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Generating oxygen vacancies (Vö) in vanadium pentoxide (V 2 O 5 ) has been demonstrated as an effective approach to tailor its electrochemical properties. The present study investigates three different kinds of conductive polymer (CP = PPy, PEDOT, and PANI) coated V 2 O 5 nanofibers with Vö generated at the interface during the polymerization process. Surface Vö form a local electric field and promote the charge transfer kinetics of the resulting Vö-V 2 O 5 /CP nanocables, and the accompanying V 4+ and V 3+ ions may also catalyze the redox reactions and improve the supercapacitor performance. The differences and similarities of three different CP coatings have been compared and discussed, and are dependent on their polymerization conditions and coating thickness. The distribution of Vö in the surface layer and in the bulk has been elaborated and the corresponding effects on the electrochemical properties and supercapacitor performance have also been investigated. Vö-V 2 O 5 /CP can deliver a high capacity of up to 614 F g −1 at a current rate of 0.5 A g −1 and supercapacitors with Vö-V 2 O 5 /CP demonstrated excellent cycling stability over 15 000 cycles at a rate of 10 A g −1 . 

Spherically‐bent crystal analyzers (SBCAs) see considerable use in very high‐resolution hard X‐ray wavelength dispersive X‐ray fluorescence spectroscopy, often called X‐ray emission spectroscopy (XES). While Si and Ge are the most frequently used diffractive components of SBCAs, we consider here the somewhat classical choice of muscovite mica as the dispersing element. We find that the various harmonics of a highest‐quality mica‐based SBCA show ~5–~40% of the integral reflectivity per unit solid angle of a typical Si or Ge SBCA in the hard X‐ray range, and that the mica SBCA have comparable energy resolution to the traditional SBCAs. Interestingly, the choice of mica comes with a practical benefit: the primary (0,0,2) reflection has sufficiently strong harmonics that are fairly tightly spaced in energy so that they span the complete energy range from ~4 to ~11 keV when used at convenient Bragg angles in a Rowland circle spectrometer. Hence, a single mica SBCA can be used for every K‐shell emission line of three dimensional transition metals and every L‐shell emission line of the lanthanide elements simply by selecting the correct mica (0,0,2) harmonic with a final energy‐dispersive solid state detector. The loss in efficiency is counteracted by an operational efficiency, i.e., the “universal” application of a single analyzer over a very large range of elements. This performance suggests future application of mica SBCAs in both laboratory‐based XES and synchrotron‐based photon‐in, photon‐out spectroscopies in the hard X‐ray range. 

Abstract A local electric field is induced to engineer the interface of vanadium pentoxide nanofibers (V₂O₅‐NF) to manipulate the charge transport behavior and obtain high‐energy and durable supercapacitors. The interface of V₂O₅‐NF is modified with oxygen vacancies (Vö) in a one‐step polymerization process of polyaniline (PANI). In the charge storage process, the local electric field deriving from the lopsided charge distribution around Vö will provide Coulombic forces to promote the charge transport in the resultant Vö‐V₂O₅/PANI nanocable electrode. Furthermore, an ≈7 nm porous PANI coating serves as the external percolated charge transport pathway. As the charge transfer kinetics are synergistically enhanced by the dual modifications, Vö‐V₂O₅/PANI‐based supercapacitors exhibit an excellent specific capacitance (523 F g⁻¹) as well as a long cycling lifespan (110% of capacitance remained after 20 000 cycles). This work paves an effective way to promote the charge transfer kinetics of electrode materials for next‐generation energy storage systems.