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141.
The critical behavior of passive mode locking has been demonstrated in a figure-eight fiber laser that performs rational harmonic mode locking (RHML). On both the repetition rate and the pulse amplitude distribution, the observed pulse trains near the threshold exhibit the same regulations as the rational harmonic mode-locked ones. The theory also shows that there should be a middle status of RHML before achieving normal mode locking. It is important to note that the results provide what we believe to be the first confirmed attempt to address a fundamental question: how does a laser become mode locking with an increase of pump power? 相似文献
142.
锂金属二次电池具有极高的能量密度,是下一代储能电池的研究热点。然而,金属锂负极在传统碳酸酯电解液1 mol·L?1 LiPF6-EC/DEC(ethylene carbonate/diethyl carbonate)中充放电时,存在严重的枝晶生长和循环效率低下等问题,阻碍了其商业化应用。因此,开发与锂负极兼容的新型电解液体系是目前重要的研究任务。与传统稀溶液相比,高浓度电解液体系具有独有的物化性质和优异的界面相容性,并且能有效抑制锂枝晶生长、显著提升锂负极的循环可逆性,因而格外受到关注。本文综述了高浓度电解液及局部高浓电解液体系的最新研究进展,分析了其溶液化学结构和物化性质,对其与锂负极的界面相容性、枝晶抑制效果、效率提升能力及界面稳定性机制进行了探讨;文章着重介绍了高浓与局部高浓电解液体系在锂金属二次电池中的应用,同时从基础科学研究和应用研究两个层面对高浓电解液和局部高浓电解液存在的主要问题进行了简要分析,并对其未来发展方向进行了展望。 相似文献
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145.
Nano-carbon connections among carbon-coated LiFe0.8Mn0.2PO4 grains are successfully constructed using polyacrylic acid and sucrose as carbon sources by sol-gel method, which can improve the electrochemical performance of LiFe0.8Mn0.2PO4. Samples were characterised by X-ray diffraction, scanning electron microscopy and electrochemical tests. The electrochemical tests show LiFe0.8Mn0.2PO4 grains connected by nano-carbon networks obtain the discharge specific capacity of 165 mA h g?1 at 0.1 C rate and excellent rate capability. Its specific capacity reaches 122 mA h g?1 at 5 C rate. Its capacity retention at 5 C rate attains 97% cycled 100 cycles. Therefore the construction of nano-carbon networks offers an effective and convenient technique to improve the specific capacities and rate capabilities of electrode materials of low electronic conductivity. 相似文献
146.
Time‐Resolved Assembly of Cluster‐in‐Cluster {Ag12}‐in‐{W76} Polyoxometalates under Supramolecular Control 下载免费PDF全文
Caihong Zhan Jamie M. Cameron Jing Gao Jamie W. Purcell De‐Liang Long Leroy Cronin 《Angewandte Chemie (International ed. in English)》2014,53(39):10362-10366
We report the time‐resolved supramolecular assembly of a series of nanoscale polyoxometalate clusters (from the same one‐pot reaction) of the form: [H(10+m)Ag18Cl(Te3W38O134)2]n, where n=1 and m=0 for compound 1 (after 4 days), n=2 and m=3 for compound 2 (after 10 days), and n=∞ and m=5 for compound 3 (after 14 days). The reaction is based upon the self‐organization of two {Te3W38} units around a single chloride template and the formation of a {Ag12} cluster, giving a {Ag12}‐in‐{W76} cluster‐in‐cluster in compound 1 , which further aggregates to cluster compounds 2 and 3 by supramolecular Ag‐POM interactions. The proposed mechanism for the formation of the clusters has been studied by ESI‐MS. Further, control experiments demonstrate the crucial role that TeO32?, Cl?, and Ag+ play in the self‐assembly of compounds 1 – 3 . 相似文献
147.
Voltage‐Driven Reversible Insertion into and Leaving from a Lipid Bilayer: Tuning Transmembrane Transport of Artificial Channels 下载免费PDF全文
Wen Si Prof. Zhan‐Ting Li Prof. Jun‐Li Hou 《Angewandte Chemie (International ed. in English)》2014,53(18):4578-4581
Three new artificial transmembrane channel molecules have been designed and synthesized by attaching positively charged Arg‐incorporated tripeptide chains to pillar[5]arene. Fluorescent and patch‐clamp experiments revealed that voltage can drive the molecules to insert into and leave from a lipid bilayer and thus switch on and off the transport of K+ ions. One of the molecules was found to display antimicrobial activity toward Bacillus subtilis with half maximal inhibitory concentration (IC50) of 10 μM which is comparable to that of natural channel‐forming peptide alamethicin. 相似文献
148.
Hui Zhang Kan Zhan Yulu Chen Guoxia Chen Xiaomei Zhou Junxiu Liu Min Wu Henmei Ni 《Journal of Sol-Gel Science and Technology》2014,71(3):597-605
Three dimensional Liesegang spherical layers of CaHPO4 in gelatin ball were performed by employing CaCl2 and Na2HPO4 as the inner and outer electrolyte, respectively. Effects of concentrations of inner and outer electrolyte as well as pH on the morphologies of Liesegang rings (LRs) were investigated. As a result, it was observed that the time law, spacing law and width law found in 1D/2D gel systems were obeyed in this 3D gelatin system. The interaction of Ca2+ and HPO4 2? with gelatin matrix played a key role to the formation of LRs due to the existence of carboxylic groups on the gelatin chains. Using Ca2+ as the inner electrolyte, LRs were prepared. However, employing HPO4 2? as inner electrolyte, LRs were not obtained. Moreover, pH of gelatin solution greatly impacted on the formation of LRs. The number of LRs increased with the decrease of pH, whereas the width inversely decreased. pH 4.40 was a turn point, from which the spacing coefficient abruptly increased as pH increased. All these results indicated that the network was created by the interaction of Ca2+ and –COO? of gelatin chains, which dominated the formation of CaHPO4 LRs in gelatin. 相似文献
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150.
Qingyi Cao Yahui Qian Handong Liang Zhanping Li Siyao Chen Liu Yang Qin Zhan 《Surface and interface analysis : SIA》2020,52(5):283-292
Pyrite is considered to be the major carrier of mercury in coal. Here, the chemical characteristics of two natural pyrite samples of different weathering degrees were characterized by time-of-flight secondary ion mass spectrometry (TOF-SIMS). Thermal stability of Hg was also analyzed via temperature programmed desorption experiment (TPD). Characteristic ions such as S−, Fe+, FeS−, and FeS2− were detected on the surface of fresh pyrite. The release temperature of Hg ranged between 180°C and 300°C, and the characteristic peak of black HgS was recorded. In addition, abundant Fe2O3−, FeSO−, SO4−, and HSO4− were detected on the surface of weathered pyrite, and the release temperature of Hg therein was mainly distributed at 260°C to 380°C and 520°C to 600°C, corresponding to the characteristic peaks of red HgS and HgSO4, respectively. The results show that pyrite is acidified during weathering and that Hg forms in pyrite are transformed from the original state (HgS) to HgSO4. 相似文献