2021
DOI: 10.1016/j.inoche.2021.108691
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Co/MoS2 nanocomposite catalyzed H2 evolution upon dimethylamine-borane hydrolysis and in situ tandem reaction

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Cited by 13 publications
(7 citation statements)
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“…The P-MoS 2 has an appreciable capacity for Co doping with a high saturation limit. Overall, our results agree with the existing theoretical studies for similar materials, [14][15][16]28,29 indicating that here the charge transfer is from Co atoms to S atoms. Dramatic magnetism (with a magnetic moment of ∼9.42 μ B per supercell) was observed, which is attributed to the strong hybridizations between Co-3d states and 3p states of neighboring S atoms.…”
Section: ■ Methods and Computational Detailssupporting
confidence: 92%
“…The P-MoS 2 has an appreciable capacity for Co doping with a high saturation limit. Overall, our results agree with the existing theoretical studies for similar materials, [14][15][16]28,29 indicating that here the charge transfer is from Co atoms to S atoms. Dramatic magnetism (with a magnetic moment of ∼9.42 μ B per supercell) was observed, which is attributed to the strong hybridizations between Co-3d states and 3p states of neighboring S atoms.…”
Section: ■ Methods and Computational Detailssupporting
confidence: 92%
“…In addition, the catalytic activity of the Pt 0.7 Ni 0.3 /CNS nanohybrid with other reported catalytic systems for H 2 generation from dimethylamineborane hydrolysis is also compared in Table . As a result, the comparison had further confirmed that Pt 0.7 Ni 0.3 /CNS exhibited the highest TOF of 16,607 h –1 at 0.3 M NaOH, which exceeded the other reported catalytic systems, in H 2 generation from dimethylamineborane hydrolysis.…”
Section: Resultsmentioning
confidence: 83%
“…In the past two decades, H 2 gas is comprehensively deemed as a green, sustainable, environmental-friendly future energy source for displacing fossil fuels, preventing further environmental deterioration, and meeting ever-increasing global energy demand. However, the large-scale practical and industrial application of H 2 has been severely limited by its ultra-low density, liquefaction problem, and high transportation costs. To overcome this difficulty, all kinds of hydrogen storage materials, e.g., HCOOH, N 2 H 4 , NaBH 4 , N 2 H 4 BH 3 , NH 3 BH 3 , and Me 2 NHBH 3 , have been designed and explored for the safe production, transport, and storage of hydrogen gas. Among them, dimethylamineborane (Me 2 NHBH 3 ) has recently attracted wide attention due to its cost-effectiveness (compared to NH 3 BH 3 ), excellent hydrogen storage capacity, non-flammability, non-toxicity, excellent stability, and solubility in water. In spite of the fact that remarkable developments have been realized in the design and development of novel nanocatalysts for H 2 evolution from dimethylamineborane hydrolysis in water (eq ), the development of “on–off” control for on-demand H 2 evolution upon dimethylamineborane hydrolysis is still a matter of supreme importance, however. Herein, we synthesized a string of MoS 2 nanosheet-supported RuNi nanohybrids (Ru x Ni 1– x /MoS 2 ), by fixation of RuNi nanoparticles at the MoS 2 surface, for H 2 evolution upon dimethylamineborane hydrolysis at 30 °C. Particularly, the thin MoS 2 nanosheet was widely applied in photocatalytic H 2 production, antibacterial agents, microwave absorption, and water treatment due to its unique optical, physicochemical, and electrical properties. These bimetallic Ru x Ni 1– x /MoS 2 exhibited higher ca...…”
Section: Introductionmentioning
confidence: 99%