低温合成二硒化钨纳米晶的羰基钨前驱体可控CO稳定化

IF 4.1 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY
Jessica Q. Geisenhoff, Hang Yin, Natacha Oget, Haeun Chang, Linfeng Chen, Alina M. Schimpf
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引用次数: 0

摘要

本文报道了以氧化三辛基膦(TOPO)为原料,以六羰基钨和二苯基二硒为原料,低温胶体法制备了WSe2纳米晶体。利用红外光谱技术鉴定了TOPO取代中间体W(CO)5TOPO和顺式W(CO)4(TOPO)2。为了证实这些定位,我们合成了氧化膦取代中间体的芳基类似物,W(CO)5TPPO(先前合成的,TPPO =三苯基氧化膦)和顺式W(CO)4(TPPO)2和顺式W(CO)3(TPPO)3(本文报道的新结构)。烷基或芳基膦氧化物将钨羰基连接,使剩余的CO易于稳定,从而使低温分解成为WSe2纳米晶体的核。与含磷化氢配体的合成相比,在含磷化氢配体的合成中,取代导致CO稳定性降低,并且需要更高的温度来诱导纳米晶体成核。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Controlled CO labilization of tungsten carbonyl precursors for the low-temperature synthesis of tungsten diselenide nanocrystals
We report a low-temperature colloidal synthesis of WSe2 nanocrystals from tungsten hexacarbonyl and diphenyl diselenide in trioctylphosphine oxide (TOPO). We identify TOPO-substituted intermediates, W(CO)5TOPO and cis-W(CO)4(TOPO)2 by infrared spectroscopy. To confirm these assignments, we synthesize aryl analogues of phosphine-oxide-substituted intermediates, W(CO)5TPPO (synthesized previously, TPPO = triphenylphosphine oxide) and cis-W(CO)4(TPPO)2 and fac-W(CO)3(TPPO)3 (new structures reported herein). Ligation of the tungsten carbonyl by either the alkyl or aryl phosphine oxides results in facile labilization of the remaining CO, enabling low-temperature decomposition to nucleate WSe2 nanocrystals. The reactivity in phosphine oxides is contrasted with syntheses containing phosphine ligands, where substitution results in decreased CO labilization and higher temperatures are required to induce nanocrystal nucleation.
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来源期刊
Frontiers in Nanotechnology
Frontiers in Nanotechnology Engineering-Electrical and Electronic Engineering
CiteScore
7.10
自引率
0.00%
发文量
96
审稿时长
13 weeks
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