Chong Yu Ruan

Direct Observation of Optically Induced Transient Structures in Graphite Using Ultrafast Electron Crystallography

We use ultrafast electron crystallography to study structural changes induced in graphite by a femtosecond laser pulse. At moderate fluences of < or =21 mJ/cm2, lattice vibrations are observed to thermalize on a time scale of approximately 8 ps. At higher fluences approaching the damage threshold, lattice vibration amplitudes saturate. Following a marked initial contraction, graphite is driven nonthermally into a transient state with sp3-like character, forming interlayer bonds. Using ab initio density functional calculations, we trace the governing mechanism back to electronic structure changes following the photoexcitation.

Ultrafast diffraction and structural dynamics: The nature of complex molecules far from equilibrium

Studies of molecular structures at or near their equilibrium configurations have long provided information on their geometry in terms of bond distances and angles. Far-from-equilibrium structures are relatively unknown—especially for complex systems—and generally, neither their dynamics nor their average geometries can be extrapolated from equilibrium values. For such nonequilibrium structures, vibrational amplitudes and bond distances play a central role in phenomena such as energy redistribution and chemical reactivity. Ultrafast electron diffraction, which was developed to study transient molecular structures, provides a direct method for probing the nature of complex molecules far from equilibrium. Here we present our ultrafast electron diffraction observations of transient structures for two cyclic hydrocarbons. At high internal energies of ≈4 eV, these molecules display markedly different behavior. For 1,3,5-cycloheptatriene, excitation results in the formation of hot ground-state structures with bond distances similar to those of the initial structure, but with nearly three times the average vibrational amplitude. Energy is redistributed within 5 ps, but with a negative temperature characterizing the nonequilibrium population. In contrast, the ring-opening reaction of 1,3-cyclohexadiene is shown to result in hot structures with a C—C bond distance of over 1.7 Å, which is 0.2 Å away from any expected equilibrium value. Even up to 400 ps, energy remains trapped in large-amplitude motions comprised of torsion and asymmetric stretching. These studies promise a new direction for studying structural dynamics in nonequilibrium complex systems.

Dynamics of Size-Selected Gold Nanoparticles Studied by Ultrafast Electron Nanocrystallography

We report the studies of ultrafast electron nanocrystallography on size-selected Au nanoparticles (2-20 nm) supported on a molecular interface. Reversible surface melting, melting, and recrystallization were investigated with dynamical full-profile radial distribution functions determined with subpicosecond and picometer accuracies. In an ultrafast photoinduced melting, the nanoparticles are driven to a nonequilibrium transformation, characterized by the initial lattice deformations, nonequilibrium electron-phonon coupling, and, upon melting, the collective bonding and debonding, transforming nanocrystals into shelled nanoliquids. The displasive structural excitation at premelting and the coherent transformation with crystal/liquid coexistence during photomelting differ from the reciprocal behavior of recrystallization, where a hot lattice forms from liquid and then thermally contracts. The degree of structural change and the thermodynamics of melting are found to depend on the size of nanoparticle.

The molecular structure of copper- and nickel-phthalocyanine as determined by gas-phase electron diffraction and ab initio/DFT computations

Abstract The structure of two metal phthalocyanines (MPcs) where M=Ni and Cu, have been determined by gas-phase electron diffraction for the first time. Structural analysis is assisted by ab initio/DFT calculations, carried out in the present work for NiPc and taken from the literature for CuPc. The focus of these studies is the position of the metal ion relative to the 16-membered C8N8 ring. Both molecules were found to be planar. Slight non-planarity found in the previous study is now removed by a new procedure of structural analysis; this is in accordance with the results of the X-ray studies and ab initio/DFT calculations for both compounds. From comparisons presented here we can conclude that there is a close structural similarity of MPcs in the gas phase and in the crystal.

ELECTRON DIFFRACTION STUDIES OF METAL PHTHALOCYANINES, MPC, WHERE M=SN, MG, AND ZN (REINVESTIGATION)

The structure of two metal phthalocyanines, MPc where M=Sn and Mg, have been determined by gas-phase electron diffraction for the first time; furthermore, the structure of ZnPc established earlier by the same technique has been reanalyzed. The focus of these studies is the position of the metal ion relative to the 16-membered C8N8 ring. Tin(II)phthalocyanine we find to be nonplanar with the Sn(II) ion 1.0(1) A above the molecular plane in accordance with its structure in crystal established earlier; the two other molecules were found to be planar. Slight nonplanarity of ZnPc found in the previous study is now removed by a new procedure of structural analysis; this is in accordance with the results of ab initio/DFT calculations for this molecule performed by Pulay. From comparisons presented here we can conclude that there is a close structural similarity of metal phthalocyanines in the gas phase and in crystal.

The development and applications of ultrafast electron nanocrystallography.

We review the development of ultrafast electron nanocrystallography as a method for investigating structural dynamics for nanoscale materials and interfaces. Its sensitivity and resolution are demonstrated in the studies of surface melting of gold nanocrystals, nonequilibrium transformation of graphite into reversible diamond-like intermediates, and molecular scale charge dynamics, showing a versatility for not only determining the structures, but also the charge and energy redistribution at interfaces. A quantitative scheme for 3D retrieval of atomic structures is demonstrated with few-particle (<1,000) sensitivity, establishing this nanocrystallographic method as a tool for directly visualizing dynamics within isolated nanomaterials with atomic scale spatio-temporal resolution.

Space charge effects in ultrafast electron diffraction and imaging

Understanding space charge effects is central for the development of high-brightness ultrafast electron diffraction and microscopy techniques for imaging material transformation with atomic scale detail at the fs to ps timescales. We present methods and results for direct ultrafast photoelectron beam characterization employing a shadow projection imaging technique to investigate the generation of ultrafast, non-uniform, intense photoelectron pulses in a dc photo-gun geometry. Combined with N-particle simulations and an analytical Gaussian model, we elucidate three essential space-charge-led features: the pulse lengthening following a power-law scaling, the broadening of the initial energy distribution, and the virtual cathode threshold. The impacts of these space charge effects on the performance of the next generation high-brightness ultrafast electron diffraction and imaging systems are evaluated.

Ultrafast imaging of photoelectron packets generated from graphite surface

We present an electron projection imaging method to study the ultrafast evolution of photoelectron density distribution and transient fields near the surface. The dynamical profile of the photoelectrons from graphite reveals an origin of a thermionic emission, followed by an adiabatic process leading to electron acceleration and cooling before a freely expanding cloud is established. The hot electron emission is found to couple with a surface charge dipole layer formation, with a sheet density several orders of magnitude higher than that of the vacuum emitted cloud.

Exploration of metastability and hidden phases in correlated electron crystals visualized by femtosecond optical doping and electron crystallography

Using femtosecond photodoping and crystallography to explore metastable and hidden quantum phases in tantalum disulfide. Characterizing and understanding the emergence of multiple macroscopically ordered electronic phases through subtle tuning of temperature, pressure, and chemical doping has been a long-standing central issue for complex materials research. We report the first comprehensive studies of optical doping–induced emergence of stable phases and metastable hidden phases visualized in situ by femtosecond electron crystallography. The electronic phase transitions are triggered by femtosecond infrared pulses, and a temperature–optical density phase diagram is constructed and substantiated with the dynamics of metastable states, highlighting the cooperation and competition through which the macroscopic quantum orders emerge. These results elucidate key pathways of femtosecond electronic switching phenomena and provide an important new avenue to comprehensively investigate optical doping–induced transition states and phase diagrams of complex materials with wide-ranging applications.

Photovoltage dynamics of the hydroxylated Si(111) surface investigated by ultrafast electron diffraction

We present a novel method to measure transient photovoltage at nanointerfaces using ultrafast electron diffraction. In particular, we report our results on the photoinduced electronic excitations and their ensuing relaxations in a hydroxyl-terminated silicon surface, a standard substrate for fabricating molecular electronics interfaces. The transient surface voltage is determined by observing Coulomb refraction changes induced by the modified space-charge barrier within a selectively probed volume by femtosecond electron pulses. The results are in agreement with ultrafast photoemission studies of surface state charging, suggesting a charge relaxation mechanism closely coupled to the carrier dynamics near the surface that can be described by a drift-diffusion model. This study demonstrates a newly implemented ultrafast diffraction method for investigating interfacial processes, with both charge and structure resolution.