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The tensor force is implemented into the time-dependent Hartree-Fock (TDHF) theory so that both exotic and stable collision partners, as well as their dynamics in heavy-ion fusion, can be described microscopically. The role of tensor force on fusion dynamics is systematically investigated for 40 Ca + 40 Ca, 40 Ca + 48 Ca, 48 Ca + 48 Ca, 48 Ca + 56 Ni, and 56 Ni + 56 Ni reactions which vary by the total number of spin-unsaturated magic numbers in target and projectile. A notable effect on fusion barriers and cross sections is observed by the inclusion of tensor force. The origin of this effect is analyzed. The influence of isoscalar and isovector tensor terms is investigated with the TIJ forces. These effects of tensor force in fusion dynamics are essentially attributed to the shift of lowlying vibration states of colliding partners and nucleon transfer in the asymmetric reactions. Our calculations of above-barrier fusion cross sections also show that tensor force does not significantly affect the dynamical dissipation at near-barrier energies.

Na-ion batteries (NIBs) have attracted increasing attention given the fact that sodium is relatively more plentiful and affordable than lithium for sustainable and large-scale energy storage systems. However, the shortage of electrode materials with outstanding comprehensive properties has limited the practical implementations of NIBs. Among all the discovered anode materials, transition-metal sulfide has been proven as one of the most competitive and promising ones due to its excellent redox reversibility and relatively high theoretical capacity. In this study, double-morphology N-doped CoS/multichannel carbon nanofibers composites (CoS/MCNFs) are precisely designed, which overcome common issues such as the poor cycling life and inferior rate performance of CoS electrodes. The conductive 3D interconnected multichannel nanostructure of CoS/MCNFs provides efficient buffer zones for the release of mechanical stresses from Na ions intercalation/deintercalation. The synergy of the diverse structural features enables a robust frame and a rapid electrochemical reaction in CoS/MCNFs anode, resulting in an impressive long-term cycling life of 900 cycles with a capacity of 620 mAh g at 1 A g (86.4% theoretical capacity) and a surprisingly high-power output. The proposed design in this study provides a rational and novel thought for fabricating electrode materials.

To explore environmentally benign solvents for the absorption of NO and NO2, a series of caprolactam tetrabutyl ammonium halide ionic liquids were synthesized. The solubility of NO and NO2 was measured at temperatures ranging from 298.2 to 363.2 K and atmospheric pressure, and the following trend in the solubility of NO and NO2 in ionic liquids with various halide anions was observed, respectively: F > Br > Cl and Br > Cl > F. Moreover, as the temperature increased from 308.15 to 363.15 K and the mole ratio of caprolactam increased from 2:1 to 6:1, the solubility of NO increased. Alternatively, the solubility of NO2 decreased as the temperature increased from 298.15 to 363.15 K, and the mole ratio of caprolactam increased from 2:1 to 6:1. The absorption and desorption of NO and NO2 was practically reversible in the ionic liquids, which was characterized by nuclear magnetic resonance. The method, which is at least partially reversible, offers interesting possibilities for the removal of NO and NO2.

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