排序方式: 共有59条查询结果,搜索用时 234 毫秒
1.
2.
M. Talebi-Esfandarani S. Rousselot M. Gauthier P. Sauriol G. Liang M. Dollé 《Journal of Solid State Electrochemistry》2016,20(7):1821-1829
LiFePO4/C material has been prepared using fast-melt synthesis method followed by grinding and carbon coating. The low-cost iron ore concentrate (IOC) and purified iron ore concentrate (IOP) were used as iron precursors in the melt process to reduce significantly the cost of LiFePO4/C. The same product was also synthesized using pure Fe2O3 under similar conditions as reference. The physical-chemical and electrochemical properties of samples were investigated. The X-ray Diffraction (XRD) results confirm the formation of an olivine structure of LiFePO4 with a minor amount of Li3PO4 and Li4P2O7 impurities for all the samples but no Fe2P. The power performances of LiFePO4/C using low-cost iron precursors were close to the sample using pure Fe2O3 precursor although capacity in mAh g?1 is somewhat lower. With the inherent presence of silicon and other metals species, multi-substitution may take place when using IOC as source of iron leading to a Li(Fe1-yMy)(P1-xSix)O4 general composition. Multi-substitution, however, allows a better cycling stability. Therefore, these iron precursors present a promising option in this field to reduce the cost of a large-scale synthesis of LiFePO4/C for Li-ion batteries application. 相似文献
3.
Morgane Rosendale Jonathan Daniel Frdric Castet Paolo Pagano Jean-Baptiste Verlhac Mireille Blanchard-Desce 《Molecules (Basel, Switzerland)》2022,27(7)
Molecular-based Fluorescent Organic Nanoparticles (FONs) are versatile light-emitting nano-tools whose properties can be rationally addressed by bottom-up molecular engineering. A challenging property to gain control over is the interaction of the FONs’ surface with biological systems. Indeed, most types of nanoparticles tend to interact with biological membranes. To address this limitation, we recently reported on two-photon (2P) absorbing, red to near infrared (NIR) emitting quadrupolar extended dyes built from a benzothiadiazole core and diphenylamino endgroups that yield spontaneously stealth FONs. In this paper, we expand our understanding of the structure-property relationship between the dye structure and the FONs 2P absorption response, fluorescence and stealthiness by characterizing a dye-related series of FONs. We observe that increasing the strength of the donor end-groups or of the core acceptor in the quadrupolar (D-π-A-π-D) dye structure allows for the tuning of optical properties, notably red-shifting both the emission (from red to NIR) and 2P absorption spectra while inducing a decrease in their fluorescence quantum yield. Thanks to their strong 1P and 2P absorption, all FONs whose median size varies between 11 and 28 nm exhibit giant 1P (106 M−1.cm−1) and 2P (104 GM) brightness values. Interestingly, all FONs were found to be non-toxic, exhibit stealth behaviour, and show vanishing non-specific interactions with cell membranes. We postulate that the strong hydrophobic character and the rigidity of the FONs building blocks are crucial to controlling the stealth nano-bio interface. 相似文献
4.
5.
6.
F. Bernard C. Rousselot L. Hirsinger P. Delobelle 《The European physical journal. Special topics》2008,158(1):187-191
The Ni2MnGa ferromagnetic alloys are one of these smart materials, that show a great interest for micro-electromechanical systems
(MEMS) and micro-opto-electromechanical systems (MOEMS) when they are
deposited as a thin film by rf sputtering. These films can be sputtered on
silicon wafer in order to be easily integrated in Si-based device. Indeed,
the use of this kind of substrate is very interesting because of the several
well-known micromachining and integration technologies. However only heat
treated thin films shows good functional properties that lay the problem of
the silicon diffusion, as usually observed in the literature. In this work,
a process (rf-sputtering process and annealing treatment) is proposed to
elaborate martensite Ni2MnGa thin films on Si substrate without silicon diffusion. This paper presents results on samples annealed at 873 K during
6 h. 相似文献
7.
Synthesis of Carbon/Sulfur Nanolaminates by Electrochemical Extraction of Titanium from Ti2SC
下载免费PDF全文
![点击此处可从《Angewandte Chemie (International ed. in English)》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Dr. Meng‐Qiang Zhao Morgane Sedran Zheng Ling Maria R. Lukatskaya Olha Mashtalir Michael Ghidiu Boris Dyatkin Darin J. Tallman Prof. Thierry Djenizian Prof. Michel W. Barsoum Prof. Yury Gogotsi 《Angewandte Chemie (International ed. in English)》2015,54(16):4810-4814
Herein we electrochemically and selectively extract Ti from the MAX phase Ti2SC to form carbon/sulfur (C/S) nanolaminates at room temperature. The products are composed of multi‐layers of C/S flakes, with predominantly amorphous and some graphene‐like structures. Covalent bonding between C and S is observed in the nanolaminates, which render the latter promising candidates as electrode materials for Li‐S batteries. We also show that it is possible to extract Ti from other MAX phases, such as Ti3AlC2 , Ti3SnC2 , and Ti2GeC, suggesting that electrochemical etching can be a powerful method to selectively extract the “M” elements from the MAX phases, to produce “AX” layered structures, that cannot be made otherwise. The latter hold promise for a variety of applications, such as energy storage, catalysis, etc. 相似文献
8.
Bibienne Thomas Maillaud Laurent Rousselot Steeve Taylor Lauren W. Pasquali Matteo Dollé Mickaël 《Journal of Solid State Electrochemistry》2017,21(5):1407-1416
Journal of Solid State Electrochemistry - The preparation of collector- and binder-free, high-energy density cathodes made from carbon-coated LiFePO4 (C-LFP) and single-walled carbon nanotubes... 相似文献
9.
10.
Dr. Toni Moragas Dr. Morgane Gaydou Prof. Ruben Martin 《Angewandte Chemie (International ed. in English)》2016,55(16):5053-5057
A user‐friendly Ni‐catalyzed reductive carboxylation of benzylic C?N bonds with CO2 is described. This procedure outperforms state‐of‐the‐art techniques for the carboxylation of benzyl electrophiles by avoiding commonly observed parasitic pathways, such as homodimerization or β‐hydride elimination, thus leading to new knowledge in cross‐electrophile reactions. 相似文献