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91.
Wei-Jie Ou Chen-Shan Kao Yih-Shing Duh Jing-Ming Hsu 《Journal of Thermal Analysis and Calorimetry》2014,116(3):1111-1116
Thermal instability of lithiated cathode materials with organic carbonate were investigated using DSC. Lithium transition metal oxides of LiFePO4, LiMn2O4, and LiCoO2 were mixed with diethyl carbonate, dimethyl carbonate, ethylene carbonate, ethyl methyl carbonate, and propylene carbonate then dynamically screened to about 500 °C. Curves were acquired and analyzed to determine exothermic onset temperatures and reaction enthalpies. These data for assessing the thermal hazards of lithium-ion batteries under discharged conditions were compared to those data published in the literature. 相似文献
92.
Highly Efficient Electrocatalysts for Oxygen Reduction Based on 2D Covalent Organic Polymers Complexed with Non‐precious Metals 下载免费PDF全文
Dr. Zhonghua Xiang Dr. Yuhua Xue Prof. Dapeng Cao Ling Huang Prof. Jian‐Feng Chen Prof. Liming Dai 《Angewandte Chemie (International ed. in English)》2014,53(9):2433-2437
A class of 2D covalent organic polymers (COPs) incorporating a metal (such as Fe, Co, Mn) with precisely controlled locations of nitrogen heteroatoms and holes were synthesized from various N‐containing metal–organic complexes (for example, metal–porphyrin complexes) by a nickel‐catalyzed Yamamoto reaction. Subsequent carbonization of the metal‐incorporated COPs led to the formation of COP‐derived graphene analogues, which acted as efficient electrocatalysts for oxygen reduction in both alkaline and acid media with a good stability and free from any methanol‐crossover/CO‐poisoning effects. 相似文献
93.
利用浸渍法制备稀土改质催化剂,用于废食用油脂催化裂解的裂解气催化改质。考察了催化剂活性组分含量、硅铝比、焙烧温度、改质反应温度对产物组成、烯烃含量及收率的影响。得最佳条件:ZSM-5作为催化剂载体,催化剂活性组分镧稀土含量为6%,催化剂焙烧温度为550℃,改质反应温度为360℃。在最佳条件下催化改质,燃料油烯烃含量降低了34.3%,汽油含量提高了14.36%,轻柴油含量提高了1.67%,重柴油含量下降了6.72%,重油含量下降了2.2%,燃料油总收率提高了7.12%,油品质显著提高。 相似文献
94.
Pingchun Wei Kai Zhang Dr. Xin Li Deying Meng Prof. Dr. Hans Ågren Prof. Dr. Zhongping Ou Prof. Dr. Seikweng Ng Prof. Dr. Hiroyuki Furuta Prof. Dr. Yongshu Xie 《Angewandte Chemie (International ed. in English)》2014,53(51):14069-14073
The first neo‐confused hexaphyrin(1.1.1.1.1.0) was synthesized by oxidative ring closure of a hexapyrrane bearing two terminal “confused” pyrroles. The new compound displays a folded conformation with a short interpyrrolic C???N distance of 3.102 Å, and thus it readily underwent ring fusion to afford a neo‐fused hexaphyrin with an unprecedented 5,5,5,7‐tetracyclic ring structure. Furthermore, coordination of CuII triggered a ring opening/contracting reaction to afford a CuII complex of an N‐linked pentaphyrin derivative. The roles of reactive N? C bonds in the porphyrinoid macrocycles were demonstrated. 相似文献
95.
96.
Yingrui Shang Jing Zhao Jingqing Li Zhonghua Wu Shichun Jiang 《Colloid and polymer science》2014,292(12):3205-3221
The influence of annealing on the microstructure and mechanical properties of β-form isotactic polypropylene (iPP) was investigated via in situ synchrotron small-angle X-ray scattering (SAXS), wide-angle X-ray diffraction (WAXD), and differential scanning calorimetry (DSC). Transition of β-iPP to α-iPP was investigated via recrystallization at high annealing temperatures (T a?>?120 °C). And crystallinity, crystal sizes, and long period of ordered structure increased with increasing annealing temperature. Abrupt changes were found in both mechanical properties and structural features at the same T a range (~120 °C). The in situ synchrotron SAXS and WAXD shows that the destruction of b phase at yielding and after yielding should account for the ductility of β-iPP. The thermodynamics and kinetics of annealing were investigated with DSC and X-ray synchrotron experiments. A characteristic annealing time was investigated, which measures the rate of phase evolution in annealing of β-iPP. Eventually, a hypothesized model can be used to describe the property/structure relations during this process. 相似文献
97.
A pair of enantiomers formulated as {Δ-cis-[Ni(en)2OAc][ClO4]} n (Δ-1) and {Λ-cis-[Ni(en)2OAc][ClO4]} n (Λ-1) (en = diaminoethane, OAc? = acetate anion) were obtained when nickel acetate was reacted with diaminoethane and sodium perchlorate in the absence of any chiral source, whereas the reactions of nickel acetate with 1,3-propanediamine and sodium perchlorate only gave a centrosymmetric complex [Ni(1,3-pn)2OAc][ClO4] (2) (1,3-pn = 1,3-propanediamine). Single-crystal X-ray diffraction analyses of all three complexes indicated that the central Ni(II) atoms all have a distorted octahedral coordination geometry, being coordinated by four nitrogen atoms of the diamine ligands, plus two oxygen atoms of OAc?. In complexes Δ-1 and Λ-1, the monomers of {Δ-cis-[Ni(en)2OAc]}+ and {Λ-cis-[Ni(en)2OAc]}+ are connected through intermolecular hydrogen bonds to generate one-dimensional right- and left-handed homochiral helical chains, respectively, while the monomers of [Ni(1,3-pn)2OAc]+ are linked by similar intermolecular hydrogen bonds to form one-dimensional zigzag chains instead of helical chains. The chiral natures of complexes Δ-1 and Λ-1 have been confirmed by circular dichroism spectroscopy. 相似文献
98.
Dr. Weihui Ou Dr. Binbin Zhou Junda Shen Dr. Tsz Wing Lo Prof. Dangyuan Lei Dr. Shengliang Li Jing Zhong Prof. Yang Yang Li Prof. Jian Lu 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(17):6856-6859
Hot carriers (HCs) and thermal effects, stemming from plasmon decays, are crucial for most plasmonic applications. However, quantifying these two effects remains extremely challenging due to the experimental difficulty in accurately measuring the temperature at reaction sites. Herein, we provide a novel strategy to disentangle HCs from photothermal effects based on the different traits of heat dissipation (long range) and HCs transport (short range), and quantitatively uncover the dominant and potential-dependent role of photothermal effect by investigating the rapid- and slow-response currents in plasmon-mediated electrochemistry at nanostructured Ag electrode. Furthermore, the plasmoelectric surface potential is found to contribute to the rapid-response currents, which is absent in the previous studies. 相似文献
99.
Dr. Linzhou Zhuang Dr. Yi Jia Hongli Liu Zhiheng Li Dr. Mengran Li Dr. Longzhou Zhang Dr. Xin Wang Prof. Dongjiang Yang Prof. Zhonghua Zhu Prof. Xiangdong Yao 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(34):14772-14778
The oxygen vacancies of defective iron–cobalt oxide (FeCoOx-Vo) nanosheets are modified by the homogeneously distributed sulfur (S) atoms. S atoms can not only effectively stabilize oxygen vacancies (Vo), but also form the Co−S coordination with Co active site in the Vo, which can modulate the electronic structure of the active site, enabling FeCoOx-Vo-S to exhibit much superior OER activity. FeCoOx-Vo-S exhibits a mass activity of 2440.0 A g−1 at 1.5 V vs. RHE in 1.0 m KOH, 25.4 times higher than that of RuO2. The Tafel slope is as low as 21.0 mV dec−1, indicative of its excellent charge transfer rate. When FeCoOx-Vo-S (anode catalyst) is paired with the defective CoP3/Ni2P (cathode catalyst) for overall water splitting, current densities of as high as 249.0 mA cm−2 and 406.0 mA cm−2 at a cell voltage of 2.0 V and 2.3 V, respectively, can be achieved. 相似文献
100.
Yiyi Ou Dr. Weijie Zhou Dr. Zece Zhu Dr. Fengkai Ma Dr. Rongfu Zhou Fang Su Dr. Lirong Zheng Prof. Li Ma Prof. Hongbin Liang 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(52):24018-24024
Optical multiplexing based on luminescent materials with tunable color/lifetime has potential applications in information storage and security. However, the available tunable luminescent materials reported so far still suffer from several drawbacks of low efficiency or poor stability, thus restraining their further applications. Herein, we demonstrate a strategy to develop efficient and stable lanthanide coordination polymers (LCPs) with tunable luminescence as a new option for optical multiplexing. Their multicolor emission from green to red and naked-eye-sensitive green emission with tunable lifetime (from ca. 300 to ca. 600 μs) can be controlled by host differential sensitization and energy transfer between lanthanide ions. The quantum efficiencies of developed samples range from around 20 % to 46 % and the luminescence intensity/lifetime appear quite stable in polar solvents up to ten weeks. Furthermore, with the aid of inkjet printing and concepts of luminescence lifetime imaging and time-gated imaging, we illustrate their promising applications of information storage and security in spatial and temporal domains. 相似文献