首页> 外文OA文献 >Free surfaces recast superconductivity in few-monolayer MgB2: Combined first-principles and ARPES demonstration
【2h】

Free surfaces recast superconductivity in few-monolayer MgB2: Combined first-principles and ARPES demonstration

机译:自由表面重铸了几层MgB2中的超导电性:结合第一性原理和ARPES演示

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Two-dimensional materials are known to harbour properties very different from those of their bulk counterparts. Recent years have seen the rise of atomically thin superconductors, with a caveat that superconductivity is strongly depleted unless enhanced by specific substrates, intercalants or adatoms. Surprisingly, the role in superconductivity of electronic states originating from simple free surfaces of two-dimensional materials has remained elusive to date. Here, based on first-principles calculations, anisotropic Eliashberg theory, and angle-resolved photoemission spectroscopy (ARPES), we show that surface states in few-monolayer MgB2 make a major contribution to the superconducting gap spectrum and density of states, clearly distinct from the widely known, bulk-like sigma-and pi-gaps. As a proof of principle, we predict and measure the gap opening on the magnesium-based surface band up to a critical temperature as high as similar to 30 K for merely six monolayers thick MgB2. These findings establish free surfaces as an unavoidable ingredient in understanding and further tailoring of superconductivity in atomically thin materials.
机译:众所周知,二维材料所具有的特性与其整体同类材料非常不同。近年来,原子薄的超导体兴起,但需注意的是,除非通过特定的底物,插层剂或吸附原子来增强,否则超导性将被严重消耗。令人惊讶的是,迄今为止,源自二维材料简单自由表面的电子态在超导中的作用仍然难以捉摸。在此,基于第一性原理计算,各向异性Eliashberg理论和角度分辨光发射光谱法(ARPES),我们显示出少数单层MgB2中的表面态对超导能隙谱和态密度起着重要作用,这明显不同于众所周知的大块状sigma和pi间隙。作为原理证明,我们仅针对六个单层厚度的MgB2预测并测量了高达30 K的临界温度的镁基表面带上的间隙开口。这些发现将自由表面确定为理解和进一步调整原子薄材料中超导性的必然成分。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号