Dual-emission center ratiometric optical thermometer based on Bi3+ and Mn4+ co-doped SrGd2Al2O7 phosphor.

In recent years, more and more attention has been paid to optical temperature sensing, and how to improve its accuracy is the most important issue. Herein, a new temperature sensing material, SrGd2Al2O7:Bi3+,Mn4+, based on fluorescence intensity ratio was designed in this work. It has both blue-purple and red luminescence under 300 nm excitation, and the dual-emitting centers with distinct colors, the different thermal sensitivities of Bi3+ and Mn4+, and the energy transfer between Bi3+ and Mn4+ give it excellent signal resolution and accurate temperature detection. The Sa of SrGd2Al2O7:0.04Bi3+,0.003Mn4+ phosphor reaches a maximum value of 8.573% K-1 at 473 K, and the corresponding Sr is 1.927% K-1, both of which are significantly better than those of most other reported optical temperature sensing materials. Taking all the results into account, the SrGd2Al2O7:0.04Bi3+,0.003Mn4+ phosphor can be regarded as a prominent FIR-type temperature sensing material.

Co/CeO2/C composites derived from bimetallic metal-organic frameworks for efficient microwave absorption.

CeO2, an n-type semiconductor material, has been widely used in microwave absorption (MA) due to its unique structural features such as oxygen vacancies and interstitial atoms. In this paper, Co/CeO2/C composites were prepared by a hydrothermal method followed by a pyrolysis process. The effect of different pyrolysis temperatures (650-950 °C) on the MA property of the composites was investigated. When the pyrolysis temperature was 850 °C, the Co/CeO2/C-850 composite exhibited outstanding MA behavior in the frequency range of 2-18 GHz, displaying a minimum reflection loss (RLmin) of -45.22 dB and an effective absorption bandwidth (EAB) of 4.61 GHz at a thin thickness of 1.75 mm. The MA performance of the Co/CeO2/C composites is mainly attributed to the dielectric loss due to interfacial polarization originating from different interfaces and dipole polarization caused by the oxygen vacancies in CeO2. In addition, the introduction of Co nanoparticles not only provides the magnetic loss but also modulates impendence matching for the current magnetoelectric coupling system.

Trumpet-Like ZnS@C Composite for High-Performance Potassium Ion Battery Anode.

ZnS has acquired increasing attention for high-performance PIBs anode because of its remarkable theoretical capacity, and redox reversibility for conversion reaction. However, the larger volume variation and delayed reaction kinetics for the ZnS in the discharge/charge processes lead to pulverization and severe capacity degradation. Herein, the trumpet-like ZnS@C composite was synthesized by template method by using sodium citrate as carbon source followed by vulcanization process. As potassium ion batteries (PIB) anode, ZnS@C composite exhibits good rate performance and long life (stable reversible capacity of 107.8 mAh/g over 2000 charge-discharge cycles at 5 A/g and high reversible capacity of 310 mAh/g at 0.1 A/g). The outstanding electrochemical performance of the ZnS@C composite is ascribed to its unique structure, which can mitigate the volume expansion of ZnS in the charge discharge process, expand the contact area between the electrode and electrolyte, and improve the conductivity of electrode materials by the introduction of carbon layer. This method of synthesizing trumpet-like ZnS@C composite provides an important strategy for obtaining potassium ion batteries anode with long cycle.

Fabrication of Nb2 O5 /Carbon Submicrostructures for Advanced Lithium-Ion Battery Anodes.

Nb2 O5 possesses superior fast Li+ storage capability for LIB anodes, benefiting from its fast pseudocapacitive behavior and low volumetric change within the cycling processes. However, the poor electric conductivity for Nb2 O5 restricts its reaction kinetics and rate property. Herein, Nb2 O5 /carbon (C) submicrostructures are fabricated by solvothermal method followed by calcination process. The Nb2 O5 /C submicrostructures exhibit outstanding rate behavior and cyclic performance (332 (194) mAh g-1 after 1000 cycles at 1 (5) A g-1 ). The superior electrochemical property is attributed to the distinctive structure for Nb2 O5 /C submicrostructures, in which Nb2 O5 nanoparticles uniformly distributed within Nb2 O5 /C composite can protect Nb2 O5 nanoparticles from agglomeration, and the porous carbon matrix can enhance electron/ion conductivity. This work furnishes a novel strategy for fabricating Nb2 O5 /C submicrostructures with superior Li+ storage performance, which can be potentially used to design other metal oxide/C submicrostructures for second battery anode.

Effect of concentration of glycidol on the properties of resorcinol-formaldehyde aerogels and carbon aerogels.

By using glycidol as a catalyst, high porosity, low-density resorcinol (R) and formaldehyde (F) aerogels and carbon aerogels (CAs) were synthesized via a sol-gel method. The effect of glycidol and water on the color, density, morphology, textual characteristics and adsorption properties of the resultant RF aerogels and CAs were investigated in detail. The results revealed that the properties of RF aerogels and CAs can be controlled by adjusting the amount of glycidol and water. The resultant RF aerogels and CAs were porous materials, the minimum densities of RF aerogels and CAs were 96 and 110 mg cm-3 respectively while the maximum specific surface areas of RF aerogels and CAs were 290 and 597 m2 g-1. The maximum adsorption capacity of CAs was about 125 mg g-1 on Rhodamine B, which was higher than that of some reported CAs catalyzed by base and acid catalysts. The sol-gel mechanisms of RF aerogels and CAs can be attributed to the opening of the epoxy group of glycidol in the mixture of R and F.

Construction of Fe7Se8@Carbon nanotubes with enhanced sodium/potassium storage.

The Fe7Se8@Carbon (C) nanotubes are successfully synthesized using Fe3O4@C nanotubes as sacrificial templates. Fe7Se8@C nanotubes exhibit excellent rate behaviour and maintainable capacity (319 mAh g-1 at 2 A g-1 upon 720 cycles), when utilized as SIBs anode. Moreover, for PIBs anode, Fe7Se8@C nanotubes also exhibit outstanding rate behaviour and maintainable capacity 222 mAh g-1 at 2 A g-1 upon 500 cycles). The superior electrochemical performance of Fe7Se8@C nanotubes is ascribed to the unique structure, where the hierarchical hollow tubular characteristic of Fe7Se8@C composites can mitigate the volume expansion of Fe7Se8 and supply effective transmission paths for both Na+(K+) and electrons within repeated cycle processes, and additionally, N-doped carbon layer can further protect the integrality of Fe7Se8@C nanotubes from destruction within the cycle processes, and enhance electronic conductivity.

Pomegranate-like structured Nb2O5/Carbon@N-doped carbon composites as ultrastable anode for advanced sodium/potassium-ion batteries.

The distinctive pomegranate-like Nb2O5/Carbon@N-doped carbon (Nb2O5/C@NC) composites are fabricated using hydrothermal method integrated with nitrogen doped carbon coating procedure. For the SIBs anode, the Nb2O5/C@NC composites present superior rate character and sustainable capacity (117 mAh g-1 upon 1000 cycles at 5 A g-1). The in-situ X-ray diffraction (XRD) is utilized to research its sodium storage mechanism. Furthermore, for PIBs, the Nb2O5/C@NC composites present sustainable capacity (81 mAh g-1 upon 1000 cycles at 1 A g-1). The outstanding performance of Nb2O5/C@NC composites is ascribed to its unique architecture, in which Nb2O5 nanocrystals embedded in porous carbon can restrain agglomeration of Nb2O5 nanocrystals, enhance electron/ion diffusion kinetics, and ensure electrolyte accessibility, and moreover, NC shell layer can provide effective active sites and further increase ions/electrons transfer.

Fabrication of ZnSe/C Hollow Polyhedrons for Lithium Storage.

ZnSe has got extensive attention for high-performance LIBs anode due to its remarkable theoretical capacity and environmental friendliness. Nevertheless, the large volume variation for the ZnSe in the discharge/charge processes brings about rapid capacity fading and poor rate performance. Herein, ZnSe/C hollow polyhedrons are successfully synthesized by selenization of zeolitic imidazolate framework-8 (ZIF-8) with resorcinol-formaldehyde (RF) coating. The protection of C layer derived from RF coating layer and Ostwald ripening during the process of selenization play important roles in promoting formation of ZnSe/C hollow polyhedrons. The ZnSe/C hollow polyhedrons exhibit good rate performance and long-term cycle stability (345 mAh g-1 up to 1000 cycles at 1 A g-1 ) for lithium ion batteries (LIBs) anode. The improved electrochemical performance is benefit from the unique ZnSe/C hollow structure, in which the hollow structure can effectively avoid terrible volume expansion, and the thin ZnSe/C shell can not only provide adequate diffusion paths of lithium ions and but also enhance the electronic conductivity.

Molten salt synthesis of single-crystalline K2Ti6O13 annular nanostructures.

Single-crystalline K2Ti6O13 ring-like structures have been synthesized via a simple molten salt method without any templates and surfactants. The annular structures have several different types, such as nanoring, wheel-like and diskette-like ring. Each type of rings was characterized individually by scanning electron microscopy (SEM), transmission electron microscopy (TEM), selected area electron diffraction (SAED) and high-resolution transmission electron microscopy (HRTEM). These annular structures are formed by the loop-by-loop self-coiling of K2Ti6O13 nanobelts in the ring plane. The driving force of self-coiling is suggested to minimize the local electrostatic energy introduced by spontaneous polarization.