Mehdi
Doğan, Meryem M.
Yavuz, Özgün
Nizam, Ü. Seleme
Makey, Ghaith
Choura, Aladin
Laçin, Mesut
Kurç, Burcu Akata
Elahi, Parviz
Ilday, F. Ömer
Ilday, Serim
author_facet Galioglu, Sezin
Hagverdiyev, Mehdi
Doğan, Meryem M.
Yavuz, Özgün
Nizam, Ü. Seleme
Makey, Ghaith
Choura, Aladin
Laçin, Mesut
Kurç, Burcu Akata
Elahi, Parviz
Ilday, F. Ömer
Ilday, Serim
contents Research has demonstrated that zeolite nucleation and growth can be controlled by fine-tuning chemical composition, temperature, and pressure, resulting in structures with diverse porosities and functionalities. Nevertheless, current energy delivery methods lack the finesse required to operate on the femto- and picosecond timescales of silica polymerisation and depolymerisation, limiting their ability to direct synthesis with high precision. To overcome this limitation, we introduce an ultrafast laser synthesis technique capable of delivering energy at these timescales with unprecedented spatiotemporal precision. Unlike conventional or emerging approaches, this method bypasses the need for specific temperature and pressure settings, as nucleation and growth are governed by dynamic phenomena arising from nonlinear light-matter interactions, such as convective flows, cavitation bubbles, plasma formation, and shock waves. These processes can be initiated, paused, and resumed within fractions of a second, effectively freezing structures at any stage of self-assembly. Using this approach, we traced the entire nucleation and growth pathway of laser-synthesized TPA-silicate-1 zeolites, from early oligomer formation to fully developed crystals. The unprecedented spatiotemporal control of this technique unlocks new avenues for manipulating reaction pathways and exploring the vast configurational space of zeolites.
format Preprint
id arxiv_https___arxiv_org_abs_2502_02292
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle Ultrafast laser synthesis of zeolites
Galioglu, Sezin
Hagverdiyev, Mehdi
Doğan, Meryem M.
Yavuz, Özgün
Nizam, Ü. Seleme
Makey, Ghaith
Choura, Aladin
Laçin, Mesut
Kurç, Burcu Akata
Elahi, Parviz
Ilday, F. Ömer
Ilday, Serim
Materials Science
Mesoscale and Nanoscale Physics
Chemical Physics
Research has demonstrated that zeolite nucleation and growth can be controlled by fine-tuning chemical composition, temperature, and pressure, resulting in structures with diverse porosities and functionalities. Nevertheless, current energy delivery methods lack the finesse required to operate on the femto- and picosecond timescales of silica polymerisation and depolymerisation, limiting their ability to direct synthesis with high precision. To overcome this limitation, we introduce an ultrafast laser synthesis technique capable of delivering energy at these timescales with unprecedented spatiotemporal precision. Unlike conventional or emerging approaches, this method bypasses the need for specific temperature and pressure settings, as nucleation and growth are governed by dynamic phenomena arising from nonlinear light-matter interactions, such as convective flows, cavitation bubbles, plasma formation, and shock waves. These processes can be initiated, paused, and resumed within fractions of a second, effectively freezing structures at any stage of self-assembly. Using this approach, we traced the entire nucleation and growth pathway of laser-synthesized TPA-silicate-1 zeolites, from early oligomer formation to fully developed crystals. The unprecedented spatiotemporal control of this technique unlocks new avenues for manipulating reaction pathways and exploring the vast configurational space of zeolites.
title Ultrafast laser synthesis of zeolites
topic Materials Science
Mesoscale and Nanoscale Physics
Chemical Physics
url https://arxiv.org/abs/2502.02292