Yuruo Qi,Junmei Zhao,Chao Yang,Huizhou Liu,Yong-Sheng Hu
Sodium vanadium fluorophosphate, Na 3 (VO 1− x PO 4 ) 2 F 1+2 x (0 ≤ x ≤ 1), is proved to be a series of very promising cathode materials for Na-ion batteries, owing to the high operating voltage and structural stability. However, the selective preparation of phase-pure Na 3 (VO 1− x PO 4 ) 2 F 1+2 x (0 ≤ x ≤ 1) with outstanding electrochemical performance still remains a big challenge. Moreover, there are lots of discrepancies concerning the Na-storage properties, including a diversity of voltage profiles and capacities reported, based on the variety of synthetic methods. Herein, a comprehensive investigation is conducted about the fabrication of phase-pure Na 3 (VO 1− x PO 4 ) 2 F 1+2 x (0 ≤ x ≤ 1) by employing different starting materials and corresponding synthetic conditions, based on a facile low-temperature hydrothermal strategy. Results show that the pH in the reaction system may be of vital importance for the successful preparation of Na 3 (VO 1− x PO 4 ) 2 F 1+2 x (0 ≤ x ≤ 1) with special microarchitecture. Furthermore, it is found that NaH 2 PO 4 ·2H 2 O is the most appropriate phosphorus source, while VCl 3 , VOSO 4 · x H 2 O, and NH 4 VO 3 are the best choices of vanadium sources to prepare Na 3 (VO 1− x PO 4 ) 2 F 1+2 x (0 ≤ x ≤ 1) with superior Na-storage performance. This is the first time that the underlying correlations between the starting materials and the Na-storage performance, are investigated and further that guidance for the selective synthesis of phase-pure Na 3 (VO 1− x PO 4 ) 2 F 1+2 x (0 ≤ x ≤ 1) with superior performance is provided.
Abstract Hierarchical VAPO-5 molecular sieves were prepared with different vanadium resources in the absence/presence of fluorine and characterized by XRD, SEM, N 2 adsorption-desorption, and NH 3 -TPD. The catalytic performances of hierarchical VAPO-5 molecular sieves were evaluated using toluene oxidation as the probe reaction and the corresponding mechanism was further proposed. The sample D-AFI-2(F) synthesized in a fluorine system with NH 4 VO 3 as metal sources show better catalytic performance than other samples in toluene oxidation, which is ascribed to the hierarchically porous structure and more acidic sites. The optimized condition of toluene oxidation was attained at the reaction temperature of 60°C, the reaction time of 5 h, the molar ratio of H 2 O 2 to toluene 2 : 1, the mass ratio of acetonitrile to toluene 6 : 1, and the mass ratio of catalyst to toluene 10%. In this case, the toluene conversion was 21.0%, and the selectivity of benzaldehyde, benzyl alcohol, and cresol was 43.3, 11.4, and 26.2%, respectively.