Multifaceted properties of Ni and Zn codoped MgO nanoparticles.

Recent advancements in material science have aimed to create novel nanomaterials with unique properties and potential applications across diverse domains. By deciphering the complexities of the versatile nanomaterial, MgO, the study aims to deepen our comprehension of the synergistic effects induced by dual doping in MgO, thus propelling the advancement of innovative technologies and materials with broad applications. The present investigation employed a facile chemical precipitation and coprecipitation approach to synthesize pure MgO and Ni, Zn dual doped MgO, varying Ni concentration ranging between 2% and 10% and maintaining a constant Zn concentration at 20%.

Harnessing Nuclear Magnetic Resonance Spectroscopy to Decipher Structure and Dynamics of Clathrate Hydrates in Confinement: A Perspective.

This perspective outlines recent developments in the field of NMR spectroscopy, enabling new opportunities for in situ studies on bulk and confined clathrate hydrates. These hydrates are crystalline ice-like materials, built up from hydrogen-bonded water molecules, forming cages occluding non-polar gaseous guest molecules, including CH, CO and even H and He gas. In nature, they are found in low-temperature and high-pressure conditions.

Surface modification of mesostructured cellular foam to enhance hydrogen storage in binary THF/H clathrate hydrate.

This study introduces solid-state tuning of a mesostructured cellular foam (MCF) to enhance hydrogen (H) storage in clathrate hydrates. Grafting of promoter-like molecules (, tetrahydrofuran) at the internal surface of the MCF resulted in a substantial improvement in the kinetics of formation of binary H-THF clathrate hydrate. Identification of the confined hydrate as sII clathrate hydrate and enclathration of H in its small cages was performed using XRD and high-pressure H NMR spectroscopy respectively.

Noncontact In Situ Multidiagnostic NMR/Dielectric Spectroscopy.

Introduction of a dielectric material in a nuclear magnetic resonance (NMR) probe head modifies the frequency response of the probe circuit, a phenomenon revealed by detuning of the probe. For NMR spectroscopy, this detuning is corrected for by tuning and matching the probe head prior to the NMR measurement. The magnitude of the probe detuning, "the dielectric shift", provides direct access to the dielectric properties of the sample, enabling NMR spectrometers to simultaneously perform both dielectric and NMR spectroscopy.

Prediction of Cu Zeolite NH-SCR Activity from Variable Temperature H NMR Spectroscopy.

Selective catalytic reduction (SCR) of NO by ammonia is one of the dominant pollution abatement technologies for near-zero NO emission diesel engines. A crucial step in the reduction of NO to N with Cu zeolite NH-SCR catalysts is the generation of a multi-electron donating active site, implying the permanent or transient dimerization of Cu ions. Cu atom mobility has been implicated by computational chemistry as a key factor in this process.

Hydrogen bonding to oxygen in siloxane bonds drives liquid phase adsorption of primary alcohols in high-silica zeolites.

Upon liquid phase adsorption of C-C primary alcohols on high silica MFI zeolites (Si/Al = 11.5-140), the concentration of adsorbed molecules largely exceeds the concentration of traditional adsorption sites: Brønsted acid and defect sites. Combining quantitative H MAS NMR, qualitative multinuclear NMR and IR spectroscopy, hydrogen bonding of the alcohol function to oxygen atoms of the zeolite siloxane bridges (Si-O-Si) was shown to drive the additional adsorption.

Reversible Parahydrogen Induced Hyperpolarization of N in Unmodified Amino Acids Unraveled at High Magnetic Field.

Amino acids (AAs) and ammonia are metabolic markers essential for nitrogen metabolism and cell regulation in both plants and humans. NMR provides interesting opportunities to investigate these metabolic pathways, yet lacks sensitivity, especially in case of N. In this study, spin order embedded in p-H is used to produce on-demand reversible hyperpolarization in N of pristine alanine and ammonia under ambient protic conditions directly in the NMR spectrometer.

Water as a tuneable solvent: a perspective.

Water is the sustainable solvent of excellence, but its high polarity limits the solubility of non-polar compounds. Confinement of water in hydrophobic pores alters its hydrogen bonding structure and related properties such as dielectric constant and solvation power. Whether this special state of confined water can be rendered useful in chemical processes is hitherto underexplored.

A Porous POSiSil Suited for Pressure-Driven Reversible Confinement of Solutions: PSS-2.

Polyoligosiloxysilicone (POSiSil; designated PSS-2) is a copolymer of double four-ring (D4R) cyclosilicate and dimethylsiloxane. It is synthesized by linking D4R units in tetrabutylammonium cyclosilicate crystals with dimethyldichlorosilane. The structure of PSS-2 was revealed using solid state NMR spectroscopy.