硼
硼酚
材料科学
溶解
合金
基质(水族馆)
结晶学
相(物质)
铝
镍
表征(材料科学)
金属
化学工程
化学物理
纳米技术
冶金
化学
单层
有机化学
工程类
地质学
海洋学
作者
Yongchang Qiu,Pietro Biasin,Pietro Mantegazza,Stefania Baronio,Martin Heinrich,Matthias Muntwiler,Erik Vesselli
出处
期刊:JPhys materials
[IOP Publishing]
日期:2024-02-08
卷期号:7 (2): 025004-025004
标识
DOI:10.1088/2515-7639/ad278c
摘要
Abstract Synthesis of a stable, well ordered honeycomb borophene (hB) phase has been achieved to date by exploiting Al(111) as a growth substrate, which provides the necessary charge doping to compensate the high hexagonal-holes density. However, B/Al(111) is governed by a strong B–Al interaction so to yield the actual formation of an AlB 2 hB phase. Dilution of aluminum by alloying could then in principle weaken the boron-support bonding. By means of a combined spectroscopy and microscopy experimental approach, we find instead that the growth of boron layers on the Ni 3 Al(111) alloy termination is driven by B dissolution into the bulk and surface segregation mechanisms. While no long-range ordered boron-induced phase is observed, locally ordered superstructural units with triangular appearance are stabilized by substrate pinning, following the chemical p (2 × 2) surface order. Oxidation involves both boron and aluminum, inducing surface segregation of B, while nickel remains in its metallic form.
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