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High-rate electrochemical energy storage through Li+ intercalation pseudocapacitance
Author(s) -
Veronica Augustyn,
Jérémy Come,
Michael A. Lowe,
Jong Woung Kim,
PierreLouis Taberna,
Sarah H. Tolbert,
Héctor D. Abruña,
Patrice Simon,
Bruce Dunn
Publication year - 2013
Publication title -
nature materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 14.344
H-Index - 483
eISSN - 1476-4660
pISSN - 1476-1122
DOI - 10.1038/nmat3601
Subject(s) - pseudocapacitance , intercalation (chemistry) , electrolyte , materials science , energy storage , redox , electrochemistry , chemical engineering , supercapacitor , nanotechnology , inorganic chemistry , electrode , chemistry , thermodynamics , metallurgy , engineering , power (physics) , physics
Pseudocapacitance is commonly associated with surface or near-surface reversible redox reactions, as observed with RuO2·xH2O in an acidic electrolyte. However, we recently demonstrated that a pseudocapacitive mechanism occurs when lithium ions are inserted into mesoporous and nanocrystal films of orthorhombic Nb2O5 (T-Nb2O5; refs 1,2). Here, we quantify the kinetics of charge storage in T-Nb2O5: currents that vary inversely with time, charge-storage capacity that is mostly independent of rate, and redox peaks that exhibit small voltage offsets even at high rates. We also define the structural characteristics necessary for this process, termed intercalation pseudocapacitance, which are a crystalline network that offers two-dimensional transport pathways and little structural change on intercalation. The principal benefit realized from intercalation pseudocapacitance is that high levels of charge storage are achieved within short periods of time because there are no limitations from solid-state diffusion. Thick electrodes (up to 40 μm thick) prepared with T-Nb2O5 offer the promise of exploiting intercalation pseudocapacitance to obtain high-rate charge-storage devices.

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