TY - JOUR
T1 - Sol-gel based synthesis and enhanced processability of MAX phase Cr2GaC
AU - Siebert, Jan Paul
AU - Bischoff, Lothar
AU - Lepple, Maren
AU - Zintler, Alexander
AU - Molina-Luna, Leopoldo
AU - Wiedwald, Ulf
AU - Birkel, Christina S.
N1 - Funding Information:
Financial support by the DFG (BI 1775/2-1) and the German federal state of Hessen through its excellence program LOEWE ‘‘RESPONSE’’ is gratefully acknowledged. A. Z. and L. M.-L. also acknowledge financial support from the Hessen State Ministry of Higher Education, Research and the Arts via LOEWE RESPONSE. L. M.-L. acknowledges financial support from DFG Grant MO 3010/3-1 and the European Research Council (ERC) ‘‘Horizon 2020’’ Program under Grant No. 805359-FOXON. The transmission electron microscope used in this work was partially funded by the German Research Foundation (DFG/INST163/2951). We thank Martin Steinbrück (Karlsruhe Institute of Technology) for conducting the thermal analysis experiments and Marina Spasova, Mehmet Acet and Michael Farle (Univ. Duisburg-Essen) for fruitful discussions. Use of the Advanced Photon Source at Argonne National Laboratory was supported by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, under Contract No. DE-AC02-06CH11357.
Publisher Copyright:
© 2019 The Royal Society of Chemistry.
PY - 2019
Y1 - 2019
N2 - MAX phases are typically prepared by high-temperature (oftentimes high-pressure) solid-state methods. Here, we report a new wet chemistry based synthesis technique starting from an aqueous solution of metal nitrates and citric acid to prepare MAX phase Cr2GaC. This solution-processable precursor mixture has the potential to be easily scaled, painted, printed or fabricated onto supports-an advantage that is demonstrated by the formation of hollow carbon microspheres which are decorated with Cr2GaC particles. A small amount of chromium carbide and oxide remains in the product, however, the amount of the latter can be reduced by a larger excess in citric acid in the precursor gel. The transformation mechanism of the initial amorphous gel into highly crystalline and anisotropic MAX phase particles is investigated by detailed thermal analysis. Transmission electron microscopy studies are conducted to elucidate the microstructure of the sol-gel-prepared particles as well as the decorated hollow microspheres. From magnetic susceptibility measurements, the density of states at the Fermi level is deduced reflecting the quality of the Pauli paramagnet Cr2GaC.
AB - MAX phases are typically prepared by high-temperature (oftentimes high-pressure) solid-state methods. Here, we report a new wet chemistry based synthesis technique starting from an aqueous solution of metal nitrates and citric acid to prepare MAX phase Cr2GaC. This solution-processable precursor mixture has the potential to be easily scaled, painted, printed or fabricated onto supports-an advantage that is demonstrated by the formation of hollow carbon microspheres which are decorated with Cr2GaC particles. A small amount of chromium carbide and oxide remains in the product, however, the amount of the latter can be reduced by a larger excess in citric acid in the precursor gel. The transformation mechanism of the initial amorphous gel into highly crystalline and anisotropic MAX phase particles is investigated by detailed thermal analysis. Transmission electron microscopy studies are conducted to elucidate the microstructure of the sol-gel-prepared particles as well as the decorated hollow microspheres. From magnetic susceptibility measurements, the density of states at the Fermi level is deduced reflecting the quality of the Pauli paramagnet Cr2GaC.
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U2 - 10.1039/c9tc01416k
DO - 10.1039/c9tc01416k
M3 - Article
AN - SCOPUS:85066125295
SN - 2050-7526
VL - 7
SP - 6034
EP - 6040
JO - Journal of Materials Chemistry C
JF - Journal of Materials Chemistry C
IS - 20
ER -