Mingliang Du

Design of Two-Dimensional, Ultrathin MoS2 Nanoplates Fabricated Within One-Dimensional Carbon nanofibers With Thermosensitive Morphology: High-Performance Electrocatalysts For The Hydrogen Evolution Reaction

Two-dimensional MoS2 nanoplates within carbon nanofibers (CNFs) with monolayer thickness, nanometer-scale dimensions and abundant edges are fabricated. This strategy provides a well-defined pathway for the precise design of MoS2 nanomaterials, offering control over the evolution of MoS2 morphology from nanoparticles to nanoplates as well as from mono- to several-layer structures, over a lateral dimension range of 5 to 70 nm. CNFs play an important role in confining the growth of MoS2 nanoplates, leading to increases in the amount of exposed edge sites while hindering the stacking and aggregation of MoS2 layers, and accelerating electron transfer. The controlled growth of MoS2 nanoplates embedded in CNFs is leveraged to demonstrate structure-dependent catalytic activity in the hydrogen evolution reaction (HER). The results suggest that increases in the number of layers and the lateral dimension result in a decrease in HER activity as a general rule. Single-layer MoS2 nanoplates with abundant edges and a lateral dimension of 7.3 nm demonstrated the lowest hydrogen evolution reaction overpotential of 93 mV (J = 10 mA/cm(2)), the highest current density of 80.3 mA/cm(2) at η = 300 mV and the smallest Tafel slope of 42 mV/decade. The ability of MoS2-CNFs hybrids to act as nonprecious metal catalysts indicates their promise for use in energy-related electrocatalytic applications.

WO3–x Nanoplates Grown on Carbon Nanofibers for an Efficient Electrocatalytic Hydrogen Evolution Reaction

The search for non-noble metal catalysts with high activity for the hydrogen evolution reaction (HER) is crucial for efficient hydrogen production at low cost and on a large scale. Herein, we report a novel WO3-x catalyst synthesized on carbon nanofiber mats (CFMs) by electrospinning and followed by a carbonization process in a tubal furnace. The morphology and composition of the catalysts were tailored via a simple method, and the hybrid catalyst mats were used directly as cathodes to investigate their HER performance. Notably, the as-prepared catalysts exhibit substantially enhanced activity for the HER, demonstrating a small overpotential, a high exchange current density, and a large cathodic current density. The remarkable electrocatalytic performances result from the poor crystallinity of WO3-x, the high electrical conductivity of WO3-x, and the use of electrospun CNFs. The present work outlines a straightforward approach for the synthesis of transition metal oxide (TMO)-based carbon nanofiber mats with promising applications for the HER.

Morphology and Structure Engineering in Nanofiber Reactor: Tubular Hierarchical Integrated Networks Composed of Dual Phase Octahedral CoMn2O4/Carbon Nanofibers for Water Oxidation

1D hollow nanostructures combine the advantages of enhanced surface-to-volume ratio, short transport lengths, and efficient 1D electron transport, which can provide more design ideas for the preparation of highly active oxygen evolution (OER) electrocatalysts. A unique architecture of dual-phase octahedral CoMn2 O4 /carbon hollow nanofibers has been prepared via a two-step heat-treatment process including preoxidation treatment and Ostwald ripening process. The hollow and porous structures provide interior void spaces, large exposed surfaces, and high contact areas between the nanofibers and electrolyte and the morphology can be engineered by adjusting the heating conditions. Due to the intimate electrical and chemical coupling between the oxide nanocrystals and integrated carbon, the dual-phase octahedral CoMn2 O4 /carbon hollow nanofibers exhibit excellent OER activity with overpotentials of 337 mV at current density of 10 mA cm-2 and Tafel slope of 82 mV dec-1 . This approach will lead to the new perception of design issue for the nanoarchitecture with fine morphology, structures, and excellent electrocatalytic activity.

Atomic‐Scale Core/Shell Structure Engineering Induces Precise Tensile Strain to Boost Hydrogen Evolution Catalysis

Tuning surface strain is a new strategy for boosting catalytic activity to achieve sustainable energy supplies; however, correlating the surface strain with catalytic performance is scarce because such mechanistic studies strongly require the capability of tailoring surface strain on catalysts as precisely as possible. Herein, a conceptual strategy of precisely tuning tensile surface strain on Co9 S8 /MoS2 core/shell nanocrystals for boosting the hydrogen evolution reaction (HER) activity by controlling the MoS2 shell numbers is demonstrated. It is found that the tensile surface strain of Co9 S8 /MoS2 core/shell nanocrystals can be precisely tuned from 3.5% to 0% by changing the MoS2 shell layer from 5L to 1L, in which the strained Co9 S8 /1L MoS2 (3.5%) exhibits the best HER performance with an overpotential of only 97 mV (10 mA cm-2 ) and a Tafel slope of 71 mV dec-1 . The density functional theory calculation reveals that the Co9 S8 /1L MoS2 core/shell nanostructure yields the lowest hydrogen adsorption energy (∆EH ) of -1.03 eV and transition state energy barrier (∆E2H* ) of 0.29 eV (MoS2 , ∆EH = -0.86 eV and ∆E2H* = 0.49 eV), which are the key in boosting HER activity by stabilizing the HER intermediate, seizing H ions, and releasing H2 gas.

A self-supported electrochemical sensor for simultaneous sensitive detection of trace heavy metal ions based on PtAu alloy/carbon nanofibers

The key issue in efficient electrochemical detection of trace heavy metal ions (HMIs) is to design hierarchical nanostructure electrodes with high sensitivity and low detection limit. In this study, bimetallic PtAu alloy nanoparticles (PtAuNPs) with uniform size and distribution were constructed in electrospun carbon nanofibers (CNFs) by combining an electrospinning procedure and an in situ thermal reduction process. The PtAu/CNF membrane can be directly used as a sensor electrode for simultaneous detection of trace Cd2+, Pb2+, and Cu2+ by square wave anodic stripping voltammetry (SWASV). The prepared PtAu/CNF membrane is capable of simultaneously detecting Cd2+, Pb2+, and Cu2+ with a sensitivity of 0.10 μM and correlation coefficients of 0.976, 0.993, and 0.976, respectively, indicating high sensitivity and good linear relation. The excellent sensitivity and low detection limit for HMI detection were ascribed to the high conductivity of CNFs, fast response of PtAu alloy NPs, and high specific surface area of the hybrid structure. The present research provides a convenient and efficient way to construct new sensors for simultaneous trace detection of HMIs.

Graphene-assisted fabrication of poly(ε-caprolactone)-based nanocomposites with high mechanical properties and self-healing functionality

Herein, high-performance and self-healing poly(e-caprolactone) (PCL) nanocomposites were fabricated using polydopamine-capped reduced graphene oxide (PDG) as a nanofiller with the aid of fold-thermal compression (termed “mechanical annealing”) cycle effect. To improve the dispersion and interfacial interactions between the PDG nanosheets and PCL matrix, PCL chains were first grafted on PDG nanosheets by ring-opening polymerization of e-caprolactone. Notably, superior mechanical performances were successfully achieved by tailoring the periodic mechanical annealing process. The tensile strength of the PCL nanocomposite reaches up to 41.6 MPa, and the yield strength is as high as 22.7 MPa after 10 cycles of mechanical annealing, which are 2.4 and 2.6 times higher than those of pure PCL, respectively. Moreover, the photothermal conversion ability of polydopamine endowed the nanocomposite with self-healing functionality. The temperature of nanocomposites can rapidly surpass the melting temperature of the polymer upon exposure to near-infrared (NIR) light and thus allows fast NIR light-induced self-healing and recovery of the mechanical properties of the nanocomposites; this finding provides a facile method to obtain and explore new graphene-based NIR light-induced self-healing nanocomposites.

Nitrogen anion-decorated cobalt tungsten disulfides solid solutions on the carbon nanofibers for water splitting

A facile method to prepare nitrogen anion-decorated cobalt tungsten disulfides solid solutions, retaining ultra-thin WS2-like nanosheet structures (The N-Co x W1-x S2) anchored on carbon nanofibers (CNFs), is developed. The synergistic effect of the WS2 nanosheets provides a secure framework for stabilizing the amorphous Co-S clusters, CNFs substrate and nitrogen anion-decoration significantly enhances the inherent conductivity of the catalyst, resulting in a significantly promoted hydrogen evolution reaction activity and stable performance compared to pure Co9S8 nanoparticles or ultra-thin WS2 nanosheets. The N-Co x W1-x S2 electrode demonstrates the excellent electrocatalytic performance, with current density of 10 mA cm-2 at a low overpotential of 93 mV and Tafel slope of 85 mV dec-1, as well as the long-term stability in acid electrolyte. The present investigation may provide a feasible strategy for incorporating other heteroatoms into transitional metal disulfides materials to design catalysts with highly active and stable performance for water splitting.

Effects of Melanin on Optical Behavior of Polymer: From Natural Pigment to Materials Applications

Melanin is a kind of ubiquitous natural pigment, which serves a variety of protective functions in many organisms. In the present study, natural melanin and synthetic melanin nanoparticles (NPs) were systematically investigated for its potential application in polymeric optical materials. A significant short-wavelength shielding and high visible light transparency polymer nanocomposite was easily obtained via tuning the melanin particle size. In particular, the nanocomposite film with melanin NPs (diameter ≈ 15 nm) loading even as low as 1 wt % blocks most ultraviolet light below 340 nm and still keeps high visible light transparency (83%) in the visible spectrum. More importantly, because of the excellent photoprotection and radical scavenging capabilities of melanin, the resulting polymer nanocomposite exhibits outstanding photostability. In effect, such fantastic melanin NPs is promising for applications in various optical materials.