Fabrication of sulfur-doped cove-edged graphene nanoribbons on Au(111)

The on-surface synthesis from predesigned organic precursors can yield graphene nanoribbons(GNRs) with atomically precise widths, edge terminations and dopants, which facilitate the tunning of their electronic structures. Here, we report the synthesis of novel sulfur-doped cove-edged GNRs(S-CGNRs) on Au(111) from a specifically designed precursor containing thiophene rings. Scanning tunneling microscopy and non-contact atomic force microscopy measurements elucidate the formation of S-CGNRs through subsequent polymerization and cyclodehydrogenation, which further result in crosslinked branched structures. Scanning tunneling spectroscopy results reveal the conduction band minimum of the S-CGNR locates at 1.2 e V. First-principles calculations show that the S-CGNR possesses an energy bandgap of 1.17 e V,which is evidently smaller than that of an undoped cove-edged GNR(1.7 e V), suggesting effective tuning of the bandgap by introducing sulfur atoms. Further increasing the coverage of precursors close to a monolayer results in the formation of linear-shaped S-CGNRs. The fabrication of S-CGNRs provides one more candidate in the GNR toolbox and promotes the future applications of heteroatom-doped graphene nanostructures.     

Substrate tuned reconstructed polymerization of naphthalocyanine on Ag(110)

The linkage structures between monomers make great influence on the properties of polymers.The synthesis of some special linkage structures can be challenging,which is often overcome by employing special reaction conditions.Here,we build dihydropentalene linkage in poly-naphthalocyanine on Ag(110)surface.Scanning tunneling microscopy(STM)and non-contact atomic force microscopy(nc-AFM)measurements confirm the dihydropentalene linkage structure and a possible formation path with reconstruction steps is proposed.The controlled experiment on Ag(100)surface shows no dihydropentalene structures formed,which indicates the grooved substrate is necessary for the reconstruction.This work provides insights into the surface restricted reactions that can yield special structures in organic polymers.     

NBN-doped nanographene embedded with five-and seven-membered rings on Au(111) surface

Nanographenes(NGs) can be embedded with predesigned dopants or nonhexagonal rings to tailor the electronic properties and provide ideal platforms to study the unique physical and chemical properties. Here, we report the onsurface synthesis of NBN-doped NG embedded with five-and seven-membered rings(NBN-575-NG) on Au(111) from a oligophenylene precursor preinstalled with a NBN unit and a heptagonal ring. Scanning tunneling microscopy and noncontact atomic force microscopy images elucidate the intramolecular cyclodehydrogenation and the existence of the fiveand seven-membered rings. Scanning tunneling spectroscopy spectra reveal that the NBN-575-NG is a semiconductor,which agrees with the density functional theory calculation results on a freestanding NBN-575-NG with the same structure.This work provides a feasible approach for the on-surface synthesis of novel NGs containing non-hexagonal rings.     

石墨烯纳米结构的原子级精准构造

相比单层石墨烯,特定构型的石墨烯纳米结构具有更加新奇的物理性质,被认为是构筑基于石墨烯功能纳米器件的基本单元。由于纳米结构的性质对其局域原子构型非常敏感,可控制备高质量的、原子级精确的石墨烯纳米结构并研究其奇特的电子学和自旋电子学性质是实现其器件应用的必要前提。目前,实验构筑锯齿形石墨烯纳米带及其面内异质结、纳米孔洞以及量子点已取得很多重要进展,但是具有复杂结构的功能化石墨烯纳米结构的构筑与物性研究仍存在挑战。文章介绍作者在原子级精确构造石墨烯纳米结构方面取得的系列科研进展。运用可控制备技术与高精度的极低温强磁场扫描隧道显微镜,探索在不同衬底上制备高质量的、具有特定构型的石墨烯纳米结构,并尝试对制备的石墨烯纳米结构进行原子级精准的操纵,实现构造“用户定制”的功能化石墨烯纳米结构。此系列工作发展了石墨烯纳米结构精确可控制备方法,为研究复杂纳米结构与物性提供了新的思路。     

STM的同胞兄弟--原子力显微镜(AFM)

介绍了在扫描隧道显微镜（ＳＴＭ）基础上发展起来的原子力显微镜（ＡＦＭ）的工作原理、关键部分、工作模式及其应用。     

Controllable growth of low-dimensional nanostructures on well-defined surfaces

The controllable growth of nanostructures with desired geometric order and well-defined shapes has stimulated great interest due to its applicability in the development of microelectronic devices. Self-assembly is an efficient and versatile way to guide the atoms or molecules into low-dimensional nanostructures as a consequence of balancing complex interplay between adsorbate-adsorbate and adsorbate-substrate interfacial interactions. The tailoring of low-dimensional nanostruc- tures by control of inter-adsorbate and adsorbate-substrate interfacial interactions is reviewed. Such inherent interactions greatly influence not only the size and shape of the growing nanostructures, but also their chemical identity. The degree of interaction between adsorbates can be controlled via preparation procedures, opening up the study of the influence of this phenomenon with respect to reactivity and catalytic behavior. The formation of well-defined molecular layers can be controlled not only by repulsive molecule-molecule interaction but also by symmetry matching or charge transfer be- tween adsorbed molecules and the substrate. It has become obvious that inter-adsorbate and adsorbate-substrate interfacial interactions can be tuned to fabricate diverse surface nanostructures from semiconductor, metallic, and molecular materials.     

Electrical Measurement Techniques in Atomic Force Microscopy

A conductive tip in an atomic force microscope (AFM) has extended the capability from conventional topographic imaging to electrical surface characterization. The conductive tip acts as a voltage electrode to provide stimuli and monitor electrical surface properties. In this review article, we have organized the AFM electrical techniques based on whether the electrical properties are monitored at the cantilever tip or across the sample. Furthermore, the techniques are organized based on probe detection signal. A number of acronyms are used in the literature, and the more commonly used ones are identified. The principle of each technique is described, and representative applications are presented. A better understanding of the spectrum of techniques should serve as the driver to expand the application of electrical techniques to study interdisciplinary phenomena at the nanoscale.     

原子力与光子扫描隧道组合显微镜

介绍了超高分辨光于扫描隧遭显微镜（PSTM）的计冗历程,为解决第一代（单光束照明）光千扫捕隧逼显傲镜中存在人为假象和样品光学图像与形貌图像难于分离两个难题,用“对称双光束照明方法消假象,用原子力与光子扫描隧道组合显微镜（AF／PSTM）图像分解方法分离样品光学透过率、折射率与形貌图像。研制成功新一代原子力与光子扫描隧道组合显微镜（AF／PSTM）样机。该样机在一次扫描中已获得两幅原子力显微镜图像（形貌与相位）和两幅光学图像（透过率和折射率）,有效地减少了假象,分解了样品光学折射率、透过率与形貌图像。     

表/界面水的扫描探针技术研究进展

表面和界面水在自然界、人们的日常生活以及现代科技中无处不在.它在物理、化学、环境学、材料学、生物学、地质学等诸多基础学科和应用领域起到至关重要的作用.因此,表面和界面水的功能与特性的研究,是水基础科学的一项核心任务.然而,由于水分子之间氢键相互作用的复杂性,及其与水-固界面相互作用的竞争,使得表(界)面水对于局域环境的影响非常敏感,往往需要深入到分子层次研究其微观结构和动力学过程.近年来,新型扫描探针技术的发展使得人们可以在单分子甚至亚分子尺度上对表(界)面水展开细致的实空间研究.本文着重介绍几种代表性的扫描探针技术及其在表(界)面水体系中的应用,包括:超高真空扫描隧道显微术、单分子振动谱技术、电化学扫描隧道显微术和非接触式原子力显微术.此外,本文还将对表(界)面水扫描探针技术研究面临的挑战和未来发展方向进行了展望.     

扫描隧道显微镜针尖调制的薄膜表面的原子扩散

采用原子尺度的模拟方法,探讨了在零偏压下扫描隧道显微镜(STM)针尖调制的金属表面岛上原子运动及岛边的层间质量输运. 研究结果显示STM的移动对岛上及岛边的原子扩散有重要的影响. 针尖与吸附原子的交互作用及岛和基体中强的形状变化影响了岛上吸附原子的跳跃扩散及岛边的跳下扩散和交换扩散过程. 研究发现,通过调节针尖与基体的垂直距离及针尖与吸附原子的水平距离,可以降低岛上吸附原子的跳跃扩散能垒及岛边的跳下扩散和交换扩散能垒,从而实现薄膜由三维生长模式向二维生长模式的转变. 关键词： 扫描隧道显微镜 原子运动 质量输运     

研究单原子分子表面扩散运动的时域隧穿电流谱方法

以单个Cu原子在Si(111)(7×7)层错半单元(FHUC)内的随机扩散运动研究为例,演示了一种新的可以测量快速扩散运动的扫描隧道显微镜方法──时域隧穿电流谱方法.运用这种方法可定量地检测纳米局域区间内单原子分子的表面扩散运动,跳跃频率的测量范围达到1—104Hz,比过去已有的用扫描隧道显微镜研究表面扩散的方法提高三个量级.这种方法将会使人们在原子尺度下对快速扩散运动比如氢原子的量子扩散运动获得更进一步的理解.     

Moiré superlattice modulations in single-unit-cell FeTe films grown on NbSe2 single crystals

Interface can be a fertile ground for exotic quantum states, including topological superconductivity, Majorana mode, fractal quantum Hall effect, unconventional superconductivity, Mott insulator, etc. Here we grow single-unit-cell (1UC) FeTe film on NbSe₂ single crystal by molecular beam epitaxy (MBE) and investigate the film in-situ with a home-made cryogenic scanning tunneling microscopy (STM) and non-contact atomic force microscopy (AFM) combined system. We find different stripe-like superlattice modulations on grown FeTe film with different misorientation angles with respect to NbSe₂ substrate. We show that these stripe-like superlattice modulations can be understood as moiré pattern forming between FeTe film and NbSe₂ substrate. Our results indicate that the interface between FeTe and NbSe₂ is atomically sharp. By STM-AFM combined measurement, we suggest that the moiré superlattice modulations have an electronic origin when the misorientation angle is relatively small (≤ 3°) and have structural relaxation when the misorientation angle is relatively large (≥ 10°).     

Electrochemical tip-enhanced Raman Spectroscopy for microscopic studies of electrochemical interfaces

The review describes electrochemical applications of tip-enhanced Raman spectroscopy (TERS). These applications combine the merits of both scanning probe microscopy (SPM) and Raman spectroscopy, which enables us to simultaneously obtain high-resolution images of surface morphology and chemical information under the electrochemical environment. This review, first summarizes the pioneering work done on the TERS systems that operate in liquid and electrochemical environments, and then gives an overview of the typical instrumentation of electrochemical TERS (EC-TERS) based on electrochemical scanning tunneling microscopy (EC-STM). Furthermore, this review summarizes the advancements in EC-TERS studies of events that occur at the interfaces. These include potential dependent structural changes and electrochemical reactions. Finally, we discuss the current issues and future prospects of EC-TERS for microscopic studies of electrochemical interfaces.     

Pulsed laser ablation in liquid of sp-carbon chains: Status and recent advances

This review provides a discussion of the current state of research on sp-carbon chains synthesized by pulsed laser ablation in liquid. In recent years, pulsed laser ablation in liquid (PLAL) has been widely employed for polyynes synthesis thanks to its flexibility with varying laser parameters, solvents, and targets. This allows the control of sp-carbon chains properties as yield, length, termination and stability. Although many reviews related to PLAL have been published, a comprehensive work reporting the current status and advances related to the synthesis of sp-carbon chains by PLAL is still missing. Here we first review the principle of PLAL and the mechanisms of formation of sp-carbon chains. Then we discuss the role of laser fluence (i.e. energy density), solvent, and target for sp-carbon chains synthesis. Lastly, we report the progress related to the prolonged stability of sp-carbon chains by PLAL encapsulated in polymeric matrices. This review will be a helpful guide for researchers interested in synthesizing sp-carbon chains by PLAL.     

高定向热解石墨表面局域导电增强现象的扫描探针显微学研究

基于导电型原子力显微镜和扫描隧道显微镜的对比观察,研究高定向热解石墨表面上残留石墨片的导电增强现象.根据样品电阻的测量数据,将这种现象归结为导电针尖与石墨表面的点接触问题,并且发现接触电导和接触点处局域的电子密度成正比,从而确定石墨表面的局域导电增强现象的原因在于残留在石墨表面的石墨片具有较高的电子密度. 关键词： 扫描隧道显微镜 导电原子力显微镜 高定向热解石墨 导电性     

Comparison of tunneling through molecules with Mott-Hubbard and with dimerization gaps

In order to study the tunneling of electrons through an interacting, 1D, dimerized molecule connected to leads, we consider the persistent current in a ring embedding this molecule. We find numerically that, for spinless fermions, a molecule with a gap mostly due to interactions, i.e. a Mott-Hubbard gap, gives rise to a larger persistent current than a molecule with the same gap, but due only to the dimerization. In both cases, the tunneling current decreases exponentially with the size of the molecule, but more slowly in the interacting case. Implications for molecular electronic are briefly discussed. Received: 17 November 1997 / Revised: 16 January 1998 / Accepted: 16 January 1998     

低维原子/分子晶体材料的可控生长、物性调控和原理性应用

本文介绍了高鸿钧课题组在物理所20年来的部分代表性工作.研究的主要方向为低维纳米功能材料的分子束外延可控制备、生长机制、物性调控及其在未来信息技术中的原理性应用.从材料的可控制备入手,结合第一性原理的理论计算,阐明材料生长机制和结构与物性的关系,进而实现物性调控和原理性应用.主要内容有:1)纳米尺度"海马"分形结构的形成及其生长机制;2)STM分辨率的提高及最高分辨Si(111)-7×7原子图像的获得;3)固体表面上功能分子的吸附、组装及其机制;4)稳定、重复、可逆的纳米尺度电导转变与超高密度信息存储;5)固体表面上单分子自旋态的量子调控及其原理性应用;6)原子尺度上朗德g因子的空间分辨及其空间分布不均匀性的发现;7)晶圆尺寸、高质量、单晶石墨烯的制备及原位硅插层绝缘化;8)几种新型二维原子晶体材料的可控构筑及其物性调控;9)"自然图案化"的新型二维原子晶体材料及其功能化.这些工作为低维量子结构的构造、物性调控及其原理性应用奠定了基础.     

Nitriding molybdenum: Effects of duration and fill gas pressure when using 100-Hz pulse DC discharge technique

Molybdenum is nitrided by a 100-Hz pulsed DC glow discharge technique for various time durations and fill gas pressures to study the effects on the surface properties of molybdenum. X-ray diffractometry(XRD), scanning electron microscopy(SEM), and atomic force microscopy(AFM) are used for the structural and morphological analysis of the nitrided layers. Vickers’ microhardness tester is utilized to investigate surface microhardness. Phase analysis shows the formation of more molybdenum nitride molecules for longer nitriding durations at fill gas pressures of 2 mbar and 3 mbar(1 bar = 105Pa). A considerable increase in surface microhardness(approximately by a factor of 2) is observed for longer duration(10 h) and 2-mbar pressure. Longer duration(10 h) and 2-mbar fill gas pressure favors the formation of homogeneous, smooth, hard layers by the incorporation of more nitrogen.     

光子扫描隧道显微镜的光电成像系统研究

本文论述了光子扫描隧道显微镜（ＰＳＴＭ）的显微成像机理、成像规律，针对具体的物理模型进行数值模拟计算，并得到了与实际探测相一致的场分布规律。采用自行研制的光子扫描隧道显微镜（ＰＳＴＭ）的显微实验系统对多种样品进行了表面显微成像研究，获得了关于样品表面三维立体图像信息，通过多种图像处理手段对原始图像进行后期处理，得到了更具视觉效果、更为逼真的样品表面图像。     

Nitriding molybdenum： Effects of duration and fill gas pressure when using lO0-Hz pulse DC discharge technique

Molybdenum is nitrided by a 100-Hz pulsed DC glow discharge technique for various time durations and fill gas pressures to study the effects on the surface properties of molybdenum. X-ray diffractometry （XRD）, scanning electron microscopy （SEM）, and atomic force microscopy （AFM） are used for the structural and morphological analysis of the nitrided layers. Vickers＇ microhardness tester is utilized to investigate surface microhardness. Phase analysis shows the formation of more molybdenum nitride molecules for longer nitriding durations at fill gas pressures of 2 mbar and 3 mbar （1 bar = 105 Pa）. A considerable increase in surface microhardness （approximately by a factor of 2） is observed for longer duration （10 h） and 2-mbar pressure. Longer duration （10 h） and 2-mbar fill gas pressure favors the formation of homogeneous, smooth, hard layers by the incorporation of more nitrogen.