Hui-Ming Cheng

More Reliable Lithium-Sulfur Batteries: Status, Solutions and Prospects

Lithium-sulfur (Li-S) batteries have attracted tremendous interest because of their high theoretical energy density and cost effectiveness. The target of Li-S battery research is to produce batteries with a high useful energy density that at least outperforms state-of-the-art lithium-ion batteries. However, due to an intrinsic gap between fundamental research and practical applications, the outstanding electrochemical results obtained in most Li-S battery studies indeed correspond to low useful energy densities and are not really suitable for practical requirements. The Li-S battery is a complex device and its useful energy density is determined by a number of design parameters, most of which are often ignored, leading to the failure to meet commercial requirements. The purpose of this review is to discuss how to pave the way for reliable Li-S batteries. First, the current research status of Li-S batteries is briefly reviewed based on statistical information obtained from literature. This includes an analysis of how the various parameters influence the useful energy density and a summary of existing problems in the current Li-S battery research. Possible solutions and some concerns regarding the construction of reliable Li-S batteries are comprehensively discussed. Finally, insights are offered on the future directions and prospects in Li-S battery field.

A Sulfur‐Rich Copolymer@CNT Hybrid Cathode with Dual‐Confinement of Polysulfides for High‐Performance Lithium–Sulfur Batteries

A sulfur-rich copolymer@carbon nanotubes hybrid cathode is introduced for lithium-sulfur batteries produced by combining the physical and chemical confinement of polysulfides. The binderfree and metal-current-collector-free cathode of dual confinement enables an efficient pathway for the fabrication of high-performance sulfur copolymer carbon matrix electrodes for lithium-sulfur batteries.

Nitrogen-Superdoped 3D Graphene Networks for High-Performance Supercapacitors

An N-superdoped 3D graphene network structure with an N-doping level up to 15.8 at% for high-performance supercapacitor is designed and synthesized, in which the graphene foam with high conductivity acts as skeleton and nested with N-superdoped reduced graphene oxide arogels. This material shows a highly conductive interconnected 3D porous structure (3.33 S cm-1 ), large surface area (583 m2 g-1 ), low internal resistance (0.4 Ω), good wettability, and a great number of active sites. Because of the multiple synergistic effects of these features, the supercapacitors based on this material show a remarkably excellent electrochemical behavior with a high specific capacitance (of up to 380, 332, and 245 F g-1 in alkaline, acidic, and neutral electrolytes measured in three-electrode configuration, respectively, 297 F g-1 in alkaline electrolytes measured in two-electrode configuration), good rate capability, excellent cycling stability (93.5% retention after 4600 cycles), and low internal resistance (0.4 Ω), resulting in high power density with proper high energy density.

Tailoring the thermal and electrical transport properties of graphene films by grain size engineering

Understanding the influence of grain boundaries (GBs) on the electrical and thermal transport properties of graphene films is essentially important for electronic, optoelectronic and thermoelectric applications. Here we report a segregation–adsorption chemical vapour deposition method to grow well-stitched high-quality monolayer graphene films with a tunable uniform grain size from ∼200u2009nm to ∼1u2009μm, by using a Pt substrate with medium carbon solubility, which enables the determination of the scaling laws of thermal and electrical conductivities as a function of grain size. We found that the thermal conductivity of graphene films dramatically decreases with decreasing grain size by a small thermal boundary conductance of ∼3.8 × 109u2009Wu2009m−2u2009K−1, while the electrical conductivity slowly decreases with an extraordinarily small GB transport gap of ∼0.01u2009eV and resistivity of ∼0.3u2009kΩu2009μm. Moreover, the changes in both the thermal and electrical conductivities with grain size change are greater than those of typical semiconducting thermoelectric materials.

Rosin-enabled ultraclean and damage-free transfer of graphene for large-area flexible organic light-emitting diodes

The large polymer particle residue generated during the transfer process of graphene grown by chemical vapour deposition is a critical issue that limits its use in large-area thin-film devices such as organic light-emitting diodes. The available lighting areas of the graphene-based organic light-emitting diodes reported so far are usually <1u2009cm2. Here we report a transfer method using rosin as a support layer, whose weak interaction with graphene, good solubility and sufficient strength enable ultraclean and damage-free transfer. The transferred graphene has a low surface roughness with an occasional maximum residue height of about 15u2009nm and a uniform sheet resistance of 560u2009Ω per square with about 1% deviation over a large area. Such clean, damage-free graphene has produced the four-inch monolithic flexible graphene-based organic light-emitting diode with a high brightness of about 10,000u2009cdu2009m−2 that can already satisfy the requirements for lighting sources and displays.

Green synthesis of graphene oxide by seconds timescale water electrolytic oxidation

Graphene oxide is highly desired for printing electronics, catalysis, energy storage, separation membranes, biomedicine, and composites. However, the present synthesis methods depend on the reactions of graphite with mixed strong oxidants, which suffer from explosion risk, serious environmental pollution, and long-reaction time up to hundreds of hours. Here, we report a scalable, safe and green method to synthesize graphene oxide with a high yield based on water electrolytic oxidation of graphite. The graphite lattice is fully oxidized within a few seconds in our electrochemical oxidation reaction, and the graphene oxide obtained is similar to those achieved by the present methods. We also discuss the synthesis mechanism and demonstrate continuous and controlled synthesis of graphene oxide and its use for transparent conductive films, strong papers, and ultra-light elastic aerogels.Graphene oxide is a graphene derivative showing wide applications, but it suffers from harsh synthetic conditions and long reaction time. Pei et al. show a green electrochemical method to fully oxidize the graphite lattice in a few seconds, which is over 100 times faster than existing methods.

Atomically Dispersed Transition Metals on Carbon Nanotubes with UltraHigh Loading for Selective Electrochemical Carbon Dioxide Reduction

Single-atom catalysts (SACs) are the smallest entities for catalytic reactions with projected high atomic efficiency, superior activity, and selectivity; however, practical applications of SACs suffer from a very low metal loading of 1-2 wt%. Here, a class of SACs based on atomically dispersed transition metals on nitrogen-doped carbon nanotubes (MSA-N-CNTs, where M = Ni, Co, NiCo, CoFe, and NiPt) is synthesized with an extraordinarily high metal loading, e.g., 20 wt% in the case of NiSA-N-CNTs, using a new multistep pyrolysis process. Among these materials, NiSA-N-CNTs show an excellent selectivity and activity for the electrochemical reduction of CO2 to CO, achieving a turnover frequency (TOF) of 11.7 s-1 at -0.55 V (vs reversible hydrogen electrode (RHE)), two orders of magnitude higher than Ni nanoparticles supported on CNTs.

Strongly Coupled High-Quality Graphene/2D Superconducting Mo2C Vertical Heterostructures with Aligned Orientation

Vertical heterostructures of two-dimensional (2D) crystals have led to the observations of numerous exciting physical phenomena and presented the possibilities for technological applications, which strongly depend on the quality, interface, relative alignment, and interaction of the neighboring 2D crystals. The heterostructures or hybrids of graphene and superconductors offer a very interesting platform to study mesoscopic superconductivity and the interplay of the quantum Hall effect with superconductivity. However, so far the heterostructures of graphene and 2D superconductors are fabricated by stacking, and consequently suffer from random relative alignment, weak interfacial interaction, and unavoidable interface contaminants. Here we report the direct growth of high-quality graphene/2D superconductor (nonlayered ultrathin α-Mo2C crystal) vertical heterostructures with uniformly well-aligned lattice orientation and strong interface coupling by chemical vapor deposition. In the heterostructure, both graphene and 2D α-Mo2C crystal show no defect, and the graphene is strongly compressed. Different from the previously reported graphene/superconductor heterostructures or hybrids, the strong interface coupling leads to a phase diagram of superconducting transition with multiple voltage steps being observed in the transition regime. Furthermore, we demonstrate the realization of highly transparent Josephson junction devices based on these strongly coupled high-quality heterostructures, in which a clear magnetic-field-induced Fraunhofer pattern of the critical supercurrent is observed.

Highly stable graphene-oxide-based membranes with superior permeability

Increasing fresh water demand for drinking and agriculture is one of the grand challenges of our age. Graphene oxide (GO) membranes have shown a great potential for desalination and water purification. However, it is challenging to further improve the water permeability without sacrificing the separation efficiency, and the GO membranes are easily delaminated in aqueous solutions within few hours. Here, we report a class of reduced GO membranes with enlarged interlayer distance fabricated by using theanine amino acid and tannic acid as reducing agent and cross-linker. Such membranes show water permeance over 10,000u2009Lu2009m−2 h−1 bar−1, which is 10–1000 times higher than those of previously reported GO-based membranes and commercial membranes, and good separation efficiency, e.g., rhodamine B and methylene blue rejection of ~100%. Moreover, they show no damage or delamination in water, acid, and basic solutions even after months.Graphene oxide membranes show great potential for water filtering, but improving their performance and stability remains difficult. Here, the authors use theanine amino acid and tannic acid to reduce and cross-link graphene oxide membranes with remarkably high permeability and stability in aqueous solution.

Ultrafast Growth of High‐Quality Monolayer WSe2 on Au

The ultrafast growth of high-quality uniform monolayer WSe2 is reported with a growth rate of ≈26 µm s-1 by chemical vapor deposition on reusable Au substrate, which is ≈2-3 orders of magnitude faster than those of most 2D transition metal dichalcogenides grown on nonmetal substrates. Such ultrafast growth allows for the fabrication of millimeter-size single-crystal WSe2 domains in ≈30 s and large-area continuous films in ≈60 s. Importantly, the ultrafast grown WSe2 shows excellent crystal quality and extraordinary electrical performance comparable to those of the mechanically exfoliated samples, with a high mobility up to ≈143 cm2 V-1 s-1 and ON/OFF ratio up to 9 × 106 at room temperature. Density functional theory calculations reveal that the ultrafast growth of WSe2 is due to the small energy barriers and exothermic characteristic for the diffusion and attachment of W and Se on the edges of WSe2 on Au substrate.