Carbon nanoparticles (CNPs) are grown on flexible carbon fabric via a simple and low‐cost flame synthesis process. The entire struture of the carbon fabric substrate retains its high flexibility after the growth of CNPs and can even be rolled‐up and twisted to a large degree without affecting the electric characteristics. No appreciable changes in the conductance can be observed under different bending curvatures after hundreds of bending cycles. The thermal conductivity of the carbon fabric with CNPs is about 2.34 W m−1 K−1, about one order of magnitude higher than that of most polymer substrates. The field emitter fabricated using the structure has a low threshold electric field of around 2.8 V μm−1, and a high field emission current density of 108 mA cm−2, which is about two to four orders of magnitude higher than that of most polymer substrate‐based flexible CNT field emitters. These results indicate that CNPs on carbon fabric have potential applications in flexible electronics devices and displays.
Two cobalt mixed-valence complexes with different substituents have been prepared and structurally characterized by single-crystal X-ray diffraction to alter slow magnetic relaxation by tailoring the transverse anisotropy. The trinuclear complexes [(L(1))4Co3(H2O)2](NO3)4·CH3OH·5H2O (1-NO3) and [(L(2))4Co3(H2O)2](NO3)4·6H2O (2-NO3) feature a distorted octahedral Co(II) strongly hindered in a trinuclear Co(III)-Co(II)-Co(III) mixed-valence array. Detailed magnetic studies of 1-NO3 and 2-NO3 have been conducted using direct- and alternating-current magnetic susceptibility data. In accordance with variable-field magnetic susceptibility data at low temperatures, high-field electron paramagnetic resonance (HF-EPR) spectroscopy reveals the presence of an easy-plane anisotropy (D > 0) with a significant transverse component, E, in complexes 1-NO3 and 2-NO3. These findings indicate that the onset of the variation of distortion within complex 2-NO3 leads to a suppression of quantum tunneling of the magnetization within the easy plane, resulting in magnetic bistability and slow relaxation behavior. Consequently, the anisotropy energy scale associated with the relaxation barrier, 5.46 cm(-1) (τo = 1.03 × 10(-5) s), is determined by the transverse E term. The results demonstrate that slow magnetic relaxation can be switched through optimization of the transverse anisotropy associated with magnetic ions that possess easy-plane anisotropy.
The magnetization and electron spin resonance (ESR) in nanocrystals of Haldane-chain antiferromagnet Gd2BaNiO5 have been investigated. It is revealed that a reduction in crystal size results in an enhancement of magnetization due to a large number of paramagnetic Gd3+ and Ni2+ ions forming on the surfaces of nanocrystals. The smallest nanoparticles with an average size of 45 nm behave like a paramagnet, as evidenced by our ESR data. Upon application of an external magnetic field, the weakly coupled spins can be well aligned along the direction of the magnetic field, giving rise to a giant entropy change of −ΔSm = 36 J⋅kg−1⋅K−1 at 2 K in a field range of 0–7 T. This value is larger than those of most rare-earth-based compounds reported. The large value of −ΔSm, together with the absence of thermal and field hysteresis, makes Gd2BaNiO5 nanocrystals very promising candidates for low-temperature magnetic refrigeration.
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