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用于全固态锂二次电池的高沸点溶剂中磷化镍的择形合成。

Phase-selective synthesis of nickel phosphide in high-boiling solvent for all-solid-state lithium secondary batteries.

机构信息

Department of Applied Chemistry, Graduate School of Engineering, Osaka Prefecture University, Sakai, Osaka 599-8531, Japan.

出版信息

Inorg Chem. 2011 Nov 7;50(21):10820-4. doi: 10.1021/ic2013733. Epub 2011 Oct 3.

Abstract

Nickel phosphide particles were synthesized by thermal decomposition of a nickel precursor in a mixed solution of trioctylphosphine and trioctylphosphine oxide. The crystal phase and morphology of samples prepared by changing the solvents, the amount of trioctylphosphine as a phosphorus source, the reaction temperature, and the nickel precursor were characterized using X-ray diffraction and transmission electron microscopy. Spherical Ni(5)P(4) particles with diameters of 500 nm were obtained using nickel acetylacetonate as a nickel precursor at 360 °C for 1 h in trioctylphosphine oxide. NiP(2) particles with diameters of 200-500 nm were obtained using nickel acetate tetrahydrate at 360 °C for 5 h in trioctylphosphine oxide. All-solid-state cells were fabricated using NiP(2) particles as an active material and 80Li(2)S·20P(2)S(5) (mol %) glass-ceramic as a solid electrolyte. The Li-In/80Li(2)S·20P(2)S(5)/NiP(2) cell exhibited an initial discharge capacity of 1100 mAh g(-1) at a current density of 0.13 mA cm(-2) and retained a discharge capacity of 750 mAh g(-1) after 10 cycles.

摘要

采用三辛基膦(TOP)和三辛基氧化膦(TOPO)的混合溶液,通过热分解镍前体合成了磷化镍颗粒。通过改变溶剂、三辛基膦作为磷源的用量、反应温度和镍前体,用 X 射线衍射和透射电子显微镜对制备的样品的晶体相和形态进行了表征。以乙酰丙酮镍为镍前体,在 360°C 下,用三辛基氧化膦反应 1 小时,得到直径为 500nm 的球形 Ni(5)P(4)颗粒。以四水合乙酸镍为镍前体,在 360°C 下,用三辛基氧化膦反应 5 小时,得到直径为 200-500nm 的 NiP(2)颗粒。采用 NiP(2)颗粒作为活性材料,80Li(2)S·20P(2)S(5)(摩尔%)玻璃陶瓷作为固体电解质,制备了全固态电池。Li-In/80Li(2)S·20P(2)S(5)/NiP(2)电池在电流密度为 0.13mA cm(-2)时,初始放电容量为 1100mAh g(-1),经过 10 次循环后,放电容量保持在 750mAh g(-1)。

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