ABSTRACT
Thermal conductive coating materials with combination of mechanical robustness, good adhesion and electrical insulation are in high demand in the electronics industry. However, very few progresses have been achieved in constructing a highly thermal conductive composites coating that can conformably coat on desired subjects for efficient thermal dissipation, due to their lack of materials design and structure control. Herein, we report a bioinspired thermal conductive coating material from cellulose nanofibers (CNFs), boron nitride (BN), and polydopamine (PDA) by mimicking the layered structure of nacre. Owing to the strong interfacial strength, mechanical robustness, and high thermal conductivity of CNFs, they do not only enhance the exfoliation and dispersion of BN nanoplates, but also bridge BN nanoplates to achieve superior thermal and mechanical performance. The resulting composites coating exhibits a high thermal conductivity of 13.8 W/(m·K) that surpasses most of the reported thermal conductive composites coating owing to the formation of an efficient thermal conductive pathway in the layered structure. Additionally, the coating material has good interface adhesion to conformably wrap around various substrates by scalable spray coating, combined with good mechanical robustness, sustainability, electrical insulation, low-cost, and easy processability, which makes our materials attractive for electronic packaging applications.
ABSTRACT
Making full use of low-energy photons and reducing photogenerated carriers' recombination rate have been considered important ways to raise photoelectrocatalysis (PEC) efficiency. In this study, Ir-doped ZnO PEC electrodes were prepared by thermal decomposition method, first principles calculations were used to study the effects of Ir content on the electronic structure and optical properties of IrxZn1-xO coatings, the PEC degradation mechanism of the IrxZn1-xO/Ti electrodes was also tentatively presented. The results indicated that with numbers of Zn atoms replaced by Ir atoms, impurity energy level appeared in ZnO band gap, which reduced the electron transition barriers and increased the number of photogenerated carriers. Besides, IrO2 nanoparticles covered on ZnO nanorods surface, acting as highly efficient electron transfer channels and electrocatalytic active sites, could separate photogenerated electron-hole pairs and enhance PEC performance effectively. PEC performance of IrxZn1-xO/Ti electrodes with different Ir contents under UV irradiation was evaluated by rhodamine B (RhB) removal rate. Compared with pure ZnO electrodes, IrxZn1-xO/Ti ones exhibited much stronger degradation capacity. Specifically, Ir0.09375Zn0.90625O/Ti electrodes showed the highest degradation rate of 99.4 %, and a relatively high rate of 95.2 % after working 100 h continuously, indicating its excellent long-term stability.
ABSTRACT
DSA-type Ti/RuxSn1-xO2 electrodes were prepared by thermal decomposition method as photoelectrocatalysts (PECs) and extensively characterized by various sophisticated techniques. First-principles calculations was employed to study the effects of Ru content on the electronic structures of the RuxSn1-xO2 coatings. The photoelectric-synergistic catalytic activity of the Ti/RuxSn1-xO2 electrodes was evaluated for the degradation of methyl orange (MO) in aqueous solution. The results show that the RuO2-SnO2 solid solution could be formed. The band gaps of the RuxSn1-xO2 coatings gradually decreased and eventually turned into metallic conductivity with the increase of ruthenium content. As a PEC electrode, reducing band gap is helpful to improve electronic conductivity and the electrocatalytic activity, but not always advantageous to increase the photocatalytic activity. Because too narrow band gap will sacrifice the photogenerated charge carriers and thus reduce photocatalytic activity of the electrode. In our experiments, the rate constant of Ti/Ru0.05Sn0.95O2 electrode increased with increasing Ru content and exhibited the maximum rate for 5% Ru loading. The stability test showed the photoelectrocatalytic activity of the Ti/Ru0.05Sn0.95O2 electrode almost had no attenuation after 100h photoelectrolysis, revealing that this electrode has good long-term stability.