RESUMEN
H2 is one of the most attractive fuel alternatives to the existing fossil fuels that cause detrimental environmental issues. Thus, there has been an upsurge in the research on the production of green hydrogen. In this view, cucurbit[7]uril (CB7)-functionalized Co:Ni alloy nanocomposites with different compositions, reported here for the first time, were synthesized to synergise the catalytic activities of a nanoalloy and CB7 and screened for hydrogen generation via hydrolysis of ammonia borane (AB). The (Co85:Ni15)50:(CB7)50 nanocomposite exhibited enhanced catalytic performance for AB hydrolysis even at room temperature as compared to the nanoalloy without CB7. Efficient release of ammonia-free green H2 is ensured by the retention of NH3 by the surface functionalized CB7 macrocycles. For sustained release, a novel and cost-effective procedure was used to regenerate AB from the by-product, and the H2 release activity was verified to be on par with commercial AB. The used nanocomposite magnetically separated from the by-product solution was shown to be an efficient electrochemical catalyst for the hydrogen evolution reaction (HER). The cucurbit[7]uril-functionalized Co:Ni nanocomposite demonstrates remarkable dual catalytic performance to generate clean hydrogen from both the hydrolysis of AB at room temperature and the electrochemical HER, thus opening new avenues in supramolecular chemistry for developing noble metal-free catalysts with high activity and long-term stability.
RESUMEN
Shell thickness dependent band-gap engineering of quasi typeâ II core-shell material with higher carrier cooling time, lower interfacial defect states, and longer charge carrier recombination time can be a promising candidate for both photocatalysis and solar cell. In the present investigation, colloidal CdSe@CdS core-shells with different shell thickness (2, 4 and 6â monolayer CdS) were synthesized through hot injection method and have been characterized by high resolution transmission electron microscope (HRTEM) followed by steady state absorption and luminescence techniques. Ultrafast transient absorption (TA) studies suggest longer carrier cooling, lower interfacial surface states, and slower carrier recombination time in CdSe@CdS core-shell with increasing shell thickness. By TA spectroscopy, the role of CdS shell in power conversion efficiency (PCE) has been explained in detail. The measured PCE was found to initially increase and then decrease with increasing shell thickness. Shell thickness has been optimized to maximize the efficiency after correlating the shell controlled carrier cooling and recombination with PCE values and a maximum PCE of 3.88 % was obtained with 4 monolayers of CdS shell, which is found to be 57 % higher than compared to bare CdSe QDs.