Avoiding the invasion of H2O into Y2Mo3O12 by coating with C3N4 to improve negative thermal expansion properties.

The hygroscopicity of Y2Mo3O12 has serious influences on its mechanic and negative thermal expansion (NTE) properties. The reported partial ion substitution for Y3+ in Y2Mo3O12 could reduce the hygroscopicity, however, the expected NTE properties disappear disappointedly. In this investigation, it is found that avoiding the invasion of crystal water and extending the NTE temperature range of Y2Mo3O12 to room temperature could be realized together by heating with CO(NH2)2. The X-ray diffraction patterns, infrared absorption spectra, scanning electron microscopy images and X-ray photoelectron spectra suggest the formation of small hydrophobic molecules (C3N4, C, etc.) coated on the surface, which could clog the microchannels in Y2Mo3O12 to avoid the invasion of crystal water. The investigation paves a way to improve the NTE properties by neglecting the influences of water molecules on the stretching vibrations of MoO4 tetrahedra and the transverse vibrations of bridge oxygen atoms.

A novel planar metamaterial design for electromagnetically induced transparency and slow light.

A novel planar plasmonic metamaterial for electromagnetically induced transparency and slow light characteristic is presented in this paper, which consists of nanoring and nanorod compound structures. Two bright modes in the metamaterial are induced by the electric dipole resonance inside nanoring and nanorod, respectively. The coupling between two bright modes introduces transparency window and large group index. By adjusting the geometric parameters of metamaterial structure, the transmittance of EIT window at 385 THz is about 60%, and the corresponding group index and Q factor can reach up to 1.2 × 10³ and 97, respectively, which has an important application in slow-light device, active plasmonic switch, SERS and optical sensing.

The study of zirconium vanadate as a cathode material for lithium ion batteries.

The electrochemical properties of ZrV2O7 (ZVO) and ZVO@C were investigated in lithium ion batteries. The first charge (or discharge) specific capacity of ZVO and ZVO@C are 279 mA h g-1, 392 mA h g-1, 208 mA h g-1 and 180 mA h g-1 for 0%, 3%, 5% and 9% of carbon, respectively. The capacity retention rates (with 0% 3%, 5% and 9% carbon content) are 33.0%, 52.5%, 56.4% and 76.1% after ten cycles, respectively. The low inner resistance relates to the good contact of the electrode rather than the high content of carbon, and the specific capacity retention rate increases with the increase of the carbon content.

Substitutions of Zr4+/V5+ for Y3+/Mo6+ in Y2Mo3O12 for Less Hygroscopicity and Low Thermal Expansion Properties.

In this investigation, ZrxY2-xVxMo3-xO12 (0 ≤ x ≤ 1.4) is developed and the effects of the substitutions of Zr4+/V5+ for Y3+/Mo6+ in Y2Mo3O12 on the hygroscopicity and thermal expansion property are investigated. For the smaller substitution content (x ≤ 0.5), their crystal structures remain orthorhombic, while there is crystal water still in the lattice. The linear coefficients of thermal expansions (CTEs), for x = 0.1, 0.3, 0.5, and 0.7, are about -4.30 × 10-6, -0.97 × 10-6, 0.85 × 10-6, and 0.77 × 10-6 K-1, respectively, from 476 to 773 K, which means that the linear CTE could be changed linearly with the substitution content of Zr4+/V5+ for Y3+/Mo6+ in Y2Mo3O12. As long as the substitution content reaches x = 1.3/1.4, almost no hygroscopicity and low thermal expansion from room temperature are obtained and are discussed in relation to the crystal structure and microstructure.

Negative thermal expansion and broad band photoluminescence in a novel material of ZrScMo2VO12.

In this paper, we present a novel material with the formula of ZrScMo2VO12 for the first time. It was demonstrated that this material exhibits not only excellent negative thermal expansion (NTE) property over a wide temperature range (at least from 150 to 823 K), but also very intense photoluminescence covering the entire visible region. Structure analysis shows that ZrScMo2VO12 has an orthorhombic structure with the space group Pbcn (No. 60) at room temperature. A phase transition from monoclinic to orthorhombic structure between 70 and 90 K is also revealed. The intense white light emission is tentatively attributed to the n- and p-type like co-doping effect which creates not only the donor- and acceptor-like states in the band gap, but also donor-acceptor pairs and even bound exciton complexes. The excellent NTE property integrated with the intense white-light emission implies a potential application of this material in light emitting diode and other photoelectric devices.