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Hunter Phillips
Hunter Phillips

Daniela Diamond

Nanosized diamond (UDD), obtained by a detonation procedure, was modified with iron from the corresponding acetylacetonate precursor under various pretreatment conditions. Nitrogen physisorption, X-ray diffraction, temperature-programmed reduction, and FTIR and Mössbauer spectroscopy were used for their characterization. The samples' catalytic behavior in methanol decomposition was also studied. The physicochemical and catalytic properties of the obtained materials (Fe/UDD) were compared with those of other iron-oxide-modified mesoporous supports with different nature and functionality (MCM-48 silica and CMK-1 carbon). The highest catalytic activity and stability was achieved with air-pretreated Fe/UDD.

daniela diamond

Color-center-hosting semiconductors are emerging as promising source materials for low-field dynamic nuclear polarization (DNP) at or near room temperature, but hyperfine broadening, susceptibility to magnetic field heterogeneity, and nuclear spin relaxation induced by other paramagnetic defects set practical constraints difficult to circumvent. Here, we explore an alternate route to color-center-assisted DNP using nitrogen-vacancy (NV) centers in diamond coupled to substitutional nitrogen impurities, the so-called P1 centers. Working near the level anticrossing condition-where the P1 Zeeman splitting matches one of the NV spin transitions-we demonstrate efficient microwave-free 13C DNP through the use of consecutive magnetic field sweeps and continuous optical excitation. The amplitude and sign of the polarization can be controlled by adjusting the low-to-high and high-to-low magnetic field sweep rates in each cycle so that one is much faster than the other. By comparing the 13C DNP response for different crystal orientations, we show that the process is robust to magnetic field/NV misalignment, a feature that makes the present technique suitable to diamond powders and settings where the field is heterogeneous. Applications to shallow NVs could capitalize on the greater physical proximity between surface paramagnetic defects and outer nuclei to efficiently polarize target samples in contact with the diamond crystal. 041b061a72


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