TY - JOUR
T1 - Ultra-high-rate pseudocapacitive energy storage in two-dimensional transition metal carbides
AU - Lukatskaya, Maria R.
AU - Kota, Sankalp
AU - Lin, Zifeng
AU - Zhao, Meng Qiang
AU - Shpigel, Netanel
AU - Levi, Mikhael D.
AU - Halim, Joseph
AU - Taberna, Pierre Louis
AU - Barsoum, Michel W.
AU - Simon, Patrice
AU - Gogotsi, Yury
N1 - Publisher Copyright:
© 2017 Nature America, Inc., part of Springer Nature. All rights reserved.
PY - 2017/7/10
Y1 - 2017/7/10
N2 - The use of fast surface redox storage (pseudocapacitive) mechanisms can enable devices that store much more energy than electrical double-layer capacitors (EDLCs) and, unlike batteries, can do so quite rapidly. Yet, few pseudocapacitive transition metal oxides can provide a high power capability due to their low intrinsic electronic and ionic conductivity. Here we demonstrate that two-dimensional transition metal carbides (MXenes) can operate at rates exceeding those of conventional EDLCs, but still provide higher volumetric and areal capacitance than carbon, electrically conducting polymers or transition metal oxides. We applied two distinct designs for MXene electrode architectures with improved ion accessibility to redox-active sites. A macroporous Ti3 C2 T x MXene film delivered up to 210 F g-1 at scan rates of 10 V s-1, surpassing the best carbon supercapacitors known. In contrast, we show that MXene hydrogels are able to deliver volumetric capacitance of ∼1,500 F cm-3 reaching the previously unmatched volumetric performance of RuO2.
AB - The use of fast surface redox storage (pseudocapacitive) mechanisms can enable devices that store much more energy than electrical double-layer capacitors (EDLCs) and, unlike batteries, can do so quite rapidly. Yet, few pseudocapacitive transition metal oxides can provide a high power capability due to their low intrinsic electronic and ionic conductivity. Here we demonstrate that two-dimensional transition metal carbides (MXenes) can operate at rates exceeding those of conventional EDLCs, but still provide higher volumetric and areal capacitance than carbon, electrically conducting polymers or transition metal oxides. We applied two distinct designs for MXene electrode architectures with improved ion accessibility to redox-active sites. A macroporous Ti3 C2 T x MXene film delivered up to 210 F g-1 at scan rates of 10 V s-1, surpassing the best carbon supercapacitors known. In contrast, we show that MXene hydrogels are able to deliver volumetric capacitance of ∼1,500 F cm-3 reaching the previously unmatched volumetric performance of RuO2.
UR - http://www.scopus.com/inward/record.url?scp=85023765308&partnerID=8YFLogxK
U2 - 10.1038/nenergy.2017.105
DO - 10.1038/nenergy.2017.105
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AN - SCOPUS:85023765308
SN - 2058-7546
VL - 6
JO - Nature Energy
JF - Nature Energy
M1 - 17105
ER -