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排序方式: 共有354条查询结果,搜索用时 15 毫秒
1.
Mathias Mallmann Sebastian Wendl Dr. Philipp Strobel Dr. Peter J. Schmidt Prof. Dr. Wolfgang Schnick 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(28):6257-6263
Nitridophosphates exhibit an intriguing structural diversity with different structural motifs, for example, chains, layers or frameworks. In this contribution the novel nitridophosphate Sr3P3N7 with unprecedented dreier double chains is presented. Crystalline powders were synthesized using the ammonothermal method, while single crystals were obtained by a high-pressure multianvil technique. The crystal structure of Sr3P3N7 was solved and refined from single-crystal X-ray diffraction and confirmed by powder X-ray methods. Sr3P3N7 crystallizes in monoclinic space group P2/c. Energy-dispersive X-ray and Fourier-transformed infrared spectroscopy were conducted to confirm the chemical composition, as well as the absence of NHx functionality. The optical band gap was estimated to be 4.4 eV using diffuse reflectance UV/Vis spectroscopy. Upon doping with Eu2+, Sr3P3N7 shows a broad deep-red to infrared emission (λem=681 nm, fwhm≈3402 cm−1) with an internal quantum efficiency of 42 %. 相似文献
2.
Meihong Zhang Yuqian Fang Shuai Yuan Liyi Shi Zhuyi Wang Yi Wang Jiefang Zhu Yin Zhao 《Surface and interface analysis : SIA》2023,55(1):63-70
The graphitic carbon nitride (g-C3N4) materials with many intriguing properties have attracted much attention in photocatalysis. The photocatalytic activity of g-C3N4 is hindered by serious aggregation and limited exposed active sites. Herein is shown that nanosized g-C3N4 can be simply obtained by a superfast high-pressure homogenization approach. The high-pressure homogenization treatment can provide strong force to cut and/or to exfoliate the bulk g-C3N4 into nanosized g-C3N4 with good dispersion. Moreover, choosing different solvents during treatment can cause a different surface structure of as-prepared nanosized g-C3N4. In addition, the narrow bandgap properties, the high photogenerated charge carrier separation, and the transport abilities are achieved in as-prepared nanosized g-C3N4 because of the retaining conjugated C3N4 system. Specifically, the photocatalytic activities of as-prepared nanosized g-C3N4 have been significantly enhanced in terms of degradation of organic dye Rhodamine B (RhB) under visible light irradiation (10 times higher than that of bulk g-C3N4). These findings can provide a promising and simple approach to the exfoliation, nanonization, and surface functionalization of 2D layered materials. 相似文献
3.
Dr. Alif Sussardi Dr. Ross J. Marshall Prof. Stephen A. Moggach Prof. Anita C. Jones Prof. Ross S. Forgan 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(60):14871-14875
Photophysical studies of chromophoric linkers in metal–organic frameworks (MOFs) are undertaken commonly in the context of sensing applications, in search of readily observable changes of optical properties in response to external stimuli. The advantages of the MOF construct as a platform for investigating fundamental photophysical behaviour have been somewhat overlooked. The linker framework offers a unique environment in which the chromophore is geometrically constrained and its structure can be determined crystallographically, but it exists in spatial isolation, unperturbed by inter-chromophore interactions. Furthermore, high-pressure studies enable the photophysical consequences of controlled, incremental changes in local environment or conformation to be observed and correlated with structural data. This approach is demonstrated in the present study of the trans-azobenzene chromophore, constrained in the form of the 4,4’-azobenzenedicarboxylate (abdc) linker, in a UiO topology framework. Previously unobserved effects of pressure-induced solvation and conformational distortion on the lowest energy, nπ* transition are reported, and interpreted the light of crystallographic data. It was found that trans-azobenzene remains non-fluorescent (with a quantum yield less than 10−4) despite the prevention of trans-cis isomerization by the constraining MOF structure. We propose that efficient non-radiative decay is mediated by the local, pedal-like twisting of the azo group that is evident as dynamic disorder in the crystal structure. 相似文献
4.
Lucien Eisenburger Prof. Dr. Oliver Oeckler Prof. Dr. Wolfgang Schnick 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(13):4461-4465
Tetrahedra-based nitrides with network structures have emerged as versatile materials with a broad spectrum of properties and applications. Both nitridosilicates and nitridophosphates are well-known examples of such nitrides that upon doping with Eu2+ exhibit intriguing luminescence properties, which makes them attractive for applications. Nitridosilicates and nitridophosphates show manifold structural variability; however, no mixed nitridosilicatephosphates except SiPN3 and SiP2N4NH have been described so far. The compounds AESiP3N7 (AE=Sr, Ba) were synthesized by a high-pressure high-temperature approach using the multianvil technique (8 GPa, 1400–1700 °C) starting from the respective alkaline earth azides and the binary nitrides P3N5 and Si3N4. The latter were activated by NH4F, probably acting as a mineralizing agent. SrSiP3N7 and BaSiP3N7 were obtained as single crystals. They crystallized in the barylite-1O (M=Sr) and barylite-2O structure types (M=Ba), respectively, with P and Si being occupationally disordered. Cation disorder was further supported by solid-state NMR spectroscopy and energy-dispersive X-ray spectroscopy (EDX) mapping of BaSiP3N7 with atomic resolution. Upon doping with Eu2+, both compounds showed blue emission under UV excitation. 相似文献
5.
Dr. Anna Pakhomova Birgit Fuchs Prof. Dr. Leonid S. Dubrovinsky Prof. Dr. Natalia Dubrovinskaia Prof. Dr. Hubert Huppertz 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(19):6007-6014
Based on the results from previous high-pressure experiments on the gadolinite-type mineral datolite, CaBSiO4(OH), the behavior of the isostructural borates β-HfB2O5 and β-ZrB2O5 have been studied by synchrotron-based in situ high-pressure single-crystal X-ray diffraction experiments. On compression to 120 GPa, both borate layer-structures are preserved. Additionally, at ≈114 GPa, the formation of a second phase can be observed in both compounds. The new high-pressure modification γ-ZrB2O5 features a rearrangement of the corner-sharing BO4 tetrahedra, while still maintaining the four- and eight-membered rings. The new phase γ-HfB2O5 contains ten-membered rings including the rare structural motif of edge-sharing BO4 tetrahedra with exceptionally short B−O and B⋅⋅⋅B distances. For both structures, unusually high coordination numbers are found for the transition metal cations, with ninefold coordinated Hf4+, and tenfold coordinated Zr4+, respectively. These findings remarkably show the potential of cold compression as a low-energy pathway to discover metastable structures that exhibit new coordinations and structural motifs. 相似文献
6.
An original experimental investigation of heat transfer with steam condensation on a surface of a horizontal cooled tube immersed in a bubbling layer was carried out. A copper test section 16 mm in diameter and 285 mm in length was placed in a bubbling column 295 mm in diameter. Experiments were made under a pressure of 0.72-3.8 MPa with volume steam content 0-0.18, steam superficial velocities 0-0.18 m/s, and liquid-wall temperature difference 38–106 K. The heat transfer process in a bubbling layer under high pressures is shown to be of considerably intensity; with moderate values of steam content heat transfer coefficients reach 10–12 kW/(m2·K). The use of the known correlations assumed for the case of air bubbling under atmospheric pressure results in systematically underestimating heat transfer by 30–80%. Data were obtained on heat transfer with film condensation of steam and natural convection of subcooled water at high temperature differences outside the range investigated earlier. Experimental data table is appended. 相似文献
7.
本文提出的采用增量理论的分析模型和方法可以定量分析应变硬化、包辛格效应和材料机械性质随温度变化等因素对自增强厚壁圆筒中残余应力和操作应力分布的影响.厚壁圆筒看成由N个同轴薄壁圆筒套在一起组成的构件;采用包括弹性、塑性和温度应变的增量型本构关系和相容条件导出了自增强圆筒的基本方程;设计了计算机程序并给出了分析实例。分析结果表明,应变硬化会减小塑性区并降低残余应力;包辛格效应使反向屈服容易出现;温度升高将使残余应力和热应力松驰. 相似文献
8.
9.
作者研制了一台可测试润滑油在高压下的粘度和密度的落柱式高压粘度装置。本装置采用了新型高压粘性动密封和新型高压流变平垫静密封,经1200MPa试压、1000MPa压力下48小时保压和使用试验证明均无泄漏。用本装置所获得的压粘数据的重现性好、灵敏度高、可比性强。 相似文献
10.
Vladimir Solozhenko 《高压研究》2013,33(2):317-318
Composite diamond anvils have been developed for high-pressure/high-temperature measurements of diamond anvil cells. The anvils are fabricated using single-crystal chemical vapor deposition (CVD) from previously used and/or slightly damaged anvils made of natural or synthetic diamond. These composite anvils can be fabricated to possess optical characteristics at least comparable to conventional diamond anvils, whereas the single-crystal CVD portion is more durable because of its enhanced toughness relative to natural diamond. The viability of such anvils is demonstrated in measurements on hydrogen at megabar pressures and high temperature. 相似文献