Ultrathin Nanoribbons Research Articles

Synthesis and Characterization of Novel 2D Ultrathin Nanoribbons Cd-Ag-MOF@ZnO Composite as Organo-Nanocatalyst for Preparation of Polyhydroquinoline Heterocycles

Novel ultrathin Cd-Ag-MOF@ZnO composite nanoribbons (Ut-Nr Cd-Ag-MOF@ZnO C) were prepared and characterized in this research to serve as organocatalyst in Hantzsch condensation for selective synthesis of asymmetric polyhydroquinolines through a one-pot multi-component condensation reaction of various substituted arylaldehyde, 5,5-dimethyl-1,3-cyclohexanedione, ammonium acetate and ethyl acetoacetate under solvent-free conventional heating in relatively short reaction times. The developed catalysts were easily recycled and reutilized at least three times under optimized reaction conditions with no noticeable decline in their initial catalytic activities. Operational simplicity and environmental compatibility, combined with the application of a reusable and affordable heterogeneous catalyst, significant efficiency, relatively short reaction time, and good yield are among the main characteristics of the proposed synthetic approach.

2D coordination unsaturated Ni-MOFs hierarchical nanosheets with internal electric fields for high-performance hybrid supercapacitors

The poor intrinsic electronic conductivity and low-exposure electroactive sites of MOFs limit their practical application in energy storage. Herein, the coordination unsaturated nickel-based metal organic frameworks (Ni-MOFs) were prepared by one-step solvothermal method via adjusting the molar ratio of metal salts to organic ligands (RM/L). The coordination unsaturated degree and morphology of the materials can be controlled by adjusting RM/L. When the RM/L is 2, the obtained Ni-MOF 2:1 is a two-dimensional (2D) hierarchical nanosheets made of interwoven ultra-thin nanoribbons. The 2D hierarchical nanosheets structure of Ni-MOF 2:1 can not only expose more electroactive sites, but also promote ions diffusion. The density functional theory (DFT) simulations reveal that the coordination unsaturated centers can narrow the band gap, thus resetting the internal electric field and improving the conductivity of Ni-MOF 2:1. Benefit from abundant electroactive sites, rapid ions diffusion and improved electrical conductivity, the Ni-MOF 2:1 shows a high specific capacity of 746 C g−1 at 1 A g−1 and excellent cycling stability of 89.7 % capacity retention after 10,000 cycles at 10 A g−1. The hybrid supercapacitor (HSC) assembled with Ni-MOF 2:1 as cathode and activated carbon (AC) as anode has a maximum energy density of 53.1 Wh Kg−1 at 799.9 W Kg−1. This work provides a promising strategy for the rational design of MOFs-based electrode materials for high performance HSC. Moreover, compared with the studies using MOFs derivatives as electrode materials, the direct use of Ni-MOFs as electrode materials in this study is of great significance to avoid energy waste and maintain the inherent advantages of MOFs.

Cooperative Cationic and Anionic Redox Reactions in Ultrathin Polyvalent Metal Selenide Nanoribbons for High-Performance Electrochemical Magnesium-Ion Storage.

Rechargeable magnesium batteries (RMBs) are considered as potential energy storage devices due to their high volumetric specific capacity, good safety, as well as source abundance. Despite extensive efforts devoted to constructing an efficient magnesium battery system, the sluggish Mg2+ diffusion in conventional cathode materials often leads to slow rate kinetics, low capacity, and poor cycling lifespan. Although transition metal selenides with soft anion frameworks have attracted extensive attention, their Mg2+ storage mechanism still needs to be clarified. Herein, we demonstrate that the ultrathin CoSe2 nanoribbons can be used as a robust cathode material for RMBs and reveal a novel Mg2+ storage mechanism based on cooperative cationic (Co) and anionic (Se) redox processes via systematic ex-situ characterizations. Compared to other metal selenide cathodes based on conversion reactions of solely metal cations, the cooperative cationic-anionic redox reactions of the CoSe2 cathode contribute to obtaining an enhanced specific capacity and boosted electrochemical kinetics. Moreover, on one hand, the ultrathin nanoribbon structure enables effective contact between the electrode material and electrolyte and on the other hand significantly reduces the length and time consumption of Mg2+ diffusion, leading to dominated surface-driven capacitance-controlled Mg2+ storage behavior and rapid Mg2+ storage kinetics. As a result, the ultrathin CoSe2 nanoribbon cathode exhibits a reversible discharge capacity of ∼130 mAh g-1 at 100 mA g-1, good rate capability (116 mAh g-1 at 300 mA g-1), and long cyclability over 600 cycles. This finding confirms the development potentiality of polyvalent metal selenide cathode materials based on a cooperative cationic-anionic redox mechanism for the construction of next-generation multivalent secondary batteries.

Atomically Dispersed Ruthenium on Nickel Hydroxide Ultrathin Nanoribbons for Highly Efficient Hydrogen Evolution Reaction in Alkaline Media.

Achieving highly efficient hydrogen evolution reaction (HER) in alkaline media is a great challenge. Single-atom catalysts with high-loading amount have attracted great interest due to their remarkable catalytic properties. Herein, by using nickel foam as the substrate, the authors design and precisely synthesize atomic ruthenium (Ru)-loaded nickel hydroxide ultrathin nanoribbons (R-NiRu) with a high atomic Ru loading amount reaching ≈7.7wt% via a one-step hydrothermal method. The presence of concentrated Cl- in the synthetic system is beneficial for constructing ultrathin nanoribbons, which, with abundant edge OH groups, make it easy to trap atomic Ru. Taking advantage of the synergy between atomic Ru and the nanoribbon morphology of nickel hydroxide, R-NiRu exhibit a low overpotential of 16mV for HER at 10mAcm-2 and a Tafel slope of 40mVdec-1 in aqueous 1.0mKOH solution, which are superior to those of commercial Pt/C (overpotential of 17mV at 10mAcm-2 , Tafel slope of 43mVdec-1 ). Density functional theory (DFT) calculation results demonstrate that atomically dispersed Ru can significantly reduce the HER energy barrier. Moreover, R-NiRu maintains exceptional stability after 5000 cyclic voltammetry cycles. This efficient and facile synthetic strategy provides a new avenue for designing efficient catalysts.

Deformation and ductile fracture of nanocrystalline gold ultrathin nanoribbon: Width effect

AbstractMolecular dynamics simulations are used to investigate the mechanical properties of finite‐width nanocrystalline gold nanoribbons with a thickness of one grain size under tensile strain. We find strong variations in the Young's modulus and flow stress especially for the sample with narrow width. With statistical analysis, Young's modulus has a trend of increase with the decrease of width. Flow stress does not follow this trend. Ductile fracture is observed at large strain in these nanocrystalline nanoribbons, but the fracture strain and mechanism are different from those of thick films as observed in existing experiments. For small widths below 80 nm, fracture is a necking effect, while for larger widths, shear bands and formation of nanovoids due to stress concentration are the main mechanism. Voids are mainly distributed in special GBs that are parallel to the direction of the maximum principal stress of the plastic deformation tensor. We find there is a width regime (about 80–130 nm) for the ultrathin nanoribbon gold, which have good ductility and large fracture strain.

Interconversion between nanoribbons and nanospheres mediated by detachable ‘invisibility suit’

Taming the ultrathin nanomaterials with the desired stability and functionality is one of the challenges of chemistry and materials science. Developing a detachable smart ’invisibility suit’ may represent an attractive strategy for coping with this dilemma. Here, a protection-deprotection strategy for ultrathin nanomaterials of hydrogen-bonded organic frameworks (HOFs), by putting on and taking off a detachable ’invisibility suit,’ is reported. Upon wearing the ’invisibility suit,’ the ultrathin nanoribbons with high crystallinity can fold into ’sturdy’ nanospheres, the latter featured with amorphous character, stimuli inertia, and excellent extreme condition resistance, achieving the challenging goal of ’stealth.’ In addition, the superior water affinity, sensitive selectivity, ultrahigh water adsorption capacity, and promising energy-saving activation steps for the ’stealth’ nanospheres have been demonstrated, suggesting a promising candidate for the real-world application as an effective dehydrator. More importantly, taking off the ’invisibility suit’ leads to the release of the initial nanoribbons, which features the promising thermal and NIR light-triggered photoluminescence and photocatalysis. These results have provided an inter-conversion cycle between nanoribbons and nanospheres, which are expected to significantly promote the demand-oriented storage, transportation, and practical application of ultrathin nanomaterials.

Chirally Twisted Ultrathin Polydopamine Nanoribbons: Synthesis and Spontaneous Assembly of Silver Nanoparticles on Them.

Polydopamine (PDA) is a synthetic polymeric material with immense potential in biomedical and surface functionalization applications. Herein, we have screened self-assemblies formed by Phenylalanine-based amphiphiles (Phe-AMPs) as soft templates for preparing chiral PDA nanostructures. Our study revealed that the amphiphile 2 endowed with a primary amine residue afforded chirally-twisted ultrathin nanoribbons of PDA under optimized conditions. The chirality at the Phe residue of 2 modulated the twist-chirality of the PDA nanoribbons; the l-2 resulted in nanoribbons with right-handed twist, whereas the d-2 induced a left-handed twist to the ribbons. The racemic mixture of these two amphiphiles produced flat, achiral tapes. The PDA ribbon thickness was ≈5.86±0.40 nm, whereas its width and length were ≈133.5±3.2 nm and >5000 nm, respectively. Upon dialysis, hollow PDA nanotubes were obtained due to curling of the PDA nanoribbons. These PDA-nanoarchitectures were employed to spontaneously form and assemble Ag-nanoparticles along the edges of the PDA nanoribbons. In this work we are reporting chirality controlled synthesis of PDA nanostructures for the first time.

Exfoliation Behavior of van der Waals Strings: Case Study of Bi2S3.

The family of crystals constituting covalently bound strings, held together by van der Waals forces, can be exfoliated into smaller entities, similar to crystals made of van der Waals sheets. Depending on the anisotropy of such crystals, as well as the spacing between their strings in each direction, van der Waals sheets or ribbons can be obtained after the exfoliation process. In this work, we demonstrate that ultrathin nanoribbons of bismuth sulfide (Bi2S3) can be synthesized via a high-power sonication process. The thickness and width of these ribbons are governed by the van der Waals spacings around the strings within the parent crystal. The lengths of the nanoribbons are initially limited by the dimensions of the starting bulk particles. Interestingly, these nanoribbons change stoichiometry and composition and are elongated when the duration of agitation increases because of Ostwald ripening. An application of the exfoliated van der Waals strings is presented for optical biosensing using photoluminescence of Bi2S3 nanoribbons, reaching detection limits of less than 10 nM L-1 in response to bovine serum albumin. The concept of exfoliating van der Waals strings could be extended to a large class of crystals for creating bodies ranging from sheets to strings, with optoelectronic properties different from that of their bulk counterparts.

High conductivity of ultrathin nanoribbons of SrRuO3 on SrTiO3 probed by infrared spectroscopy

SrRuO3 (SRO) is a perovskite increasingly used in oxide-based electronics both for its intrinsic metallicity, which remains unaltered in thin films and for the ease of deposition on dielectric perovskites like SrTiO3, (STO) to implement SRO/STO microcapacitors and other devices. In order to test the reliability of SRO/STO also as high-current on-chip conductor, when the SRO dimensions are pushed to the nanoscale, here we have measured the electrodynamic properties of arrays of nanoribbons, fabricated by lithography starting from an ultrathin film of SRO deposited on a STO substrate. The nanoribbons are 6 or 4 nm thick, 400, 200 and 100 nm wide and 5 mm long. The measurements have been performed by infrared spectroscopy, a non-contact weakly perturbing technique which also allows one to separately determine the carrier density and their scattering rate or mobility. Far-infrared reflectivity spectra have been analyzed by Rigorous Coupled-Wave Analysis (RCWA) and by an Effective Medium Theory, obtaining consistent results. With the radiation polarized along the nanoribbons, we obtain a carrier density similar to that of a flat film used as reference, which in turn is similar to that of bulk SRO. Moreover, in the nanoribbons the carrier scattering rate is even smaller than in the unpatterned film by about a factor of 2. This shows that the transport properties of SRO deposited on STO remain at least unaltered down to nanometric dimensions, with interesting perspectives for implementing on-chip nano-interconnects in an oxide-based electronics. When excited in the perpendicular direction, the nanoribbons appear instead virtually transparent to the radiation field, as predicted by RCWA.

Magnetotransport in antidot arrays of three-dimensional topological insulators

Three-dimensional topological insulators are a new kind of quantum matter featured with gapless Dirac-like energy-dispersive surface states in the insulating bulk band gaps. However, in experiment, it is difficult to study quantum interference effect of surface states due to considerable contribution from bulk carriers in thick bulk material. To suppress such a bulk state contribution, nanostructures, such as ultra-thin films, nanowires and nanoribbons, have been employed in the study of quantum interference effects of the surface states. Here, we report on a magnetotransport measurement study of nanoscaled antidot array devices made from three-dimensional topological insulator Bi2Se3 thin films. The antidot arrays with hundreds of nanometers in diameter and edge-to-edge distance are fabricated in the thin films by utilizing the focused-ion beam technique, and the magnetotransport properties of the fabricated devices are measured at low temperatures. The results of the magnetotransport measurements for three representative devices, denoted as Dev-1 (with no antidot array fabricated), Dev-2 (with an antidot array of a relatively large period), and Dev-3 (with an antidot array of a relatively small period), are reported in this work. Weak anti-localization indicated by a sharp peak of conductivity at zero magnetic field is observed in all the three devices. Through theoretical fitting to the measurement data, the transport parameters in the three devices, such as spin-orbit coupling length Lso, phase coherence length L, and the number of conduction channels , are extracted. The extracted Lso value is tens of nanometers, which is consistent with the presence of the strong spin-orbit interaction in the Bi2Se3 thin film. The extracted L value is hundreds of nanometers and increases exponentially with temperature decreasing. It is found that the magnetotransports in Dev-1 and Dev-2 are well characterized by the coherent transport through a single conduction channel. For Dev-3, the magnetotransport at low temperatures is described by the coherent transport through two independent conduction channels, while at elevated temperatures the magnetotransport is dominantly described by the transport through one single conduction channel. Unlike the case where the transport occurs dominantly through a single conduction channel, the transport through two independent conduction channels in Dev-3 implies that at least one surface channel is present in the device.

Nanoribbons and nanoscrolls intertwined three-dimensional vanadium oxide hydrogels for high-rate lithium storage at high mass loading level

Ultrathin layered nanomaterials show promising advantages to promote the Li+ diffusion kinetics, however, the self-aggregation/stacking of nanomaterials lead to large capacity loss and limited rate capability, which urgently needs to be addressed. Herein, we report a three-dimensional (3D) novel vanadium oxide (H2V3O8) hydrogel nanostructure composed of intertwined ultrathin nanoribbons and self-coiled nanoscrolls, synthesized by a universal modified liquid exfoliation method. The hydrogels display largely enhanced rate capability and cycling stability, compared to those of the pure nanowires and nanoribbons. Based on the geometrical features of hydrogels, the intertwined hydrogels/carbon nanotubes (CNTs) flexible film is fabricated and delivers remarkable lithium storage performance: a high capacity of 310mAhg−1 at 0.1Ag−1, excellent rate capability (145mAhg−1 at 12Ag−1) and stable cycling performance. Moreover, at a high mass loading up to 13mgcm−2, the hydrogels/CNTs film delivers an area capacity ~ 2.7mAhcm−2 (at 0.91mAcm−2), high rate capability (an area capacity of 1.16mAhcm−2 at 18.2mAcm−2). The scalable hydrogels/CNTs films provide a promising route towards high performance flexible electrodes at high mass loading.

Ultrathin Nanoribbons of in Situ Carbon-Coated V3O7·H2O for High-Energy and Long-Life Li-Ion Batteries: Synthesis, Electrochemical Performance, and Charge–Discharge Behavior

The ever-growing demands of Li-ion batteries (LIBs) for high-energy and long-life applications, such as electrical vehicles, have prompted great research interest. Herein, by applying an interesting one-step high-temperature mixing method under hydrothermal conditions, ultrathin V3O7·H2O@C nanoribbons with good crystallinity and robust configuration are in situ synthesized as promising cathode materials of high-energy, high-power, and long-life LIBs. Their capacity is up to 319 mA h/g at a current density of 100 mA/g. Moreover, the capacity of 262 mA h/g can be delivered at 500 mA/g, and 94% of capacity can be retained after 100 cycles. Even at a large current density of 3000 mA/g, they can still deliver a high capacity of 165 mA h/g, and 119% of the initial capacity can be kept after 600 cycles. Importantly, their energy density is up to 800 Wh/kg, which is 48-60% higher than those of conventional cathode materials (such as LiCoO2, LiMn2O4, and LiFePO4), and they can maintain an energy density of 355 Wh/kg at a high power density of 8000 W/kg. Furthermore, based on ex situ X-ray diffraction and X-ray photoelectron spectroscopy technology, their exact charge-discharge behavior is reasonably described for the first time. Excitingly, it is found for the first time that the as-synthesized V3O7·H2O@C nanoribbons are also great promising cathode materials for Na-ion batteries.

Ti3C2 MXene-Derived Sodium/Potassium Titanate Nanoribbons for High-Performance Sodium/Potassium Ion Batteries with Enhanced Capacities.

Sodium and potassium ion batteries hold promise for next-generation energy storage systems due to their rich abundance and low cost, but are facing great challenges in optimum electrode materials for actual applications. Here, ultrathin nanoribbons of sodium titanate (M-NTO, NaTi1.5O8.3) and potassium titanate (M-KTO, K2Ti4O9) were successfully synthesized by a simultaneous oxidation and alkalization process of Ti3C2 MXene. Benefiting from the suitable interlayer spacing (0.90 nm for M-NTO, 0.93 nm for M-KTO), ultrathin thickness (<11 nm), narrow widths of nanoribbons (<60 nm), and open macroporous structures for enhanced ion insertion/extraction kinetics, the resulting M-NTO exhibited a large reversible capacity of 191 mAh g-1 at 200 mA g-1 for sodium storage, higher than those of pristine Ti3C2 (178 mAh g-1) and commercial TiC derivatives (86 mAh g-1). Notably, M-KTO displayed a superior reversible capacity of 151 mAh g-1 at 50 mA g-1 and 88 mAh g-1 at a high rate of 300 mA g-1 and long-term stable cyclability over 900 times, which outperforms other Ti-based layered materials reported to date. Moreover, this strategy is facile and highly flexible and can be extended for preparing a large number of MXene-derived materials, from the 60+ group of MAX phases, for various applications such as supercapacitors, batteries, and electrocatalysts.

Atomically Dispersed Ru on Ultrathin Pd Nanoribbons.

We report a one-pot synthesis of atomically dispersed Ru on ultrathin Pd nanoribbons. By using synchrotron radiation photoemission spectroscopy (SRPES) and extended X-ray absorption fine structure (EXAFS) measurements in combination with aberration corrected high-resolution transmission electron microscopy (HRTEM), we show that atomically dispersed Ru with content up to 5.9% was on the surface of the ultrathin nanoribbon. Furthermore, the ultrathin Pd/Ru nanoribbons could remarkably prohibit the hydrogenolysis in chemoselective hydrogenation of C═C bonds, leading to an excellent catalytic selectivity compared with commercial Pd/C and Ru/C.

Controllable Growth of Ultrathin P-doped ZnO Nanosheets.

Ultrathin phosphor (P)-doped ZnO nanosheets with branched nanowires were controllably synthesized, and the effects of oxygen and phosphor doping on the structural and optical properties were systematically studied. The grown ZnO nanosheet exhibits an ultrathin nanoribbon backbone with one-side-aligned nanoteeth. For the growth of ultrathin ZnO nanosheets, both oxygen flow rate and P doping are essential, by which the morphologies and microstructures can be finely tuned. P doping induces strain relaxation to change the growth direction of ZnO nanoribbons, and oxygen flow rate promotes the high supersaturation degree to facilitate the growth of nanoteeth and widens the nanoribbons. The growth of P-doped ZnO in this work provides a new progress towards the rational control of the morphologies for ZnO nanostructures.

Enhanced microwave absorption properties of MnO2 hollow microspheres consisted of MnO2 nanoribbons synthesized by a facile hydrothermal method

MnO2 hollow microspheres consisted of nanoribbons were successfully fabricated via a facile hydrothermal method with SiO2 sphere templates. The crystal structure, morphology and microwave absorption properties in X and Ku band of the as-synthesized samples were characterized by powder X-ray diffraction (XRD), transmission electron microscopy (TEM) and a vector network analyzer. The results show that the three-dimensional (3D) hollow microspheres are assembled by ultra thin and narrow one-dimensional (1D) nanoribbons. A rational process for the formation of hollow microspheres is proposed. The 3D MnO2 hollow microspheres possess improved dielectric and magnetic properties than the 1D nanoribbons prepared by the same procedures with the absence of SiO2 hard templates, which are closely related to their special nanostructures. The MnO2 microspheres also show much better microwave absorption properties in X (8–12 GHz) and Ku (12–18 GHz) microwave band compared with 1D MnO2 nanoribbons. The minimum reflection loss of −40 dB for hollow microsphere can be observed at 14.2 GHz and reflection loss below −10 dB is 3.5 GHz with a thickness of only 4 mm. The possible mechanism for the enhanced microwave absorption properties is also discussed.

Coexistence of an anatase/TiO2(B) heterojunction and an exposed (001) facet in TiO2 nanoribbon photocatalysts synthesized via a fluorine-free route and topotactic transformation

In this work, we report a novel approach to fabricate hierarchical TiO2 microspheres (HTMS) assembled by ultrathin nanoribbons where an anatase/TiO2(B) heterojunction and high energy facet coexist. The as-adopted approach involves (1) nonaqueous solvothermal treatment of a mixture of tetrabutyl titanate and acetic acid and (2) topotactical transformation into HTMS via thermal annealing. By this approach, the TiO2(B) phase usually synthesized from an alkaline treatment route could be initially formed. Subsequently, phase transition from TiO2(B) to anatase TiO2 occurs upon thermal treatment. It is demonstrated that such phase transition is accompanied by crystallographic orientation along the c-axis of anatase and TiO2(B) crystals, resulting in not only a coherent interface between two phases but also oriented attachment of anatase mesocrystals along the [001] direction, and finally high-energy (001) facet exposure. Interestingly, this work provides an alternative fluorine-free route for the synthesis of TiO2 crystals with high-energy (001) facet exposure. The structural analysis reveals that lattice-match induced topotactic transformation from TiO2(B) to anatase is the sole reason for the (001) facet exposure of anatase TiO2. The photocatalytic test for acetaldehyde decomposition shows that HTMS with anatase/TiO2(B) heterojunction and high-energy (001) facet exhibits superior photocatalytic efficiency compared with the relevant commercial product P25, which can be ascribed to the synergistic effect of large surface area, anatase/TiO2(B) heterojunction as well as high-energy facet exposure.

Design and Synthesis of High Performance Multifunctional Ultrathin Hematite Nanoribbons

1D porous ultrathin nanoribbons of hematite (α-Fe2O3) were prepared by controlled annealing of different oxides and hydroxides of iron obtained from a solvothermal synthesis method. It is found that calcination at a temperature of 500 °C for 150 min decomposes these iron hydroxides into their most stable oxide form, i.e., α-Fe2O3. Driven by different attractive forces, these porous α-Fe2O3 nanoparticles get aggregated in an ordered fashion to form an ultrathin 1D nanoribbon structure, as observed by detailed time dependent TEM and HRTEM analysis. It has been found that the high aspect ratio and porous surface morphology of these nanoribbons have significantly improved their electronic and spintronic properties as manifested by their photocatalysis, gas sensing, electrochemical, and magnetic behaviors. These hematite nanoribbons exhibit a weak ferromagnetic behavior due to surface spin disorder and shape anisotropy. Lateral confinement of electrons increases the band gap of the nanoribbons, as evident from the UV absorption analysis, which in turn improves their photocatalytic degradation efficiency (rate constant ∼0.95 h(-1)) by delaying the electron-hole recombination process. However, their liquid petroleum gas sensing properties have been found to be mainly governed by the improved (porous) surface of the hematite nanoribbons that provides huge interaction sites for the analyte gas. Most of all, these hematite nanoribbons show a significantly enhanced pseudocapacitive performance exhibited by their high specific capacitance of about 145 F g(-1) at a current density of 1 A g(-1), high rate capability, and also long cycle stability (nearly 96% of capacity retention after 1600 charging/discharging cycles).

Self-Adjustable Crystalline Inorganic Nanocoils

Biomacromolecules such as proteins, although extremely complex in microstructure, can crystallize into macro-sized crystals after self-adjusting their shapes, based on which the structure of biology is built. Inorganic nanowires/nanoribbons with a similar one-dimensional topology but much simpler structures can hardly be as flexible as macromolecules when constructing superlattice structures because of their inherent rigidity. Here we report the synthesis of crystalline indium sulfide nanoribbon-based nanocoils that are formed by spontaneous self-coiling of ultrathin nanoribbons. The nanostructures are flexible and appear as relatively random coils because of their ultrathin ribbon structures (~0.9 nm in thickness) with high aspect ratios. Moreover, the nanocoils can self-adjust their shapes and assemble into two-dimensional superlattices and three-dimensional supercrystals in solution. The ultrathin nanocoils are expected to bring new insights into the use of flexible nanocrystals as building blocks for constructing superstructures.

Facile and effective synthesis of hierarchical TiO2 spheres for efficient dye-sensitized solar cells

Three-dimensional (3D) crystalline anatase TiO2 hierarchical spheres were successfully derived from Ti foils via a fast, template-free, low-temperature hydrothermal route followed by a calcination post-treatment. These dandelion-like TiO2 spheres are composed of numerous ultrathin nanoribbons, which were subsequently split into fragile nanoflakes as a result of the decomposition of Ti-complex intermediates to TiO2 and H2O at high temperature. The dye-sensitized solar cells (DSSCs) employing such hierarchically structured TiO2 spheres as the photoanodes exhibited a light-to-electricity conversion efficiency of 8.50%, yielding a 28% enhancement in comparison with that (6.64%) of P25-based DSSCs, which mainly benefited from the enhanced capacity of dye loading in combination with effective light scattering and trapping from hierarchical architecture.