Integrating Molecular Simulations with Machine Learning Guides in the Design and Synthesis of [BMIM][BF4]/MOF Composites for CO2/N2 Separation

离子液体 选择性 材料科学 四氟硼酸盐 复合数 吸附 复合材料 物理化学 有机化学 催化作用 化学
作者
Hilal Daglar,Hasan Can Gülbalkan,Nitasha Habib,Özce Durak,Alper Uzun,Seda Keskın
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:15 (13): 17421-17431 被引量:33
标识
DOI:10.1021/acsami.3c02130
摘要

Considering the existence of a large number and variety of metal-organic frameworks (MOFs) and ionic liquids (ILs), assessing the gas separation potential of all possible IL/MOF composites by purely experimental methods is not practical. In this work, we combined molecular simulations and machine learning (ML) algorithms to computationally design an IL/MOF composite. Molecular simulations were first performed to screen approximately 1000 different composites of 1-n-butyl-3-methylimidazolium tetrafluoroborate ([BMIM][BF4]) with a large variety of MOFs for CO2 and N2 adsorption. The results of simulations were used to develop ML models that can accurately predict the adsorption and separation performances of [BMIM][BF4]/MOF composites. The most important features that affect the CO2/N2 selectivity of composites were extracted from ML and utilized to computationally generate an IL/MOF composite, [BMIM][BF4]/UiO-66, which was not present in the original material data set. This composite was finally synthesized, characterized, and tested for CO2/N2 separation. Experimentally measured CO2/N2 selectivity of the [BMIM][BF4]/UiO-66 composite matched well with the selectivity predicted by the ML model, and it was found to be comparable, if not higher than that of all previously synthesized [BMIM][BF4]/MOF composites reported in the literature. Our proposed approach of combining molecular simulations with ML models will be highly useful to accurately predict the CO2/N2 separation performances of any [BMIM][BF4]/MOF composite within seconds compared to the extensive time and effort requirements of purely experimental methods.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
Neoshine完成签到,获得积分10
刚刚
称心的不言完成签到,获得积分10
刚刚
花开富贵完成签到,获得积分10
1秒前
hjhhjh完成签到,获得积分10
1秒前
又见白龙完成签到,获得积分10
1秒前
哈哈哈完成签到,获得积分10
1秒前
黄黄完成签到,获得积分0
1秒前
1秒前
杨冰完成签到,获得积分10
1秒前
嘿嘿哈完成签到,获得积分10
1秒前
徐先生完成签到,获得积分10
2秒前
幽默的煎饼完成签到,获得积分10
2秒前
研友_ZGAWYL完成签到,获得积分10
2秒前
2秒前
xmhxpz完成签到,获得积分10
3秒前
Lvy完成签到,获得积分10
3秒前
yuhaha完成签到,获得积分10
3秒前
科研通AI6.1应助海鑫王采纳,获得10
3秒前
生物科研小白完成签到 ,获得积分10
4秒前
meiting发布了新的文献求助10
4秒前
快乐疯样完成签到,获得积分10
4秒前
小明同学应助缠流子采纳,获得10
4秒前
嘿嘿哈发布了新的文献求助10
4秒前
nan完成签到,获得积分10
4秒前
4秒前
24号甜冰茶完成签到,获得积分10
4秒前
慕青应助金锐采纳,获得10
5秒前
HAHA完成签到,获得积分10
5秒前
渴望成功的学术残废完成签到,获得积分10
6秒前
lll完成签到 ,获得积分10
6秒前
柠静樨完成签到,获得积分10
6秒前
东木耳语完成签到,获得积分10
7秒前
xzgwbh完成签到,获得积分10
7秒前
烯灯完成签到,获得积分10
7秒前
DXK完成签到 ,获得积分10
7秒前
11111发布了新的文献求助10
7秒前
许多多完成签到,获得积分10
8秒前
记名字完成签到,获得积分10
8秒前
风中的蛋卷完成签到 ,获得积分10
8秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Burger's Medicinal Chemistry, Drug Discovery and Development, Volumes 1 - 8, 8 Volume Set, 8th Edition 1800
Cronologia da história de Macau 1600
Contemporary Debates in Epistemology (3rd Edition) 1000
International Arbitration Law and Practice 1000
文献PREDICTION EQUATIONS FOR SHIPS' TURNING CIRCLES或期刊Transactions of the North East Coast Institution of Engineers and Shipbuilders第95卷 1000
BRITTLE FRACTURE IN WELDED SHIPS 1000
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 纳米技术 计算机科学 化学工程 生物化学 物理 复合材料 内科学 催化作用 物理化学 光电子学 细胞生物学 基因 电极 遗传学
热门帖子
关注 科研通微信公众号,转发送积分 6159220
求助须知:如何正确求助?哪些是违规求助? 7987423
关于积分的说明 16599191
捐赠科研通 5267688
什么是DOI,文献DOI怎么找? 2810802
邀请新用户注册赠送积分活动 1790856
关于科研通互助平台的介绍 1657996