材料科学
纳米尺度
图层(电子)
钻石
比例(比率)
曲面(拓扑)
化学工程
复合材料
碳纤维
纳米技术
光电子学
金刚石材料性能
类金刚石碳
纳米颗粒
纳米结构
表层
化学气相沉积
碳纳米管
作者
Anonymous,Xi Kong,Haoyu Sun,Yunxia Wang,Guanyu Qu,Pei Yu,Tianyu Xie,Zhiyuan Zhao,Ya Wang,Guosheng Shi,Fazhan Shi,Du Jiang-Feng
摘要
The chemical environment at interfaces plays an important role in controlling the structure, properties, and performance of low-dimensional materials. The water environment and adsorbates on solid surfaces are the most common interface environments that are prevalent in nonultrahigh vacuum conditions. Despite their ubiquitous presence, the structural and dynamic properties of these surface adsorbates are difficult to be directly characterized in situ at the atomic scale. Here, we report a dissection method leveraging shallow nitrogen-vacancy centers to quantitatively characterize nanoscale adsorbate layers on diamond surfaces with distinct structural and dynamical signatures. Our results reveal that under ambient conditions, a tightly bound organic adsorbate layer and an icelike interfacial water layer coexist on diamond surfaces. We further demonstrate that the rigidity of the interfacial water layer originates from its interaction with specific surface adsorption sites, such as the dangling bonds on the diamond surface. These findings establish new insights for investigating the structure and dynamics of low-dimensional adsorbates, as well as surface properties modulated by adsorbates under native conditions.
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