Jiachen Liu

Structure formation process, heat-insulation property and cyclic compression–resilience performance of mullite fibres/whiskers frameworks

Mullite fibres/whiskers frameworks (MF/MW frameworks) were prepared by mixed-slurry-filtration and heat-treating. Hierarchical fibres/whiskers structure formed in the frameworks through fluorine-catalyzed gas-phase reaction. Topaz rods as a transient product first formed in the frameworks, and then gradually transformed into mullite whiskers. Intersected mullite whiskers served as lap-jointing points of the fibres. The volume density, apparent porosity and thermal conductivity of the samples heat-treated at 1100–1500 °C were 0.402–0.541 g cm−3, 81.2–85% and 0.1191–0.1647 W m−1 k−1, respectively. Cyclic compression–resilience performance (maximum stress = 0.4 MPa) of the samples was tested at room temperature. The compression ratio, permanent deformation ratio and resilience ratio of the samples in the first circle compression–resilience test were 2.031–3.833%, 0.125–0.042% and 93.85–98.28%, respectively. The excellent thermal/mechanical properties indicated that the MF/MW frameworks were suitable for being applied as high temperature heat-insulation/sealing materials.

Facile synthesis of free-standing Fe2O3/carbon nanotube composite films as high-performance anodes for lithium-ion batteries

Continuous Fe nanoparticles (NPs)/carbon nanotube (CNTs) composite films have been fabricated with the CVD gas flow reaction using ferrocene as a catalyst and ethanol as a carbon precursor. The as-spun Fe NPs/CNTs films are converted to Fe2O3 NPs/CNTs films by an annealing process in air at a temperature of 500 °C. The as-prepared Fe2O3 NPs/CNTs films are still highly flexible. Scanning electron microscopy (SEM) and transmission electron microscopy observations reveal the Fe2O3 NPs are homogeneously bonded with the CNT network. In addition, the flexible and conductive 3D CNTs networks endow the as-synthesized composite with increased electrical conductivity and mechanical stability. As a result, the as-synthesized flexible and transferrable composite films deliver an initial reversible capacity of 985.8 mA h g−1 at a current density of 30 mA g−1, and maintain a high reversible capacity of 392.4 mA h g−1 even at a current density up to 3 A g−1. Meanwhile, Fe2O3 NPs/CNTs films exhibit an excellent cycling performance with a reversible capacity of 375.5 mA h g−1 after 800 cycles at a current density of 3 A g−1.

Joining of silicon carbide by a heat-resistant phosphate adhesive

In this paper, SiC was bonded with a phosphate inorganic adhesive prepared from H3PO4 and Al(OH)3 as the matrix and Si and B4C as the inorganic fillers. The properties of the obtained adhesive were analyzed by XRD, TG-DSC, IR, shear strength tests and SEM. The results showed that the phosphate adhesive exhibited outstanding heat-resistant properties and excellent bonding strength. The addition of B4C could greatly improve the adhesives mechanical properties due to the formation of borosilicate glass and the volume compensation came from B4Cs oxidation. The shear strength of bonded specimens could be up to about 10 MPa after heat treatment at 1300 °C, attributed to the generation of mullite and borosilicate as well as the reasonable compensation for the adhesives volume.

Hierarchical Mesoporous NiO/MnO2@PANI Core–Shell Microspheres, Highly Efficient and Stable Bifunctional Electrocatalysts for Oxygen Evolution and Reduction Reactions

We report on the new facile synthesis of mesoporous NiO/MnO2 in one step by modifying inverse micelle templated UCT (University of Connecticut) methods. The catalyst shows excellent electrocatalytic activity and stability for both the oxygen evolution reaction (OER) and the oxygen reduction reaction (ORR) in alkaline media after further coating with polyaniline (PANI). For electrochemical performance, the optimized catalyst exhibits a potential gap, ΔE, of 0.75 V to achieve a current of 10 mA cm-2 for the OER and -3 mA cm-2 for the ORR in 0.1 M KOH solution. Extensive characterization methods were applied to investigate the structure-property of the catalyst for correlations with activity (e.g., XRD, BET, SEM, HRTEM, FIB-TEM, XPS, TGA, and Raman). The high electrocatalytic activity of the catalyst closely relates to the good electrical conductivity of PANI, accessible mesoporous structure, high surface area, as well as the synergistic effect of the specific core-shell structure. This work opens a new avenue for the rational design of core-shell structure catalysts for energy conversion and storage applications.