Organic functionalization of Ti3C2Tx MXene for urea adsorption in aqueous solutions
Two-dimensional MXene materials with the composition Ti3C2Tx, where T represents a surface termination species, have become popular for many applications due to their large surface areas, unique mechanical and electrochemical properties, and the ability to create thin single-layer systems. The high...
Saved in:
Main Authors: | , , , , |
---|---|
Other Authors: | |
Format: | Article |
Language: | English |
Published: |
2024
|
Subjects: | |
Online Access: | https://hdl.handle.net/10356/174212 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Nanyang Technological University |
Language: | English |
id |
sg-ntu-dr.10356-174212 |
---|---|
record_format |
dspace |
spelling |
sg-ntu-dr.10356-1742122024-03-22T15:46:09Z Organic functionalization of Ti3C2Tx MXene for urea adsorption in aqueous solutions Yen, Zhihao Bradley, David G. Wang, Yamin Hanna, John V. Lam, Yeng Ming School of Materials Science and Engineering Engineering Ti3C2Tx, MXene Urea adsorption Solid state NMR XPS Amino acid Surface functionalization Two-dimensional MXene materials with the composition Ti3C2Tx, where T represents a surface termination species, have become popular for many applications due to their large surface areas, unique mechanical and electrochemical properties, and the ability to create thin single-layer systems. The high surface area and hydrophilicity of this material renders it a viable option as a molecular adsorber in aqueous solutions. In recent studies using a simplified synthesis method called minimally intensive layer delamination (MILD), we have shown how the surface functionalization (T) affects the material's ability to adsorb urea. Here we present a new approach to enhancing urea adsorption by functionalizing the surface with amino acid and ‘amino acid-like’ moieties such as glutamic acid, lysine, and L-dopa. The differences between these functionalized MXenes are probed using PXRD, XPS, FTIR/Raman and solid state 13C MAS NMR, and appear to emanate from distinct steric bonding configurations between each amino acid and the MXene surface, thus facilitating a variety of organic-urea interactions in these regions. In particular, solid state 13C MAS NMR offers a detailed picture of each amino acid’s bonding configuration based on peak shifting/broadening due to paramagnetic interactions with the Ti3+ positions within the MXene surface. Furthermore, corresponding solid state 7Li MAS NMR measurements verified that the surface functionalization does, in fact, deintercalate Li+ ions, not only from Cu functionalization derivatives, but also for particular organic-functionalized systems. It was found that glutamic acid functionalized MXene has a maximum urea adsorption capability of 23.5 mg/g in aqueous media. This adsorption capacity was found to be superior compared to previous studies on using pristine MXene for urea adsorption. Ministry of Education (MOE) Submitted/Accepted version J.V.H. acknowledges financial support for the solid-state NMR instrumentation at Warwick used in this research, which was funded by EPSRC (grant nos. EP/M028186/1 and EP/K024418/1), the University of Warwick, and the Birmingham Science City AM1 and AM2 projects, which were supported by Advantage West Midlands (AWM) and the European Regional Development Fund (ERDF). We would like to acknowledge the Ministry of Education Research Scholarship, Singapore, for supporting the project. 2024-03-21T05:34:40Z 2024-03-21T05:34:40Z 2024 Journal Article Yen, Z., Bradley, D. G., Wang, Y., Hanna, J. V. & Lam, Y. M. (2024). Organic functionalization of Ti3C2Tx MXene for urea adsorption in aqueous solutions. ACS Applied Nano Materials. https://dx.doi.org/10.1021/acsanm.4c00119 2574-0970 https://hdl.handle.net/10356/174212 10.1021/acsanm.4c00119 en ACS Applied Nano Materials © 2024 American Chemical Society. All rights reserved. This article may be downloaded for personal use only. Any other use requires prior permission of the copyright holder. The Version of Record is available online at http://doi.org/10.1021/acsanm.4c00119. application/pdf |
institution |
Nanyang Technological University |
building |
NTU Library |
continent |
Asia |
country |
Singapore Singapore |
content_provider |
NTU Library |
collection |
DR-NTU |
language |
English |
topic |
Engineering Ti3C2Tx, MXene Urea adsorption Solid state NMR XPS Amino acid Surface functionalization |
spellingShingle |
Engineering Ti3C2Tx, MXene Urea adsorption Solid state NMR XPS Amino acid Surface functionalization Yen, Zhihao Bradley, David G. Wang, Yamin Hanna, John V. Lam, Yeng Ming Organic functionalization of Ti3C2Tx MXene for urea adsorption in aqueous solutions |
description |
Two-dimensional MXene materials with the composition Ti3C2Tx, where T represents a surface termination species, have become popular for many applications due to their large surface areas, unique mechanical and electrochemical properties, and the ability to create thin single-layer systems. The high surface area and hydrophilicity of this material renders it a viable option as a molecular adsorber in aqueous solutions. In recent studies using a simplified synthesis method called minimally intensive layer delamination (MILD), we have shown how the surface functionalization (T) affects the material's ability to adsorb urea.
Here we present a new approach to enhancing urea adsorption by functionalizing the surface with amino acid and ‘amino acid-like’ moieties such as glutamic acid, lysine, and L-dopa. The differences between these functionalized MXenes are probed using PXRD, XPS, FTIR/Raman and solid state 13C MAS NMR, and appear to emanate from distinct steric bonding configurations between each amino acid and the MXene surface, thus facilitating a variety of organic-urea interactions in these regions. In particular, solid state 13C MAS NMR offers a detailed picture of each amino acid’s bonding configuration based on peak shifting/broadening due to paramagnetic interactions with the Ti3+ positions within the MXene surface. Furthermore, corresponding solid state 7Li MAS NMR measurements verified that the surface functionalization does, in fact, deintercalate Li+ ions, not only from Cu functionalization derivatives, but also for particular organic-functionalized systems. It was found that glutamic acid functionalized MXene has a maximum urea adsorption capability of 23.5 mg/g in aqueous media. This adsorption capacity was found to be superior compared to previous studies on using pristine MXene for urea adsorption. |
author2 |
School of Materials Science and Engineering |
author_facet |
School of Materials Science and Engineering Yen, Zhihao Bradley, David G. Wang, Yamin Hanna, John V. Lam, Yeng Ming |
format |
Article |
author |
Yen, Zhihao Bradley, David G. Wang, Yamin Hanna, John V. Lam, Yeng Ming |
author_sort |
Yen, Zhihao |
title |
Organic functionalization of Ti3C2Tx MXene for urea adsorption in aqueous solutions |
title_short |
Organic functionalization of Ti3C2Tx MXene for urea adsorption in aqueous solutions |
title_full |
Organic functionalization of Ti3C2Tx MXene for urea adsorption in aqueous solutions |
title_fullStr |
Organic functionalization of Ti3C2Tx MXene for urea adsorption in aqueous solutions |
title_full_unstemmed |
Organic functionalization of Ti3C2Tx MXene for urea adsorption in aqueous solutions |
title_sort |
organic functionalization of ti3c2tx mxene for urea adsorption in aqueous solutions |
publishDate |
2024 |
url |
https://hdl.handle.net/10356/174212 |
_version_ |
1794549342856544256 |