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In order to achieve elemental and chemical sensitivity in scanning tunneling microscopy (STM), synchrotron x-rays have been applied to excite core-level electrons during tunneling. The x-ray photo-excitations result in tip currents that are superimposed onto conventional tunneling currents. While carrying important physical information, the varying x-ray induced currents can destabilize the feedback loop causing it to be unable to maintain a constant tunneling current, sometimes even causing the tip to retract fully or crash. In this paper, we report on an easy-to-implement filter circuit that can separate the x-ray induced currents from conventional tunneling currents, thereby allowing simultaneous measurements of topography and chemical contrasts. The filter and the schematic presented here can also be applied to other variants of light-assisted STM such as laser STM.
In order to achieve elemental and chemical sensitivity in scanning tunneling microscopy (STM), synchrotron x-rays have been applied to excite core-level electrons during tunneling. The x-ray photo-excitations result in tip currents that are superimposed onto conventional tunneling currents. While carrying important physical information, the varying x-ray induced currents can destabilize the feedback loop causing it to be unable to maintain a constant tunneling current, sometimes even causing the tip to retract fully or crash. In this paper, we report on an easy-to-implement filter circuit that can separate the x-ray induced currents from conventional tunneling currents, thereby allowing simultaneous measurements of topography and chemical contrasts. The filter and the schematic presented here can also be applied to other variants of light-assisted STM such as laser STM.
Scanning tunneling microscopy (STM) combined with brilliant X-rays from synchrotron radiation (SR) can provide various possibilities of original and important applications, such as the elemental analysis on solid surfaces at an atomic scale. The principle of the elemental analysis is based on the inner-shell excitation of an element-specific energy level "under STM observation". A key to obtain an atomic locality is to extract the element-specific modulation of the local tunneling current (not emission that can damage the spatial resolution), which is derived from the inner-shell excitation [1]. On this purpose, we developed a special SR-STM system and smart tip. To surmount a tiny core-excitation efficiency by hard X-rays, we focused two-dimensionally an incident beam having the highest photon density at the SPring-8.After successes in the elemental analyses by SR-STM [1,2] on a semiconductor hetero-interface (Ge on Si) and metal-semiconductor interface (Cu on Ge), we succeeded in obtaining the elemental contrast between Co nano-islands and Au substrate. The results on the metallic substrate suggest the generality of the method and give some important implications on the principle of contrast. For all cases of three samples, the spatial resolution of the analysis was estimated to be ∼1 nm or less, and it is worth noting that the measured surface domains had a deposition thickness of less than one atomic layer (Fig. 1, left and center).jmicro;63/suppl_1/i14-a/DFU045F1F1DFU045F1Fig. 1.(left) Topographic image and (center) beam-induced tip current image of Ge(111)-Cu (-2V, 0.2 nA). (right) X-ray- induced atomic motion tracks on Ge(111) that were newly imaged by the Xray-STM. On the other hand, we found that the "X-ray induced atomic motion" can be observed directly with atomic scale using the SR-STM system effectively under the incident photon density of ∼2 x10(15) photon/sec/mm(2) [3]. SR-STM visualized successfully the track of the atomic motion (Fig. 1, right), which enabled the further analysis on the mechanism of the atomic motion. It is worth comparing our results with past conventional thermal STM observations on the same surface [4], where the atomic motion was found to occur in the 2-dimensional domain. However, our results show the atomic track having a local chain distribution [3].The above mentioned results will allow us to investigate the chemical analysis and control of the local reaction with the spatial resolution of STM, giving hope of wide applications.
Scanning probe microscopy (SPM) is widely used for analysis of structures on substrate surfaces. Particularly, scanning tunneling microscopy (STM) and noncontact atomic force microscopy (NC-AFM) enable real-space observations of solid surfaces at the atomic level with high spatial resolution. However, these microscopic measurement methods still involve difficulties in elemental analysis at the nanoscale for general purposes, although several validated solutions have already been proposed for well-defined cases. This brief review explains issues and their resolution, including topics related to the development of chemical analysis methodologies based on STM/NC-AFM, such as inelastic tunneling spectroscopy (IETS)-STM for spectroscopy of individual molecules, STM combined with synchrotron radiation X-ray sources for elemental analysis of surface structures, and force spectroscopy with atom tracking technology, as well as X-ray-aided noncontact atomic force microscopy (XANAM). Particularly, the review describes details of XANAM including recently obtained results on X-ray energy dependence of force spectroscopy and its twodimensional recording as XANAM imaging, suggesting XANAM offers great potential to contribute to nanoscale investigations of chemical analysis for various purposes. IntroductionScanning probe microscopy (SPM) is a powerful tool to observe surface structures on substrate surfaces with measurement of physical parameters of different interactions between a tip and a sample surface. Among the SPM techniques, scanning tunneling microscopy (STM) 1 and noncontact atomic force microscopy (NC-AFM) 2,3 enable real-space observations of solid surfaces at the atomic level with high spatial resolution. Actually, STM can visualize surface structures of conductive materials with projection of electron density of states near the Fermi level. A sharpened metal tip is scanned with sensing tunneling current for imaging. Using a tiny tip, NC-AFM can visualize structures even on insulator surfaces by tracing corrugations of substances through sensing weak attractive force interactions. Many books 19 have described experimental and theoretical studies of the development of STM and NC-AFM, and have provided numerous examples of SPM applications in the fields of semiconductor devices, catalysis, sensors, and biochemistry. In addition, an upward trend is apparent in the number of studies in spectroscopy used to examine characteristic features of surfaces at the nanoscale. They have presented important new insights into surface physics and chemistry. Particularly, the identification of chemical characteristics on individual atoms and molecules on surfaces has persistently underlain SPM studies.Studies of the development of such chemically sensitive SPM are classifiable into two approaches: enhancing chemical sensitivity of tipsurface mutual interactions of SPM, and introducing extra probes of light/electron beam sources that can stimulate responses in the tipsurface interactions of SPM. As an example for the former, inelast...
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