磷化物
材料科学
过渡金属
纳米颗粒
金属
氯化物
无机化学
纳米技术
冶金
催化作用
有机化学
化学
作者
Alexandre Sodreau,Hooman Ghazi Zahedi,Rıza Dervişoğlu,Liqun Kang,Julia Menten,Johannes Zenner,Nicole Terefenko,Serena DeBeer,Thomas Wiegand,Alexis Bordet,Walter Leitner
标识
DOI:10.1002/adma.202306621
摘要
Abstract Metal chloride complexes react with tris(trimethylsilyl)phosphine under mild condition to produce metal phosphide (TMP) nanoparticles (NPs), and chlorotrimethylsilane as a byproduct. The formation of Si–Cl bonds that are stronger than the starting M‐Cl bonds acts as a driving force for the reaction. The potential of this strategy is illustrated through the preparation of ruthenium phosphide NPs using [RuCl 2 (cymene)] and tris(trimethylsilyl)phosphine at 35 °C. Characterization with a combination of techniques including electron microscopy (EM), X‐ray absorption spectroscopy (XAS), and solid‐state nuclear magnetic resonance (NMR) spectroscopy, evidences the formation of small (diameter of 1.3 nm) and amorphous NPs with an overall Ru 50 P 50 composition. Interestingly, these NPs can be easily immobilized on functional support materials, which is of great interest for potential applications in catalysis and electrocatalysis. Mo 50 P 50 and Co 50 P 50 NPs can also be synthesized following the same strategy. This approach is simple and versatile and paves the way toward the preparation of a wide range of transition metal phosphide nanoparticles under mild reaction conditions.
科研通智能强力驱动
Strongly Powered by AbleSci AI