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The present work delves into the spin-polarized transport property of organic radicals sandwiched between two zigzag-graphene nanoribbon (ZGNR) electrodes by employing density functional theory and nonequilibrium Green's function technique. We demonstrated that the magnetic center(s) of the radical can manipulate the localized edge states of the ZGNR in the scattering region, causing ferromagnetic coupling. Such manipulation of the magnetic edges results in a high spin-filter effect in molecular junctions, and even the antiferromagnetic diradicals serve as nearly perfect spin filters. We have confirmed that this is a general phenomenon of ZGNR by analyzing two antiferromagnetic diradicals and a doublet. The spin-polarized density of states, transmission spectra, and current vs voltage curves of the systems provide strong evidence for our findings. This research strongly suggests that ZGNRs attached with organic radicals could be the perfect building blocks for spintronic materials. [ABSTRACT FROM AUTHOR]

Third order polarizability, (γ) taken from the collective electronic oscillator (CEO) method was used to calculate the two-photon absorption (TPA) of tetrastyryl-[2,2]paracyclophane derivatives with different through-space charge transfer configurations considering various donor and acceptor combinations at the terminal styryl groups. For the virtually same linear absorption, different TPA spectra were obtained. For controlling and fine-tuning frequency and cross-sections of TPA the through-space charge transfer interactions can be used. The results are explained by the electronic density matrices corresponding to governing oscillators in one- and two-photon absorption and the ground state. It is indicated that for the studied systems mainly the lowest four oscillators are responsible for the TPA cross-sections rather than a simple effective three-state model.

X-ray diffraction signals from the time-evolving molecular charge density induced by selective core excitation of chemically inequivalent carbon atoms are calculated. A narrowband X-ray pulse selectively excites the carbon K-edge of the -CH3 or -CH2F groups in fluoroethane (CH3-CH2F). Each excitation creates a distinct core coherence which depends on the character of the electronic transition. Direct propagation of the reduced single-electron density matrix, using real-time time-dependent density functional theory, provides the time-evolving charge density following interactions with external fields. The interplay between partially filled valence molecular orbitals upon core excitation induces characteristic femtosecond charge migration which depends on the core-valence coherence, and is monitored by the sum-frequency generation diffraction signal. This article is part of the theme issue Measurement of ultrafast electronic and structural dynamics with X-rays.

Homodyne X-ray diffraction signals produced by classical light and classical detectors are given by the modulus square of the charge density in momentum space |σ(q)|2, missing its phase, which is required in order to invert the signal to real space. We show that quantum detection of the radiation field yields a linear diffraction pattern that reveals σ(q) itself, including the phase. We further show that repeated diffraction measurements with variable delays constitute a novel multidimensional measure of spontaneous charge-density fluctuations. Classical diffraction, in contrast, only reveals a subclass of even-order correlation functions. Simulations of two-dimensional signals obtained by two diffraction events are presented for the amino acid cysteine.

The ultrafast spontaneous electron-density fluctuation dynamics in molecules is studied theoretically by off-resonant multiple X-ray diffraction events. The time- and wavevector-resolved photon-coincidence signals give an image of electron-density fluctuations expressed through the four-point correlation function of the charge density in momentum space. A Fourier transform of the signal provides a real-space image of the multipoint charge-density correlation functions, which reveal snapshots of the evolving electron density in between the diffraction events. The proposed technique is illustrated by ab initio simulations of the momentum- and real-space inelastic scattering signals from a linear cyanotetracetylene molecule.

The ultrafast spontaneous electron-density fluctuation dynamics in molecules is studied theoretically by off-resonant multiple X-ray diffraction events. The time- and wavevector-resolved photon-coincidence signals give an image of electron-density fluctuations expressed through the four-point correlation function of the charge density in momentum space. A Fourier transform of the signal provides a real-space image of the multipoint charge-density correlation functions, which reveal snapshots of the evolving electron density in between the diffraction events. The proposed technique is illustrated by ab initio simulations of the momentum- and real-space inelastic scattering signals from a linear cyanotetracetylene molecule.

Cobalt(II) and copper(II) complexes supported by 4‐(quinolin‐2‐ylmethyl)morpholine (L) were characterized, and their reactivity toward the ring‐opening polymerization (ROP) of rac‐lactide (rac‐LA) was studied. The use of [LMCl2]/LiOiPr and [LMCl2]/LiMe (M = Co, Cu) resulted in over 95% conversion within 10 min at 25 °C. The effect of the initiating group and geometry of the metal complexes steered the heterotactic enchainment of the resultant polylactide(PLA). The Co(II)/LiMe system represents the first example of the ROP of rac‐LA with high heterotactic enchainment (Pr = 0.92) with 98% conversion at 0 °C. [ABSTRACT FROM AUTHOR]

The harsh operating conditions of the oxygen evolution reaction (OER) in water electrolysis severely degrade the activity and stability of the electrocatalysts due to elemental leaching or particle agglomeration. Therefore, it is crucial to incorporate support materials that effectively immobilize catalyst particles for developing efficient OER catalysts. This review aims to highlight the role of MXene as a support material to improve the performance of OER catalysts. First, the extended OER mechanism is briefly described in terms of the effect of MXene support on OER catalysts. Then, various synthesis methods of MXene and catalyst‐MXene compounds are introduced, and important properties of MXene that are beneficial to improve OER performances are discussed. The electrocatalytic results of the enhanced OER catalysts due to the effective MXene support are also summarized. Finally, future challenges and prospects are proposed for utilizing MXene as an excellent support material for various electrocatalysis. [ABSTRACT FROM AUTHOR]

Analogous to conventional carbon nanotubes, single-walled, chiral, γ-graphyne nanotubes (C-γGyNTs) are modeled based on the synthesized 2D γ-graphyne motif, and their electronic properties are investigated via density-functional tight-binding calculations for the first time. The resulting γGyNTs are predicted to be excellent semiconductors with moderate bandgaps ranging from 1.291 eV to 1.928 eV. In addition, the bandgaps of zigzag γGyNTs and armchair γGyNTs show damped oscillatory behaviour, while those of C-γGyNTs do not show any chirality- or diameter-dependent oscillatory behaviour. Interestingly, it is revealed that the (2a, m)-γGyNTs, where a is a positive integer, have nearly identical bandgap values, which provides a fresh method of bandgap manipulation for semiconductor devices that has not yet been reported. [ABSTRACT FROM AUTHOR]

Electrical control of magnetic exchange coupling interactions is central to designing magnetic materials. In this study, we performed density functional theory calculations to investigate the magnetic spin configuration, magnetic moment, and magnetic coupling strength of zigzag MoS2 nanoribbons (zMoS2NRs) with different edge passivation, that is, pristine (Pristine), hydrogen termination (H-tem), sulfur termination (S-term), and sulfhydryl termination (SH-term). Further, we investigated the influence of an external electric field (FExt) on the magnetic properties. Pristine and H-term showed an AFM ground configuration with considerably weak magnetic coupling strength while S-term and SH-term showed a single edge FM ground configuration in the absence of the electric field. When the external electric field was applied, the positive field intensified the original spin configuration, thus increasing the magnetic moment of the system while the negative field weakened the original spin configuration, thus decreasing the magnetic moment and further reversed the spin configuration from AFM to FM and vice versa in most systems. The magnetic coupling strength of the system increased for both Pristine and H-term regardless of the direction of the field. However, the extent of increase was much higher in Pristine due to the existence of relatively easily transferable dangling electrons compared with the constrained electrons of H-term restricted to chemical bonds. Our results demonstrate a possibility of reversible spin control from AFM to FM and vice versa by applying an electric field and the enhancement of the magnetic coupling strength of zMoS2NRs. [ABSTRACT FROM AUTHOR]