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单晶级别的水收集。

Water Harvesting at the Single-Crystal Level.

机构信息

Department of Chemistry and Center for NanoScience (CeNS), Ludwig-Maximilians-Universität München, Butenandtstr. 5-13, 81377 Munich, Germany.

Department of Chemistry and Kavli Energy Nanoscience Institute, University of California-Berkeley, Berkeley, California 94720, United States.

出版信息

J Am Chem Soc. 2023 Jul 5;145(26):14324-14334. doi: 10.1021/jacs.3c02902. Epub 2023 Jun 23.

DOI:10.1021/jacs.3c02902
PMID:37353221
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10326874/
Abstract

Metal-organic frameworks (MOFs) have emerged as a class of porous materials with facile uptake and release of water, turning them into excellent substrates for real-world atmospheric water harvesting applications. The performance of different MOF systems was experimentally characterized at the bulk level by assessing the total amount of water taken up and the release kinetics, leaving the question behind of what the upper limit of the pristine materials actually is. Moreover, recent devices rely on fluidized bed reactors that exploit the harvesting capacities of MOFs at the single-crystal (SC) level. In this publication, we present a novel methodology based on Raman spectroscopy, for acquiring water adsorption isotherms and kinetic curves with a sub-micrometer resolution that provides valuable insights into the material behavior probing the pristine MOF at the SC level. We investigated isolated MOF-801 particles in situ and could dissect contributions of intra- and inter-particle effects on the water harvesting performance of MOF-801 via adsorption-desorption isotherms and kinetic curves. Using spontaneous Raman spectroscopy, we found an almost 20-fold faster uptake for the undisturbed crystalline material. Correlative imaging based on four-wave mixing and coherent anti-Stokes Raman scattering further localized the uptaken water inside MOF-801 and identified inter-particle condensation as the main source for the discrepancies between the performance at the bulk and SC level. Our studies determined an upper limit of around 91.9 L/kg/day for MOF-801.

摘要

金属-有机骨架(MOFs)作为一类多孔材料,具有易于吸收和释放水的特点,因此成为实际大气水收集应用的理想基质。通过评估吸收的总水量和释放动力学,不同 MOF 体系的性能在体相水平上进行了实验表征,而原始材料的实际上限问题仍未得到解决。此外,最近的设备依赖于流化床反应器,利用 MOF 在单晶(SC)水平上的收集能力。在本出版物中,我们提出了一种基于拉曼光谱的新方法,用于以亚微米分辨率获得水吸附等温线和动力学曲线,从而深入了解材料行为,在 SC 水平上探测原始 MOF。我们原位研究了孤立的 MOF-801 颗粒,并通过吸附-解吸等温线和动力学曲线来剖析内颗粒和颗粒间效应对 MOF-801 水收集性能的贡献。使用自发拉曼光谱,我们发现未受干扰的结晶材料的吸收速度快了近 20 倍。基于四波混频和相干反斯托克斯拉曼散射的相关成像进一步将吸收的水定位在 MOF-801 内,并确定颗粒间凝结是体相和 SC 水平性能差异的主要原因。我们的研究确定 MOF-801 的上限约为 91.9 L/kg/天。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b209/10326874/2835ee65f7b6/ja3c02902_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b209/10326874/ca136faad4eb/ja3c02902_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b209/10326874/f826504f22e6/ja3c02902_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b209/10326874/cf6d0178a6ed/ja3c02902_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b209/10326874/31955655f287/ja3c02902_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b209/10326874/3915a2436092/ja3c02902_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b209/10326874/2835ee65f7b6/ja3c02902_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b209/10326874/ca136faad4eb/ja3c02902_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b209/10326874/f826504f22e6/ja3c02902_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b209/10326874/cf6d0178a6ed/ja3c02902_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b209/10326874/31955655f287/ja3c02902_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b209/10326874/3915a2436092/ja3c02902_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b209/10326874/2835ee65f7b6/ja3c02902_0007.jpg

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