A general dealloying strategy is developed to prepare multi-component alloys with high thermal stability, electrochemical durability, and catalytic activity.

Ir‐based binary and ternary alloys are effective catalysts for the electrochemical oxygen evolution reaction (OER) in acidic solutions. Nevertheless, decreasing the Ir content to less than 50 at% while maintaining or even enhancing the overall electrocatalytic activity and durability remains a grand challenge. Herein, by dealloying predesigned Al‐based precursor alloys, it is possible to controllably incorporate Ir with another four metal elements into one single nanostructured phase with merely ≈20 at% Ir. The obtained nanoporous quinary alloys, i.e., nanoporous high‐entropy alloys (np‐HEAs) provide infinite possibilities for tuning alloy's electronic properties and maximizing catalytic activities owing to the endless element combinations. Particularly, a record‐high OER activity is found for a quinary AlNiCoIrMo np‐HEA. Forming HEAs also greatly enhances the structural and catalytic durability regardless of the alloy compositions. With the advantages of low Ir loading and high activity, these np‐HEA catalysts are very promising and suitable for activity tailoring/maximization.

A superparamagnetic graphene oxide-Fe 3 O 4 hybrid composite (GO-Fe 3 O 4 ) was prepared via a simple and effective chemical method. Amino-functionalized Fe 3 O 4 (NH 2 -Fe 3 O 4 ) particles are firmly deposited on the graphene oxide sheets. The graphene oxide sheets could prevent NH 2 -Fe 3 O 4 particles from agglomeration and enable a good dispersion of these oxide particles. The as-prepared GO-Fe 3 O 4 hybrid composite had a much higher thermal stability than graphene oxide. The amount of NH 2 -Fe 3 O 4 loaded on GO was estimated to be 23.6 wt% by atomic absorption spectrometry. The specific saturation magnetization (M s ) of the GO-Fe 3 O 4 hybrid composite is 15 emu g À1 . The magnetic GO-Fe 3 O 4 composite has been employed as adsorbent for the magnetic separation of dye contaminants from water. The adsorption test of dyes (Methylene Blue (MB) and Neutral Red (NR)) demonstrates that it only takes 30 min for MB and 90 min for NR to attain equilibrium. The adsorption capacities for MB and NR in the concentration range studied are 167.2 and 171.3 mg g À1 , respectively. The GO-Fe 3 O 4 hybrid composite can be easily manipulated in magnetic field for desired separation, leading to the removal of dyes from polluted water. These GO-Fe 3 O 4 hybrid composites have great potential applications in removing organic dyes from polluted water.

Developing highly efficient catalysts for oxygen evolution reactions (OER) is a key step for rechargeable metal− oxygen batteries and water splitting. Usually, binary NiFe or ternary NiCoFe nano-alloys are used as the OER catalysts. Herein, combining the precursor alloy design with chemical etching, a simple dealloying route is developed to controllably incorporate five or more nonprecious metals into one nanostructured alloy with a naturally oxidized surface, that is, nanoporous high entropy alloys (np-HEAs) covered with high-entropy (oxy)hydroxides (HEOs). It is found that the alloy composition plays a dominant role in the OER activity enhancement with the np-AlNiCoFeX (X = Mo, Nb, Cr) combination showing the highest activity. Forming quinary HEAs also greatly enhances the electrochemical cycling stabilities compared with the ternary and quaternary counterparts. The result indicates the significance of synergistically incorporating five or more metal elements in one single-phase nanostructure, which provides more structural and chemical degrees of freedom to boost the catalytic performance, overcoming the restriction of normal binary or ternary alloys. Multinary transition metal-based np-HEA is a new class of promising catalyst for various important reactions.

In this study, we present the synthesis of reduced graphene oxide/hydroxyapatite (RGO/HA) hybrid materials by an environmental-friendly route. Graphene oxide (GO) was first simultaneously reduced and surface functionalized by one-step oxidative polymerization of dopamine (PDA). The bioinspired surface was further used for biomimetic mineralization of hydroxyapatite. When incubated in a simulated body fluid (SBF), the PDA layer enabled efficient interaction between the RGO surface and the mineral ions to improve the bioactivity, promoted the formation of the HA nanoparticles. A detailed structural and morphological characterization of the mineralized composite was performed. The HA-based hybrid materials exhibited no cytotoxic effect on L929 fibroblast cells, showing potential capacity of being a scaffold material for bone tissue regeneration and implantation. This facile strategy also can be a useful platform for other RGO-based nanocomposites.