Fabrication of Zn-Air Battery with High Output Capacity Under Ultra-Large Current.

Zn-air battery (ZAB) is advocated as a more viable option in the new-energy technology. However, the limited-output capacity at a high current density impedes the driving range in power batteries substantially. Here, a novel heterojunction-based graphdiyne (GDY) and Ag29Cu7 alloy quantum dots (Ag29Cu7 QDs/GDY) for constructing a high-performance aqueous ZAB are fabricated. The as-fabricated ZAB achieves discharge at up to 100 mA cm-2 (the highest value ever reported) along with a remarkable output specific capacity of 786.2 mAh g-1 Zn, which is mainly benefitted from the binary-synergistic effect toward a stable triple-phase interface for air electrode induced by the Ag29Cu7 QDs and GDY in harsh base, together with the decreasing reaction energy barrier and polarization. The results outperform the superior reports discharging at low current and will bring breakthrough progress toward the practical applications of ZAB on large power supply facilities.

The Underlying Function and Structural Organization of the Intracellular Protein Corona on Graphdiyne Oxide Nanosheet for Local Immunomodulation.

Nanomaterial-biology interaction is the critical step in the fate of biomedical nanomedicines, influencing the consequent biological outcomes. Herein, we present two-dimensional carbon-based nanomaterials-graphdiyne oxide (GDYO) nanosheets that interact with an intracellular protein corona consisting of signal transducer and activator of transcription 3 (STAT3), inducing the reeducation of immunosuppressive macrophages. The interaction at the GDYO-STAT3 interface, driven by structure matching, hydrogen bonding, and salt bridges, simultaneously triggers the immune response in the tumor microenvironment, facilitating cancer immunotherapy. For the first time, our data reveal an interaction mechanism between the nanoparticle-protein interfaces inevitably formed inside the cells that determines the macrophage phenotype. Our results suggest that GDYO nanosheets could be applied for local immunomodulation due to their function and structural organization of the intracellular protein corona occurred inside macrophages.

Progress in Research into 2D Graphdiyne-Based Materials.

Graphynes (GYs) are carbon allotropes with single-atom thickness that feature layered 2D structure assembled by carbon atoms with sp - and sp2 - hybridization form. Various functional theories have predicted GYs to have natural band gap with Dirac cones structure, presumably originating from inhomogeneous π-bonding between those carbon atoms with different hybridization and overlap of the carbon 2p z orbitals. Among all the GYs, graphdiyne (GDY) was the first reported to be prepared practically and, hence, attracted the attention of many researchers toward this new planar, layered material, as well as other GYs. Several approaches have been reported to be able to modify the band gap of GDY, containing invoking strain, boron/nitrogen doping, nanoribbon architectures, hydrogenation, and so on. GDY has been well-prepared in many different morphologies, like nanowires, nanotube arrays, nanowalls, nanosheets, ordered stripe arrays, and 3D framwork. The fascinating structure and electronic properties of GDY make it a potential candidate carbon material with many applications. It has recently revealed the practicality of GDY as catalyst; in rechargeable batteries, solar cells, electronic devices, magnetism, detector, biomedicine, and therapy; and for gas separation as well as water purification.

Graphdiyne: synthesis, properties, and applications.

Graphdiyne (GDY), a new two-dimensional (2D) carbon allotrope, has been receiving increased attention. Its unique sp-sp2 carbon atoms, uniform pores, and highly π-conjugated structure provide promising potential in practical applications, such as gas separation, catalysis, water remediation, humidity sensor, and energy-related fields. In the recent years, considerable efforts have been expended toward the development of well-defined GDY. However, GDY materials still face numerous challenges, including the need for a more thorough understanding of the growth mechanism, strategies for synthesizing one- or few-layer single-crystalline GDY films, characterization of basic physicochemical properties, and achievement of promising applications. This review aims at providing a comprehensive update on the synthesis of GDY and GDY-based materials, as well as their properties, including structural, electronic, mechanical, and spectral properties, and their applications in nanotechnology.

Graphdiyne:Structure of Fluorescent Quantum Dots.

Graphdiyne (GDY) as an emerging two-dimensional carbon allotrope exhibits excellent performance in energy chemistry, catalytic chemistry, optoelectronics, electronics, etc. because of the unique structure combining an sp- and sp2 -hybrid carbon network. However, the poor solubility of pristine GDY is a major obstacle to its applications in many fields. Proposed here is a facile strategy to control the preparation of GDY quantum dots (GDY-Py QDs), in which pyrene groups are covalently linked to GDY by using a Sonogashira cross-coupling reaction. The as-prepared GDY-Py QDs, with an average diameter of about 3±0.1 nm, show superior dispersibility in many organic solvents and water. The GDY-Py QDs display not only bright fluorescent with a high relative quantum yield (QY) of 42.82 %, but they are also well-behaved as contrast agents in cell imaging. The GDY-Py QDs are bestowed with high stability and non-cytotoxicity, and exhibit long fluorescent times, and have potential for optical imaging and biomedical applications.

High-Yield and Damage-free Exfoliation of Layered Graphdiyne in Aqueous Phase.

The two-dimensional carbon material graphdiyne (GDY) holds great promise as a semiconductor and porous material, however, exfoliation of bulk GDY into single- or few-layered GDY in the aqueous phase remains a challenge. We report an efficient method for the damage-free exfoliation of bulk GDY into single- or few-layered GDY with high yield in an aqueous solution of inorganic salts (e.g., Li2 SiF6 ). This was confirmed by spherical-aberration-corrected scanning transmission electron microscopy, scanning/transmission electron microscopy, atomic force microscopy, Fourier transform infrared/Raman spectroscopy, X-ray photoelectron spectroscopy. The method gives high exfoliation efficiency (75 wt %) without creating additional structural defects or oxides in the exfoliated GDY. Theoretical calculations suggest that non-covalent adsorption of the anion, diffusion of the cation, and subsequent repulsive forces between adjacent flakes are the main driving force for the efficient exfoliation.

Synthesis and Properties of 2D Carbon-Graphdiyne.

Graphdiyne (GDY) is a flat material comprising sp2- and sp-hybridized carbon atoms with high degrees of π conjugation that features uniformly distributed pores. It is interesting not only from a structural point of view but also from the perspective of its electronic, chemical, mechanical, and magnetic properties. We have developed an in situ homocoupling reaction of hexaethynylbenzene on Cu foil for the fabrication of large-area ordered films of graphdiyne. These films are uniform and composed of graphdiyne multilayers. The conductivity of graphdiyne films, calculated at 2.52 × 10-4 S m-1, is comparable to that of Si, suggesting excellent semiconducting properties. Through morphology-controlled syntheses, we have prepared several well-defined graphdiyne structures (e.g., nanotubes, nanowires, and nanowalls) having distinct properties. The graphdiyne nanotube arrays and graphdiyne nanowalls exhibited excellent field emission performance, higher than that of some other semiconductors such as graphite and carbon nanotubes. These structures have several promising applications, for example, as energy storage materials and as anode materials in batteries. The unique atomic arrangement and electronic structure of graphdiyne also inspired us to use it to develop highly efficient catalysts; indeed, its low reduction potential and highly conjugated electronic structure allow graphdiyne to be used as a reducing agent and stabilizer for the electroless deposition of highly dispersed and surfactant-free Pd clusters. GDY-based three-dimensional (3D) nanoarchitectures featuring well-defined porous network structures can function as highly active cathodes for H2 evolution. Heteroatom-doped GDY structures are excellent metal-free electrocatalysts for the oxygen reduction reaction (ORR). Its excellent electrocatalytic activity and inexpensive, convenient, and scalable preparation make GDY a promising candidate for practical and efficient energy applications; indeed, we have explored the application of GDY as a highly efficient lithium storage material and have elucidated the method through which lithium storage occurs in multilayer GDY. Lithium-ion batteries featuring GDY-based electrodes display excellent electrochemical performance, including high specific capacity, outstanding rate performance, and long cycle life. We have also explored the application of GDY in energy conversion and found that it exhibits excellent conductivity. In this Account, we summarize the relationships between the functions of graphdiyne and its well-defined nanostructures. Our results suggest that GDY is a novel 2D carbon material possessing many attractive properties. It can be designed into new nanostructures and materials across a range of compositions, sizes, shapes, and functionalities and can be applied in the fields of electronics, optics, energy, and optoelectronics.

Ultrathin Graphdiyne Nanosheets Grown In†Situ on Copper Nanowires and Their Performance as Lithium-Ion Battery Anodes.

A method is presented for the scalable preparation of high-quality graphdiyne nanotubes and ultrathin graphdiyne nanosheets (average thickness: ca. 1.9 nm) using Cu nanowires as a catalyst. For the storage of Li+ ions, the graphdiyne nanostructures show a high capacity of 1388 mAh g-1 and high rate performance (870 mA h g-1 at 10 A g-1 , and 449.8 mA h g-1 at 20 A g-1 ) with robust stability, demonstrating outstanding overall potential for its applications.

Carbon Atom Hybridization Matters: Ultrafast Humidity Response of Graphdiyne Oxides.

Graphdiyne oxide (GDO), the oxidized form of graphdiyne (GDY), exhibits an ultrafast humidity response with an unprecedented response speed (ca. 7 ms), which is three times faster than that of graphene oxide (GO) with the same thickness and O/C ratio. The ultrafast humidity response of GDO is considered to benefit from the unique carbon hybridization of GDO, which contains acetylenic bonds that are more electron-withdrawing than ethylenic bonds in GO, consequently giving rise to a faster binding rate with water. This distinctive structure-based property enables the fabrication of a novel GDO-based humidity sensor with an ultrafast response speed and good selectivity against other kinds of gas molecules as well as high sensitivity. These properties allow the sensor to accurately monitor the respiration rate change of human and hypoxic rats.

Graphdiyne as Electrode Material: Tuning Electronic State and Surface Chemistry for Improved Electrode Reactivity.

Graphdiyne (GDY) is recently synthesized two-dimensional carbon allotrope with hexagonal rings cross-linked by diacetylene through introducing butadiyne linkages (-C≡C-C≡C-) to form 18-C hexagons and is emerging to be fundamentally interesting and particularly useful in various research fields. In this study, we for the first time find that GDY can be used as an electrode material with reactivity tunable by electronic states and surface chemistry of GDY. To demonstrate this, GDY is oxidized into graphdiyne oxide (GDYO) that is then chemically and electrochemically reduced into chemically reduced GDYO (cr-GDYO) and electrochemically reduced GDYO (er-GDYO), respectively. Electrode reactivity of GDY and its derivatives (i.e., GDYO, cr-GDYO, and er-GDYO) is studied with hexaammineruthenium chloride ([Ru(NH3)6]Cl3) and potassium ferricyanide (K3Fe(CN)6) as redox probes. We find that electron transfer kinetics of the redox probes employed here at GDYs depends on the density of electronic state (DOS) and the synergetic effects of the surface chemistry as well as the hydrophilicity of the materials, and that the electron transfer kinetics at cr-GDYO and er-GDYO are faster than those at GDY and GDYO, and quite comparable with those at carbon nanotubes and graphene and its derivatives (i.e., GO, cr-GO, and er-GO). These properties, combined with the unique electronic and chemical structures of GDY, essentially enable GDY as a new kind of electrode material for fundamental studies on carbon electrochemistry and various electroanalytical applications.

Graphdiyne-Supported NiCo2 S4 Nanowires: A Highly Active and Stable 3D Bifunctional Electrode Material.

The oxygen evolution reaction (OER), hydrogen evolution reaction (HER), and overall water splitting are major energy and chemical conversion efforts. Progress in electrocatalytic reactions have shown that the future is limitless in many fields. However, it is urgent to develop efficient electrocatalysts. Here, the first graphdiyne-supported efficient and bifunctional electrocatalyst is reported using 3D graphdiyne foam as scaffolds, and NiCo2 S4 nanowires as building blocks (NiCo2 S4 NW/GDF). NiCo2 S4 NW/GDF exhibits outstanding catalytic activity and stability toward both OER and HER, as well as overall water splitting in alkaline media. Remarkably, it enables a high-performance alkaline water electrolyzer with 10 and 20 mA cm-2 at very low cell voltages of 1.53 and 1.56 V, respectively, and remarkable stability over 140 h of continuous electrolysis operation at 20 mA cm-2 . The results indicate that this catalyst has a bifunction that overcomes all reported bifunctional, nonprecious-metal-based ones.

Superlyophilicity-Facilitated Synthesis Reaction at the Microscale: Ordered Graphdiyne Stripe Arrays.

As a new member of carbon allotropes, graphdiyne is a promising material with excellent electronic performance and high elasticity, indicating the possibility of graphdiyne to serve as the building blocks in flexible electronics. However, precise positioning/patterning of graphdiyne is still a challenge for the realization of large-area and flexible organic electronic devices and circuits. Here, the direct in situ synthesis of patterning graphdiyne stripe arrays dominated by the superlyophilic grooved templates is reported, whereas the superlyophilicity of grooved templates plays a key role in allowing continuous mass transport of raw reactants into the microscale spacing. After the completion of cross-coupling reaction procedure, precisely patterned graphdiyne stripes can be generated accordingly. The size of graphdiyne stripe arrays is depending on the silicon substrate size (1 cm × 1.5 cm), and the layer thickness can be manipulated from just several nanometers to hundreds of nanometers by varying the primary concentration of hexaethynylbenzene monomers. As a proof-of-principle demonstration, a stretchable sensor based on the graphdiyne stripe arrays is performed to monitor the human finger motion. It is expected that this wettability-facilitated strategy will provide new insights into the controlled synthesis of graphdiyne toward promising flexible electronics and other optoelectronic applications.

Multinuclear Phthalocyanine-Fused Molecular Nanoarrays: Synthesis, Spectroscopy, and Semiconducting Property.

The post-cyclization strategy rather than the conventional ante-cyclotetramerization method was employed for the synthesis of multinuclear phthalocyanine-fused molecular nanoarrays. Reaction of 2,3,9,10,16,17-hexakis(2,6-dimethylphenoxy)-23,24-diaminophthalocyaninato zinc(II) with 2,7-di-tert-butylpyrene-4,5-dione, 2,7-di-tert-butylpyrene-4,5,9,10-tetraone, and hexaketocyclohexane in refluxing acetic acid afforded the corresponding mono-, bi-, and trinuclear phthalocyanine-fused zinc complexes (Pz-pyrene){Zn[Pc(OC8 H9 )6 ]} (1), (Pz2 -pyrene){Zn[Pc(OC8 H9 )6 ]}2 (2), {(HAT){Zn[Pc(OC8 H9 )6 ]}3 } (3) in 46, 13, and 25 % yield, respectively, which extend the scope of multinuclear phthalocyanine-fused nanoarrays with different molecular skeletons. The self-assembly behavior of trinuclear phthalocyanine 3 in THF/CH3 CN was investigated by electronic absorption spectroscopy and SEM, and the fabricated nanorods showed interesting semiconducting properties, which suggest good application potential of these multinuclear phthalocyanine-fused molecular nanoarrays.

Mixed Phthalocyanine-Porphyrin Fused Conjugated Pentameric Nanoarrays.

The largest phthalocyanine-porphyrin-fused pentameric molecular arrays have been synthesized and spectroscopically characterized. The saddled molecular conformation revealed for the pentamer by DFT-D3 calculation in combination with the bulky peripheral substituents precludes effective face-to-face π-π intermolecular interaction. As a consequence, intermolecular C-H⋅⋅⋅π interactions together with the ubiquitous dispersion force arrays help to self-assemble the representative metal-free pentameric molecules into the three-dimensional supramolecular structures with nanorod morphology in CHCl3 and n-butanol. Powder X-ray diffraction (XRD) analysis and selected area electron diffraction (SAED) disclose the gradually increased long range of molecular ordering in the nanorods along with the increase in the substrate temperature from 30, 40, 50, to 60 °C. This in turn results in an increase in the semiconductivity of the single nanorod in the same order from 9.4×10-9 to 3.8×10-8 , 7.6×10-7 , and 6.3×10-5  S m-1 .

Highly efficient electron transport obtained by doping PCBM with graphdiyne in planar-heterojunction perovskite solar cells.

Organic-inorganic perovskite solar cells have recently emerged at the forefront of photovoltaics research. Here, for the first time, graphdiyne (GD), a novel two dimension carbon material, is doped into PCBM layer of perovskite solar cell with an inverted structure (ITO/PEDOT:PSS/CH3NH3PbI(3-x)Cl(x)/PCBM:GD/C60/Al) to improve the electron transport. The optimized PCE of 14.8% was achieved. Also, an average power conversion efficiency (PCE) of PCBM:GD-based devices was observed with 28.7% enhancement (13.9% vs 10.8%) compared to that of pure PCBM-based ones. According to scanning electron microscopy, conductive atomic force microscopy, space charge limited current, and photoluminescence quenching measurements, the enhanced current density and fill factor of PCBM:GD-based devices were ascribed to the better coverage on the perovskite layer, improved electrical conductivity, strong electron mobility, and efficient charge extraction. Small hysteresis and stable power output under working condition (14.4%) have also been demonstrated for PCBM:GD based devices. The enhanced device performances indicated the improvement of film conductivity and interfacial coverage based on GD doping which brought the high PCE of the devices and the data repeatability. In this work, GD demonstrates its great potential for applications in photovoltaic field owing to its networks with delocalized π-systems and unique conductivity advantage.

Graphdiyne oxides as excellent substrate for electroless deposition of Pd clusters with high catalytic activity.

Graphdiyne (GDY), a novel kind of two-dimensional carbon allotrope consisting of sp- and sp(2)-hybridized carbon atoms, is found to be able to serve as the reducing agent and stabilizer for electroless deposition of highly dispersed Pd nanoparticles owing to its low reduction potential and highly conjugated electronic structure. Furthermore, we observe that graphdiyne oxide (GDYO), the oxidation form of GDY, can be used as an even excellent substrate for electroless deposition of ultrafine Pd clusters to form Pd/GDYO nanocomposite that exhibits a high catalytic performance toward the reduction of 4-nitrophenol. The high catalytic performance is considered to benefit from the rational design and electroless deposition of active metal catalysts with GDYO as the support.

Synthesis of Graphdiyne Nanowalls Using Acetylenic Coupling Reaction.

Synthesizing graphdiyne with a well-defined structure is a great challenge. We reported herein a rational approach to synthesize graphdiyne nanowalls using a modified Glaser-Hay coupling reaction. Hexaethynylbenzene and copper plate were selected as monomer and substrate, respectively. By adjusting the ratio of added organic alkali along with the amount of monomer, the proper amount of copper ions was dissolved into the solution, thus forming catalytic reaction sites. With a rapid reaction rate of Glaser-Hay coupling, graphdiyne grew vertically at these sites first, and then with more copper ions dissolved, uniform graphdiyne nanowalls formed on the surface of copper substrate. Raman spectra, UV-vis spectra, and HRTEM results confirmed the features of graphdiyne. These graphdiyne nanowalls also exhibited excellent and stable field-emission properties.

Self-assembly of intramolecular charge-transfer compounds into functional molecular systems.

Highly polarized compounds exhibiting intramolecular charge transfer (ICT) are used widely as nonlinear optical (NLO) materials and red emitters and in organic light emitting diodes. Low-molecular-weight donor/acceptor (D/A)-substituted ICT compounds are ideal candidates for use as the building blocks of hierarchically structured, multifunctional self-assembled supramolecular systems. This Account describes our recent studies into the development of functional molecular systems with well-defined self-assembled structures based on charge-transfer (CT) interactions. From solution (sensors) to the solid state (assembled structures), we have fully utilized intrinsic and stimulus-induced CT interactions to construct these functional molecular systems. We have designed some organic molecules capable of ICT, with diversity and tailorability, that can be used to develop novel self-assembled materials. These ICT organic molecules are based on a variety of simple structures such as perylene bisimide, benzothiadiazole, tetracyanobutadiene, fluorenone, isoxazolone, BODIPY, and their derivatives. The degree of ICT is influenced by the nature of both the bridge and the substituents. We have developed new methods to synthesize ICT compounds through the introduction of heterocycles or heteroatoms to the π-conjugated systems or through extending the conjugation of diverse aromatic systems via another aromatic ring. Combining these ICT compounds featuring different D/A units and different degrees of conjugation with phase transfer methodologies and solvent-vapor techniques, we have self-assembled various organic nanostructures, including hollow nanospheres, wires, tubes, and ribbonlike architectures, with controllable morphologies and sizes. For example, we obtained a noncentrosymmetric microfiber structure that possessed a permanent dipole along its fibers' long axis and a transition dipole perpendicular to it; the independent NLO responses of this material can be separated and tuned spectroscopically and spatially. The ready processability and intrinsically high NLO efficiency of these microfibers offer great opportunities for applications in photonic devices. We have also designed molecular sensors based on changes in the efficiency of the ICT process upon complexation of an analyte with the D or A moieties in the ICT compounds. Such sensors, which display evident Stokes shifts or changes in quantum yields or fluorescence lifetimes, have promise for applications in chemical and biological recognition and sensing. In this Account, we shed light on the structure-function relationships of these functional molecular systems with well-defined self-assembled structures based on ICT interactions. The encouraging results that we have obtained suggest that such self-assembled ICT molecular materials can guide the design of new nanostructures and materials from organic systems, and that these materials, across a range of compositions, sizes, shapes, and functionalities, can potentially be applied in the fields of electronics, optics, and optoelectronics.

Growth of axial nested P-N heterojunction nanowires for high performance diodes.

Heterojunction nanomaterials have attracted the interest of numerous scientists and engineers to explore the fundamental scientific understanding of the formation of heterojunction nanostructures, their special properties with enhanced electrical and optical performance and the relationship between the functionality and the molecular structures. In this work, we synthesized novel axial nested P-N heterojunction nanowires combining the inorganic semiconductor PbS and the organic conjugated polymer polypyrrole (PPy). The nested P-N heterojunction nanowires (NWs) show a higher rectification ratio (exceeding 100), long-term stability and high unilateral conductivity due to the bigger area of junction produced.

Pristine graphdiyne-hybridized photocatalysts using graphene oxide as a dual-functional coupling reagent.

Advanced functional hybrids based on carbon materials (CMs) represent one of the main achievements of scientific communities. To achieve the hybridization, pristine CMs have to be chemically modified, or surfactants, which are nonfunctional for the performances of the hybrids, have to be employed as a cross-linkage. The construction of pristine CM-based hybrids using dual-functional coupling reagents, which work not only as a glue for hybridization but also as a functional component for enhanced performance, is strongly desired. Here, we report that pristine graphdiyne (GD), a recently synthesized new carbon allotrope, can be facilely hybridized with Ag/AgBr using graphene oxide (GO) as a cross-linkage. We demonstrate that compared to Ag/AgBr, Ag/AgBr/GO, and Ag/AgBr/GD, our Ag/AgBr/GO/GD exhibits an enhanced photocatalytic performance toward the degradation of methyl orange (MO) pollutant under visible light irradiation. In our Ag/AgBr/GO/GD, GO serves not only as a glue for a successful hybridization, but also as a functional component for enhanced catalytic performance. Beyond GD, our work likely paves a new avenue for the fabrication of advanced functional hybrids based on pristine carbon allotropes, wherein desired functions or properties might be achieved by choosing desired CMs and desired hybridized components.