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The deformation behavior of nanoporous metal (NPM) is important for their wide range of applications. Strain hardening can effectively enhance the resistance to the deformation. Here we report a novel nanoporous CrFe alloy with ordered structure, which is fabricated by selective phase dissolution of the two-phase Al–Ni–Fe–Cr high entropy alloy. The formation mechanism, microstructure and deformation behavior are investigated in details. The ordered nanoporous CrFe alloy behaves rapid strain hardening and high resistance to deformation. The regular skeletons can be entirely compacted between parallel two sides, which facilitates the densification of nanoporous alloy. Lots of internal boundaries are generated and act as barriers for the dislocation motion. This would favor of the improvement of strain hardening.

Abstract Due to low cost, high capacity, and high energy density, lithium–sulfur (Li–S) batteries have attracted much attention; however, their cycling performance was largely limited by the poor redox kinetics and low sulfur utilization. Herein, predicted by density functional theory calculations, single‐atomic Co‐B2N2 site‐imbedded boron and nitrogen co‐doped carbon nanotubes (SA‐Co/BNC) were designed to accomplish high sulfur loading, fast kinetic, and long service period Li–S batteries. Experiments proved that Co‐B2N2 atomic sites can effectively catalyze lithium polysulfide conversion. Therefore, the electrodes delivered a specific capacity of 1106 mAh g−1 at 0.2 C after 100 cycles and exhibited an outstanding cycle performance over 1000 cycles at 1 C with a decay rate of 0.032% per cycle. Our study offers a new strategy to couple the combined effect of nanocarriers and single‐atomic catalysts in novel coordination environments for high‐performance Li–S batteries.

The unique bicontinuous porous structure and superior electrical conductivity of nanoporous gold (NPG) make it a highly promising material for energy storage and conversion. Although the number of articles on the study of NPG-based materials in energy fields has increased significantly in recent years, the collation and review of these articles are still lacking. Herein, we address this gap by reviewing recent research activities on dealloyed NPG for energy storage and conversion applications. Firstly, the typical dealloying process for forming NPG is introduced. Subsequently, NPG-based composite catalysts used to catalyze water splitting and fuel cells electrode reactions are presented. Afterward, the applications of NPG for different types of electrodes of supercapacitors (SCs) and batteries are discussed. Finally, the studies on NPG for catalyzing CO2 reduction reaction (CO2RR) are reviewed. In a word, the recent research progress of NPG-based materials is reviewed and the future research directions are outlined, laying the cornerstone for the preparation of more advanced energy storage and conversion devices in the future.

Metal oxide anode materials are affected by severe volume expansion and cracking in the charging/discharging process, resulting in low capacity and poor cycle stability, which limits their application in lithium-ion batteries (LIBs). Herein, a new strategy is uncovered for a preparing spinel-structured, multi-component transition metal oxide, (Ni,Co,Mn)Fe2O4−x, with oxygen vacancies as an LIB anode material. The as-fabricated material presented excellent reversible capacity and cycling stability, delivering a discharge capacity of 1240.2 mAh g−1 at 100 mA g−1 for 200 cycles and then at 300 mA g−1 for 300 additional cycles. It presented extremely long cycle stability even at 2 A g−1, revealing 650.5 mAh g−1 after 1200 cycles. The good lithium storage capacity can be ascribed to the entropy stabilization effect, the multi-cation synergistic effect, abundant oxygen vacancies and the spinel structure. This study provides a new opportunity to fabricate and optimize conversion-type anodes for LIBs with satisfactory electrochemical performance.

Today, the development of new self-supporting electrode materials with high porosity and excellent degradation properties is of great importance for the removal of dye pollutants. Herein, this work synthesized nanoporous nickel@nickel oxide (np-Ni@NiO) electrode containing an amorphous alloy in the middle interlayer. The nanoporous structure endowed the electrode with more active sites and facilitated the ion/electron transport. The electrochemical active surface area was about 185.5 cm2. The electrochemical degradation of rhodamine B (RhB) using a np-Ni@NiO electrode was systematically investigated. The effects of technology paraments (NaCl concentration, the applied potential and pH) on electro-catalytic degradation were explored. An RhB removal rate of 99.68% was achieved in 30 s at optimized conditions, which was attributed to the unique bicontinuous ligament/pore structure and more active sites on the surface, as well as lower charge transfer resistance. In addition, the degradation mechanism of RhB in electrochemical oxidation was proposed, according to active species capture tests and EPR measurements.

Developing a facile and environmentally friendly approach to the synthesis of nanostructured Ni(OH)2 electrodes for high-performance supercapacitor applications is a great challenge. In this work, we report an extremely simple route to prepare a Ni(OH)2 nanopetals network by immersing Ni nanofoam in water. A binder-free composite electrode, consisting of Ni(OH)2 nanopetals network, Ni nanofoam interlayer and Ni-based metallic glass matrix (Ni(OH)2/Ni-NF/MG) with sandwich structure and good flexibility, was designed and finally achieved. Microstructure and morphology of the Ni(OH)2 nanopetals were characterized. It is found that the Ni(OH)2 nanopetals interweave with each other and grow vertically on the surface of Ni nanofoam to form an “ion reservoir”, which facilitates the ion diffusion in the electrode reaction. Electrochemical measurements show that the Ni(OH)2/Ni-NF/MG electrode, after immersion in water for seven days, reveals a high volumetric capacitance of 966.4 F/cm3 at a current density of 0.5 A/cm3. The electrode immersed for five days exhibits an excellent cycling stability (83.7% of the initial capacity after 3000 cycles at a current density of 1 A/cm3). Furthermore, symmetric supercapacitor (SC) devices were assembled using ribbons immersed for seven days and showed a maximum volumetric energy density of ca. 32.7 mWh/cm3 at a power density of 0.8 W/cm3, and of 13.7 mWh/cm3 when the power density was increased to 2 W/cm3. The fully charged SC devices could light up a red LED. The work provides a new idea for the synthesis of nanostructured Ni(OH)2 by a simple approach and ultra-low cost, which largely extends the prospect of commercial application in flexible or wearable devices.

Designing a novel photocatalytic composite for the efficient degradation of organic dyes remains a serious challenge. Herein, the multi-layered Co3O4@NP-CuO photocatalyst with unique features, i.e., the self-supporting, hierarchical porous network as well as the construction of heterojunction between Co3O4 and CuO, are synthesized by dealloying-electrodeposition and subsequent thermal treatment techniques. It is found that the interwoven ultrathin Co3O4 nanopetals evenly grow on the nanoporous CuO network (Co3O4@NP-CuO). The three-dimensional (3D) hierarchical porous structure for the catalyst provides more surface area to act as active sites and facilitates the absorption of visible light in the photodegradation reaction. Compared with the commercial CuO and Co3O4 powders, the newly designed Co3O4@NP-CuO composite exhibits superior photodegradation performance for RhB. The enhanced performance is mainly due to the construction of heterojunction of Co3O4/CuO, greatly promoting the efficient carrier separation for photocatalysis. Furthermore, the possible photocatalytic mechanism is analyzed in detail. This work provides a promising strategy for the fabrication of a new controllable heterojunction to improve photocatalytic activity.

With the deterioration of the ecological environment and the depletion of fossil energy, fuel cells, representing a new generation of clean energy, have received widespread attention. This review summarized recent progress in noble metal-based core–shell catalysts for oxygen reduction reactions (ORRs) in proton exchange membrane fuel cells (PEMFCs). The novel testing methods, performance evaluation parameters and research methods of ORR were briefly introduced. The effects of the preparation method, temperature, kinds of doping elements and the number of shell layers on the ORR performances of noble metal-based core–shell catalysts were highlighted. The difficulties of mass production and the high cost of noble metal-based core–shell nanostructured ORR catalysts were also summarized. Thus, in order to promote the commercialization of noble metal-based core–shell catalysts, research directions and prospects on the further development of high performance ORR catalysts with simple synthesis and low cost are presented.

In the present work, nanoporous Ag (np Ag) ribbons are prepared by chemical etching Cu60-xAg40Lax (x = 0, 3, 6 at.%) precursor alloys. The effects of precursor crystal structure on the morphology and mechanical properties of nanoporous Ag (np Ag) ribbons are investigated. The addition of La element inhibits the nucleation and growth of the crystal phases, then controls the phase compositions of the Cu-Ag-(La) precursors. The corroded np Ag with various ligament connectivity and homogeneity exhibits the different mechanical properties. Current study provides a general strategy for strengthening the np Ag metals by increasing the ligament connectivity and uniformity of the nanoporous metals.

Abstract Due to the severe volume expansion and poor cycle stability, transition metal oxide anode is still not meeting the commercial utilization. We herein demonstrate the synthetic method of core-shell pomegranate-shaped Fe2O3/C nano-composite via one-step hydrothermal process for the first time. The electrochemical performances were measured as anode material for Li-ion batteries. It exhibits excellent cycling performance, which sustains 705 mAh g−1 reversible capacities after 100 cycles at 100 mA g−1. The anodes also showed good rate stability with discharge capacities of 480 mAh g−1 when cycling at a rate of 2000 mA g−1. The excellent Li storage properties can be attributed to the unique core-shell pomegranate structure, which can not only ensure good electrical conductivity for active Fe2O3, but also accommodate huge volume change during cycles as well as facilitate the fast diffusion of Li ion.

The development of facile preparation methods and novel three-dimensional structured anodes to improve cycling stability of lithium ion batteries (LIBs) is urgently needed. Herein, a dual-network ferroferric oxide/nickel oxide (Fe3O4/NiO) anode was synthesized through a facile dealloying technology, which is suitable for commercial mass manufacturing. The dual-network with high specific surface area contains a nanoplate array network and a bimodal nanoporous urchin network. It exhibits excellent electrochemical performance as an anode material for LIB, delivering a reversible capacity of 721 mAh g−1 at 100 mA g−1 after 100 cycles. The good lithium storage performance is related to the ample porous structure, which can relieve stress and mitigate the volume change in the charge/discharge process, the interconnected porous network that enhances ionic mobility and permeability, and synergistic effects of two kinds of active materials. The paper provides a new idea for the design and preparation of anode materials with a novel porous structure by a dealloying method and may promote the development of the dealloying field.

Mg-based metallic glasses (MGs) are widely studied due to their high elasticity and high strength originating from their amorphous nature. However, their further application in many potential fields is limited by poor corrosion resistance. In order to improve this property, an MgO nanoplate array layer is first constructed on the surface of Mg-based MGs by cyclic voltammetry (CV) treatments. In this situation, the corrosion resistance and hydrophilicity of the material are enhanced. Then, stearic acid (SA) can effectively adhere onto the surface of the MgO layer to form a superficial hydrophobic film with a water contact angle (WCA) of 131°. As a result, the SA coated MgO hydrophobic film improves the corrosion resistance of Mg-based MGs in 3.5 wt.% NaCl solution obviously. In addition, the effects of four technological parameters (solution concentration, sweep rate, cycle number, and reaction temperature) in the CV process on the morphology and size of nano-products are investigated in detail. The work proposes a new method for the creation of nanostructures on the surface of materials and provides a new idea to increase the corrosion resistance of MGs. The related method is expected to be applied in wider fields in future.

To improve glucose electrocatalytic performance, one efficient manner is to develop a novel Cu-Ag bimetallic composite with fertile porosity and unique architecture. Herein, the self-supported electrode with CuxO/Ag2O (x = 1, 2) nanowires grown in-situ on a nanoporous Cu-Ag network (CuxO/Ag2O@NP-CuAg) has been successfully designed by a facile two-step approach. The integrated hierarchical porous structure, the tip-converged CuxO/Ag2O nanowires combined with the interconnected porous conductive substrate, are favorable to provide more reactive sites and improve ions or electrons transportation. Compared with monometallic Cu2O nanowires integrated with nanoporous Cu matrix (Cu2O@NP-Cu), the bimetallic CuxO/Ag2O@NP-CuAg composites exhibit the enhanced electrocatalytic performance for glucose. Moreover, the higher sensitivity of ~1.49 mA mM−1 cm−2 in conjunction with a wider linear range of 17 mM for the CuxO/Ag2O@NP-CuAg electrode anodized for 10 min are attributed to the synergistic effect of porous structure and bimetallic CuxO/Ag2O nanowires. Particularly, the integrated CuxO/Ag2O@NP-CuAg composites possess good flexibility, which has been reported for the first time. Accordingly, the CuxO/Ag2O@NP-CuAg with excellent glucose electrocatalytic performance and good flexibility is promising to further develop as a candidate electrode material of glucose sensors.

Dealloying, a famous ancient etching technique, was used to produce nanoporous metals decades ago. With the development of dealloying techniques and theories, various interesting dealloying products including nanoporous metals/alloys, metal oxides and composites, which exhibit excellent catalytic, optical and sensing performance, have been developed in recent years. As a result, the research on dealloying products is of great importance for developing new materials with superior physical and chemical properties. In this paper, typical dealloying products from Cu-based metallic glasses after dealloying in hydrofluoric acid and hydrochloric acid solutions are summarized. Several potential application fields of these dealloying products are discussed. A promising application of nanoporous Cu (NPC) and NPC-contained composites related to the energy storage field is introduced. It is expected that more promising dealloying products could be developed for practical energy storage applications.

Free dealloying of Cu-Hf-Al metallic glasses in HCl electrolytes are studied in this paper. The results show that the electrolyte concentration and dealloying time strongly influence the type of dealloying products. A superficial dealloying happens in diluted HCl electrolytes while a complete dealloying occurs in concentrated HCl electrolytes. The results present that Cu2O microparticles with regular morphology can be tailored on glassy surfaces in 0. 05 M HCl solution by controlling the dealloying time. Furthermore, the designable products of nanoporous Cu, Cu2O nanoplates and CuO microwires can be fabricated in 1. 2 M HCl electrolyte with the dealloying time. Due to a big difference of examined Cu-Hf-Al alloys in the electrolyte concentration and dealloying time, one or mixed dealloying products (Cu, Cu2O and CuO), which depend on the progress of relative chemical reactions and the different dealloying route, will finally be produced.

High-entropy alloys (HEAs) present excellent mechanical properties. However, the exploitation of chemical properties of HEAs is far less than that of mechanical properties, which is mainly limited by the low specific surface area of HEAs synthesized by traditional methods. Thus, it is vital to develop new routes to fabricate HEAs with novel three-dimensional structures and a high specific surface area. Herein, we develop a facile approach to fabricate nanoporous noble metal quasi-HEA microspheres by melt-spinning and dealloying. The as-obtained nanoporous Cu30Au23Pt22Pd25 quasi-HEA microspheres present a hierarchical porous structure with a high specific surface area of 69.5 m2/g and a multiphase approximatively componential solid solution characteristic with a broad single-group face-centered cubic XRD pattern, which is different from the traditional single-phase or two-phase solid solution HEAs. To differentiate, these are named quasi-HEAs. The synthetic strategy proposed in this paper opens the door for the synthesis of porous quasi-HEAs related materials, and is expected to promote further applications of quasi-HEAs in various chemical fields.

Mg-Zn-Ca amorphous alloys are considered as potential bone implants. A large number of works have focused on the alloys under free corrosion environment. However, the real service environment of bone implants is a kind of chemistry-mechanics interactive environment in which the materials not only suffer corrosion by body fluids but also bear applied force induced by body movement. In order to imitate the real service environment, surface morphologies and mechanical properties of Mg-Zn-Ca amorphous alloys were studied under different chemistry-mechanics interactive environments in this paper. It was found that cracks and Ca/Mg phosphates formed on the surface of amorphous alloys. The compressive strength of the alloys decreased seriously but could still reach an acceptable value to avoid material failure. Fan-shaped patterns found on all the samples implied that brittle fracture was the main fracture form. Moreover, vein-like patterns could still be found in some areas, showing a locally plastic deformation. This was the reason why the alloy could maintain a high compressive strength after severe and interactive treatments. The study could guide related works in the establishment of experimental environments in the future, which will facilitate a more accurate biomedical evaluation of bone implants.

Cu xO(x = 1,2)/amorphous compounds have been successfully synthesized by chemical free dealloying and spontaneous oxidation method. Technological parameters, such as the acid concentration and dealloying time strongly influence the crystal type, size and morphology of coppery oxide. The further study shows that with the increase of HCl concentration, the surface coverage rate of Cu2O micro-flowers increases and the sizes of Cu2O micro-flowers get bigger. Moreover, it is observed that cracks are formed on the etched ribbon surface and plentiful Cu2O/CuO particles grow up from these crack walls if the dealloying time extends to long enough. Considering many fascinating properties of Cu2O/CuO particles and the amorphous alloy carrier, potential application fields of these amazing compounds will be developed in future.

A wedge-shaped copper mold was used to fabricate micro quasicrystals(QCs). Stable Mg-Zn-Y-based nano-QCs were directly synthesized through this simple route instead of crystallization from metallic glasses or complicated forming processes at high temperature. The study showed that on the tips of the wedge-shaped ingots, the minimum diameter of nano-QCs approach to 4~6 nm. The main size of nano-QCs is about 10~30 nm. The maximum microhardness of QCs has been dramatically improved to about HV440 which increased by about 280% compared with that of the petal-like QCs fabricated under common cast iron mold cooling conditions. Possessing a certain negative enthalpy of mixing and existence of Frank-Kasper-type phases determined the formation of Mg-Zn-Y-based nano-QCs. The further electrochemical studies showed that Mg71Zn26Y2Cu1 nano-QC alloy possess high corrosion resistance in simulated seawater and its corrosion resistance is much better than those of the Mg72Zn26Y2 and Mg71Zn26Y2Cu0.5 Ni0.5 nano-QC alloys.

Mg‒Zn‒Ca metallic glasses are regarded as promising biodegradable materials. Previous studies on this alloy system have mostly focused on the composition regions with a large critical size (Dc) for the formation of metallic glasses, while this paper investigates the composition regions with a small Dc, which has been overlooked by researchers for a long time. The effects of the addition of Ag, Nd, and Yb elements on the microstructure and mechanical properties of Mg‒Zn‒Ca metallic glasses were studied. It was found that the Mg‒Zn‒Ca metallic glass exhibits a single and uniform amorphous structure with a compressive strength of 590 MPa. After the addition of a small amount of Ag into the alloy, the amorphous matrix is retained and new precipitate phases that lead to the decrease of the compressive strength are formed. The addition of the rare earth elements Nd and Yb changes the microstructure from a single amorphous matrix to a large number of quasicrystal phases, which results in an increase in compressive strength. The compressive strength of the Mg‒Zn‒Ca‒Yb alloy increases to 606.2 MPa due to the formation of multi-layered swirling solidified structure and a large number of small quasicrystals with high microhardness. Moreover, this study can be considered as a useful supplement to the existing studies on the Mg‒Zn‒Ca alloy system; it also provides new ideas for designing the microstructure and spatial structure of quasicrystal containing alloys with high performances.

Metallic glasses represent an interesting group of materials as they possess outstanding physical, chemical and mechanical properties compared to their crystalline counterparts. Currently, with well designed compositions it is possible to cast liquid alloys into the glassy state at low critical cooling rates from 100 K•s-1 to 1 K•s-1 and in large critical sample sizes up to several centimeters, which significantly enhances the promise for possible applications as advanced engineering materials. This paper reviews the development of (ZrCu)-based bulk metallic glasses with large sizes by copper mold casting and their unique properties. Additionally, the ex-situ and in-situ second phases reinforced BMG composites with large plasticity are also presented.

CuS is a metal sulfide anode material used in constructing lithium ion batteries (LIBs) with great promise. However, its practical application is limited by rapid capacity decline, poor cycling, and rate performance. In this work, the CuS nanowire-on-nanoplate network is synthesized through an improved dealloying method under two contrasting reaction temperatures. When used as an LIB anode, the as-obtained CuS network exhibits superior cycling performance (420 mAh·g−1 retained after 100 cycles at 0.2 C). When at 3 C, it still delivers a capacity of around 350 mAh·g−1. The improved electrochemical performances of the CuS anode should be attributed to the well-designed nanowire-on-nanoplate network structure in which the introduction of nanowires improves Li storage sites, shortens Li-ion diffusion distance, enhances the conductivity of active materials, and offers multiscale spaces for buffering the volume variation. The fabrication route adopted in this paper has an important significance for developing the dealloying technique and designing more suitable anode structures for LIBs.

The mechanical properties and degradation behavior of both as-cast and extruded Mg(100−7x)Zn6xYx alloys (x = 0.2, 0.4, 0.6, 0.8 at %) were systematically studied in this paper. The results indicated that with the increase in x value, the mechanical properties and corrosion resistance of the Mg(100−7x)Zn6xYx alloys were improved. The extruded Mg95.8Zn3.6Y0.6 alloy exhibited excellent mechanical properties, showing a tensile strength of 320 MPa, yield strength of 240 MPa, and elongation of 16%, which is much higher than that of commercially extruded AZ31 alloy. The weight loss experiment presented a higher degradation rate for the extruded Mg95.8Zn3.6Y0.6 alloy compared with the wrought AZ31 alloy, indicating a good bioactivity and biocompatibility. More detailed and long-term studies for evaluating and further controlling the degradation behavior of Mg–Zn–Y-based alloys remain to be performed.

Cu50Zr45Al5 bulk metallic glass (BMG) presents high fracture strength. For improving its plasticity and controlling its mechanical properties, superficial dealloying of the BMG was performed. A composite structure containing an inner rod-shaped Cu-Zr-Al amorphous core with high strength and an outer dealloyed nanoporous layer with high energy absorption capacity was obtained. The microstructures and mechanical properties of the composites were studied in detail. It was found, for the first time, that the mechanical properties of Cu50Zr45Al5 BMG can be controlled by adjusting the width of the buffer deformation zone in the dealloyed layer, which can be easily manipulated with different dealloying times. As a result, the compressive strength, compressive strain, and energy absorption capacity of the BMGs can be effectively modulated from 0.9 to 1.5 GPa, from 2.9% to 4.7%, and from 29.1 to 40.2 MJ/m3, respectively. The paper may open a door for developing important engineering materials with regulable and comprehensive performances.