
NSF Org: |
DMR Division Of Materials Research |
Recipient: |
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Initial Amendment Date: | August 6, 2014 |
Latest Amendment Date: | August 8, 2018 |
Award Number: | 1435241 |
Award Instrument: | Standard Grant |
Program Manager: |
John Schlueter
jschluet@nsf.gov (703)292-7766 DMR Division Of Materials Research MPS Directorate for Mathematical and Physical Sciences |
Start Date: | October 1, 2014 |
End Date: | September 30, 2020 (Estimated) |
Total Intended Award Amount: | $503,622.00 |
Total Awarded Amount to Date: | $603,622.00 |
Funds Obligated to Date: |
FY 2018 = $100,000.00 |
History of Investigator: |
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Recipient Sponsored Research Office: |
1500 HORNING RD KENT OH US 44242-0001 (330)672-2070 |
Sponsor Congressional District: |
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Primary Place of Performance: |
Kent OH US 44242-0001 |
Primary Place of
Performance Congressional District: |
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Unique Entity Identifier (UEI): |
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Parent UEI: |
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NSF Program(s): | DMREF |
Primary Program Source: |
01001819DB NSF RESEARCH & RELATED ACTIVIT |
Program Reference Code(s): |
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Program Element Code(s): |
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Award Agency Code: | 4900 |
Fund Agency Code: | 4900 |
Assistance Listing Number(s): | 47.049 |
ABSTRACT
DMREF: Collaborative Research: Chemoresponsive Liquid Crystals Based on Metal Ion-Ligand Coordination
Non-Technical Description: Computer-based methods that can predict materials properties have the potential to transform the current materials design paradigm into one based on integrated "cycles" of computation, experimentation and data analysis, thereby substantially accelerating materials development while decreasing costs. This DMREF project seeks to advance this vision through the formation of an interdisciplinary team with deep insight in computational chemistry (Mavrikakis), synthetic organic chemistry (Twieg) and physical property measurement (Abbott). The team will tackle the challenge of accelerating deployment of promising classes of chemically-responsive materials that are based on liquid crystals (LCs). In addition to addressing fundamental scientific questions related to the design of chemically functionalized LCs and interfaces, the project will advance the enormous technological and societal potential of these materials as the basis of new classes of sensors and actuators that can, for example, be used in the context of environmental monitoring of climate change, detection of toxic industrial chemicals or chemical warfare agents, and measurement of volatile gases in breath as an indicator of disease. The multi-disciplinary environment created by this DMREF project will also contribute to the training of a next generation workforce fully versed in the new materials deployment paradigm that integrates computational chemistry, synthesis and property characterization to rapidly design and realize functional materials. The project will be leveraged by the investigators to develop new university-level educational materials as well as new programs for public outreach efforts and engagement of underrepresented groups. Members of this DMREF team have a record of entrepreneurism; students and postdoctoral fellows engaged in this project will be provided with opportunities to participate in entrepreneurial activities. All of the efforts of the group will be integrated by an approach to data management that is designed also to interface to key US national databases and thus contribute to the Materials Genome Initiative national infrastructure by providing unfettered access to data and metadata for the broader scientific and industrial community.
Technical Description: Laborious and slow experimental efforts over the past decade have demonstrated the promise of chemoresponsive liquid crystals (LCs) in the context of sensing one important class of chemical targets (organophosphonates). The principles, however, are far more general and thus an opportunity exists to design chemically tailored LCs and interfaces that respond selectively to many other classes of target molecules. This DMREF project will address this broad opportunity by integrating cycles of computation (performed at several levels, called Generations), organic synthesis of novel mesogens and physical property evaluation to accelerate the timeline for design of LC materials that respond selectively to societally important chemical species such as HCN, (CH3)2CO, HCHO, O3, CO, NH3, NO, ClCN, CO2, NO2 and H2O. A key aspect of the intellectual merit of this DMREF project lies in the development of new knowledge that will enable integration of computation, experiment and data analysis for the design of functional materials. The close feedback between computation (at the level of electronic structure), synthesis of functional mesogens and property characterization, which will lead to advances in each methodology, will define new principles for the design of chemoresponsive liquid crystalline materials based on metal-ligand coordination. It will also provide fundamental advances in our understanding of hierarchical design of chemically responsive materials, interfacial ordering of soft matter, and the use of metal ion-ligand coordination interactions to control the interfacial ordering of LCs.
PUBLICATIONS PRODUCED AS A RESULT OF THIS RESEARCH
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PROJECT OUTCOMES REPORT
Disclaimer
This Project Outcomes Report for the General Public is displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed in this Report are those of the PI and do not necessarily reflect the views of the National Science Foundation; NSF has not approved or endorsed its content.
A collaborative team of chemists, chemical engineers and computational researchers have shown that it is possible to exploit the interactions of liquid crystals on ionic surfaces to make chemical sensors. Liquid crystals are a special class of condensed matter that are fluids but still retain some structural order. To build highly sensitive sensor devices, the team has exploited liquid crystals because they are able to not only detect but also amplify targeted surface interactions with environmental chemicals into easily visualized optical outputs. The critical combination of liquid crystal materials and the ionic surfaces are being optimized via cycles of feedback amongst synthesis, device experiments and computations. From these studies personal wearable sensors for chlorine gas at concentrations as low as 200 ppb and with a 15-minute response time using commercial cyanobiphenyl liquid crystals have been demonstrated (satisfying OSHA personal exposure limits).
The liquid crystal class which has been most widely utilized for research on these sensor applications are the alkylcyanobiphenyls and especially cyanopentylbiphenyl (commonly known as K15 or 5CB) which has a cyano group for surface interaction and a short nematic phase just above ambient temperature (K 22 N 25 I; where K = crystal, N = nematic, I = isotropic). The nematic phase is the least ordered liquid crystal phase with orientational order but no positional order. Another related class are the alkoxycyanobiphenyls, which have an additional ether oxygen atom such as cyanopentyloxybiphenyl (commonly known as M15) which also has a short nematic phase but further above room temperature (K 53 N 67 I). Neither of these substances is suitable individually for use in a practical device because the temperature range of the nematic phase is not at ambient temperature (15-25 deg C) and is also too narrow. One way to overcome this problem is to mix different nematic materials together. If the right materials are mixed in the right proportion a broad temperature range mixture can result. Contemporary commercial liquid crystal displays contain multiple individual substances chosen to deliver a range of physical properties including a broad nematic phase between at least 0 deg C and 50 deg C.
We are exploring modifications of cyanobiphenyls by adding fluorine atoms in strategic locations in the molecules. As seen in the image, the phase behavior of a series of 4′-ω-fluoroalkoxy-4-cyanobiphenyls FnOCB are shown. Here n represents the number of carbon atoms in the tail portion of the molecule and a single fluorine atom is introduced on the terminal carbon of the tail. The F2OCB, F3OCB and F4OCB are monotropic (nematic phase exists only on cooling) and cooling cycles are shown. However, F5OCB through F12OCB are thermotropic (nematic phase exists on heating and cooling) and heating cycles are shown. The F3OCB and F4OCB are especially interesting as the nematic phases (red bars in the image) exist near ambient and thus attractive for making device mixtures. Another feature of the FnOCB cyanobiphenyls shown is that they possess only the nematic phase required for the sensor device. Notably, the cyanobiphenyls with n greater than or equal to eight with only hydrogen termination (not shown) may also possess layered and more highly organized smectic phases which are eliminated by selective fluorination. Smectic phases have positional order in addition to orientational order and have no benefit in the current sensor designs.
Combinations of different surfaces with custom fluorinated liquid crystal structures are being examined to enhance the sensitivity and specificity of these sensor devices so that they can respond to a still broader range of volatile analytes (ozone, HCl, etc.).
Last Modified: 08/20/2021
Modified by: Robert J Twieg
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