Black BiOCl with oxygen vacancies was prepared by UV light irradiation with Ar blowing. The as-prepared black BiOCl sample showed 20 times higher visible light photocatalytic activity than white BiOCl for RhB degradation. The trapping experiment showed that the superoxide radical (O(2)(•-)) and holes (h(+)) were the main active species in aqueous solution under visible light irradiation.
We present a two-step synthesis process to produce hierarchical ZnO nanoarchitectures that involves the preparation of ZnO nanosheet arrays by the pyrolysis of the precursor Zn5(OH)8Cl2 electrodeposited on conductive glass substrates, followed by the aqueous chemical growth (ACG) of dense ZnO single-crystalline nanowires on the surfaces of the primary ZnO nanosheets. The dye-sensitized solar cell (DSSC) based on the hierarchical ZnO nanowire−nanosheet architectures showed a power conversion efficiency of 4.8%, which is nearly twice as high as that of the DSSC constructed using a photoanode of bare ZnO nanosheet arrays. The better photovoltaic performance of hierarchical ZnO nanoarchitecture DSSC was due to a better dye loading and light harvesting as a consequence of the enlargement of the internal surface area within the photoanode. Moreover, the improved performance for the DSSC with the hierarchical ZnO nanowire−nanosheet architectures may be also ascribed to more light scattering behavior through extending the optical path length within the photoanode so as to increase the light harvesting. The results demonstrate potential application of the hierarchical ZnO nanoarchitectures derived from ZnO nanosheet arrays for highly efficient DSSCs.
Hollandites (OMS-2) are an intriguing class of sorbents, catalysts, and energy storage materials with a tunnel structure permitting one-dimensional insertion and deinsertion of ions and small molecules along the c direction. A 7-fold increase in delivered capacity for Li/AgxMn8O16 electrochemical cells (160 versus 23 mAh/g) observed upon a seemingly small change in silver content (x ∼1.1 (L-Ag-OMS-2) and 1.6 (H-Ag-OMS-2)) led us to characterize the structure and defects of the silver hollandite material. Herein, Ag hollandite nanorods are studied through the combined use of local (atomic imaging, electron diffraction, electron energy-loss spectroscopy) and bulk (synchrotron based X-ray diffraction, thermogravimetric analysis) techniques. Selected area diffraction and high resolution transmission electron microscopy show a structure consistent with that refined by XRD; however, the Ag occupancy varies significantly even within neighboring channels. Both local and bulk measurements indicate a greater quantity of oxygen vacancies in L-Ag-OMS-2, resulting in lower average Mn valence relative to H-Ag-OMS-2. Electron energy loss spectroscopy shows a lower Mn oxidation state on the surface relative to the interior of the nanorods, where the average Mn valence is approximately Mn(3.7+) for H-Ag-OMS-2 and Mn(3.5+) for L-Ag-OMS-2 nanorods, respectively. The higher delivered capacity of L-Ag-OMS-2 may be related to more oxygen vacancies compared to H-Ag-OMS-2. Thus, the oxygen vacancies and MnO6 octahedra distortion are assumed to open the MnO6 octahedra walls, facilitating Li diffusion in the ab plane. These results indicate crystallite size and surface defects are significant factors affecting battery performance.
Bismuth
has garnered tremendous interest for Na-ion batteries (NIBs)
due to potentially high volumetric capacity. Yet, the bismuth upon
sodiation/desodiation experiencing structure and phase transitions
remains unclear, which sets a challenge for accessing nanotechnology
and nanofabrication to achieve its applicability. Here, we use in
situ transmission electron microscopy to disclose the structure and
phase transitions of layered bismuth (few-layer bismuth nanosheets)
during Na+ intercalation and alloying processes. Multistep
phase transitions from Bi → NaBi → c-Na3Bi
(cubic) → h-Na3Bi (hexagonal) are clearly identified,
during which the Na+ migration from interlayer to in-plane
evokes the structure transition from ABCABC stacking type of c-Na3Bi to ABABAB stacking type of h-Na3Bi. It is found
that the metastable c-Na3Bi devotes to buffer the dramatic
structure changes from thermodynamic stable h-Na3Bi, which
unveils the origin of volume expansion for bismuth and has important
consequences for 2D in-plane structure. As the lateral ductility can
efficiently alleviate the in-plane mechanical strain caused by the
Na+ migration, the few-layer bismuth nanosheet exhibits
a potential cyclability for NIBs. Our findings will encourage more
attention to bismuthene as a novel anode material for secondary batteries.
Abstract. The Airborne Multiangle SpectroPolarimetric Imager (AirMSPI) is an eight-band (355, 380, 445, 470, 555, 660, 865, 935 nm) pushbroom camera, measuring polarization in the 470, 660, and 865 nm bands, mounted on a gimbal to acquire multiangular observations over a ±67° along-track range. The instrument has been flying aboard the NASA ER-2 high altitude aircraft since October 2010. AirMSPI employs a photoelastic modulator-based polarimetric imaging technique to enable accurate measurements of the degree and angle of linear polarization in addition to spectral intensity. A description of the AirMSPI instrument and ground data processing approach is presented. Example images of clear, hazy, and cloudy scenes over the Pacific Ocean and California land targets obtained during flights between 2010 and 2012 are shown, and quantitative interpretations of the data using vector radiative transfer theory and scene models are provided to highlight the instrument's capabilities for determining aerosol and cloud microphysical properties and cloud 3-D spatial distributions. Sensitivity to parameters such as aerosol particle size distribution, ocean surface wind speed and direction, cloud-top and cloud-base height, and cloud droplet size is discussed. AirMSPI represents a major step toward realization of the type of imaging polarimeter envisioned to fly on NASA's Aerosol-Cloud-Ecosystem (ACE) mission in the next decade.
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