MoS2 Hollow Multishelled Nanospheres Doped Fe Single Atoms Capable of Fast Phase Transformation for Fast-charging Na-ion Batteries.

Low Na+ and electron diffusion kinetics severely restrain the rate capability of MoS2 as anode for sodium-ion batteries (SIBs). Slow phase transitions between 2H and 1T, and from NaxMoS2 to Mo and Na2S as well as the volume change during cycling, induce a poor cycling stability. Herein, an original Fe single atom doped MoS2 hollow multishelled structure (HoMS) is designed for the first time to address the above challenges. The Fe single atom in MoS2 promotes the electron transfer, companying with shortened charge diffusion path from unique HoMS, thereby achieving excellent rate capability. The strong adsorption with Na+ and self-catalysis of Fe single atom facilitates the reversible conversion between 2H and 1T, and from NaxMoS2 to Mo and Na2S. Moreover, the buffering effect of HoMS on volume change during cycling improves the cyclic stability. Consequently, the Fe single atom doped MoS2 quadruple-shelled sphere exhibits a high specific capacity of 213.3 mAh g-1 at an ultrahigh current density of 30 A g-1, which is superior to previously-reported results. Even at 5 A g-1, 259.4 mAh g-1 (83.68 %) was reserved after 500 cycles. Such elaborate catalytic site decorated HoMS is also promising to realize other "fast-charging" high-energy-density rechargeable batteries.

Surface Crystal Modification of Na3 V2 (PO4 )3 to Cast Intermediate Na2 V2 (PO4 )3 Phase toward High-Rate Sodium Storage.

The two-phase reaction of Na3 V2 (PO4 )3 - Na1 V2 (PO4 )3 in Na3 V2 (PO4 )3 (NVP) is hindered by low electronic and ionic conductivity. To address this problem, a surface-N-doped NVP encapsulating by N-doped carbon nanocage (N-NVP/N-CN) is rationally constructed, wherein the nitrogen is doped in both the surface crystal structure of NVP and carbon layer. The surface crystal modification decreases the energy barrier of Na+ diffusion from bulk to electrolyte, enhances intrinsic electronic conductivity, and releases lattice stress. Meanwhile, the porous architecture provides more active sites for redox reactions and shortens the diffusion path of ion. Furthermore, the new interphase of Na2 V2 (PO4 )3 is detected by in situ XRD and clarified by density functional theory (DFT) calculation with a lower energy barrier during the fast reversible electrochemical three-phase reaction of Na3 V2 (PO4 )3 - Na2 V2 (PO4 )3 - Na1 V2 (PO4 )3 . Therefore, as cathode of sodium-ion battery, the N-NVP/N-CN exhibited specific capacities of 119.7 and 75.3 mAh g-1 at 1 C and even 200 C. Amazingly, high capacities of 89.0, 86.2, and 84.6 mAh g-1 are achieved after overlong 10000 cycles at 20, 40, and 50 C, respectively. This approach provides a new idea for surface crystal modification to cast intermediate Na2 V2 (PO4 )3 phase for achieving excellent cycling stability and rate capability.

Rapid fluorescent color analysis of copper ions on a smart phone via ratiometric fluorescence sensor.

A smartphone-assisted fluorescence color sensing system for rapid, convenient, and on-site detection of copper ions was developed. The ratiometric fluorescence sensor was fabricated by using silica-coated blue-light-emitting carbon dots and surface-grafted red-light-emitting cadmium-telluride quantum dots. After exposure to Cu2+ in 20 s, the red fluorescence was quenched obviously, while the blue fluorescence remained unchanged, and the sensor color changes continuously from red to blue under the ultraviolet lamp. The concentration (50-1200 nM) of copper ions could be measured by the fluorescence spectrum (excitation at 360 nm, dual-emission at 441 and 640 nm) with a detection limit of 7.7 nM. The fluorescence colors were converted to digital RGB values to calculate the concentration of copper ions by a smartphone with a detection limit of 9.6 nM. The method was applied to detecting copper ions spiked in real samples with recovery from 97.9 to 108.0% and RSD from 3.8 to 8.9%. Thus, this convenient and practical fluorescence color sensing system presents a new strategy for rapid, sensitive, and on-site determination of copper ions in environmental or biological samples.

Boron nitride modified reduced graphene oxide as solid-phase microextraction coating material for the extraction of seven polycyclic aromatic hydrocarbons from water and soil samples.

A novel hexagonal boron nitride modified reduced graphene oxide material was synthesized and used as the adsorbent for the solid-phase microextraction of seven polycyclic aromatic hydrocarbons from water and soil samples prior to their detection by gas chromatography-flame ionization detector. Under optimal conditions, the linear response range of the analytes for water sample is 0.25-50 ng/mL with the correlation coefficients (r) ranging between 0.9953 and 0.9996. The linear range for soil sample is 1.0-400 ng/g with r ranging from 0.9959 to 0.9999. On the basis of the signal-to-noise ratio of 3, the limits of detections for the analytes ranged from 0.05 to 0.15 ng/mL for water samples, and from 0.3 to 0.5 ng/g for soil samples. The relative recoveries of the seven polycyclic aromatic hydrocarbons for water and soil samples were in the range of 79.55-120.0 and 78.76-120.8%, respectively. The relative standard deviations for the determination of the analytes in water and soil samples were lower than 11 and 10%, respectively. The method is simple and suitable for the determination of polycyclic aromatic hydrocarbon residues in water and soil samples.