Ultrafast imaging of spontaneous symmetry breaking in a photoionized molecular system.

The Jahn-Teller effect is an essential mechanism of spontaneous symmetry breaking in molecular and solid state systems, and has far-reaching consequences in many fields. Up to now, to directly image the onset of Jahn-Teller symmetry breaking remains unreached. Here we employ ultrafast ion-coincidence Coulomb explosion imaging with sub-10 fs resolution and unambiguously image the ultrafast dynamics of Jahn-Teller deformations of [Formula: see text] cation in symmetry space.

Degradation of recalcitrant organic matter in SAARB leachate by a combined process of coagulation and catalytic ozonation.

A combined coagulation and γ-AlO catalytic ozonation process was used to treat semi-aerobic aged refuse biofilter (SAARB) effluent from treating mature landfill leachate. First, the coagulant providing the best pretreatment performance was selected. Then, the coagulated SAARB leachate was further treated in an optimized γ-AlO-catalyzed ozonation process.

Revealing the effect of atomic orbitals on the phase distribution of an ionizing electron wave packet with circularly polarized two-color laser fields.

We theoretically study the interference of photoelectrons released from atomic p orbitals in co-rotating and counter-rotating circularly polarized two-color laser pulses consisting of a strong 400-nm field and a weak 800-nm field. We find that in co-rotating fields the interference fringes in the photoelectron momentum distributions are nearly the same for p orbitals, while in counter-rotating fields the interference fringes for p and p orbitals oscillate out of phase with respect to the electron emission angle. The simulations based on the strong-field approximation show a good agreement with the numerical solutions of the time-dependent Schrödinger equation.

Photoelectron Holographic Interferometry to Probe the Longitudinal Momentum Offset at the Tunnel Exit.

Laser-induced electron tunneling underlies numerous emerging spectroscopic techniques to probe attosecond electron dynamics in atoms and molecules. The improvement of those techniques requires an accurate knowledge of the exit momentum for the tunneling wave packet. Here we demonstrate a photoelectron interferometric scheme to probe the electron momentum longitudinal to the tunnel direction at the tunnel exit by measuring the photoelectron holographic pattern in an orthogonally polarized two-color laser pulse.

Detecting and Characterizing the Nonadiabaticity of Laser-Induced Quantum Tunneling.

The nonadiabaticity of quantum tunneling through an evolving barrier is relevant to resolving laser-driven dynamics of atoms and molecules at an attosecond timescale. Here, we propose and demonstrate a novel scheme to detect the nonadiabatic behavior of tunnel ionization studied in an attoclock configuration, without counting on the laser intensity calibration or the modeling of the Coulomb effect. In our scheme, the degree of nonadiabaticity for tunneling scenarios in elliptically polarized laser fields can be steered continuously simply with the pulse ellipticity, while the critical instantaneous vector potentials remain identical.

Photoelectron holography and forward scattering in atomic ionization by elliptically polarized laser pulses.

We report on the scaling of the photoelectron holography with the laser ellipticity in strong-field atomic ionization. We find that the spacing of the holographic fringe gradually decreases with increasing of the ellipticity. In terms of the strong-field approximation, the scaling of the fringe spacing with the laser ellipticity is explained by the effect of the initial transverse momenta at the tunnel exit.

Controlling nonsequential double ionization of Ne with parallel-polarized two-color laser pulses.

We measure the recoil-ion momentum distributions from nonsequential double ionization of Ne by two-color laser pulses consisting of a strong 800-nm field and a weak 400-nm field with parallel polarizations. The ion momentum spectra show pronounced asymmetries in the emission direction, which depend sensitively on the relative phase of the two-color components. Moreover, the peak of the doubly charged ion momentum distribution shifts gradually with the relative phase.

Horseradish peroxidase inactivation: heme destruction and influence of polyethylene glycol.

Horseradish peroxidase (HRP) mediates efficient conversion of many phenolic contaminants and thus has potential applications for pollution control. Such potentially important applications suffer however from the fact that the enzyme becomes quickly inactivated during phenol oxidation and polymerization. The work here provides the first experimental data of heme consumption and iron releases to support the hypothesis that HRP is inactivated by heme destruction.

Comparison of lignin peroxidase and horseradish peroxidase for catalyzing the removal of nonylphenol from water.

Concentrations of aqueous-phase nonylphenol (NP), a well-known endocrine-disrupting chemical, are shown to be reduced effectively via reaction with lignin peroxidase (LiP) or horseradish peroxidase (HRP) and hydrogen peroxide. We systematically assessed their reaction efficiencies at varying conditions, and the results have confirmed that the catalytic performance of LiP toward NP was more efficient than that of HRP under experimental conditions. Mass spectrum analysis demonstrated that polymerization through radical-radical coupling mechanism was the pathway leading to NP transformation.