Published June 30, 2015 | Version Published + Supplemental Material
Journal Article Open

Rescaling of metal oxide nanocrystals for energy storage having high capacitance and energy density with robust cycle life

  • 1. ROR icon Korea Advanced Institute of Science and Technology
  • 2. ROR icon California Institute of Technology
  • 3. ROR icon Lawrence Berkeley National Laboratory
  • 4. ROR icon The University of Texas at Austin

Abstract

Nanocrystals are promising structures, but they are too large for achieving maximum energy storage performance. We show that rescaling 3-nm particles through lithiation followed by delithiation leads to high-performance energy storage by realizing high capacitance close to the theoretical capacitance available via ion-to-atom redox reactions. Reactive force-field (ReaxFF) molecular dynamics simulations support the conclusion that Li atoms react with nickel oxide nanocrystals (NiO-n) to form lithiated core–shell structures (Ni:Li_2O), whereas subsequent delithiation causes Ni:Li_2O to form atomic clusters of NiO-a. This is consistent with in situ X-ray photoelectron and optical spectroscopy results showing that Ni^(2+) of the nanocrystal changes during lithiation–delithiation through Ni^0 and back to Ni^(2+). These processes are also demonstrated to provide a generic route to rescale another metal oxide. Furthermore, assembling NiO-a into the positive electrode of an asymmetric device enables extraction of full capacitance for a counter negative electrode, giving high energy density in addition to robust capacitance retention over 100,000 cycles.

Additional Information

© 2015 National Academy of Sciences. Contributed by William A. Goddard III, May 20, 2015 (sent for review December 9, 2014) Published online before print June 15, 2015, doi: 10.1073/pnas.1503546112. This research was supported by the Global Frontier R&D Program (2013M3A6B1078865) on Center for Hybrid Interface Materials funded by the Ministry of Science, Information and Communication Technology and Future Planning, and the National Research Foundation of Korea (2011-0028737, 2012M1A2A2671813). The work at the Molecular Foundry was supported by the US Department of Energy (DOE) under Contract DE-AC02-05CH11231. D.J.M. was supported by DOE Advanced Research Projects Agency-Energy under the same contract. Support for T.C. and W.A.G. was provided by National Science Foundation (CBET-1067848). Author contributions: H.M.J. and J.K.K. designed research; H.M.J., K.M.C., R.Z., I.W.O., and J.K.K. performed research; D.K.L. and I.W.O. contributed new reagents/analytic tools; T.C. and W.A.G. analyzed data; and H.M.J., K.M.C., T.C., D.J.M., W.A.G., and J.K.K. wrote the paper. The authors declare no conflict of interest. This article contains supporting information online at www.pnas.org/lookup/suppl/doi:10.1073/pnas.1503546112/-/DCSupplemental.

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Published - PNAS-2015-Jeong-7914-9.pdf

Supplemental Material - pnas.1503546112.sapp.pdf

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Additional details

Identifiers

PMCID
PMC4491738
Eprint ID
58263
Resolver ID
CaltechAUTHORS:20150615-151220941

Funding

Ministry of Science, Information and Communication Technology and Future Planning (Korea)
2013M3A6B1078865
National Research Foundation of Korea
2011-0028737
National Research Foundation of Korea
2012M1A2A2671813
Department of Energy (DOE)
DE-AC02-05CH11231
NSF
CBET-1067848

Dates

Created
2015-06-15
Created from EPrint's datestamp field
Updated
2022-06-01
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