Results 171 to 180 of about 1,687,826 (388)

Mixed‐Metal Promotion in a Manganese‐Molybdenum Oxynitride as Catalyst to Integrate C─C and C─N Coupling Reactions for the Direct Synthesis of Acetonitrile from Syngas and Ammonia

open access: yesAdvanced Materials, EarlyView.
Transition metal oxy/carbo‐nitrides show great promise as catalysts for sustainable processes. A Mn‐Mo mixed‐metal oxynitride attains remarkable performance for the direct synthesis of acetonitrile, an important commodity chemical, via sequential C─N and C─C coupling from syngas (C1) and ammonia (N1) feedstocks.
M. Elena Martínez‐Monje   +7 more
wiley   +1 more source

NH3‐Guided Low‐Temperature Nanostructural Refinement Boosts Visible‐Light‐Driven H2O2 Synthesis in Ionic Carbon Nitrides

open access: yesAdvanced Materials, EarlyView.
A nanostructural refinement strategy is reported for KPHI photocatalysts using NH4Cl in a molten salt environment to induce coherent domain fragmentation and controlled cyano defect formation. This dual modification promotes n→π* transitions, enhances charge separation, and accelerates ORR kinetics, yielding exceptional AQY values of 49% (410 nm) and 5%
Jaya Bharti   +9 more
wiley   +1 more source

Implied volatility and future market return [PDF]

open access: yesInsurance Markets and Companies, 2010
Ping Hsiao, Ming Li
doaj  

Prediction of realized volatility and implied volatility indices using AI and machine learning: A review

open access: yesInternational Review of Financial Analysis
Elias Søvik Gunnarsson   +5 more
semanticscholar   +1 more source

Reactive Carbide‐Based Synthesis and Microstructure of NASICON Sodium Metal All Solid‐State Electrolyte

open access: yesAdvanced Materials, EarlyView.
Sodium Metal All‐Solid State Batteries (Na‐ASSBs) are enabled by the synthesis of the solid state electrolyte, NASICON (Na1+xZr2SixP3‐xO12), using carbide‐based precursor compounds (ZrC and SiC); resulting in dense, pure, and mechanically improved microstructure.
Callum J. Campbell   +10 more
wiley   +1 more source

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