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        Covalent bonding of ZnO nanostructures with dispersible carbon nanotubes for self-assembly photocatalytic heterostructures

        Tie, Weiwei,Jin, Jiaming,Bhattacharyya, Surjya Sarathi,Yue, Hongwei,Lei, Yan,Zheng, Zhi,He, Weiwei,Lee, Seung Hee Elsevier BV * North-Holland 2019 Applied Surface Science Vol.492 No.-

        <P><B>Abstract</B></P> <P>This work demonstrates the fabrication of zinc oxide‑carbon nanotube (ZnO/CNT) heterostructures with tunable photocatalytic activity via microstructure modulation. The ZnO/CNT heterostructures are constructed in one-step hydrothermal procedure consisting of in situ anchoring of ZnO nanostructures with dispersible CNTs in an aqueous alkali solution containing bile salts as a dispersant. Observation via scanning (SEM) and transmission (TEM) electron microscopy reveals self-assembled heterostructures of monodispersible CNTs tightly surrounding ZnO nanostructures with multimorphology. The XRD, FT-IR, Raman and XPS analysis confirm that the CNTs were successfully incorporated into the ZnO nanostructures with strong interfacial contact of covalent bonding rather than simple mixing. A series of ZnO/CNT heterostructures, which varies according to their degree of doping with dispersible CNTs, exhibit distinct sunlight-induced photocatalytic activity onto the degradation of Rhodamine B (RhB). The superior photocatalytic performance of ZnO/CNT heterostructures originates from synergistic effects of sufficient interfacial bonding, self-assembly microstructures, and continuous conducting pathways between ZnO nanostructures and CNTs, which acquires better sunlight utilization and more efficient separation of electron-hole pair, confirmed by UV–Visible diffuse reflectance spectra as well as photocurrent and photovoltage analysis. This study also proposes a photocatalytic degradation mechanism of RhB dyes through detection of active species confirmed by electron-spin-resonance analysis.</P> <P><B>Highlights</B></P> <P> <UL> <LI> ZnO nanostructures covalently linking with dispersible carbon nanotubes for self-assembly heterostructures are synthesized. </LI> <LI> This sunlight-driven self-assembly heterostructures possess tunable photocatalytic activity via microstructure modulation. </LI> <LI> The charge separation and transfer process are monitored by transient photovoltaic and photocurrent measurement. </LI> </UL> </P>

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        Discovery of the Early Paleozoic Akechukesai high-Mg diorites in the western segment of East Kunlun Orogenic Belt and its constraints on the mechanism of break-off from Proto-Tethys oceanic subducted slab

        Chao Wang,Fengyue Sun,Dongwei Liu,Lei Zuo,Tuofei Zhao,Jiaming Yan 한국지질과학협의회 2022 Geosciences Journal Vol.26 No.1

        High-Mg andesites (HMAs) and their cognate intrusive rocks constitute volumetrically very small proportions of the total earth, and are mainly distributed along the edges of convergent plates. Petrogenetic studies can provide possible solutions for discrepancies in the geodynamics and subduction zone evolution. This paper presents the first ever reports of the newly discovered high-Mg diorite in Akechukesai area, the western part of the East Kunlun Orogenic Belt, and provides a reference for the evolutionary history and subduction mechanism of the Proto-Tethys Ocean. Akechukesai high-Mg diorites yielded a weighted mean zircon U-Pb dating age of 427.3 ± 2.3Ma (Middle Silurian). Results of the geochemical analyses show that the high-Mg diorites were high-K calc-alkaline series with the SiO2 content ranging 50.40 to 55.41 wt%. They are characterized by high values of Mg# (67–77), high MgO (6.92–10.58 wt%), TiO2 (0.53–0.87 wt%), Cr (286–615 ppm), Ni (61–124 ppm), Ba (570–927 ppm) contents, and low FeOtotal/MgO ratios (0.54–0.89). Furthermore, they exhibit nearly flat right-declined rare-earth element (REE) patterns with slight LREE enrichment. The samples are enriched in large ion lithophile elements (e.g., Ba, Rb, and Th) and depleted in high field strength elements (e.g., Ta, Nb, and Ti). These geochemical features are analogous to the sanukitic high-Mg andesites. The mean value of the initial εHf(t) is –1.3, indicating that the source is enriched mantle. The values of Rb/Cs, Ba/La, and La/Sm ratios suggest that subducting sediments formed an important component of the magmatic source. The presence of water-bearing minerals such as amphibole and biotite indicate a water-rich and oxygen-rich primitive magma system. Petrogenetic analysis indicates that the Akechukesai high-Mg diorites probably formed by melts and aqueous fluids produced from partial melting of the subducting sediments interacting with mantle peridotites. We hypothesize that, after the closure of the Proto-Tethys Ocean Basin in the Middle Silurian, the deep subducted slab broke-off and formed a slab window, asthenospheric material upwelled heating the subducting sediments and causing them to melt. Thus, we suggest that the emplacement of the Akechukesai high-Mg diorites mark the commencement of post-collisional magmatism.

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