Abstract:Chiral junctions of carbon nanotubes have the potential of serving as optically or electrically controllable switches. To investigate optoelectronic tuning of a chiral junction, we stamp carbon nanotubes onto a transparent gold surface and locate a tube with a semiconducting-metallic junction. We image topography, laser absorption at 532 nm, and measure I-V curves of the junction with nanometer spatial resolution. The bandgaps on both sides of the junction depend on the applied tip field (Stark effect), so the… Show more
“…These are the result of the short tip-sample distance on the order of nanometers required for quantum tunneling. 35 It has previously been shown that activation energies below 1 eV are sufficient to displace ions in the perovskite material and distort the perovskite lattice where the migration activation energies are the lowest for the halides followed by the A-site cations. [55][56][57][58] This results in various, and most of the time unpredictable and unforeseen, surface and bulk structures depending on the strength and polarity of the electric field.…”
Section: Resultsmentioning
confidence: 99%
“…In addition, strong electric fields emerge at the tip/sample junction due to the mandatory voltage which must be applied to either the tip or to the sample in STM experiments. 35 These requirements pose significant challenges with respect to lead halide perovskites where the ABX 3 crystal structure (A-site: organic or inorganic cation[s], B-site: lead, C-site: halides, eg, Cl, Br, I) also mirrors the weak point in these materials: the soft, dynamic and ionic bonding character of the crystal lattice. 36,37 In this critical review, we highlight the recent progress in applying STM-based techniques to organic/inorganic and all-inorganic lead halide perovskites, both in form of single crystals and thin films.…”
Section: Introductionmentioning
confidence: 99%
“…In particular, to obtain atomic resolution a flat surface is required in addition to the overall requirement of the sample's (semi‐)conductivity to enable the process of quantum tunneling. In addition, strong electric fields emerge at the tip/sample junction due to the mandatory voltage which must be applied to either the tip or to the sample in STM experiments 35 . These requirements pose significant challenges with respect to lead halide perovskites where the ABX 3 crystal structure (A‐site: organic or inorganic cation[s], B‐site: lead, C‐site: halides, eg, Cl, Br, I) also mirrors the weak point in these materials: the soft, dynamic and ionic bonding character of the crystal lattice 36,37 …”
Since the introduction of lead halide perovskites, tremendous progress has been made regarding their stability, reproducibility and durability. However, one of the issues that remains is related to the interfacial atomic structure arrangement and structure-property relationship under optical and electrical stimuli. In this critical review, we highlight the recent progress using scanning tunneling microscopy (STM) to understand the nanoscale properties and dynamic processes occurring in these halide perovskite materials. STM is known to be a very challenging technique, which is reflected by the low number of relevant publications in the last years. These initial reports mirror the unique potential of STM to give Ångstrom-scale insight into the (opto)electronic properties, morphology and underlying electronic structure and provide a path toward harnessing the full potential of these materials. However, care must be taken to understand the effects of the perturbations caused by STM and tailor the measurement conditions accordingly.
“…These are the result of the short tip-sample distance on the order of nanometers required for quantum tunneling. 35 It has previously been shown that activation energies below 1 eV are sufficient to displace ions in the perovskite material and distort the perovskite lattice where the migration activation energies are the lowest for the halides followed by the A-site cations. [55][56][57][58] This results in various, and most of the time unpredictable and unforeseen, surface and bulk structures depending on the strength and polarity of the electric field.…”
Section: Resultsmentioning
confidence: 99%
“…In addition, strong electric fields emerge at the tip/sample junction due to the mandatory voltage which must be applied to either the tip or to the sample in STM experiments. 35 These requirements pose significant challenges with respect to lead halide perovskites where the ABX 3 crystal structure (A-site: organic or inorganic cation[s], B-site: lead, C-site: halides, eg, Cl, Br, I) also mirrors the weak point in these materials: the soft, dynamic and ionic bonding character of the crystal lattice. 36,37 In this critical review, we highlight the recent progress in applying STM-based techniques to organic/inorganic and all-inorganic lead halide perovskites, both in form of single crystals and thin films.…”
Section: Introductionmentioning
confidence: 99%
“…In particular, to obtain atomic resolution a flat surface is required in addition to the overall requirement of the sample's (semi‐)conductivity to enable the process of quantum tunneling. In addition, strong electric fields emerge at the tip/sample junction due to the mandatory voltage which must be applied to either the tip or to the sample in STM experiments 35 . These requirements pose significant challenges with respect to lead halide perovskites where the ABX 3 crystal structure (A‐site: organic or inorganic cation[s], B‐site: lead, C‐site: halides, eg, Cl, Br, I) also mirrors the weak point in these materials: the soft, dynamic and ionic bonding character of the crystal lattice 36,37 …”
Since the introduction of lead halide perovskites, tremendous progress has been made regarding their stability, reproducibility and durability. However, one of the issues that remains is related to the interfacial atomic structure arrangement and structure-property relationship under optical and electrical stimuli. In this critical review, we highlight the recent progress using scanning tunneling microscopy (STM) to understand the nanoscale properties and dynamic processes occurring in these halide perovskite materials. STM is known to be a very challenging technique, which is reflected by the low number of relevant publications in the last years. These initial reports mirror the unique potential of STM to give Ångstrom-scale insight into the (opto)electronic properties, morphology and underlying electronic structure and provide a path toward harnessing the full potential of these materials. However, care must be taken to understand the effects of the perturbations caused by STM and tailor the measurement conditions accordingly.
“…An additional application of CNTs is as nano-probes. Here, carbon nano-probes can be exploited as atomic force microscopy [174,175] or scanning tunnelling microscope [176,177] tips.…”
Carbon has long been applied as an electrochemical sensing interface owing to its unique electrochemical properties. Moreover, recent advances in material design and synthesis, particularly nanomaterials, has produced robust electrochemical sensing systems that display superior analytical performance. Carbon nanotubes (CNTs) are one of the most extensively studied nanostructures because of their unique properties. In terms of electroanalysis, the ability of CNTs to augment the electrochemical reactivity of important biomolecules and promote electron transfer reactions of proteins is of particular interest. The remarkable sensitivity of CNTs to changes in surface conductivity due to the presence of adsorbates permits their application as highly sensitive nanoscale sensors. CNT-modified electrodes have also demonstrated their utility as anchors for biomolecules such as nucleic acids, and their ability to diminish surface fouling effects. Consequently, CNTs are highly attractive to researchers as a basis for many electrochemical sensors. Similarly, synthetic diamonds electrochemical properties, such as superior chemical inertness and biocompatibility, make it desirable both for (bio) chemical sensing and as the electrochemical interface for biological systems. This is highlighted by the recent development of multiple electrochemical diamond-based biosensors and bio interfaces.Keywords: bio sensors; carbon nanomaterials; carbon nanotubes; electrochemical sensing; synthetic diamond Users without a subscription are not able to see the full content. Please, subscribe or login to access all content.
“…Due to the unique electronic properties of single-walled carbon nanotubes (SWCNT) [1][2][3] , these quasi-one-dimensional materials have been widely investigated and applied in various device systems, such as field effect transistors (FET) 4 , optical switches 5 , organic photovoltaics (OPV) 6 and organic light emitting diodes (OLED) 7 . Charge dynamics at the interface between SWCNT and organic molecules/metals is of particular importance for the fundamental understanding of carbon-based electronic materials as well as for the development of new types of devices in organic electronics.…”
Single-walled carbon nanotubes (SWCNT) are a promising material for future optoelectronic applications, including flexible electrodes and field-effect transistors. Molecular doping of carbon nanotube surface can be an effective way to control the electronic structure and charge dynamics of these material systems. Herein, two organic semiconductors with different energy level alignment in respect to SWCNT are used to dope the channel of the SWCNT-based transistor. The effects of doping on the device performance are studied with a set of optoelectronic measurements. For the studied system, we observed an opposite change in photo-resistance, depending on the type (electron donor vs electron acceptor) of the dopants. We attribute this effect to interplay between two effects: (i) the change in the carrier concentration and (ii) the formation of trapping states at the SWCNT surface. We also observed a modest ~4 pA photocurrent generation in the doped systems, which indicates that the studied system could be used as a platform for multi-pulse optoelectronic experiments with photocurrent detection.
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