Seeking borophene on Ni3Al(111): an experimental characterization of boron segregation and oxidation

Yan Yan Grisan Qiu, P. Biasin, Paola Mantegazza, Stefania Baronio, Martin Heinrich, M. Muntwiler, E. Vesselli
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Abstract

Synthesis of a stable, well ordered honeycomb borophene 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 AlB2 honeycomb borophene 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 Ni3Al(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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在 Ni3Al(111)上寻找硼吩:硼偏析和氧化的实验表征
迄今为止,利用铝(111)作为生长基底,已经合成了稳定、有序的蜂窝状硼吩相,铝(111)提供了必要的电荷掺杂以补偿高六方孔密度。然而,B/Al(111)受强烈的 B-Al 相互作用的支配,因此实际形成的是 AlB2 蜂窝硼吩相。通过合金化稀释铝,原则上可以削弱硼支撑键。通过光谱和显微镜相结合的实验方法,我们发现硼层在 Ni3Al(111)合金终止层上的生长是由硼溶解到块体和表面偏析机制所驱动的。虽然没有观察到长程有序的硼诱导相,但具有三角形外观的局部有序超结构单元通过基底针销稳定,遵循化学 p(2  2) 表面有序。氧化涉及硼和铝,导致硼的表面偏析,而镍则保持其金属形态。
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