1f:T4e4,Increasing the complexity of hollow structures, in terms of chemical composition and shell architecture, is highly desirable for both fundamental studies and realization of various functionalities. Starting with metal-organic frameworks (MOFs), we demonstrate a general approach toward the large-scale and facile synthesis of complex hollow microboxes via manipulation of the template-engaged reactions between the Prussian blue (PB) template and different alkaline substances. The reaction between PB microcubes with NaOH solution leads to the formation of Fe(OH)3 microboxes with controllable multishelled structure. In addition, PB microcubes will react with the conjugate bases of metal oxide based weak acids, generating multicompositional microboxes (Fe2O3/SnO2, Fe2O3/SiO2, Fe2O3/GeO2, Fe2O3/Al2O3, and Fe2O3/B2O3), which consist of uniformly dispersed oxides/hydroxides of iron and another designed element. Such complex hollow structures and atomically integrated multiple compositions might bring the usual physiochemical properties. As an example, we demonstrate that these complex hollow microboxes, especially the Fe2O3/SnO2 composite microboxes, exhibit remarkable electrochemical performance as anode materials for lithium ion batteries.20:T513,Noble metals manifest themselves with unique electronic structures and irreplaceable activity toward a wide range of catalytic applications but are unfortunately restricted by limited choice of geometric structures spanning single atoms, clusters, nanoparticles, and bulk crystals. Herein, we propose how to overcome this limitation by integrating noble metal atoms into the lattice of transition metal oxides to create a new type of hybrid structure. This study shows that iridium single atoms can be accommodated into the cationic sites of cobalt spinel oxide with short-range order and an identical spatial correlation as the host lattice. The resultant Ir_0.06Co_2.94O₄ catalyst exhibits much higher electrocatalytic activity than the parent oxide by 2 orders of magnitude toward the challenging oxygen evolution reaction under acidic conditions. Because of the strong interaction between iridium and cobalt oxide support, the Ir_0.06Co_2.94O₄ catalyst shows significantly improved corrosion resistance under acidic conditions and oxidative potentials. This work eliminates the "close-packing" limitation of noble metals and offers promising opportunity to create analogues with desired topologies for various catalytic applications.21:T4d0,This review focuses on the electrosynthesis, in situ characterization, and technological applications of Prussian blue analogues with the generic formula AhMk[Fe(CN)6]l·mH2O, where h, k, l, and m are stoichiometric numbers, A = alkali metal cation, and M is a transition metal. Six such metal hexacyanoferrate (MHCF) compounds derived from Cu, Pd, In, V, Co, and Ni are featured in this article against the backdrop of the Prussian blue parent compound itself and other related compounds. The use of cyclic voltammetry and complementary techniques including scanning probe microscopies, quartz crystal microgravimetry, and ac impedance spectroscopy, for studying the growth of MHCF films on targeted substrates, is discussed. Spectroelectrochemical in situ characterization of these films in the UV−visible and IR regions is then reviewed. Finally, the use of Prussian blue and its analogues in devices for displays and “smart” windows, photoimaging, environmental remediation, chemical/biological sensing, energy conversion, and magneto-optic/opto-magnetic switching is described. Electrocatalysis of targeted reactions and structural changes upon ion uptake by the MHCF compounds constitute the other topics in this review.22:T60c,

	Year	Citations

References