The
research of fast scintillators in positron emission tomography
and other applications based on time-of-flight technology promotes
the development of radiation detection. However, because of the current
lack of efficient and fast carrier radiation recombination pathways,
the research on scintillator radioluminescence (RL) still faces severe
challenges. Here, we propose an effective interface carrier transport
mechanism: CsI:Na crystal and Cs4PbBr6 nanocrystals
(NCs) interface to form a new phase and a continuous heterostructure,
providing an effective channel for X-ray excited carrier transfer
to Cs4PbBr6. Then, the excited carriers realize
efficient recombination luminescence through the self-trapped excitons
inside Cs4PbBr6. On the basis of this mechanism,
the heterostructure composite scintillator composed of CsI:Na/Cs4PbBr6 exhibits high-efficiency radiant fluorescence
and an ultrafast photoluminescence (PL) decay time of 1.22 ns. The
effective interface carrier transport shown in this work provides
an optimization idea that can be used for reference in the research
of fast scintillators.
A high-efficiency sky-blue radioluminescence, large-size, eco-friendly hybrid scintillator made of CsI:Na and Cs3Cu2I5 single crystals is expected to become a potential ionizing radiation detection scintillator.
Recently, tin disulfide (SnS2) has become a hot research
focus in various fields due to its advantages of a high transistor
switching ratio, an adjustable band gap in visible light range, excellent
Li storage performance, sensitive gas recognition, and efficient photocatalytic
capability. However, at present, studies of its basic structure mostly
stay on the regulation related to the number of layers. To maximize
the value of SnS2 in the application design, this paper
analyzes the angle-resolved polarized Raman spectra of SnS2 crystals grown under high-temperature sealing systems. Under the
parallel scattering configuration test of both the sample basal plane
and the cross plane, we observed that how the Raman scattering intensity
of the two test planes varies with the polarization angle is different.
Combining this experimental result with theory support allows us to
reach a conclusion that the differential polarizability of the phonon
vibration mode along the z-axis of the cross plane
of SnS2 is proven to be the strongest. This finding is
expected to provide favorable support for the application of structural
regulation of SnS2 and work as a reference for studying
other van der Waals layered materials with greater potential.
An urgent demand for electronic and optoelectronic devices able to work in extreme environments promotes a series of research studies on semiconductor materials. Cubic boron phosphide (BP) as a semiconductor material with excellent characteristics shows great application potential. However, since the synthesis conditions required are difficult to achieve and the growth mechanism of BP is still unclear, there are few reports on the basic properties of BP and pure isotope BP, resulting in a narrow understanding of their special physical properties. Here, we successfully obtained highly pure isotopic 10 BP crystals by a vapor−liquid−solid (VLS) method unconventionally designed, which successfully overcomes the thermodynamic conflict between the high melting point of the boron element and low sublimation temperature of the phosphorus element. The 10 BP achieved owns an aspect ratio as high as 10 4 and a hardness up to 41 GPa. Besides, as an indirect bandgap semiconductor, it has ultrawide red emission spectra, a p-type conductivity with extremely low resistivity, and excellent photoelectronic and piezoelectric characteristics. Furthermore, compared with other superhard semiconductors like cubic BN and diamond, 10 BP has an obvious advantage of lower growth temperature (1200 °C). All these characteristics confirm the prospects owned by 10 BP in its applications to the field of high-conductivity, optoelectronic, strain-sensing, and superhard semiconductors.
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