Enhanced polarization via Joule heating in wood-derived carbon materials for absorption-dominated EMI shielding.

To cope with sophisticated application scenarios, carbon materials can provide opportunities for integrating multi-functionalities into superior electromagnetic interference (EMI) shielding properties. Nevertheless, carbon materials usually possess high electrical conductivity, which allows them to counteract electromagnetic waves by reflection. Moreover, the identification of factors that dominate the shielding mechanisms has typically been result-oriented, leading to a reliance on a trial-and-error approach for the development of shielding materials. Thus, it is crucial to identify the dominant factors for EMI shielding and elucidate the mechanism underlying the coordination of the balance between reflection and absorption in carbon materials. In this study, we developed a promising and viable approach to create Co@CNTs embedded in carbonized wood (CW) via chemical vapor deposition, producing Co@CNTs/CW foams. The CNTs, densely grown on the CW surface, tightly encapsulated the Co nanoparticles within them. By manipulating the Co content, the defect density and CNT length varied within the Co@CNTs. Through first-principles calculations, these variations substantially influenced the work function, charge density, and dipole moment of the Co@CNTs. Thus, defect-induced and interfacial polarizations were improved, inducing a transformation of the shielding mechanism from reflection to absorption. Regarding the Co@CNTs/CW foams, while high conductivity was essential for achieving satisfactory shielding performance, the enhanced polarization loss dominated the contribution of absorption to the overall shielding effectiveness. Taking advantage of the enhanced polarizations, the Co@CNTs/CW foams exhibited an impressive shielding effectiveness of 42.0 dB, along with an absorptivity of 0.64, which were instrumental in effectively minimizing secondary reflections. Remarkably, these as-prepared foams possessed outstanding hydrophobicity and Joule heating features with a water contact angle of 138° and a saturation temperature of 85.5 °C (2.5 V). Through the stimulation of voltage-driven Joule heating, the absorptivity of Co@CNTs/CW foams can be significantly enhanced to a range of 0.61 to 0.73, irrespective of the Co content. This research would provide a new avenue for designing carbon materials with an absorption-dominated mechanism integrated into EMI shielding performance.

Ultrathin and Highly Crumpled/Porous CoP Nanosheet Arrays Anchored on Graphene Boosts the Capacitance and Their Synergistic Effect toward High-Performance Battery-Type Hybrid Supercapacitors.

Constructing novel electrode materials with supernal specific capacitance and cycle stability is important for the practical applications of supercapacitors. Herein, ultrathin and highly crumpled CoP/reduced graphene oxide (rGO) nanosheet arrays are grown on nickel foam (NF) through a hydrothermal-phosphidation route. Benefitting from the synergistic effects of CoP with large specific capacity and rGO with high conductivity and ultrathin nanosheet arrays structure, CoP/rGO shows extraordinary electrochemical performance. The CoP/rGO electrode possesses a superior specific capacity of 1438.0 C g-1 (3595.0 F g-1) at 1 A g-1, which is 3.43, 2.05, and 2.26 times larger than those of Co(OH)2/rGO, Co3O4/rGO, and bare CoP. In particular, the CoP/rGO nanosheet arrays show the highest specific capacities among the monometallic phosphide-based nanostructures reported so far. The CoP/rGO retains 1198.9 C g-1 (2997.2 F g-1) at 10 A g-1, revealing the outstanding rate capability of 83%. Theoretical calculations reveal that rGO can adequately reduce the absorption energy of OH- on CoP, which makes CoP/rGO have strong adsorption capacity of OH-, resulting in boosting electrochemical performance. A hybrid supercapacitor of CoP/rGO/NF//AC was designed, which presents a superior energy density of 43.2 Wh kg-1 at a power density of 1010.5 W kg-1. After 10 000 cycles, the CoP/rGO/NF//AC supercapacitor reveals excellent cycling durability with a capacitance retention of 89%. This work provides a new insight into the design of high-performance electrode materials by combining high capacitive metal phosphides with conductive carbon, which is of great significance for energy storage systems.

Enhanced Metal-Insulator Transition in Freestanding VO2 Down to 5 nm Thickness.

Ultrathin freestanding membranes with a pronounced metal-insulator transition (MIT) have huge potential for future flexible electronic applications as well as provide a unique aspect for the study of lattice-electron interplay. However, the reduction of the thickness to an ultrathin region (a few nm) is typically detrimental to the MIT in epitaxial films, and even catastrophic for their freestanding form. Here, we report an enhanced MIT in VO2-based freestanding membranes, with a lateral size up to millimeters and the VO2 thickness down to 5 nm. The VO2 membranes were detached by dissolving a Sr3Al2O6 sacrificial layer between the VO2 thin film and the c-Al2O3(0001) substrate, allowing the transfer onto arbitrary surfaces. Furthermore, the MIT in the VO2 membrane was greatly enhanced by inserting an intermediate Al2O3 buffer layer. In comparison with the best available ultrathin VO2 membranes, the enhancement of MIT is over 400% at a 5 nm VO2 thickness and more than 1 order of magnitude for VO2 above 10 nm. Our study widens the spectrum of functionality in ultrathin and large-scale membranes and enables the potential integration of MIT into flexible electronics and photonics.

Doping effect and oxygen defects boost room temperature ferromagnetism of Co-doped ZnO nanoparticles: experimental and theoretical studies.

Co-doped ZnO nanoparticles with different dosage concentrations were fabricated by a thermal decomposition method. The nanoparticles show a pure wurtzite structure without the formation of a secondary phase or Co clusters, in which Co ions present as Co2+ and occupy Zn2+ tetrahedral sites within the ZnO matrix. All the samples show ferromagnetic properties at room temperature with nonzero coercivity and remanence magnetization. Besides, the magnetic data is also fitted by the model of bound magnetic polarons (BMP). By increasing the Co2+ doping concentration, the saturation magnetization values of Co-doped ZnO nanoparticles increase first and then decreases, which is related to the variation tendency of oxygen defects on the surface and the number of BMPs. This phenomenon can be ascribed to the formation of defect-induced BMPs, in which ferromagnetic coupling occurs at lower Co2+ concentration and Co2+-O2--Co2+ antiferromagnetic coupling arises at higher Co2+ concentration. Air annealing experiments further demonstrate this result, in which the saturation magnetization of Co-doped ZnO nanoparticles is reduced after annealing in Air. The doping effect and oxygen defects on the magnetic ordering of Co-doped ZnO were calculated using density functional theory. The calculation results reveal that stable long-range magnetic ordering in Co-doped ZnO nanoparticles is mainly attributed to the localized spin moments from 3d electrons of Co2+ ions. Both the experimental and theoretical studies demonstrate that the ferromagnetism in Co-doped ZnO nanoparticles is originated from the combined effects of Co doping and oxygen vacancies. These results provide an experimental and theoretical view to understand the magnetic origination and tune the magnetic properties of diluted magnetic semiconductors, which is of great significance for spintronics.