Emerging two-dimensional MXenes have been extensively studied in a wide range of fields thanks to their superior electrical and hydrophilic attributes as well as excellent chemical stability and mechanical flexibility. Among them, the ultrahigh electrical conductivity (σ) and tunable band structures of benchmark TiCT MXene demonstrate its good potential as thermoelectric (TE) materials. However, both the large variation of σ reported in the literature and the intrinsically low Seebeck coefficient (S) hinder the practical applications. Herein, this study has for the first time systematically investigated the TE properties of neat TiCT films, which are finely modulated by exploiting different dispersing solvents, controlling nanosheet sizes and constructing composites. First, deionized water is found to be superior for obtaining closely packed MXene sheets relative to other polar solvents. Second, a simultaneous increase in both S and σ is realized via elevating centrifugal speed on MXene aqueous suspensions to obtain small-sized nanosheets, thus yielding an ultrahigh power factor up to ~ 156 μW m K. Third, S is significantly enhanced yet accompanied by a reduction in σ when constructing MXene-based nanocomposites, the latter of which is originated from the damage to the intimate stackings of MXene nanosheets. Together, a correlation between the TE properties of neat TiCT films and the stacking of nanosheets is elucidated, which would stimulate further exploration of MXene TEs.
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http://dx.doi.org/10.1007/s40820-024-01594-z | DOI Listing |
Photochem Photobiol
September 2015
Department of Chemistry, Indian Institute of Technology, Patna, India.
This study reported the photophysics of 7-(diethylamino)coumarin-3-carboxylic acid N-succinimidyl ester (7-DCCAE) in different neat solvents of varying polarity using steady-state absorption, fluorescence emission and picosecond time-resolved spectroscopy. In nonpolar solvents, the dye molecule predominantly exists in nonpolar structure and exhibits very low value of nonradiative decay rate constant (k(nr)), demonstrating the emission takes place from S(1) -LE to S(0) ground state. The fluorescence quantum yields, lifetime values of 7-DCCAE in different solvents are rationalized on the basis of intramolecular charge transfer (ICT) followed by twisted intramolecular charge transfer state formation (TICT) as well as specific solute-solvent interactions.
View Article and Find Full Text PDFJ Phys Chem B
April 2013
National Renewable Energy Laboratory, Golden, Colorado 80401, USA.
In order to identify optimal conditions for singlet fission, we are examining the photophysics of 1,3-diphenylisobenzofuran (1) dimers covalently coupled in various ways. In the two dimers studied presently, the coupling is weak. The subunits are linked via the para position of one of the phenyl substituents, in one case (2) through a CH2 linker and in the other (3) directly, but with methyl substituents in ortho positions forcing a nearly perpendicular twist between the two joint phenyl rings.
View Article and Find Full Text PDFJ Phys Chem B
May 2009
Department of Chemistry, Indian Institute of Technology, Kharagpur 721 302, West Bengal, India.
In this paper, we have investigated the photophysics of 1-ethyl-2-(4-(p-dimethylaminophenyl)-1,3-butadienyl)pyridinium perchlorate (LDS-698) molecule in dioxane-water mixture and in a room temperature ionic liquid (RTIL) 1-butyl-3-methylimidazolium tetrafluoroborate ([bmim][BF4]). Both photoisomerization and twisted intramolecular charge transfer (TICT) are possible in this molecule. We have shown that TICT is favorable in this molecule in the dioxane-water mixture and in neat [bmim][BF4].
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