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All the materials exhibited high strain rate superplasticity at a relatively low temperature of 777 K.
Accordingly, the materials exhibited high glass transition temperatures and thermogravimetric data revealed high thermal stability.
The organic inorganic hybrid materials exhibited high catalytic activity and excellent thermal stability in the alkylation of aromatics with olefins.
The two host materials exhibited high triplet energy level (> 2.65 eV) and the benzofuran-substituted derivative presented suitable glass transition temperature (> 130 °C).
As expected, both materials exhibited high triplet energy over 2.8 eV, indicating they could act as suitable blue hosts in phosphorescent organic light-emitting diodes.
The CoS2/rGO hybrid materials exhibited high catalytic activity for HER: overpotential of −150 mV versus RHE and a Tafel slope of 48 mV/dec for CoS2/rGO (2.3 mg/mL GO).
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In DSC measurement, 180°C heat-treated hybrid materials exhibited higher miscibility as compared to untreated materials.
The core-shell materials exhibited higher electrocatalytic activity towards the ORR, and longer-term durability when compared to pure Pd.
The results showed that the N-doped materials exhibited higher catalytic activity than the un-doped one due to those physicochemical changes.
The titanium oxide catalysts prepared on these porous materials exhibited higher photocatalytic reactivities than TiO2 powder and titanium oxide catalysts prepared by a conventional impregnation method.
At comparable molar compositions, these materials exhibited higher water contents than the corresponding hydrogels containing N-vinyl-2-pyrrolidone in place of DMA.
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