Search Results (4)

Controlling spin dynamics conventionally requires external magnetic fields, strong electric bias, or material-specific spin–orbit interactions, while the temporal reference frame remains fixed. Here we introduce curved-time spintronics, a framework in which a synthetic lapse field, implemented through GHz surface-acoustic-wave (SAW) modulation, reshapes the effective flow of time experienced by spinor, magnonic, and photon–spin degrees of freedom. Using a curved-time Schrödinger–Pauli model, we show that it renormalizes the Larmor frequency, modifies SOC-driven splittings, and produces helicity-dependent spin precession under circularly polarized excitation. Strikingly, a spatial lapse gradient induces a Hall-like transverse drift even when in the absence of any external electric field or intrinsic Berry curvature, demonstrating that time geometry alone can generate transverse transport. Time-domain simulations confirm curvature-driven Hall response across graphene, carbon nanotubes, and generic Dirac platforms, establishing a material-agnostic, field-free mechanism for transverse spin manipulation. We further predict curvature-dependent spin diffusion, temporal magnon focusing, and helicity-selective entanglement generation, and propose pump–probe detection via ultrafast Kerr rotation synchronized to SAW-driven lapse modulation. These results position engineered time geometry as a new spintronic control axis, enabling Hall-like effects, spin transport, and chiral phase manipulation without relying on intrinsic material properties, magnetic fields, or electric gating. Full article

Effective residue management is crucial for maintaining soil organic carbon (SOC) in upland rice systems, particularly under diverse fertilization and planting management practices. This study investigates the impacts of residue management in upland rice fields using the CQESTR model through simulation of SOC dynamics over a 20-year period. The first 10 years served as a spin-up period for carbon pool stabilization in the model, followed by simulations under varying nitrogen (N) application rates and planting date management strategies. Experiments for various N application rates and planting times were conducted during 2018–2019 and 2019–2020. In 2019, 30% and in 2020, 100% of the residue was returned, and these data were used for evaluating model performance. Subsequently, we modeled predictions for residue retention levels of 100%, 70%, 50%, and 30% to assess their effects on SOC. The results indicated a good agreement between the simulated and observed data for model performance evaluation with an MSD value of 9.13. Lack of correlation (0.44) accounted for 5% of MSD, indicating a good agreement between the simulated and observed SOC values. The highest change in SOC was observed at 100% residue return under moderately delayed planting, potentially due to higher crop productivity and residue retention, and moderate climatic conditions. Reduced residue retention gradually declined the SOC stocks, especially under low N input. Delays in planting exacerbated negative impacts, possibly due to low crop productivity and reduced residue return. Despite the limited number of years of data and inconsistent management practices, the overall trends highlight the importance of residue retention under different N fertilization and planting management strategies. This research serves as a preliminary study for sustainable management practices to enhance long-term soil carbon sequestration in upland rice systems in southern Thailand. Long-term evaluations are necessary using the observed data and the CQESTR model application for applicable recommendations. Full article

To scale down semiconductor devices to a size less than the design rule of 10 nm, lithography using a carbon polymer hard-mask was applied, e.g., spin-on-carbon (SOC) film. Spin coating of the SOC film produces a high surface topography induced by pattern density, requiring chemical–mechanical planarization (CMP) for removing such high surface topography. To achieve a relatively high polishing rate of the SOC film surface, the CMP principally requires a carbon–carbon (C-C) bond breakage on the SOC film surface. A new design of CMP slurry evidently accomplished C-C bond breakage via transformation from a hard surface with strong C-C covalent bonds into a soft surface with a metal carbon complex (i.e., C=Fe=C bonds) during CMP, resulting in a remarkable increase in the rate of the SOC film surface transformation with an increase in ferric catalyst concentration. However, this surface transformation on the SOC film surface resulted in a noticeable increase in the absorption degree (i.e., hydrophilicity) of the SOC film CMP slurry on the polished SOC film surface during CMP. The polishing rate of the SOC film surface decreased notably with increasing ferric catalyst concentration. Therefore, the maximum polishing rate of the SOC film surface (i.e., 272.3 nm/min) could be achieved with a specific ferric catalyst concentration (0.05 wt%), which was around seven times higher than the me-chanical-only CMP. Full article

A meso-mesityl-2,6-iodine substituted boron dipyrromethene (BODIPY) dye is investigated using a suite of computational methods addressing its functionality as photosensitizer, i.e., in the scope of light-driven hydrogen evolution in a two-component approach. Earlier reports on the performance of the present iodinated BODIPY dye proposed a significantly improved catalytic turn-over compared to its unsubstituted parent compound based on the population of long-lived charge-separated triplet states, accessible due to an enhanced spin-orbit coupling (SOC) introduced by the iodine atoms. The present quantum chemical study aims at elucidating the mechanisms of both the higher catalytic performance and the degradation pathways. Time-dependent density functional theory (TDDFT) and multi-state restricted active space perturbation theory through second-order (MS-RASPT2) simulations allowed identifying excited-state channels correlated to iodine dissociation. No evidence for an improved catalytic activity via enhanced SOCs among the low-lying states could be determined. However, the computational analysis reveals that the activation of the dye proceeds via pathways of the (prior chemically) singly-reduced species, featuring a pronounced stabilization of charge-separated species, while low barriers for carbon-iodine bond breaking determine the photostability of the BODIPY dye. Full article