Tunable Reaction Potentials in Open Framework Nanoparticle Battery Electrodes for Grid-Scale Energy Storage
AuthorsWessells, Colin D.
McDowell, Matthew T.
Peddada, Sandeep V.
Huggins, Robert A.
KAUST Grant NumberKUS-I1-001-12
Online Publication Date2012-02-06
Print Publication Date2012-02-28
Permanent link to this recordhttp://hdl.handle.net/10754/600091
MetadataShow full item record
AbstractThe electrical energy grid has a growing need for energy storage to address short-term transients, frequency regulation, and load leveling. Though electrochemical energy storage devices such as batteries offer an attractive solution, current commercial battery technology cannot provide adequate power, and cycle life, and energy efficiency at a sufficiently low cost. Copper hexacyanoferrate and nickel hexacyanoferrate, two open framework materials with the Prussian Blue structure, were recently shown to offer ultralong cycle life and high-rate performance when operated as battery electrodes in safe, inexpensive aqueous sodium ion and potassium ion electrolytes. In this report, we demonstrate that the reaction potential of copper-nickel alloy hexacyanoferrate nanoparticles may be tuned by controlling the ratio of copper to nickel in these materials. X-ray diffraction, TEM energy dispersive X-ray spectroscopy, and galvanostatic electrochemical cycling of copper-nickel hexacyanoferrate reveal that copper and nickel form a fully miscible solution at particular sites in the framework without perturbing the structure. This allows copper-nickel hexacyanoferrate to reversibly intercalate sodium and potassium ions for over 2000 cycles with capacity retentions of 100% and 91%, respectively. The ability to precisely tune the reaction potential of copper-nickel hexacyanoferrate without sacrificing cycle life will allow the development of full cells that utilize the entire electrochemical stability window of aqueous sodium and potassium ion electrolytes. © 2012 American Chemical Society.
CitationWessells CD, McDowell MT, Peddada SV, Pasta M, Huggins RA, et al. (2012) Tunable Reaction Potentials in Open Framework Nanoparticle Battery Electrodes for Grid-Scale Energy Storage. ACS Nano 6: 1688–1694. Available: http://dx.doi.org/10.1021/nn204666v.
SponsorsThe authors acknowledge support from the King Abdullah University of Science and Technology (KAUST) Investigator Award (No. KUS-I1-001-12). They also acknowledge the Department of Energy, Office of Basic Energy Sciences, Division of Materials Sciences and Engineering under contract DE-AC02-76SF00515 through the SLAC National Accelerator Laboratory LDRD project.
PublisherAmerican Chemical Society (ACS)
CollectionsPublications Acknowledging KAUST Support
- Nickel hexacyanoferrate nanoparticle electrodes for aqueous sodium and potassium ion batteries.
- Authors: Wessells CD, Peddada SV, Huggins RA, Cui Y
- Issue date: 2011 Dec 14
- Copper hexacyanoferrate battery electrodes with long cycle life and high power.
- Authors: Wessells CD, Huggins RA, Cui Y
- Issue date: 2011 Nov 22
- Full open-framework batteries for stationary energy storage.
- Authors: Pasta M, Wessells CD, Liu N, Nelson J, McDowell MT, Huggins RA, Toney MF, Cui Y
- Issue date: 2014
- Effect of the alkali insertion ion on the electrochemical properties of nickel hexacyanoferrate electrodes.
- Authors: Lee HW, Pasta M, Wang RY, Ruffo R, Cui Y
- Issue date: 2014
- Combination of lightweight elements and nanostructured materials for batteries.
- Authors: Chen J, Cheng F
- Issue date: 2009 Jun 16