The ultrafast demagnetization dynamics of 3d and 4f spins, respectively, in FeCo and Tb of TbFeCo alloy film are studied independently by employing a dual-color time-resolved magneto-optical Kerr spectroscopy. The demagnetization dynamics of 3d and 4f spins are independently probed, respectively, by 800 and 400 nm light. Two-step demagnetization dynamics are observed for both the 3d and 4f spins under the excitation of 800 nm laser. In particular, the onset of 4f spin dynamics presents a delayed time with respect to the one of 3d spin dynamics. Those results clearly reveal a strong inter-atomic 3d–5d–4f exchange coupling which drives the first-step subpicosecond ultrafast demagnetization process of 4f spins, and a spin(4f)-lattice coupling which drives the second-step slower demagnetization process of 4f spins. A numerical calculation based on four temperature model reproduces the coupling characteristics in the demagnetization dynamics, and reveals the energy evolution dynamics among the different subsystems. These results provide a direct demonstration of strong coupling dynamics between the two spin subsystems in rare earth-transition metal alloy occurring within subpicosecond timescale, and show a new approach for ultrafast control of 4f spins via an indirect excitation.

In this work, we studied influence of post thermal annealing on the performance and charge photogeneration processes of PffBT4T-2OD/PC₇₁BM solar cells. As-prepared device exhibits a high-power conversion efficiency of 9.5%, much higher than that after thermal annealing. To understand this phenomenon, we studied charge photogeneration processes in these solar cells by means of time resolved spectroscopy. We associate the degradation of solar cell performance with the reduction of exciton dissociation efficiency and with increased bimolecular recombination of photogenerated charges as a result of annealing. We correlate the generation of localized PffBT4T-2OD polarons observed via spectro-electrochemical measurements with enhancement of the bimolecular charge recombination of annealed solar cells.

Magnetic skyrmions are promising potential information carriers for future spintronic devices owing to their nanoscale size, non-volatility and high mobility. In this work, we demonstrate the controlled manipulation of skyrmion motion and its implementation in a new concept of racetrack logical device by introducing an inhomogeneous perpendicular magnetic anisotropy (PMA) via micromagnetic simulation. Here, the inhomogeneous PMA can be introduced by a capping nano-island that serves as a tunable potential barriers/well which can effectively modulate the size and shape of isolated skyrmion. Using the inhomogeneous PMA in skyrmion-based racetrack enables the manipulation of skyrmion motion behaviors, for instance, blocking, trapping or allowing passing the injected skyrmion. In addition, the skyrmion trapping operation can be further exploited in developing special designed racetrack devices with logic AND and NOT, wherein a set of logic AND operations can be realized via skyrmion–skyrmion repulsion between two skyrmions. These results indicate an effective method for tailoring the skyrmion structures and motion behaviors by using inhomogeneous PMA, which further provide a new pathway to all-electric skyrmion-based memory and logic devices.

A large area of randomly distributed nanospike as nanostructured template was induced by femtosecond (fs) laser on a silicon substrate in water. Copper oxide (CuO) and palladium (Pd) heterostructured nanofilm were coated on the nanospikes by magnetron sputtering technology and vacuum thermal evaporation coating technology respectively for the construction of a p-type hydrogen sensor. Compared with the conventional gas sensor based on CuO working at high temperature, nanostructured CuO/Pd heterostructure exhibited promising detection capability to hydrogen at room temperature. The detection sensitivity to 1% H₂ was 10.8%, the response time was 198 s, and the detection limit was as low as 40 ppm, presenting an important application prospect in the clean energy field. The excellent reusability and selectivity of the CuO/Pd heterostructure sensor toward H₂ at room temperature were also demonstrated by a series of cyclic response characteristics. It is believed that our room-temperature hydrogen sensor fabricated with a waste-free green process, directly on silicon substrate, would greatly promote the future fabrication of a circuit-chip integrating hydrogen sensor.

In this work, charge photogeneration dynamics in PTQ10:Y6 solar cells were studied by steady-state and time-resolved spectroscopies. For neat donor and acceptor films, we determined the exciton diffusion coefficients of PTQ10 and Y6 as 1.3 × 10⁻³ cm²·s⁻¹ and 6.8 × 10⁻³ cm²·s⁻¹, respectively. Furthermore, we find the LUMO and HOMO level offsets of 0.14 eV and 0.11 eV are sufficient for the dissociation of donor and acceptor excitons, respectively. For PTQ10:Y6 blend films, we find DIO additive could increase the scales of acceptor and donor phases. The acceptor phase increased slightly from 17.2 nm to 20.0 nm, while the donor phase increased from 2.3 nm to 5.8 nm. In addition, we find bimolecular recombination is a critical form for carrier recombination and DIO additive can significantly suppress the carrier recombination rate of PTQ10:Y6 active layer in an ultrafast time scale. This work is helpful for understanding the charge photogeneration processes in non-fullerene polymer solar cells.

The fundamental mechanisms of ultrafast demagnetization and magnetization recovery processes in ferromagnetic materials remain incompletely understood. The investigation of different dynamic features which depend on various physical quantities requires a more systematic approach. Here, the femtosecond laser-induced demagnetization and recovery dynamics in L1₀-Fe_0.5Pt_0.5 alloy film are studied by utilizing time-resolved magneto-optical Kerr measurements, focusing on their dependences of excitation fluence and ambient temperature over broad ranges. Ultrafast demagnetization dominated by Elliott-Yafet spin-flip scattering, and two-step magnetization recovery processes are found to be involved in all observations. The fast recovery time corresponding to spin–lattice relaxation is much shorter than that of many ferromagnets and increase with excitation fluence. These can be ascribed to the strong spin–orbit coupling (SOC) demonstrated in FePt and the reduction of transient magnetic anisotropy, respectively. Surprisingly, the demagnetization time exhibits no discernible correlation with ambient temperature. Two competitive factors are proposed to account for this phenomenon. On the other hand, the spin–lattice relaxation accelerates as temperature decreases due to enhanced SOC at lower ambient temperature. A semiquantitative analysis is given to get a visualized understanding. These results offer a comprehensive understanding of the dynamic characteristics of ultrafast demagnetization and recovery processes in iron-based materials with strong SOC, highlighting the potential for regulating the magnetization recovery process through temperature and laser fluence adjustments.