Qunhong Weng

Boron Nitride Porous Microbelts for Hydrogen Storage

Layered boron nitrides (BNs) are usually viewed as excellent protective coatings and reinforcing materials due to their chemical inertness and high mechanical strength. However, the attention paid to their potential applications in gas sorption, especially in case of hydrogen, has obviously been insufficient. Herein, a novel BN material (i.e., porous microbelts), with the highest specific surface area ever reported for any BN system, up to 1488 m² g⁻¹, is obtained through one-step template-free reaction of a boron acid-melamine precursor with ammonia. Comprehensive high-resolution transmission electron microscopy, X-ray diffraction, and Raman characterizations all confirm that the obtained BN phase is partially disordered, shows an enlarged average spacing between adjacent (0002) layers (d₀₀₀₂ = 0.38 nm, compared to normal 0.33 nm for a bulk layered BN), and belongs to an intermediate state between hexagonal (h-BN) and amorphous (a-BN) phases. By changing the synthesis temperatures, the textures of obtained porous microbelts are adjustable. H₂ sorption evaluations demonstrate that the materials exhibit high and reversible H₂ uptake from 1.6 to 2.3 wt % at 77 K and at a relatively low pressure of 1 MPa.

Amorphous Phosphorus/Nitrogen-Doped Graphene Paper for Ultrastable Sodium-Ion Batteries

As the most promising anode material for sodium-ion batteries (SIBs), elemental phosphorus (P) has recently gained a lot of interest due to its extraordinary theoretical capacity of 2596 mAh/g. The main drawback of a P anode is its low conductivity and rapid structural degradation caused by the enormous volume expansion (>490%) during cycling. Here, we redesigned the anode structure by using an innovative methodology to fabricate flexible paper made of nitrogen-doped graphene and amorphous phosphorus that effectively tackles this problem. The restructured anode exhibits an ultrastable cyclic performance and excellent rate capability (809 mAh/g at 1500 mA/g). The excellent structural integrity of the novel anode was further visualized during cycling by using in situ experiments inside a high-resolution transmission electron microscope (HRTEM), and the associated sodiation/desodiation mechanism was also thoroughly investigated. Finally, density functional theory (DFT) calculations confirmed that the N-doped graphene not only contributes to an increase in capacity for sodium storage but also is beneficial in regards to improved rate performance of the anode.

Large-surface-area BN nanosheets and their utilization in polymeric composites with improved thermal and dielectric properties.

High-throughput few-layered BN nanosheets have been synthesized through a facile chemical blowing route. They possess large lateral dimensions and high surface area, which are beneficial to fabricate effectively reinforced polymeric composites. The demonstrated composites made of polymethyl methacrylate and BN nanosheets revealed excellent thermal stability, 2.5-fold improved dielectric constant, and 17-fold enhanced thermal conductivity. The results indicate multifunctional practical applications of such polymeric composites in many specific fields, such as thermoconductive insulating long-lifetime packaging for electrical circuits.

“Protrusions” or “holes” in graphene: which is the better choice for sodium ion storage?

The main challenge associated with sodium-ion battery (SIB) anodes is a search for novel candidate materials with high capacity and excellent rate capability. The most commonly used and effective route for graphene-based anode design is the introduction of in-plane “hole” defects via nitrogen-doping; this creates a spacious reservoir for storing more energy. Inspired by mountains in nature, herein, we propose another way – the introduction of blistering in graphene instead of making “holes”; this facilitates adsorbing/inserting more Na+ ions. In order to properly answer the key question: ““protrusions” or “holes” in graphene, which is better for sodium ion storage?”, two types of anode materials with a similar doping level were designed: a phosphorus-doped graphene (GP, with protrusions) and a nitrogen-doped graphene (GN, with holes). As compared with GN, the GP anode perfectly satisfies all the desired criteria: it reveals an ultrahigh capacity (374 mA h g−1 after 120 cycles at 25 mA g−1) comparable to the best graphite anodes in a standard Li-ion battery (∼372 mA h g−1), and exhibits an excellent rate capability (210 mA h g−1 at 500 mA g−1). In situ transmission electron microscopy (TEM) experiments and density functional theory (DFT) calculations were utilized to uncover the origin of the enhanced electrochemical activity of “protrusions” compared to “holes” in SIBs, down to the atomic scale. The introduction of protrusions through P-doping into graphene is envisaged to be a novel effective way to enhance the capacity and rate performance of SIBs.

Hollow boron nitride nanospheres as boron reservoir for prostate cancer treatment

High global incidence of prostate cancer has led to a focus on prevention and treatment strategies to reduce the impact of this disease in public health. Boron compounds are increasingly recognized as preventative and chemotherapeutic agents. However, systemic administration of soluble boron compounds is hampered by their short half-life and low effectiveness. Here we report on hollow boron nitride (BN) spheres with controlled crystallinity and boron release that decrease cell viability and increase prostate cancer cell apoptosis. In vivo experiments on subcutaneous tumour mouse models treated with BN spheres demonstrated significant suppression of tumour growth. An orthotopic tumour growth model was also utilized and further confirmed the in vivo anti-cancer efficacy of BN spheres. Moreover, the administration of hollow BN spheres with paclitaxel leads to synergetic effects in the suppression of tumour growth. The work demonstrates that hollow BN spheres may function as a new agent for prostate cancer treatment.

In situ electrochemical formation of core–shell nickel–iron disulfide and oxyhydroxide heterostructured catalysts for a stable oxygen evolution reaction and the associated mechanisms

For electrochemical production of H2 fuels from water splitting, the development of efficient and economic catalysts for the oxygen evolution reaction (OER) is still a challenging issue. This is because an OER process usually involves multiple electron-transfer and reaction steps; these result in large overpotentials and significant energy loss. Thus, a smart design of highly efficient, stable and cheap OER electrocatalysts is important for the improvement of energy conversion efficiency and reduction of water splitting procedure cost. In this work, we find that a thin crystalline oxyhydroxide layer has been in situ electrochemically formed on the surfaces of conductive nickel–iron disulfide nanostructures; such a heterostructure takes advantage of highly catalytically active oxyhydroxide surfaces and excellent conductivity of the interior disulfide phase. This results in a very low overpotential of 230 mV at a current density of 10 mA cm−2, which is among the best OER catalysts in alkaline electrolyte ever reported. The crystalline oxyhydroxide layer can effectively prevent the disulfide core from further oxidation, maintains the core–shell structure of the catalyst and is considered to be critical for stable and efficient OER performances.

Tuning of the Optical, Electronic, and Magnetic Properties of Boron Nitride Nanosheets with Oxygen Doping and Functionalization

Engineering of the optical, electronic, and magnetic properties of hexagonal boron nitride (h-BN) nanomaterials via oxygen doping and functionalization has been envisaged in theory. However, it is still unclear as to what extent these properties can be altered using such methodology because of the lack of significant experimental progress and systematic theoretical investigations. Therefore, here, comprehensive theoretical predictions verified by solid experimental confirmations are provided, which unambiguously answer this long-standing question. Narrowing of the optical bandgap in h-BN nanosheets (from ≈5.5 eV down to 2.1 eV) and the appearance of paramagnetism and photoluminescence (of both Stokes and anti-Stokes types) in them after oxygen doping and functionalization are discussed. These results are highly valuable for further advances in semiconducting nanoscale electronics, optoelectronics, and spintronics.

Magnetically Assembled Ni@Ag Urchin‐Like Ensembles with Ultra‐Sharp Tips and Numerous Gaps for SERS Applications

Dequan Liu , Xi Wang , * Deyan He , * Thang Duy Dao , adaaki T Nagao , * Qunhong Weng , Daiming ang , T Xuebin Wang , Wei Tian , Dmitri Gol berg , and Yoshio Bando *

Construction of Polarized Carbon–Nickel Catalytic Surfaces for Potent, Durable, and Economic Hydrogen Evolution Reactions

Electrocatalytic hydrogen evolution reaction (HER) in alkaline solution is hindered by its sluggish kinetics toward water dissociation. Nickel-based catalysts, as low-cost and effective candidates, show great potentials to replace platinum (Pt)-based materials in the alkaline media. The main challenge regarding this type of catalysts is their relatively poor durability. In this work, we conceive and construct a charge-polarized carbon layer derived from carbon quantum dots (CQDs) on Ni3N nanostructure (Ni3N@CQDs) surfaces, which simultaneously exhibit durable and enhanced catalytic activity. The Ni3N@CQDs shows an overpotential of 69 mV at a current density of 10 mA cm-2 in a 1 M KOH aqueous solution, lower than that of Pt electrode (116 mV) at the same conditions. Density functional theory (DFT) simulations reveal that Ni3N and interfacial oxygen polarize charge distributions between originally equal C-C bonds in CQDs. The partially negatively charged C sites become effective catalytic centers for the key water dissociation step via the formation of new C-H bond (Volmer step) and thus boost the HER activity. Furthermore, the coated carbon is also found to protect interior Ni3N from oxidization/hydroxylation and therefore guarantees its durability. This work provides a practical design of robust and durable HER electrocatalysts based on nonprecious metals.

Electronic and Optical Properties of 2D Materials Constructed from Light Atoms

Boron, carbon, nitrogen, and oxygen atoms can form various building blocks for further construction of structurally well-defined 2D materials (2DMs). Both in theory and experiment, it has been documented that the electronic structures and optical properties of 2DMs are well tunable through a rational design of the material structure. Here, the recent progress on 2DMs that are composed of B, C, N, and O elements is introduced, including borophene, graphene, h-BN, g-C3 N4 , organic 2D polymers (2DPs), etc. Attention is put on the band structure/bandgap engineering for these materials through a variety of methodologies, such as chemical modifications, layer number and atomic structure control, change of conjugation degree, etc. The optical properties, such as photoluminescence, thermoluminescence, single photon emission, as well as the associated applications in bioimaging and sensing, are discussed in detail and highlighted.