The Limited Incorporation and Role of Fluorine in Mn-rich Disordered Rocksalt Cathodes
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Here we have experimentally shown by neutron diffraction significant shortening of both $sp^3$- and $sp^2$-hybridized C–H bonds to 1.092(2) and 1.081(1) Å in a hydrogen-bonded crystal of a difluorinated compound, 4-((2,2-difluoroethoxy)methyl)pyridinium saccharinate. Both MP2 and DFT calculations affirmed the C–H bond shrinkages. Sanderson’s electronegativity equalization principle provides insight into the shortening of the C–H covalent bond lengths for both $sp^3$- and $sp^2$-hybridized carbon atoms. To the best of our knowledge, this neutron diffraction study has revealed the largest extents of $sp^3$ and $sp^2$ C–H bond shrinkages with a 3-sigma rule being satisfied.
A mechanism of Ni redeposition during dealloying corrosion of Ni-Cr is investigated. A model Ni20Cr (wt%) metal alloy was exposed to molten LiF-NaF-KF eutectic (FLiNaK) at 600 °C and at an applied potential of +2.1 VK+/K, above the critical potential for onset of dealloying. Upon extended exposure times (up to 12 h), prominent salt-filled corrosion channels emerge along grain boundaries. A unique grain boundary corrosion mechanism, with respect to the exposed faces of the grains, a central focus of this investigation, is intrinsically connected to the formation of high purity Ni-rich de-alloyed regions within the salt-filled channel. We implement microscale techniques such as energy dispersive spectroscopy (EDS) and electron backscatter diffraction (EBSD) to uncover morphological and compositional variations in relevance to the formation of bicontinuous porosity from corrosion dealloying. To rationalize our findings, a phase-field model is developed and discovers a mechanism in which dissolved Ni from one grain can be redeposited on an adjacent grain at a given difference in interfacial energies. The interaction of chemical and structural factors at the grain boundaries plays a central role in elucidating the dynamics of this phenomenon and its implications towards corrosion.
Proper kinetic and thermodynamic models are important in addressing durability as a major issue facing PGM-free ORR electrocatalysts.
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Highly crystalline anatase TiO 2 nanosheets, made by controlled oxidation of TiS 2 nanosheets, expose the {001} and {100} facets, giving rise to enhancement in HER as compared to Degussa P25 TiO 2 nanoparticles. No enhancement in ORR was observed.
Synthesis of a series of hydrocarbon-soluble triarylamines bearing F, CF 3 , and Br substituents showing quasi-reversible redox events in the 0.59–1.32 V range is reported. A few have been isolated as [HCB 11 Cl 11 ] − salts.
Delivered capacities of non-flammable LHCE vs. flammable LiPF 6 EC:DMC electrolyte at low temperature, high voltage charge, and fast charge.
We investigate switching of photoluminescence from PbS quantum dots crosslinked with photochromic diarylethene molecules with different degree of halogenation.
The development of theranostic agents for radiopharmaceuticals based on therapeutic alpha emitters marks an important clinical need.
CF 3 alteration in FMOF-1 to different X groups yields enhanced porosity and selectivity for specific guests (e.g., CO 2 adsorption was improved for all X variants; for X = COOH, CO 2 /CH 4 = 59.6 & CO 2 /N 2 = 128.7, >40× vs . FMOF-1).
Superhydrophobicity of MeMOFs, methylated analogues of FMOFs (CF 3 → CH 3 ) is predicted by GCMC simulations (high-RH CO 2 or CH 4 adsorption in MeMOFs > FMOFs) validated experimentally (H 2 O contact angle ∼172° for MeMOF@plastic dry-coated substrates).