Etching-Induced Surface Reconstruction of NiMoO4 for Oxygen Evolution Reaction.

Rational reconstruction of oxygen evolution reaction (OER) pre-catalysts and performance index of OER catalysts are crucial but still challenging for universal water electrolysis. Herein, we develop a double-cation etching strategy to tailor the electronic structure of NiMoO4, where the prepared NiMoO4 nanorods etched by H2O2 reconstruct their surface with abundant cation deficiencies and lattice distortion. Calculation results reveal that the double cation deficiencies can make the upshift of d-band center for Ni atoms and the active sites with better oxygen adsorption capacity. As a result, the optimized sample (NMO-30M) possesses an overpotential of 260 mV at 10 mA cm-2 and excellent long-term durability of 162 h. Importantly, in situ Raman test reveals the rapid formation of high-oxidation-state transition metal hydroxide species, which can further help to improve the catalytic activity of NiMoO4 in OER. This work highlights the influence of surface remodification and shed some light on activating catalysts.

Significant Change of Metal Cations in Geometric Sites by Magnetic-Field Annealing FeCo2 O4 for Enhanced Oxygen Catalytic Activity.

The application of magnetic fields in the oxygen reduction/evolution reaction (ORR/OER) testing for electrocatalysts has attracted increasing interest, but it is difficult to characterize on-site surface reconstruction. Here, a strategy is developed for annealing-treated FeCo2 O4 nanofibers at a magnetic field of 2500 Oe, named FeCo2 O4 -M, showing a right-shifted half-wave potential of 20 mV for the ORR and a left-shifted overpotential of 60 mV at 10 mV cm-2 for the OER as compared with its counterpart. Magnetic characterizations indicate that FeCo2 O4 -M shows the spin-state transition of cations from a low-spin state to an intermediate-spin state compared with FeCo2 O4 . Mössbauer spectra show that the Fe3+ ion in the octahedral site (0.76) of FeCo2 O4 -M is more than that of FeCo2 O4 (0.71), indicating the effective stimulus of metal cations in geometric sites by magnetic-field annealing. Furthermore, theoretical calculations demonstrate that the d-band centers (εd ) of Co 3d and Fe 3d in the tetrahedral and octahedral sites of the FeCo2 O4 -M nanofibers shift close to the Fermi level, revealing the enhanced mechanism of the ORR/OER activity.

Tunable Fe3O4 Nanorods for Enhanced Magnetic Hyperthermia Performance.

Magnetic hyperthermia is one of the most promising techniques for treating gynecological cancer, where magnetite (Fe3O4) is the most common nanomaterial used as a magnetic hyperthermia agent. Here, we demonstrate that optimal Fe3O4 nanorods (NRs) can act as a magnetic hyperthermia agent with higher specific absorption rate (SAR), which is mostly attributed to their enhanced surface anisotropy. As a result, Fe3O4 NRs could effectively hinder the growth of gynecological cancer cells in nude mice models, again demonstrating its good magnetic heating properties. These results provide a powerful basis for the development of an ideal magnetic hyperthermia agent with enhanced SAR, thereby effectively treating gynecological cancer in clinical practice.

Interfacial Engineering of NiO/NiCo2O4 Porous Nanofibers as Efficient Bifunctional Catalysts for Rechargeable Zinc-Air Batteries.

To meet the crucial demand of regenerative Zn-air (ZA) batteries, low cost, highly efficient, and durable electrocatalysts for the oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) are needed to replace the noble metal. Herein, porous NiO/NiCo2O4 nanofibers with superior electrocatalytic performance are synthesized by a facile electrospinning strategy with precursor transition metal salts in nonstoichiometric ratio, which confers the heterostructured NiO/NiCo2O4 with abundant interface-related active sites and electronic transmission channels. Density functional calculation results reveal the chemical bonds easily form between NiO and NiCo2O4 to facilitate the charge transfer, while X-ray absorption fine spectroscopy and X-ray photoelectron spectroscopy results demonstrate there are abundant Ni3+ and Co3+ species in NiO/NiCo2O4 due to the interfacial engineering. As a result, the NiO/NiCo2O4 porous nanofibers exhibit highly efficient and durable performances of OER and ORR in KOH solution, including a lower overpotential of 357 mV at 10 mA cm-2 (OER) and half-wave potential of 0.73 V (ORR) than that of the individual. What's more, the NiO/NiCo2O4-based ZA battery displays excellent specific capacities of 814.4 mA h g-1, and good cycling stability of 175 h. Additionally, the flexible ZA battery displays a long cycling life of 14 h and decent flexibility. This work shows that construction of the heterostructure could provide a feasible method to optimize their electrocatalytic performance and make them widely used in power source devices.

Efficient electrocatalyst of α-Fe2O3 nanorings for oxygen evolution reaction in acidic conditions.

Large-scale application of sustainable energy devices urgently requires cost-effective electrocatalysts to overcome the sluggish kinetics related to the oxygen evolution reaction (OER) under acidic conditions. Here, we first report the highly efficient electrocatalytic characteristics of α-Fe2O3 nanorings (NRs), which exhibits prominent OER electrocatalytic activity with lower overpotential of 1.43 V at 10 mA cm-2 and great stability in 1 M HCl, surpassing the start-of-the art Ir/C electrocatalyst. The significantly optimized OER activity of the α-Fe2O3 NRs mainly attributes to the synergistic effect of the excellent electrical conductivity and a large effective active surface because of their unique nanoring structure, disordered surface, and the dynamic stability of α-Fe2O3 NRs in acidic conditions.

Bifunctional Electrocatalytic Activity of Nitrogen-Doped NiO Nanosheets for Rechargeable Zinc-Air Batteries.

In order to improve the efficiencies and service lifetimes of rechargeable Zn-air batteries, it is necessary to develop highly efficient air electrocatalysts. In the present study, we prove that the bifunctional electrocatalytic activity in NiO nanosheets is effectively improved by the synergistic effects of N dopants and considerably porous structure. As an electrocatalyst for oxygen evolution reaction (OER) and oxygen reduction reaction (ORR), the as-prepared porous N-doped NiO nanosheets exhibit good activities with the small overpotential and ideal half-wave potential, which is superior to Ir/C electrocatalyst. Besides, it is proved that the process of HO* being oxidized to O* is the OER potential rate-determining step; also the OER electrocatalytic performance of NiO can be markedly promote by the doping of N atoms using the density functional theory calculations. Furthermore, the fabricated Zn-air battery based on the porous N-doped NiO nanosheets also exhibits superior activities, outperforming many reported NiO-based electrocatalyst materials. Two series Zn-air cells with a voltage of 2.80 V can power a red light-emitting diode, which shows their large potential for various applications.

Co and CeO2 co-decorated N-doping carbon nanofibers for rechargeable Zn-air batteries.

The heterogeneous Co and CeO2 co-decorated N-doping carbon nanofibers (Co-CeO2-N-C) were synthesized via the electrospinning technique. As the bifunctional electrocatalyst, Co-CeO2-N-C nanofibers show excellent oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) performance, owing to the higher degree of graphitization of carbon, the N-doping, and the formation of an interface between Co and CeO2. The liquid Zn-air battery based on Co-CeO2-N-C nanofibers displays excellent specific capacities (815.9 mA h g-1 at 5 mA cm-2), higher open circuit voltages (1.47 V), and good cycling stability (113 h). The corresponding flexible solid state Zn-air battery shows excellent cycling stability (11 h), and good flexibility. Our finding suggests that Co-CeO2-N-C nanofibers could serve as a new group of bifunctional electrocatalysts for OER and ORR with excellent performance, and make them promising for use in future electric vehicles, off-grid power sources, and portable electronics.

Research on the Preparation and Chromaticity Coordinates Shift Mechanism of Organic White Light Top-Emitting Devices.

The top emission organic light-emitting devices were fabricated on the multi-layers metal anode with co-doping method in single host system. In experiment, the multilayer Al/Mo/MoO(3) anode on silicon are deposited, systematically analyzed the effect MoO(3) thickness on the reflectance and found the mechanism of the MoO(3) thickness variation to the reflectivity of Al/Mo/MoO(3) on silicon. Experimental results showed that the luminous intensity of blue, green and red appear to change according to the current density increase, and compared with the red intensity, the luminous intensity of blue and green gradually increased. The emission in this host-guest co-doping system is considered to usually involve two emission mechanisms, energy transfer and carrier trapping, and the energy transfer and carrier trapping between the host-guest should be responsible for chromaticity coordinates shift of organic white emitting light devices. In addition, through further study, it is proved the electroluminescence intensity of dopant linearly decrease with the driving voltage applied to the device by theoretical and experimental results.