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71.
The polarization of a D-shaped fiber is modulated after immersing it in magnetic fluid(MF)and applying a magnetic field.Theoretical analysis predicts that magneto-optical dichroism of MF plays a key role in light polarization modulation.During light polarization modulation,the evanescent wave polarized parallel to the magnetic field has greater loss than its orthogonal component.Light polarization of a D-shaped fiber with a wide polished surface can be modulated easily.High concentration MF and a large magnetic field all have great ability to modulate light polarization. 相似文献
72.
QiuHong Wang Abdusalam Abdukerim Wei Chen Xun Chen YunHua Chen XiangYi Cui YingJie Fan DeQing Fang ChangBo Fu LiSheng Geng Karl Giboni Franco Giuliani LinHui Gu XuYuan Guo Ke Han ChangDa He Di Huang Yan Huang YanLin Huang Zhou Huang Peng Ji XiangDong Ji YongLin Ju YiHui Lai Kun Liang HuaXuan Liu JiangLai Liu WenBo Ma YuGang Ma YaJun Mao Yue Meng Parinya Namwongsa KaiXiang Ni JinHua Ning XuYang Ning XiangXiang Ren ChangSong Shang Lin Si AnDi Tan AnQing Wang HongWei Wang Meng Wang SiGuang Wang XiuLi Wang Zhou Wang MengMeng Wu ShiYong Wu JingKai Xia MengJiao Xiao PengWei Xie BinBin Yan JiJun Yang Yong Yang ChunXu Yu Jumin Yuan Dan Zhang HongGuang Zhang Tao Zhang Li Zhao QiBin Zheng JiFang Zhou Ning Zhou XiaoPeng Zhou 《中国科学:物理学 力学 天文学(英文版)》2020,(3):54-63
In dark matter direct detection experiments,neutron is a serious source of background,which can mimic the dark matter-nucleus scattering signals.In this paper,we present an improved evaluation of the neutron background in the PandaX-II dark matter experiment by a novel approach.Instead of fully relying on the Monte Carlo simulation,the overall neutron background is determined from the neutron-induced high energy signals in the data.In addition,the probability of producing a dark-matter-like background per neutron is evaluated with a complete Monte Carlo generator,where the correlated emission of neutron(s)andγ(s)in the(α,n)reactions and spontaneous fissions is taken into consideration.With this method,the neutron backgrounds in the Run 9(26-ton-day)and Run 10(28-ton-day)data sets of PandaX-II are estimated to be(0.66±0.24)and(0.47±0.25)events,respectively. 相似文献
73.
Xia Caifen Fu Boqiao Jin Jian-Cheng 《Journal of Thermal Analysis and Calorimetry》2022,147(22):12561-12567
Journal of Thermal Analysis and Calorimetry - Nd compounds have been widely used for the promotion of growth of plant due to their excellent biophysical and biochemical properties. Mitochondria are... 相似文献
74.
Xinfeng Zhu Yanli Mao Hongpan Liu Haiyan Kang Biao Liu Zhongxian Song Xueping Liu Yifei Guo Huixian Du Qiulin Zhang 《应用有机金属化学》2020,34(2):e5285
FeOx, TiO2, and Fe–Ti–Ox catalysts were synthesized and used in the catalytic hydrolysis of hydrogen cyanide (HCN). Nearly 100% HCN conversion was achieved at 250 °C over the Fe–Ti–Ox catalyst. TiO2 rutile was detected over TiO2, but not over Fe–Ti–Ox, which suggested that the interaction between Fe and Ti species could inhibit the TiO2 phase transition. Furthermore, the interaction between Fe and Ti species over Fe–Ti–Ox could promote the selectivity of NH3 and CO. The mechanism of hydrolysis of HCN over FeOx, TiO2, and Fe–Ti–Ox can be given as follows: HCN + H2O → methanamide → ammonium formate → formic acid → H2O + CO. 相似文献
75.
Xiao Ma Chongying Xu Zhibiao Mao Peiyu Ji Chenggang Jin Dongsheng Xu Yuqiang Ding 《应用有机金属化学》2020,34(2):e5349
A series of chemical vapor deposition (CVD) precursors have been synthesized by a single-step reaction of 1,1,3,3-tetramethylguanidine and a variety of silicon chlorides. The structures of the 1,1,3,3-tetramethylguanidinate-based compounds were verified by 1H NMR, 13C NMR, XPS, EI-MS, and elemental analysis. The thermal stability, transport behavior, and vapor pressures of these compounds were evaluated by simultaneous thermal analyses (STA). These compounds are highly stable and those in liquid form are very volatile. Silicon carbonitride (SiCN) thin films were prepared by using bis (tetramethylguanidine)-dimethyl-silane as the precursor in helicon wave plasma chemical vapor deposition (HWP-CVD). The properties of the films were investigated by SEM, AFM, and XPS. The results showed that the films have good uniformities, low friction coefficient, and high hardness, enabling the films for fabrication of semiconductor devices. 相似文献
76.
Zhongxian Song Yun Xing Tingji Zhang Jinggang Zhao Junkai Wang Yanli Mao Baolin Zhao Xuejun Zhang Min Zhao Ziang Ma 《应用有机金属化学》2020,34(3):e5446
A series of Ce-Fe-Ox catalysts prepared by the different calcination temperatures (marked as CF-X, where X represented calcination temperature) were used to the selectivity catalytic reduction of NOx by NH3. The results explained the relationship between calcination temperature and the sulfate species over Ce-Fe-Ox, and then investigated the surface acidity and catalytic performance. The large amounts of sulfate species were formed over CF-450 and CF-550 while it was decomposed with further the increasing of calcination temperature, which resulted in the loss of surface acidity, causing a decrease in the catalytic activity over Ce-Fe-Ox. Thereby, the CF-450 catalyst showed the best catalytic activity and over 90% NOx conversion was obtained at 244–450 °C. Besides, the favored pore structure, more Fe3+ active species, higher Ce3+ concentration and the abundance of chemical adsorbed oxygen species, as well as the surface acid sites, would together contribute to the excellent catalytic activity of CF-450 catalyst. 相似文献
77.
Wei-Zhen Sun Lin-Lin Dai Xiang-He Kong Yu Mao Zhi-Lin Wu Li-Fu Liao Xi-Lin Xiao Chang-Ming Nie 《应用有机金属化学》2020,34(4):e5486
The design of new uranyl-ligands (uranyl-Ls) is of great significance for the separation and utilization of uranium. In this paper, the triazole group was introduced into uranyl-salophen (uranyl-S) to form new asymmetric uranyl-unilateral benzotriazole salophen (uranyl-UBS); we further replaced two oxygen atoms of uranyl-UBS with two sulfur atoms to generate uranyl-unilateral benzotriazole thio-salophen (uranyl-UBTS) as a new receptor. Then, we comprehensively explored coordination models of uranyl-UBS and uranyl-UBTS with R/S-triadimefons (R/S-TDFs) enantiomers as the guests using density functional theory calculations at the B3LYP//RECP/6-311G** level; we then investigated enantioselectivity recognition of the new receptors to the guests R/S-TDFs. The results indicated that the uranium atoms of the receptors uranyl-S, uranyl-UBS and uranyl-UBTS could coordinate with the carbonyl oxygens in guests R/S-TDFs to form complexes of guest-receptors R/S-TDFs-uranyl-Ls that exhibited two stable V-shaped structures with quite different properties. It was found that the coordination ability to the guests R/S-TDFs is uranyl-UBTS > uranyl-UBS > uranyl-S, while the enantioselectivity for the guests is uranyl-UBTS > uranyl-S > uranyl-UBS and, when the receptor is the same, R-TDF has stronger coordination ability than S-TDF. These results provide information and theoretical supports for the experiments of asymmetric uranyl-UBS with R/S-TDFs, and produce a reference for further exploring the coordination characteristics of asymmetric uranyl-salophen with the triazole derivatives. 相似文献
78.
Dr. Xue Feng Lu Prof. Bao Yu Xia Prof. Shuang-Quan Zang Prof. Xiong Wen Lou 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(12):4662-4678
In view of the clean and sustainable energy, metal–organic frameworks (MOFs) based materials, including pristine MOFs, MOF composites, and their derivatives are emerging as unique electrocatalysts for oxygen reduction reaction (ORR). Thanks to their tunable compositions and diverse structures, efficient MOF-based materials provide new opportunities to accelerate the sluggish ORR at the cathode in fuel cells and metal–air batteries. This Minireview first provides some introduction of ORR and MOFs, followed by the classification of MOF-based electrocatalysts towards ORR. Recent breakthroughs in engineering MOF-based ORR electrocatalysts are highlighted with an emphasis on synthesis strategy, component, morphology, structure, electrocatalytic performance, and reaction mechanism. Finally, some current challenges and future perspectives for MOF-based ORR electrocatalysts are also discussed. 相似文献
79.
Dr. Xue Liu Dr. Yi Luo Wenting Mao Dr. Jingang Jiang Dr. Hao Xu Prof. Lu Han Prof. Junliang Sun Prof. Peng Wu 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(3):1182-1186
A novel crystalline high-silica zeolite with 12×8-membered ring (R) channel system is prepared with the aid of the 3D electron diffraction (3D ED) technique. A crystal with the same topology as one of the predicted daughter structures of CIT-13 germanosilicate, named ECNU-23 (East China Normal University 23) was coincidentally detected by the 3D ED investigation during the structure characterization of the “pure” powder sample of existing one-dimension (1D) 10-R ECNU-21. By controlling the alkaline-assisted hydrolysis under moderate conditions, we purified the phase of ECNU-23 by selectively breaking and removing the chemically weak Ge(Si)-O-Ge and metastable Si-O-Si bonds. Its structure was determined based on the 3D ED data, and confirmed by high-resolution TEM images and powder X-ray diffraction (PXRD) data. The aluminosilicate Al-ECNU-23 shows unique catalytic properties in the isomerization/ disproportionation of m-xylene as solid-acid catalyst. 相似文献
80.
Wenjun Yang Bo Ling Bowen Hu Haolin Yin Prof. Dr. Jianyou Mao Prof. Dr. Patrick J. Walsh 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(1):167-172
An umpolung 1,4-addition of aryl iodides to enals promoted by cooperative (terpy)Pd/NHC catalysis was developed that generates various bioactive β,β-diaryl propanoate derivatives. This system is not only the first reported palladium-catalyzed arylation of NHC-bound homoenolates but also expands the scope of NHC-induced umpolung transformations. A diverse array of functional groups such as esters, nitriles, alcohols, and heterocycles are tolerated under the mild conditions. This method also circumvents the use of moisture-sensitive organometallic reagents. 相似文献