TY - JOUR
T1 - Interaction of Polar and Nonpolar Polyfluorenes with Layers of Two-Dimensional Titanium Carbide (MXene)
T2 - Intercalation and Pseudocapacitance
AU - Boota, Muhammad
AU - Pasini, Mariacecilia
AU - Galeotti, Francesco
AU - Porzio, William
AU - Zhao, Meng Qiang
AU - Halim, Joseph
AU - Gogotsi, Yury
N1 - Publisher Copyright:
© 2017 American Chemical Society.
PY - 2017/4/11
Y1 - 2017/4/11
N2 - This article provides insight into the interaction of synthetic conjugated polymers [polyfluorene derivatives (PFDs)] with layers of two-dimensional titanium carbide (Ti3C2Tx). Three derivatives with nonpolar, polar, and charged nitrogen-containing functionalities were synthesized via the Suzuki polycondensation reaction. The organic-inorganic PFD/Ti3C2Tx hybrids were prepared and characterized using X-ray diffraction and a range of microscopic and spectroscopic techniques to elucidate the host-guest interaction mechanism. We show that polar polymers with charged nitrogen-containing ends have the strongest interaction with the Ti3C2Tx layers, yielding an increase in interlayer spacing and large shifts in spectroscopic peaks. Furthermore, the effect of polymer backbone juxtaposition between Ti3C2Tx layers on pseudocapacitance is discussed in detail. Our results suggest that new organic materials capable of intercalation between the layers of Ti3C2Tx and other MXenes may be used in the design of hybrid structures for high-performance energy storage applications and beyond.
AB - This article provides insight into the interaction of synthetic conjugated polymers [polyfluorene derivatives (PFDs)] with layers of two-dimensional titanium carbide (Ti3C2Tx). Three derivatives with nonpolar, polar, and charged nitrogen-containing functionalities were synthesized via the Suzuki polycondensation reaction. The organic-inorganic PFD/Ti3C2Tx hybrids were prepared and characterized using X-ray diffraction and a range of microscopic and spectroscopic techniques to elucidate the host-guest interaction mechanism. We show that polar polymers with charged nitrogen-containing ends have the strongest interaction with the Ti3C2Tx layers, yielding an increase in interlayer spacing and large shifts in spectroscopic peaks. Furthermore, the effect of polymer backbone juxtaposition between Ti3C2Tx layers on pseudocapacitance is discussed in detail. Our results suggest that new organic materials capable of intercalation between the layers of Ti3C2Tx and other MXenes may be used in the design of hybrid structures for high-performance energy storage applications and beyond.
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U2 - 10.1021/acs.chemmater.6b03933
DO - 10.1021/acs.chemmater.6b03933
M3 - Article
AN - SCOPUS:85017551819
SN - 0897-4756
VL - 29
SP - 2731
EP - 2738
JO - Chemistry of Materials
JF - Chemistry of Materials
IS - 7
ER -