Publications by authors named "Janice E Reutt-Robey"

Article Synopsis
  • The text discusses a new technique called pascalammetry that helps understand ion transport in solid-state electrochemical devices by applying stress and measuring current responses.
  • This method has been tested on specific microbattery models, revealing that stress can influence lithium diffusion, which may lead to battery degradation.
  • The findings suggest that pascalammetry could be a valuable tool for detecting stress in solid-state batteries and other electrochemical systems, providing insights that go beyond traditional methods.
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A carbon-nanotube-enabling scanning probe technique/nanotechnology for manipulating and measuring lithium at the nano/mesoscale is introduced. Scanning Li-nanopipette and probe microscopy (SLi-NPM) is based on a conductive atomic force microscope (AFM) cantilever with an open-ended multi-walled carbon nanotube (MWCNT) affixed to its apex. SLi-NPM operation is demonstrated with a model system consisting of a Li thin film on a Si(111) substrate.

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Surface self-assembly process of 9-anthracene carboxylic acid (AnCA) on Ag(111) was investigated using STM. Depending on the molecular surface density, four spontaneously formed and one annealed AnCA ordered phases were observed, namely a straight belt phase, a zigzag double-belt phase, two simpler dimer phases, and a kagome phase. The two high-density belt phases possess large unit cells on the scale length of 10 nm, which are seldom observed in molecular self-assembled structures.

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Nanoscale structure-electric potential relations in films of the organic molecular semiconductors C(60) and titanyl phthalocyanine (TiOPc) on Ag(111) have been measured under UHV conditions. Noncontact force methods were utilized to image domain structures and boundaries with molecular resolution, while simultaneously quantifying the local surface electric potential. Sensitivity and spatial resolution for the local potential measurement were first established on Ag(111) through direct observation of the electrical dipole and potential step, φ(step) = 10 ± 3 mV, of monatomic crystallographic steps.

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Article Synopsis
  • Depositing titanyl phthalocyanine (TiOPc) on a silver surface forms a honeycomb structure with two tilt angles, serving as a template for directing C(70) growth.
  • The resulting C(70) films exhibit unique kagome lattice patterns, which are analyzed using advanced imaging techniques.
  • This approach leverages electrostatic features of molecular templates to effectively control the organization of nanoscale films through anisotropic interactions.
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By controlled deposition, TiOPc, a molecular semiconductor with anisotropic interactions can generate a molecular film with a characteristic pattern repeat size of 15 nm. This structure then served as a nanotemplate for a superlattice of C(60) clusters with characteristic diameters of 7 nm. As a result, C(60) deposition on the TiOPc film template forms a pattern of nanophase-separated C(60) and TiOPc domains with a characteristic domain size of 7 nm.

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Article Synopsis
  • The study investigates how mobile pentacene precursors contribute to forming a co-crystalline structure of C(60) and pentacene on a silver surface (Ag(111)).
  • Researchers found that this unique structure can form readily at room temperature from a two-dimensional mixture, rather than only at low temperatures, as previously thought.
  • The results demonstrate a self-limiting assembly process in which pentacene and C(60) molecules organize into a specific network with defined pores, refining the overall understanding of this co-crystallization mechanism.
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The dependence of supramolecular structure on fractional molecular coverage has been investigated for acridine-9-carboxylic acid (ACA) and the C(60):ACA binary molecular system. The coverage-dependent phase diagram for ACA is first determined from room-temperature STM imaging. At low molecular coverages (theta < 0.

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We have demonstrated a method for fabricating C60 overlayers with controlled spacing and chirality by reactive coadsorption with the aromatic molecule acridine-9-carboxylic acid (ACA). Structural control is achieved by the mismatched symmetries of the coadsorbates, as well as specific intermolecular and adsorbate-substrate interactions. The resulting supramolecular structure has a C60 period nearly three times as large as the normal C60 2D packing of 1 nm and exists in enantiopure domains with robust chirality.

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