Enhancement of Isotropic Heat Dissipation of Polymer Composites by Using Ternary Filler Systems Consisting of Boron Nitride Nanotubes, h-BN, and Al2O3.

In this research article, a poly(dimethylsiloxane) (PDMS)-based composite was postulated adapting an interactive ternary filler system consisting of Al2O3, hexagonal boron nitride (h-BN), and boron nitride nanotubes (BNNT) to construct a continuous three-dimensional (3D) structure for thermal attenuation. Al2O3 was imposed as a main filler, while h-BN and BNNT were assimilated to form interconnected heat conduction pathways for effective thermal dissipation. The structured framework articulates a profound improvement in isotropic thermal conductivity considering both axial and radial heat dissipation. The presence of h-BN entails uniform heat distribution in a planar mode, eliminating the occurrence of hotspots, while BNNT constructed a connecting phonon pathway in various directions, which insinuates effective overall thermal transport. The generated ternary filler composites attained an isotropic ratio of 1.35 and a thermal conductivity of 7.50 W/mK, which is a 36-fold (∼3650%) increase compared to neat PDMS resin and almost 3-fold (∼297%) that of the Al2O3 unary filler composite and ∼53% that of its binary counterpart, partaking interfacial thermal gaps of ∼36.15 and ∼62.24% on practical heating performance relative to its counterparts. Moreover, the incorporation of BNNT on a traditional spherical and planar filler offers an advantage not only in thermal conductivity but also in thermal and structural stability. Improvement in thermal stability is stipulated due to a melting point (Tm) shift of ∼11 °C upon the assimilation of BNNT. Mechanical permeance reinforcement was also observed with the presence of BNNT, showcasing a 31.5% increase in tensile strength and a 53% increase in Young's modulus relative to the singular filler composite. This exploration administers a new insight into heat dissipation phenomena in polymeric composites and proposes a simple approach to their design and assembly.

Noble Metal Nanoparticles Decorated Boron Nitride Nanotubes for Efficient and Selective Low-Temperature Catalytic Reduction of Nitric Oxide with Carbon Monoxide.

Parallel to CO2 emission, NOx emission has become one of the menacing problems that seek a simple, durable, and high-efficiency deNOx catalyst. Herein, we demonstrated simple syntheses of platinum group metal nanoparticle-decorated f-BNNT (PGM = Pd, Pt, and Rh, and f-BNNT stands for -OH-functionalized boron nitride nanotubes) as a catalyst for efficient and selective reduction of NO by CO at low-temperature conditions. PGM/f-BNNT with a low amount of noble metal nanoparticles (0.7-0.8 wt %) presents very efficient catalytic activity for NO reduction as well as CO oxidation during their removal process. The removal efficiencies of NO and CO with Pd/f-BNNT, Pt/f-BNNT, and Rh/f-BNNT catalysts were investigated under various temperatures, flow rates, and reaction times, respectively. For most cases, NO catalytic reduction with CO reaction was >99% at a temperature as low as ∼200 °C. The catalyst robustness and efficiency were also verified by presenting almost 100% conversion of NO using a Rh/f-BNNT catalyst, which was aged under humid air at 600 and 700 °C for 24 h, respectively. The synergic effect of the catalytic efficacy of the well-dispersed noble metal nanoparticles and the excellent surface properties of BNNT are reasons for the high selectivity and catalytic property at a low temperature. On the basis of this investigation, we demonstrated that the noble metal nanoparticle-decorated f-BNNT catalysts are possible to save expensive PGM catalysts, such as Pt, Pd, and Rd, as much as 100 times while presenting similar or better catalytic performance for simultaneous NO and CO removals.

Nanohole-Structured and Palladium-Embedded 3D Porous Graphene for Ultrahigh Hydrogen Storage and CO Oxidation Multifunctionalities.

Atomic-scale defects on carbon nanostructures have been considered as detrimental factors and critical problems to be eliminated in order to fully utilize their intrinsic material properties such as ultrahigh mechanical stiffness and electrical conductivity. However, defects that can be intentionally controlled through chemical and physical treatments are reasonably expected to bring benefits in various practical engineering applications such as desalination thin membranes, photochemical catalysts, and energy storage materials. Herein, we report a defect-engineered self-assembly procedure to produce a three-dimensionally nanohole-structured and palladium-embedded porous graphene hetero-nanostructure having ultrahigh hydrogen storage and CO oxidation multifunctionalities. Under multistep microwave reactions, agglomerated palladium nanoparticles having diameters of ∼10 nm produce physical nanoholes in the basal-plane structure of graphene sheets, while much smaller palladium nanoparticles are readily impregnated inside graphene layers and bonded on graphene surfaces. The present results show that the defect-engineered hetero-nanostructure has a ∼5.4 wt % hydrogen storage capacity under 7.5 MPa and CO oxidation catalytic activity at 190 °C. The defect-laden graphene can be highly functionalized for multipurpose applications such as molecule absorption, electrochemical energy storage, and catalytic activity, resulting in a pathway to nanoengineering based on underlying atomic scale and physical defects.

3D networked graphene-ferromagnetic hybrids for fast shape memory polymers with enhanced mechanical stiffness and thermal conductivity.

A novel 3D networked graphene-ferromagnetic hybrid can be easily fabricated using one-step microwave irradiation. By incorporating this hybrid material into shape memory polymers, the synergistic effects of fast speed and the enhancement of thermal conductivity and mechanical stiffness can be achieved. This can be broadly applicable to designing magneto-responsive shape memory polymers for multifunction applications.

Graphene--nanotube--iron hierarchical nanostructure as lithium ion battery anode.

In this study, we report a novel route via microwave irradiation to synthesize a bio-inspired hierarchical graphene--nanotube--iron three-dimensional nanostructure as an anode material in lithium-ion batteries. The nanostructure comprises vertically aligned carbon nanotubes grown directly on graphene sheets along with shorter branches of carbon nanotubes stemming out from both the graphene sheets and the vertically aligned carbon nanotubes. This bio-inspired hierarchical structure provides a three-dimensional conductive network for efficient charge-transfer and prevents the agglomeration and restacking of the graphene sheets enabling Li-ions to have greater access to the electrode material. In addition, functional iron-oxide nanoparticles decorated within the three-dimensional hierarchical structure provides outstanding lithium storage characteristics, resulting in very high specific capacities. The anode material delivers a reversible capacity of ~1024 mA · h · g(-1) even after prolonged cycling along with a Coulombic efficiency in excess of 99%, which reflects the ability of the hierarchical network to prevent agglomeration of the iron-oxide nanoparticles.

Defect-engineered three-dimensional graphene-nanotube-palladium nanostructures with ultrahigh capacitance.

The development of three-dimensional carbon-based nanostructures is the next step forward for boosting industrial applications of carbon nanomaterials such as graphenes and carbon nanotubes. Some defects, which have been considered as detrimental factors for maintaining exceptional materials properties of two-dimensional graphene, can be actively used to synthesize three-dimensional graphene-based carbon nanostructures. Here we describe a fast and heretofore unreported defect-engineered method to synthesize three-dimensional carbon nanohybrid structures with strong bonding between graphene nanoplatelets and carbon nanotubes using simple microwave irradiation and an ionic liquid. Our one-pot method utilizes defect-engineered sequential processes: microwave-based defect generation on graphene nanoplatelets, anchoring of palladium nanoparticles on these defects, and subsequent growth of carbon nanotubes by use of an ionic liquid. The unique three-dimensional nanostructures showed an ultrahigh redox capacitance due to high porosity, a high surface-to-volume ratio from the spacer role of vertically standing one-dimensional carbon nanotubes on graphene sheets, and capacitance-like redox response of the palladium nanoparticles. The proposed defect-engineered method could lead to novel routes to synthesizing three-dimensional graphene-based nanostructures with exceptionally high performance in energy storage systems.