Award Abstract # 1336716
Collaborative Research: Hybrid Block Copolymer Electrodes for Electrochemical Energy Storage

NSF Org: CBET
Division of Chemical, Bioengineering, Environmental, and Transport Systems
Recipient: TEXAS A&M ENGINEERING EXPERIMENT STATION
Initial Amendment Date: July 24, 2013
Latest Amendment Date: June 10, 2015
Award Number: 1336716
Award Instrument: Standard Grant
Program Manager: Carole Read
cread@nsf.gov
 (703)292-2418
CBET
 Division of Chemical, Bioengineering, Environmental, and Transport Systems
ENG
 Directorate for Engineering
Start Date: September 1, 2013
End Date: August 31, 2017 (Estimated)
Total Intended Award Amount: $203,672.00
Total Awarded Amount to Date: $210,172.00
Funds Obligated to Date: FY 2013 = $203,672.00
FY 2015 = $6,500.00
History of Investigator:
  • Jodie Lutkenhaus (Principal Investigator)
    jodie.lutkenhaus@tamu.edu
Recipient Sponsored Research Office: Texas A&M Engineering Experiment Station
3124 TAMU
COLLEGE STATION
TX  US  77843-3124
(979)862-6777
Sponsor Congressional District: 10
Primary Place of Performance: Texas Engineering Experiment Station
TX  US  77843-3122
Primary Place of Performance
Congressional District:
10
Unique Entity Identifier (UEI): QD1MX6N5YTN4
Parent UEI: QD1MX6N5YTN4
NSF Program(s): EchemS-Electrochemical Systems
Primary Program Source: 01001314DB NSF RESEARCH & RELATED ACTIVIT
01001516DB NSF RESEARCH & RELATED ACTIVIT
Program Reference Code(s): 046E, 147E, 9251
Program Element Code(s): 764400
Award Agency Code: 4900
Fund Agency Code: 4900
Assistance Listing Number(s): 47.041

ABSTRACT

PI: Lutkenhaus, Jodie / Verduzco, Rafael
Proposal Number: 1336716 / 1336073
Institution: Texas Engineering Experiment Station/
William Marsh Rice University
Title: Collaborative Research: Hybrid Block Copolymer Electrodes for Electrochemical Energy Storage

Storage of energy through electrochemical means (batteries, capacitors) is critical to providing power for advanced transportation and portable electronics. Next-generation energy storage materials must simultaneously satisfy a number of criteria: excellent charge and ion transport, high capacity, and reversible charge transfer. For this reason, electron- and ion-conducting polymers are often explored as additives in cathodes such as V2O5, LiCoO2, LiFePO4, etc. to form hybrid electrodes. Unfortunately, it remains extremely difficult to obtain a hybrid electrode that successfully balances electron and ion transport with charge transfer because of large-scale phase separation and poor structure control among the electrode?s various components.

This project will investigate a model system of hybrid electrodes for energy storage based on nanostructured blends of poly(3-alkylthiophene)-block-poly(ethylene oxide) (P3AT-b-PEO) multifunctional block copolymers and V2O5. P3AT-b-PEO is capable of simultaneous electron and ion transport, and V2O5 is a commonly explored high-capacity cathode material for Li-ion batteries. V2O5 will be synthesized within selected polymer blocks using ?structure directed? synthesis. The PIs hypothesize that through bottom- up assembly methods, the resulting hybrid materials will exhibit favorable properties characteristic of both organic and inorganic components.

This project will determine the relationship between block copolymer composition and morphology as it is affected by V2O5, side chain functionalization, and electrochemical performance. The relationship between block copolymer morphology and charge transfer, electron transport, and ion transport has never before been systematically investigated as a whole, so the proposed research will establish a broad knowledge base to guide the development of multifunctional block copolymers for energy storage. First, the PIs will establish relationships between the morphology of hybrid electrodes containing block copolymer bearing a single type of side chain and V2O5 and electrochemical performance (Objectives 1 and 2). This knowledge will then be applied to a wider family of block copolymers of varying side chain chemistry so as to balance electrochemical properties with processability.

The proposed work will have broader impacts within the scientific community as well as the general public through educational activities and outreach. Within the scientific community, this work will establish a knowledge base for multifunctional block copolymers in electrodes, where several processes (reaction and diffusion) must be balanced.


The PIs will pursue educational activities including hosting high school teacher(s) through Enrichment Experiences in Engineering, providing summer research opportunities for talented, underrepresented groups from the Houston Community College system, hosting Nova-sponsored, materials science-themed Science Cafés at Houston-area high schools, and organizing Texas Soft Matter Meetings at TAMU and Rice University.

PUBLICATIONS PRODUCED AS A RESULT OF THIS RESEARCH

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An, H., Mike, J., Smith, K.A., Swank, L., Lin, Y.-H., L. Pesek, S., Verduzco, R., & Lutkenhaus, J.L., "Highly Flexible Self-Assembled V2O5 Cathodes Enabled by Conducting Diblock Copolymers" Scientific Reports , v.5 , 2015 , p.14166 10.1038/srep14166
Chalker, Cody J.An, HyosungZavala, JoseParija, AbhishekBanerjee, SarbajitLutkenhaus, Jodie L.Batteas, James D. "Fabrication and Electrochemical Performance of Structured Mesoscale Open Shell V2O5 Networ" Langmuir , v.33 , 2017 , p.5975 10.1021/acs.langmuir.6b04163
Hyosung AnXiaoyi LiCody ChalkerMaria StrackeRafael VerduzcoJodie L. Lutkenhaus "Conducting Block Copolymer Additives for Carbon-Free Hybrid Vanadium Pentoxide Cathodes with Enhance Performance" ACS Applied Materials & Interfaces , v.8 , 2016 , p.28585 10.1021/acsami.6b08028
Lin ShaoJu-Won JeonJodie L. Lutkenhaus "Polyaniline nanofiber/vanadium pentoxide sprayedlayer-by-layer electrodes for energy storage" Journal of Materials Chemistry A , v.2 , 2014 , p.14421 DOI: 10.1039/c4ta02911a
Melody A Morris, Hyosung An, Jodie L Lutkenhaus, Thomas H Epps III "Harnessing the Power of Plastics: Nanostructured Polymer Systems in Lithium-Ion Batteries" ACS Energy Letters , v.2 , 2017 , p.1919 10.1021/acsenergylett.7b00368

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.

Technological advances have produced tremendous growth in alternative energy utilization along with a steep drop in the cost of energy from both renewable and fossil fuel based resources. However, the capacity to store this energy for later use remains extremely limited, and as a result it is challenging and costly to supply energy for portable needs and applications. Batteries are electrochemical devices that can store electricity for use at a later time, and they are comprised of several components. First, there is an active electrochemical material that can store and/or generate charge through an electrochemical reaction, a conductive additive for transporting charges, an electrolyte for transporting ions between electrodes, and finally a binder for holding the electrode together and maintaining mechanical rigidity. Much of the research into batteries overlooks the impact of the binder, which comprises typically about 10 % of the entire battery. While this may appear to be a small fraction, the binder plays an incommensurate role in mechanical properties, rigidity, and stability. Prior studies have typically relied on nonactive polymeric binders, which contain no electrical or ionic conductivity. In this work, we proposed that the development of new polymeric binder materials could enhance battery storage capacities, improve mechanical properties, and lead to more flexible and portable devices for energy storage. Specifically, we focused on the use of electroactive polymers, which have both electrical and ionic conductivities. Our work demonstrated that electroactive polymers can enhance storage capacities and produce more robust and long-lasting electrodes for energy storage. We produced prototype batteries that were flexible and bendable, and demonstrated their use in a simple device. This work will lead to a new class of polymeric binders that simultaneously address ion and electron conduction, mechanical properties, and stability in the pursuit of high capacity battery cathodes.

Beyond the research accomplishments of this project, students at various levels from undergraduate to post-doctoral level received training and education related to the development of materials for energy storage. Five different graduate students were involved in the development of polymer binders, three of which have graduated and moved on to positions in industry and academia. These students received invaluable training on electrochemistry, polymer chemistry, materials chemistry, and device fabrication and testing. One undergraduate student worked on the project and received training on the development and application of electroactive materials. One post-doctoral researcher was trained in device fabrication of flexible batteries. Of all the participants, five were women. Participants in the lab also connected with the local community through outreach activities and events, including Expand Your Horizons, which serves to stimulate interest in science, technology, engineering, and mathematics (STEM) for school-age girls. Another activity was participation in the Science-As-Art Competition for the Materials Research Society, which stimulated public interest in STEM through graphic design. These various activities served to inspire young scientists to pursue careers in STEM, fostered lasting mentoring relationships for students, and to grow a vibrant pipeline students committed to the future of our community and capable of being articulate, engaged and transformative STEM leaders.

 

 


Last Modified: 12/31/2017
Modified by: Jodie Lutkenhaus

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