类金刚石
X射线光电子能谱
磷化氢
材料科学
纳米复合材料
碳纤维
纳米技术
分析化学(期刊)
化学工程
复合数
化学
分子
复合材料
有机化学
工程类
催化作用
作者
Moad Bouzid,Didier Poinsot,Clève Dionel Mboyi,Anna Krystianiak,Frédéric Herbst,Olivier Heintz,B. Domenichini,Marcel Bouvet,Jean‐Cyrille Hierso
标识
DOI:10.1002/admt.202301456
摘要
Abstract The assembly of hybrid materials combining a pure sp 3 ‐C platform from nano‐and microcrystals of molecularly‐defined nanometer‐sized functionalized diamondoids (nanodiamonds) coated with a gold transition metal nanolayer is conducted from the gas phase, following a two‐steps vapor phase dry construction process. By using first the controlled vapor phase self‐assembly of primary phosphine diamantane derivatives, followed by a chemical vapor decomposition of a suited gold organometallic complex the synthesis of the nanocomposite Au@H 2 P–DiamOH 2 is achieved. The gold deposit surface analysis reveals the formation of a Au–P covalent bonding, which excludes the formation of phosphine oxide, as confirmed at higher depth into the nanocomposite by Hard X‐ray Photoelectron Spectroscopy analysis (HaXPES). The thickness d of the gold layers deposited onto the surface of diamondoids is estimated to be around d = 0.8 ± 10% nm from XPS data, which allows combining the composite Au@H 2 P–DiamOH 2 with ITO interdigitated electrodes, to produce a long‐life, highly stable and reproducible, n‐type behavior sensor for ammonia detection. A relative response (RR) of 150% at 30 ppm and a limit of detection of 6 ppm are measured at room temperature (20 to 25 °C) and at 45% of relative humidity.
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