Bismuth oxide can store energy electrochemically in seventeen aqueous metal ion electrolytes with high capacity based on a “quasi-conversion reaction”.

A set of Co x Pt100−x nanoparticles (NPs) was synthesized by the sol–gel method. The structure and magnetic properties of the produced samples were investigated by x-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), selected area electron diffraction (SAED) and a vibrating sample magnetometer. When the Co content ranged from 25 to 75 at%, the results of XRD, HRTEM and SAED revealed the formation of L12 CoPt3, L10 CoPt and face-centred cubic Co3Pt NPs. Magnetic measurements indicated that CoPt3 and Co3Pt had soft magnetic properties. When the Co composition was 50 at%, the sample coercivity reached a giant value of ∼470 kA m−1.

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Titanium(IV)-based metal-organic frameworks (Ti-MOFs) have received significant attention in recent years because of their numerous photocatalytic applications; however, the synthesis of new Ti-MOFs with precise crystal structures is still challenging. Herein, three new Ti-MOFs with single-crystal structures (denoted as FIR-125−FIR-127) are rationally synthesized by employing a large Ti 44 -oxo cluster as the precursor to assembly with the organic ligand. Big single-crystals can be successfully obtained and structurally determined by single-crystal X-ray diffraction. During the synthesis, the large Ti 44 -oxo cluster is transferred to small Ti 8 O 8 (CO 2 ) 16 building units in the Ti-MOF. In addition, FIR-125 exhibit high stability, permanent porosity, and photocatalytic activity. This work provides a new strategy toward the big crystal growth of Ti-MOFs through the slow transformation of large titanium-oxo clusters.