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991.
Guangyin Li Zhanjun Zhang Zhenlei Huang Chengkai Yang Zicheng Zuo Henghui Zhou 《Journal of Solid State Electrochemistry》2017,21(3):673-682
Effect of secondary particle fracture on the accumulated cycle capacity fade of LiNi1-x-yCoxMnyO2 cathode is difficult to evaluate since performance degradation of electrode material is always caused by several factors simultaneously. Herein, LiNi0.5Co0.2Mn0.3O2 single particles (Sin-P) are prepared and introduced as a reference to understand the accumulated cycle capacity fade caused by the secondary particle fracture of LiNi0.5Co0.2Mn0.3O2 secondary particles (Sec-P). Sec-P exhibited accumulated cycle capacity fade compared to Sin-P when cycled at high rate, high voltage, and high temperature. The accumulated cycle capacity fade was mainly caused by the secondary particle fracture of Sec-P, which was confirmed by the X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and scanning electron microscope (SEM) analysis. Further, XPS and electrochemical impedance spectroscopy (EIS) analysis indicated that the surface property changes and resistance rise were responsible for the accumulated cycle capacity fade. The study provides a novel way to analyze the accumulated cycle capacity fade caused by the secondary particle fracture and is helpful for understanding the performance degradation mechanism of electrode material. 相似文献
992.
Shu Xia Wang Yan Qin Yongqiang Yu Cuiping Zhang Jianfang Zhao Jiebo Cui Jiewu Cui Lihua Zheng Hongmei Zhang Yong Wang Wenfang Wu Yucheng 《Journal of Solid State Electrochemistry》2017,21(5):1489-1497
Journal of Solid State Electrochemistry - Binder-free, high-performance electrode materials play a critical role for supercapacitors. In this paper, through the electrochemical anodization process,... 相似文献
993.
Zhang Ya Zhou Zhifeng Wen Fangfang Yuan Kechun Tan Jin Zhang Zilan Wang Honggui 《Journal of Solid State Electrochemistry》2017,21(12):3649-3657
Journal of Solid State Electrochemistry - Bacterial cellulose (BC) is a polysaccharide with tubular structure and can be produced by various species of bacteria particularly Acetobacter xylinum. It... 相似文献
994.
Wang Jiajia Yin Haixia Chen Jingshuai Niu Helin Mao Changjie Song Jiming Jin Baokang Tian Yupeng Zhang Shengyi 《Journal of Solid State Electrochemistry》2017,21(8):2381-2391
Journal of Solid State Electrochemistry - A hydrophilic polypyrrole/tellurium (PPy/Te) nanocomposite was synthesized by a facile approach in which H2TeO3 was used as the oxidizing agent of pyrrole... 相似文献
995.
Wolfram Kohs Jürgen Kahr Anwar Ahniyaz Ningxin Zhang Atanaska Trifonova 《Journal of Solid State Electrochemistry》2017,21(12):3389-3401
The electrolyte/electrode interactions on the anode side of a lithium-ion cell and the formation of the solid electrolyte interphase (SEI) have been investigated intensively in the past and are fairly well understood. Present knowledge about the reactions on the cathode side and the resulting cathode electrolyte interphase (CEI) is less detailed. In this study, the electrolyte/electrode interactions on the surface of the high-voltage cathode material LiNi0.5Mn1.5O4 (LNMO), both bare and FePO4-coated, were investigated. The gases evolving upon first time charging of the system were investigated using a GC/MS combination. The degradation products included THF, dimethyl peroxide, phosphor trifluoride, 1,3-dioxolane and dimethyl difluor silane, formed in the GC’s column as its coating reacts with HF from the experiments. Although these substances and their formation are in themselves interesting, the absence of many degradation products which have been mentioned in the existing literature is of equal interest. Our results clearly indicate that coating a cathode material can have a major influence on the amount and composition of the gaseous decomposition products in the formation phase. 相似文献
996.
Longlu Wang Xia Liu Jinming Luo Xidong Duan Prof. John Crittenden Prof. Chengbin Liu Shuqu Zhang Prof. Yong Pei Yunxiong Zeng Prof. Xiangfeng Duan 《Angewandte Chemie (International ed. in English)》2017,56(26):7610-7614
The metallic 1T-MoS2 has attracted considerable attention as an effective catalyst for hydrogen evolution reactions (HERs). However, the fundamental mechanism about the catalytic activity of 1T-MoS2 and the associated phase evolution remain elusive and controversial. Herein, we prepared the most stable 1T-MoS2 by hydrothermal exfoliation of MoS2 nanosheets vertically rooted into rigid one-dimensional TiO2 nanofibers. The 1T-MoS2 can keep highly stable over one year, presenting an ideal model system for investigating the HER catalytic activities as a function of the phase evolution. Both experimental studies and theoretical calculations suggest that 1T phase can be irreversibly transformed into a more active 1T′ phase as true active sites in photocatalytic HERs, resulting in a “catalytic site self-optimization”. Hydrogen atom adsorption is the major driving force for this phase transition. 相似文献
997.
Dr. Changkun Zhang Yu Ding Leyuan Zhang Xuelan Wang Prof. Yu Zhao Prof. Xiaohong Zhang Prof. Guihua Yu 《Angewandte Chemie (International ed. in English)》2017,56(26):7454-7459
Nonaqueous redox-flow batteries are an emerging energy storage technology for grid storage systems, but the development of anolytes has lagged far behind that of catholytes due to the major limitations of the redox species, which exhibit relatively low solubility and inadequate redox potentials. Herein, an aluminum-based deep-eutectic-solvent is investigated as an anolyte for redox-flow batteries. The aluminum-based deep-eutectic solvent demonstrated a significantly enhanced concentration of circa 3.2 m in the anolyte and a relatively low redox potential of 2.2 V vs. Li+/Li. The electrochemical measurements highlight that a reversible volumetric capacity of 145 Ah L−1 and an energy density of 189 Wh L−1 or 165 Wh kg−1 have been achieved when coupled with a I3−/I− catholyte. The prototype cell has also been extended to the use of a Br2-based catholyte, exhibiting a higher cell voltage with a theoretical energy density of over 200 Wh L−1. The synergy of highly abundant, dendrite-free, multi-electron-reaction aluminum anodes and environmentally benign deep-eutectic-solvent anolytes reveals great potential towards cost-effective, sustainable redox-flow batteries. 相似文献
998.
Ki Dong Yang Woo Ri Ko Jun Ho Lee Prof. Sung Jae Kim Prof. Hyomin Lee Prof. Min Hyung Lee Prof. Ki Tae Nam 《Angewandte Chemie (International ed. in English)》2017,56(3):796-800
The electrocatalytic conversion of CO2 to value-added hydrocarbons is receiving significant attention as a promising way to close the broken carbon-cycle. While most metal catalysts produce C1 species, such as carbon monoxide and formate, the production of various hydrocarbons and alcohols comprising more than two carbons has been achieved using copper (Cu)-based catalysts only. Methods for producing specific C2 reduction outcomes with high selectivity, however, are not available thus far. Herein, the morphological effect of a Cu mesopore electrode on the selective production of C2 products, ethylene or ethane, is presented. Cu mesopore electrodes with precisely controlled pore widths and depths were prepared by using a thermal deposition process on anodized aluminum oxide. With this simple synthesis method, we demonstrated that C2 chemical selectivity can be tuned by systematically altering the morphology. Supported by computational simulations, we proved that nanomorphology can change the local pH and, additionally, retention time of key intermediates by confining the chemicals inside the pores. 相似文献
999.
Changping Wang Prof. Qiang Zhang Xinyu Wang Hong Chang Prof. Sanjun Zhang Yuankai Tang Prof. Jianhua Xu Ruijuan Qi Prof. Yiyun Cheng 《Angewandte Chemie (International ed. in English)》2017,56(24):6767-6772
Engineering near-infrared (NIR) light-sensitive enzymes remains a huge challenge. A photothermal effect-associated method is developed for tailoring the enzymatic activity of enzymes by exposure to NIR light. An ultrasmall platinum nanoparticle was anchored in an enzyme to generate local heating upon NIR irradiation, which enhanced the enzyme activity without increasing bulk temperature. Following NIR irradiation, the enzyme activity was tailored rapidly and reversibly, and was modulated by varying laser power density and irradiation time. Four enzymes were engineered, including glucoamylase, glucose oxidase, catalase, and proteinase K with NIR-light sensitivity, and demonstrated their utility in practical applications such as photolithography and NIR light-responsive antibacterial or anticancer actions. Our investigation suggests that this approach could be broadly used to engineer enzymes with NIR-light sensitivity for many biological applications. 相似文献
1000.
Microencapsulated phase change materials with paraffin as the core material were synthesized by interfacial polymerization of isophorone diisocyanate with diethylene triamine. The particle size and particle size distribution, morphology, thermal performance and the encapsulation efficiency of the prepared materials were investigated. The results of Fourier transform infrared spectrometer and X-ray photoelectron spectroscopy suggested that the paraffin core was well encapsulated by the polyurea resin. The particle size of the prepared materials decreased and its distribution became narrow with the increase of the emulsification time, stirring speed and emulsifier amount. The thermal gravimetric analysis indicated that the prepared materials exhibited good thermal stability, while the differential scanning calorimetry their high encapsulation efficiency. 相似文献