Two Birds with One Stone: Metal–Organic Framework Derived Micro‐/Nanostructured Ni2P/Ni Hybrids Embedded in Porous Carbon for Electrocatalysis and Energy Storage

The construction of bifunctional electrode materials for hydrogen evolution reaction (HER) and lithium‐ion batteries (LIBs) has been a hot topic of research. Herein, metal–organic frameworks (MOFs) derived micro‐/nanostructured Ni₂P/Ni hybrids with a porous carbon coating (denoted as Ni₂P/Ni@C) are prepared using a feasible pyrolysis–phosphidation strategy. On the one hand, the optimal Ni₂P/Ni@C catalyst exhibits superior HER performance with a low overpotential of 149 mV versus a reversible hydrogen electrode (RHE) at 10 mA cm^?2 and excellent durability. The density functional theory computations verify that the strong synergistic effect between Ni₂P and Ni could optimize the electronic structure, thus rendering the enhanced electrocatalytic performance. On the other hand, the Ni₂P/Ni@C electrode displays a reversible capacity of 597 mAh g^?1 after 1000 cycles at 1000 mA g^?1 and improved rate capability as an anode for LIBs, owing to the well‐organized micro‐/nanostructure and conductive Ni core. In addition, the electrochemical reaction mechanism of the Ni₂P/Ni@C electrode upon lithiation/delithiation is investigated in detail via ex situ X‐ray powder diffraction and X‐ray photoelectron spectroscopy methods. It is expected that the facile and controllable approach can be extended to fabricate other MOF‐based metal phosphides/metal hybrids for electrochemical energy storage and conversion systems.     

Synthesis and Optical Properties of KYF4/Yb,Er Nanocrystals,and their Surface Modification with Undoped KYF4

KYF₄/Yb³⁺, Er³⁺ nanocrystals with a mean diameter of approximately 13 nm were synthesized at 200 °C in the high boiling organic solvent N‐(2‐hydroxyethyl)ethylenediamine (HEEDA). The particles crystallize in the cubic phase known from α‐NaYF₄ and form transparent colloidal solutions in tetraethylene glycol (TEG) or propanol. Solutions containing 1 wt % of the nanocrystals in TEG display visible upconversion emission upon continuous wave (CW) excitation at 978 nm. Growing undoped KYF₄ on the surface of the KYF₄/Yb³⁺, Er³⁺ nanocrystals increases the upconversion efficiency by more than a factor of 20. The XRD data of these particles, display a slight increase in the mean particle size from 13 to 15.5 nm, indicating that only a part of the subsequently added KYF₄ shell material is deposited onto the particle surface. Nevertheless the performed surface modification obviously leads to core/shell structured particles.     

A Facile Synthesis and Characterization of Monodisperse Spherical Pigment Particles with a Core/Shell Structure

In this paper, a facile sol–gel process for producing monodisperse, spherical, and nonaggregated pigment particles with a core/shell structure is reported. Spherical silica particles (245 and 385 nm in diameter) and Cr₂O₃, α‐Fe₂O₃, ZnCo₂O₄, CuFeCrO₄, MgFe₂O₄, and CoAl₂O₄ pigments are selected as cores and shells, respectively. The obtained core/shell‐structured pigment samples, denoted as SiO₂@Cr₂O₃ (green), SiO₂@α‐Fe₂O₃ (red), SiO₂@MgFe₂O₄ (brown), SiO₂@ZnCo₂O₄ (dark green), SiO₂@CoAl₂O₄ (blue), and SiO₂@CuFeCrO₄ (black), are well characterized by using X‐ray diffraction (XRD), field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), and UV‐vis diffuse reflection, as well as by investigating the magnetic properties. The results of XRD and high‐resolution TEM (HRTEM) demonstrate that the pigment shells crystallize well on the surface of SiO₂ particles. The thickness of the pigment shell can be tuned by the number of coatings, to some extent. These pigment particles can be well dispersed in some solvents (such as glycol) to form relatively more stable suspensions than the commercial products. Apart from the color characteristics, some of pigments like SiO₂@Cr₂O₃, SiO₂@MgFe₂O₄, and SiO₂@CuFeCrO₄ also show magnetic properties with coercivities of 1098 Oe (5 K), 648 Oe (5 K), and 91 Oe (298 K), respectively.