标题:High Performance Hollow Metal-Organic Framework Nanoshell-Based Etalons for Volatile Organic Compounds Detection
作者:Li, Cheng; Li, Limei; Yu, Shimo; Jiao, Xiuling; Chen, Dairong
作者机构:[Li, Cheng; Li, Limei; Yu, Shimo; Jiao, Xiuling; Chen, Dairong] Shandong Univ, Natl Engn Res Ctr Colloidal Mat, Sch Chem & Chem Engn, Shandanan Rd 27, 更多
通讯作者:Li, C;Jiao, XL;Chen, DR
通讯作者地址:[Li, C; Jiao, XL; Chen, DR]Shandong Univ, Natl Engn Res Ctr Colloidal Mat, Sch Chem & Chem Engn, Shandanan Rd 27, Jinan 250100, Shandong, Peoples R Ch 更多
来源:ADVANCED MATERIALS TECHNOLOGIES
出版年:2016
卷:1
期:7
DOI:10.1002/admt.201600127
摘要:A novel high performance optical metal-organic framework (MOF) sensor is presented by means of hollow MOF nanoshell-based etalon (HMNSE), which allows for selective volatile organic compound (VOC) detection with distinct color output and high efficiency of optical transduction. The HMNSE is constructed by integrating hollow MOF nanoshell arrays between the reflective surfaces of silicon wafer and metal layer, and features ultrathin shell thickness (<100 nm) and macropores within a submicron thin film, which provides appropriate optical thickness, tunable interference color, and fast mass transport all at one time. Due to the rational design of optical motif, the HMNSE has attained the largest optical response so far for ultrathin MOF toward VOC detection. Selective detection on vapor phase alcohols, ketones, nitriles, cyclohexane/benzene, and xylene isomers has been exhibited, which reflected well the characteristic effect of size exclusion and chemical interaction between the MOF and VOCs. The synergistic combination of enhanced reflectance peak and optical shift has led to visible color change with unprecedented high saturation upon VOC exposure. Wide dynamic range, ultrafast kinetics, and excellent reversibility and stability have also been achieved, rendering HMNSE promising for low-cost, real-time, and on-site detection.
收录类别:SCOPUS;SCIE
WOS核心被引频次:2
Scopus被引频次:4
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85021814221&doi=10.1002%2fadmt.201600127&partnerID=40&md5=8a3281559bbbe075ae855e57ebc92b4a
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