Evaluation of surface passivating solvents for single and mixed halide perovskites.

Surface passivation is one of the commonly used approaches to reduce the density of defects on the surfaces and interfaces hindering the performance and stability of perovskite optoelectronic devices. Although surface passivation leads to performance improvement for the targeted devices, details of the complex intermolecular interactions occurring between the molecules and perovskites are not entirely known. Here, we investigated a variety of commonly used solvents in the post-processing of perovskites by using photoluminescence (PL) spectroscopy on single and mixed halide perovskites (MAPbI3, MAPbBr3 and MAPb(Br0.5I0.5)3). Our results show that solvents with medium and low Gutmann donor and acceptor numbers provide PL intensity increase for both single halide perovskites by passivating the surface defect sites. Among the single halide perovskites, MAPbBr3 is more attracted to hydrogen bonding solvents, in contrast to MAPbI3 that is preferred by Lewis bases. This halide selective attraction also has an influence on the mixed-halide composition. Identifying these interaction mechanisms provides new insights into passivating the surface of perovskites for future device design.

The composition and structure of the ubiquitous hydrocarbon contamination on van der Waals materials.

The behavior of single layer van der Waals (vdW) materials is profoundly influenced by the immediate atomic environment at their surface, a prime example being the myriad of emergent properties in artificial heterostructures. Equally significant are adsorbates deposited onto their surface from ambient. While vdW interfaces are well understood, our knowledge regarding atmospheric contamination is severely limited. Here we show that the common ambient contamination on the surface of: graphene, graphite, hBN and MoS2 is composed of a self-organized molecular layer, which forms during a few days of ambient exposure. Using low-temperature STM measurements we image the atomic structure of this adlayer and in combination with infrared spectroscopy identify the contaminant molecules as normal alkanes with lengths of 20-26 carbon atoms. Through its ability to self-organize, the alkane layer displaces the manifold other airborne contaminant species, capping the surface of vdW materials and possibly dominating their interaction with the environment.

Molecular Encapsulation from the Liquid Phase and Graphene Nanoribbon Growth in Carbon Nanotubes.

Growing graphene nanoribbons from small organic molecules encapsulated in carbon nanotubes can result in products with uniform width and chirality. We propose a method based on encapsulation of 1,2,4-trichlorobenzene from the liquid phase and subsequent annealing. This procedure results in graphene nanoribbons several tens of nanometers long. The presence of nanoribbons was proven by Raman spectra both on macroscopic samples and on the nanoscale by tip-enhanced Raman scattering and high-resolution transmission electron microscopic images.

Direct Visualization of Ultrastrong Coupling between Luttinger-Liquid Plasmons and Phonon Polaritons.

Ultrastrong coupling of light and matter creates new opportunities to modify chemical reactions or develop novel nanoscale devices. One-dimensional Luttinger-liquid plasmons in metallic carbon nanotubes are long-lived excitations with extreme electromagnetic field confinement. They are promising candidates to realize strong or even ultrastrong coupling at infrared frequencies. We applied near-field polariton interferometry to examine the interaction between propagating Luttinger-liquid plasmons in individual carbon nanotubes and surface phonon polaritons of silica and hexagonal boron nitride. We extracted the dispersion relation of the hybrid Luttinger-liquid plasmon-phonon polaritons (LPPhPs) and explained the observed phenomena by the coupled harmonic oscillator model. The dispersion shows pronounced mode splitting, and the obtained value for the normalized coupling strength shows we reached the ultrastrong coupling regime with both native silica and hBN phonons. Our findings predict future applications to exploit the extraordinary properties of carbon nanotube plasmons, ranging from nanoscale plasmonic circuits to ultrasensitive molecular sensing.

Enhancement of X-ray-Excited Red Luminescence of Chromium-Doped Zinc Gallate via Ultrasmall Silicon Carbide Nanocrystals.

X-ray-activated near-infrared luminescent nanoparticles are considered as new alternative optical probes due to being free of autofluorescence, while both their excitation and emission possess a high penetration efficacy in vivo. Herein, we report silicon carbide quantum dot sensitization of trivalent chromium-doped zinc gallate nanoparticles with enhanced near-infrared emission upon X-ray and UV-vis light excitation. We have found that a ZnGa2O4 shell is formed around the SiC nanoparticles during seeded hydrothermal growth, and SiC increases the emission efficiency up to 1 order of magnitude due to band alignment that channels the excited electrons to the chromium ion.

New design and calibration method for a tunable single-grating spatial heterodyne spectrometer.

In our paper, we present a new design for a single-grating tunable spatial heterodyne spectrometer (SHS). Our design simplifies the change of the center wavelength (Littrow wavelength) thus one can quickly tune the system to an arbitrary spectral range. Furthermore, we introduce a new calibration method that provides superior calibration accuracy over the generally used formulas involving small angle approximations. We also present considerations about the general usability of the SHS technique in broadband measurements and propose different strategies to improve the signal-to-noise ratio.

Near-field infrared microscopy of nanometer-sized nickel clusters inside single-walled carbon nanotubes.

Nickel nanoclusters grown inside single-walled carbon nanotubes (SWCNT) were studied by infrared scattering-type scanning near-field optical microscopy (s-SNOM). The metal clusters give high local contrast enhancement in near-field phase maps caused by the excitation of free charge carriers. The experimental results are supported by calculations using the finite dipole model, approximating the clusters with elliptical nanoparticles. Compared to magnetic force microscopy, s-SNOM appears much more sensitive to detect metal clusters inside carbon nanotubes. We estimate that these clusters contain fewer than ≈700 Ni atoms.

Optical detection of charge dynamics in CH3NH3PbI3/carbon nanotube composites.

We have investigated the optical absorption of metallic and semiconducting carbon nanotubes/CH3NH3PbI3 micro- and nanowire composites. Upon visible light illumination semiconducting carbon nanotube based samples show a photo-induced doping, originating from the charge carriers created in the perovskite while this kind of change is absent in the composites containing metallic nanotubes, due to their strikingly different electronic structure. The response in the nanotubes shows, beside a fast diffusion of photo-generated charges, a slow component similar to that observed in pristine CH3NH3PbI3 attributed to structural rearrangement, and leading to slight, light induced changes of the optical gap of the perovskite. This charge transfer from the illuminated perovskite confirms that carbon nanotubes (especially semiconducting ones) can form efficient charge-transporting layers in the novel organometallic perovskite based optoelectronic devices.

Networks of semiconducting SWNTs: contribution of midgap electronic states to the electrical transport.

Single-walled carbon nanotube (SWNT) thin films provide a unique platform for the development of electronic and photonic devices because they combine the advantages of the outstanding physical properties of individual SWNTs with the capabilities of large area thin film manufacturing and patterning technologies. Flexible SWNT thin film based field-effect transistors, sensors, detectors, photovoltaic cells, and light emitting diodes have been already demonstrated, and SWNT thin film transparent, conductive coatings for large area displays and smart windows are under development. While chirally pure SWNTs are not yet commercially available, the marketing of semiconducting (SC) and metallic (MT) SWNTs has facilitated progress toward applications by making available materials of consistent electronic structure. Nevertheless the electrical transport properties of networks of separated SWNTs are inferior to those of individual SWNTs. In particular, for semiconducting SWNTs, which are the subject of this Account, the electrical transport drastically differs from the behavior of traditional semiconductors: for example, the bandgap of germanium (E = 0.66 eV) roughly matches that of individual SC-SWNTs of diameter 1.5 nm, but in the range 300-100 K, the intrinsic carrier concentration in Ge decreases by more than 10 orders of magnitude while the conductivity of a typical SC-SWNT network decreases by less than a factor of 4. Clearly this weak modulation of the conductivity hinders the application of SC-SWNT films as field effect transistors and photodetectors, and it is the purpose of this Account to analyze the mechanism of the electrical transport leading to the unusually weak temperature dependence of the electrical conductivity of such networks. Extrinsic factors such as the contribution of residual amounts of MT-SWNTs arising from incomplete separation and doping of SWNTs are evaluated. However, the observed temperature dependence of the conductivity indicates the presence of midgap electronic states in the semiconducting SWNTs, which provide a source of low-energy excitations, which can contribute to hopping conductance along the nanotubes following fluctuation induced tunneling across the internanotube junctions, which together dominate the low temperature transport and limit the resistivity of the films. At high temperatures, the intrinsic carriers thermally activated across the bandgap as in a traditional semiconductor became available for band transport. The midgap states pin the Fermi level to the middle of the bandgap, and their origin is ascribed to defects in the SWNT walls. The presence of such midgap states has been reported in connection with scanning tunneling spectroscopy experiments, Coulomb blockade observations in low temperature electrical measurements, selective electrochemical deposition imaging, tip-enhanced Raman spectroscopy, high resolution photocurrent spectroscopy, and the modeling of the electronic density of states associated with various defects. Midgap states are present in conventional semiconductors, but what is unusual in the present context is the extent of their contribution to the electrical transport in networks of semiconducting SWNTs. In this Account, we sharpen the focus on the midgap states in SC-SWNTs, their effect on the electronic properties of SC-SWNT networks, and the importance of these effects on efforts to develop electronic and photonic applications of SC-SWNTs.

Effect of Lanthanide Metal Complexation on the Properties and Electronic Structure of Single-Walled Carbon Nanotube Films.

We spectroscopically analyze the effect of e-beam deposition of lanthanide metals on the electronic structure and conductivities of films of semiconducting (SC) single-walled carbon nanotubes (SWNTs) in high vacuum. We employ near-infrared and Raman spectroscopy to interpret the changes in the electronic structure of SWNTs on exposure to small amounts of the lanthanides (Ln = Sm, Eu, Gd, Dy, Ho, Yb), based on the behavior of the reference metals (M = Li, Cr) which are taken to exemplify ionic and covalent bonding, respectively. The analysis shows that while the lanthanides are more electropositive than the transition metals, in most cases they exhibit similar conductivity behavior which we interpret in terms of the formation of covalent bis-hexahapto bonds [(η(6)-SWNT)M(η(6)-SWNT), where M = La, Nd, Gd, Dy, Ho]. However, only M = Eu, Sm, Yb show the continually increasing conductivity characteristic of Li, and this supports our contention that these metals provide the first examples of mixed covalent-ionic bis-hexahapto bonds [(η(6)-SWNT)M(η(6)-SWNT), where M = Sm, Eu, Yb].

Effect of atomic interconnects on percolation in single-walled carbon nanotube thin film networks.

The formation of covalent bonds to single-walled carbon nanotube (SWNT) or graphene surfaces usually leads to a decrease in the electrical conductivity and mobility as a result of the structural rehybridization of the functionalized carbon atoms from sp(2) to sp(3). In the present study, we explore the effect of metal deposition on semiconducting (SC-) and metallic (MT-) SWNT thin films in the vicinity of the percolation threshold and we are able to clearly delineate the effects of weak physisorption, ionic chemisorption with charge transfer, and covalent hexahapto (η(6)) chemisorption on these percolating networks. The results support the idea that for those metals capable of forming bis-hexahapto-bonds, the generation of covalent (η(6)-SWNT)M(η(6)-SWNT) interconnects provides a conducting pathway in the SWNT films and establishes the transition metal bis-hexahapto organometallic bond as an electronically conjugating linkage between graphene surfaces.

Hexahapto-lanthanide interconnects between the conjugated surfaces of single-walled carbon nanotubes.

We report the response of the electrical conductivity of semiconducting single-walled carbon nanotube (SWNT) thin films on exposure to metal vapors of the early lanthanides under high vacuum conditions. We attribute the strongly enhanced conductivities observed on deposition of samarium and europium to charge transfer from the metals to the SWNT backbone, thereby leading to the first examples of mixed covalent-ionic bis-hexahapto bonds [(η(6)-SWNT)M(η(6)-SWNT), where M = Sm, Eu].

Electronic properties of propylamine-functionalized single-walled carbon nanotubes.

We present resonant Raman measurements on single-walled carbon nanotubes (SWCNT) functionalized with propylamine groups at different degrees. Direct nucleophilic addition based on in situ generated primary amides is used for attaching n-propylamine to the sidewalls of SWCNTs. The influence of the amino functionalities on the electronic structure of the nanotubes is investigated. From the Raman resonance profiles of the radial breathing modes (RBMs), the chiral indices of the corresponding tubes are assigned. We observe significant redshifts of the transition energies and a broadening of the resonance windows due to chemical modification of SWCNTs. Similar redshifts are derived from the analysis of the NIR/Vis transmission spectrum. The relative Raman intensities of the functionalized samples and the evaluation of their transmission spectra indicate a diameter dependence of the reactivity as it has been observed for other moieties. By analyzing the defect induced D mode we observe a considerable degree of functionalization accompanied by an almost unharmed tube structure, which ensures that the observed effects are mainly driven by changes of the electronic structure.