Nickel-Tin Nanoalloy Supported ZnO Catalysts from Mixed-Metal Zeolitic Imidazolate Frameworks for Selective Conversion of Glycerol to 1,2-Propanediol.

The successful synthesis of finely tuned Ni1.5 Sn nanoalloy phases containing ZnO catalyst with a small particle size (6.7 nm) from a mixed-metal zeolitic imidazolate framework (MM-ZIF) is investigated. The catalyst was evaluated for the efficient production of 1,2-propanediol (1,2-PDO) from crude glycerol and comprehensively characterized using several analytical techniques. Among the catalysts, 3Ni1Sn/ZnO (Ni/Sn=3/1) showed the best catalytic performance and produced the highest yield (94.2 %) of 1,2-PDO at ~100 % conversion of glycerol; it also showed low apparent activation energy (15.4 kJ/mol) and excellent stability. The results demonstrated that the synergy between Ni-Sn alloy, finely dispersed Ni metallic sites, and the Lewis acidity of SnOx species-loaded ZnO played a pivotal role in the high activity and selectivity of the catalyst. The confirmation of acetol intermediate and theoretical calculations verify the Ni1.5 Sn phases provide the least energetic pathway for the formation of 1,2-PDO selectively. The reusability of solvent for successive ZIF synthesis, along with the excellent recyclability of the ZIF-derived catalyst, enables an overall sustainable process. We believe that the present synthetic protocol that uses MM-ZIF for the conversion of various biomass-derived platform chemicals into valuable products can be applied to various nanoalloy preparations.

Atomic Layer Deposition of an Effective Interface Layer of TiN for Efficient and Hysteresis-Free Mesoscopic Perovskite Solar Cells.

Perovskite solar cells (PSCs) have experienced outstanding advances in power conversion efficiencies (PCEs) by employing new electron transport layers (ETLs), interface engineering, optimizing perovskite morphology, and improving charge collection efficiency. In this work, we study the role of a new ultrathin interface layer of titanium nitride (TiN) conformally deposited on a mesoporous TiO2 (mp-TiO2) scaffold using the atomic layer deposition method. Our characterization results revealed that the presence of TiN at the ETL/perovskite interface improves the charge collection as well as reduces the interface recombination. We find that the morphology (grain size) and optical properties of the perovskite film deposited on the optimized mp-TiO2/TiN ETL are improved drastically, leading to devices with a maximum PCE of 19.38% and a high open-circuit voltage (Voc) of 1.148 V with negligible hysteresis and improved environmental (∼40% RH) and thermal (80 °C) stabilities.

Lichen-like anchoring of MoSe2 on functionalized multiwalled carbon nanotubes: an efficient electrode for asymmetric supercapacitors.

In the present study, we have developed a composite electrode of MSNT using a simple and scalable two-step scheme to synthesize a composite electrode material comprising MoSe2/multiwalled carbon nanotubes (MoSe2/MWCNTs) for supercapacitor applications. First, a MWCNT thin film was deposited on a stainless steel substrate by using a "dip and dry" coating technique. Subsequently, MoSe2 was deposited onto the MWCNT thin film using the successive ionic layer adsorption and reaction method. The lichen-like growth of MoSe2 on the MWCNT network provided dual charge storage and an effective ion transfer path. The composite electrode of MSNT has been studied systematically with different electrolytes and concentrations of electrolyte. As a result, the MoSe2/MWCNT (MSNT) electrode exhibited excellent electrochemical properties such as a specific capacity of 192 mA h g-1 and a capacitance retention of 88% after 2000 cycles in 1 M LiCl electrolyte. The results demonstrated the huge potential of the MSNT composite electrode for practical application in supercapacitors. The aqueous symmetric cell fabricated using the MSNT composite as both the anode and cathode showed an energy density of 17.9 W h kg-1. Additionally, the energy density improved by designing an asymmetric device of MSNT//MnO2 and notably, it reveals two-fold improvement in the energy density compared to a symmetric MSNT cell. The MSNT//MnO2-based asymmetric cell exhibited a maximum specific capacitance of 112 F g-1 with a high energy density of 35.6 W h kg-1.