Electrospinning is a versatile and viable technique for generating ultrathin fibers. Remarkable progress has been made with regard to the development of electrospinning methods and engineering of electrospun nanofibers to suit or enable various applications. We aim to provide a comprehensive overview of electrospinning, including the principle, methods, materials, and applications. We begin with a brief introduction to the early history of electrospinning, followed by discussion of its principle and typical apparatus. We then discuss its renaissance over the past two decades as a powerful technology for the production of nanofibers with diversified compositions, structures, and properties. Afterward, we discuss the applications of electrospun nanofibers, including their use as "smart" mats, filtration membranes, catalytic supports, energy harvesting/conversion/storage components, and photonic and electronic devices, as well as biomedical scaffolds. We highlight the most relevant and recent advances related to the applications of electrospun nanofibers by focusing on the most representative examples. We also offer perspectives on the challenges, opportunities, and new directions for future development. At the end, we discuss approaches to the scale-up production of electrospun nanofibers and briefly discuss various types of commercial products based on electrospun nanofibers that have found widespread use in our everyday life.

Electrospinning and Electrospun Nanofibers: Methods, Materials, and Applications

Hydrogen fuel is considered as the cleanest renewable resource and the primary alternative to fossil fuels for future energy supply. Sustainable hydrogen generation is the major prerequisite to realize future hydrogen economy. The electrocatalytic hydrogen evolution reaction (HER), as the vital step of water electrolysis to H2 production, has been the subject of extensive study over the past decades. In this comprehensive review, we first summarize the fundamentals of HER and review the recent state-of-the-art advances in the low-cost and high-performance catalysts based on noble and non-noble metals, as well as metal-free HER electrocatalysts. We systemically discuss the insights into the relationship among the catalytic activity, morphology, structure, composition, and synthetic method. Strategies for developing an effective catalyst, including increasing the intrinsic activity of active sites and/or increasing the number of active sites, are summarized and highlighted. Finally, the challenges, perspectives, and research directions of HER electrocatalysis are featured.

Recent Advances in Electrocatalytic Hydrogen Evolution Using Nanoparticles.

Herein, we demonstrate the use of heterostructures comprised of Co/β-Mo2 C@N-CNT hybrids for the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) in an alkaline electrolyte. The Co can not only create a well-defined heterointerface with β-Mo2 C but also overcomes the poor OER activity of β-Mo2 C, thus leading to enhanced electrocatalytic activity for HER and OER. DFT calculations further proved that cooperation between the N-CNTs, Co, and β-Mo2 C results in lower energy barriers of intermediates and thus greatly enhances the HER and OER performance. This study not only provides a simple strategy for the construction of heterostructures with nonprecious metals, but also provides in-depth insight into the HER and OER mechanism in alkaline solution.

Heterostructures Composed of N‑Doped Carbon Nanotubes Encapsulating Cobalt and β‑Mo 2 C Nanoparticles as Bifunctional Electrodes for Water Splitting

Water-splitting electrolyzers that can convert electricity into storable hydrogen are a fascinating and scalable energy conversion technology for the utilization of renewable energies. To speed up the sluggish hydrogen and oxygen evolution reactions (HER and OER), electrocatalysts are essential for reducing their kinetic energy barriers and eventually improving the energy conversion efficiency. As efficient strategies for modulating the binding ability of water-splitting intermediates on electrocatalyst surface, the support effect and interface effect are drawing growing attention. Herein, some of the recent research progress on the support and interface effects in HER, OER, and overall water-splitting electrocatalysts is highlighted. Specifically, the correlation between the electronic interaction of the constituent components and the electrocatalytic water-splitting performance of electrocatalysts is profoundly discussed, with the aim of advancing the development of highly efficient water-splitting electrocatalysts, which may eventually replace the noble-metal-based electrocatalysts and bring the practically widespread utilization of water-splitting electrolyzers into a reality.

Support and Interface Effects in Water-Splitting Electrocatalysts

Although electrocatalysts based on transition metal phosphides (TMPs) with cationic/anionic doping have been widely studied for hydrogen evolution reaction (HER), the origin of performance enhancement still remains elusive mainly due to the random dispersion of dopants. Herein, we report a controllable partial phosphorization strategy to generate CoP species within the Co-based metal-organic framework (Co-MOF). Density functional theory calculations and experimental results reveal that the electron transfer from CoP to Co-MOF through N-P/N-Co bonds could lead to the optimized adsorption energy of H2 O (ΔG H 2 O * ) and hydrogen (ΔGH* ), which, together with the unique porous structure of Co-MOF, contributes to the remarkable HER performance with an overpotential of 49 mV at a current density of 10 mA cm-2 in 1 m phosphate buffer solution (PBS, pH 7.0). The excellent catalytic performance exceeds almost all the documented TMP-based and non-noble-metal-based electrocatalysts. In addition, the CoP/Co-MOF hybrid also displays Pt-like performance in 0.5 m H2 SO4 and 1 m KOH, with the overpotentials of 27 and 34 mV, respectively, at a current density of 10 mA cm-2 .

CoP-Doped MOF-Based Electrocatalyst for pH-Universal Hydrogen Evolution Reaction

Transition-metal phosphides (TMPs) have emerged as promising catalyst candidates for the hydrogen evolution reaction (HER). Although numerous methods have been investigated to obtain TMPs, most rely on traditional synthetic methods that produce materials that are inherently deficient with respect to electrical conductivity. An electrospinning-based reduction approach is presented, which generates nickel phosphide nanoparticles in N-doped porous carbon nanofibers (Ni2 P@NPCNFs) in situ. Ni2 P nanoparticles are protected from irreversible fusion and aggregation in subsequent high-temperature pyrolysis. The resistivity of Ni2 P@NPCNFs (5.34 Ω cm) is greatly decreased by 104 times compared to Ni2 P (>104  Ω cm) because N-doped carbon NFs are incorporated. As an electrocatalyst for HER, Ni2 P@NPCNFs reveal remarkable performance compared to other previously reported catalysts in acidic media. Additionally, it offers excellent catalytic ability and durability in both neutral and basic media. Encouraged by the excellent electrocatalytic performance of Ni2 P@NPCNFs, a series of pea-like Mx P@NPCNFs, including Fe2 P@NPCNFs, Co2 P@NPCNFs, and Cu3 P@NPCNFs, were synthesized by the same method. Detailed characterization suggests that the newly developed method could render combinations of ultrafine metal phosphides with porous carbon accessible; thereby, extending opportunities in electrocatalytic applications.

Nanosized Metal Phosphides Embedded in Nitrogen‐Doped Porous Carbon Nanofibers for Enhanced Hydrogen Evolution at All pH Values

Double-Shelled NiO-NiCo2O4 Heterostructure@Carbon Hollow Nanocages as an Efficient Sulfur Host for Advanced Lithium–Sulfur Batteries

Circuit board-like CoS/MXene composite with superior performance for sodium storage

Metal-organic framework (MOF)-derived hollow cobalt sulfides have attracted extensive attention due to their porous shell that provides rich redox reactions for energy storage. However, their ultradispersed structure and the large size of MOF precursors result in relatively low conductivity, stability, and tap density. Therefore, the construction of an array of continuous hollow cages and tailoring of the inner cavity of MOF-derived materials is very effective for enhancing the electrochemical performance. Herein, we in situ assembled small Co-based zeolitic imidazolate framework (ZIF-67) on the both sides of negatively charged MnO2 nanosheets to fabricate a hierarchical sandwich-type composite with hollow cobalt sulfide nanocages/graphene-like MnO2. The graphene-like MnO2 nanosheets acted not only as a structure-directing agent to grow a ZIF-67 array but also as a promising electroactive material of electrochemical capacitors to provide capacitance. As an electrode material of supercapacitors, the as-pre...

Heng Liu

Papers

Nanosized Metal Phosphides Embedded in Nitrogen‐Doped Porous Carbon Nanofibers for Enhanced Hydrogen Evolution at All pH Values

Double-Shelled NiO-NiCo2O4 Heterostructure@Carbon Hollow Nanocages as an Efficient Sulfur Host for Advanced Lithium–Sulfur Batteries

Circuit board-like CoS/MXene composite with superior performance for sodium storage

Assembling Hollow Cobalt Sulfide Nanocages Array on Graphene-like Manganese Dioxide Nanosheets for Superior Electrochemical Capacitors.

Chinese knot-like electrode design for advanced Li-S batteries