Synthesis of Ultralong Carbon Nanotubes with Ultrahigh Yields.

Ultralong carbon nanotubes (CNTs) are in huge demand in many cutting-edge fields due to their macroscale lengths, perfect structures, and extraordinary properties, while their practical application is limited by the difficulties in their mass production. Herein, we report the synthesis of ultralong CNTs with a dramatically increased yield by a simple but efficient substrate interception and direction strategy (SIDS), which couples the advantages of floating-catalyst chemical vapor deposition with the flying-kite-like growth mechanism of ultralong CNTs. The SIDS-assisted approach prominently improves the catalyst utilization and significantly increases the yield. The areal density of the ultralong CNT arrays with length of over 1 cm reached a record-breaking value of ∼6700 CNTs mm-1, which is 2-3 orders of magnitude higher than the previously reported values obtained by traditional methods. The SIDS provides a solution for synthesizing high-quality ultralong CNTs with high yields, laying the foundation for their mass production.

A Facile Strategy To Construct Au@VxO2x+1 Nanoflowers as a Multicolor Electrochromic Material for Adaptive Camouflage.

Transition metal oxides (TMOs) are promising inorganic electrochromic materials (ECMs) that can be widely used in electronic displays and adaptive camouflage. However, there are still huge challenges for TMOs to simultaneously achieve multicolor transformation capability and good cycling stability. Herein, we assemble Au-modified (0.01 wt %) VxO2x+1 (x > 2) nanoflowers (Au@VxO2x+1 NFs) composed of two-dimensional porous nanosheets containing two valences states of vanadium (V4+ and V5+). The Au@VxO2x+1 NFs exhibits outstanding electrochromic performance with five reversible color transformations (orange, yellow, green, gray, and blue) at a voltage less than 1.5 V and excellent cycling stability (2000 cycles without significant decay). To the best of our knowledge, this is the first time that a single vanadium oxide ECM, rather than a device, realizes five color changes. This work provides a feasible way for the efficient preparation of multicolor electrochromic TMOs. The newly developed Au@VxO2x+1 NFs demonstrate the potential application in adaptive camouflage.

Mixture Phases Engineering of PtFe Nanofoams for Efficient Hydrogen Evolution.

Phase engineering is a promising but challenging approach to construct PtFe-based catalysts with efficient hydrogen evolution reaction (HER) performance. Herein, the authors successfully synthesize PtFe nanofoams with face center cubic (fcc) phase, with simple cubic crystalline (scc) phase and with the mixture phases of fcc and scc phases (PtFe-mix) by hydrogen-assisted calcination for the first time. By benchmarking the HER activity, PtFe-mix exhibits excellent activity in 1.0 m KOH, requiring an overpotential of 28 mV to achieve 10 mA cm-2 , which is better than the commercial Pt/C (34 mV). PtFe-mix also possesses remarkable stability up to 24 h. Density functional theory calculations further verify that PtFe-mix shows a more suitable d-band center and lower energy barrier for the initial water dissociation, facilitating the HER process. This work provides a meaningful strategy to design PtFe-based catalysts with efficient activity for hydrogen evolution.

Noble Metal (Pt, Rh, Pd, Ir) Doped Ru/CNT Ultra-Small Alloy for Acidic Hydrogen Evolution at High Current Density.

There are still great challenges to prepare high-efficiency Ru-based catalysts that are superior to Pt/C under acidic conditions, especially under high current conditions. In this work, a series of surfactant-free noble metal doped Ru/CNT (M-Ru/CNT, M = Pt, Rh, Pd, Ir, CNT stands for carbon nanotube) are prepared by microwave reduction method in 1 minute with ≈3-3.5 nm in size for the first time. In 0.5 m H2 SO4 , the overpotential of Pt-Ru/CNT (Pt: 4.94 at %) is only 12 mV. What's more, it also has much larger electrochemical surface area and intrinsic activity than Pt/C. Pt-Ru/CNT still has an ultra-small overpotential under high current density (113 mV at 500 mA cm-2 , 155 mV at 1000 mA cm-2 ). At the same time, it possesses excellent stability regardless of high current or low current after the durability test of 100 h. Theoretical calculation also deeply reveals that Ru is the main adsorption site of H+ . The comparison of the electronic structure of a series of noble metals adjusted by Ru shows that Pt has the most excellent Gibbs free energy of the adsorbed hydrogen and promotes the desorption of the product.

Ordered Vacancies on the Body-Centered Cubic PdCu Nanocatalysts.

Defect engineering has become one of the important considerations in today's electrocatalyst design. However, the vacancies in the ordered crystal structure (especially body-centered cubic (bcc) and the effect of ordered vacancies (OVs) on the electronic fabric have not been researched yet. In this work, we report the inaugural time of the generation of OVs in the bcc architecture and discuss the insight of the modulation system of the material and its part in the electrochemical N2 reduction reaction (NRR). OV-PdCu-2 achieves the highest Faradaic efficiency value of 21.5% at 0.05 V versus RHE. When the potential increases to 0 V versus RHE, the highest ammonia yield is 55.54 µg h-1 mgcat-1, which is significantly better than the unetched PdCu nanoparticles (12.83 µg h-1 mgcat-1). It is the latest reported catalyst to date in the NRR process at 0 V versus RHE (see Supporting Information).

Electronic states of defect with impurity and infrared emission on black silicon prepared by an ns-laser.

It is found that the optimum annealing temperature is about 1000°C for the infrared emission of defect states at room temperature on black silicon (BS) prepared by using a nanosecond-pulsed laser. In addition, it is observed that the suitable annealing time is 6∼8 min at 1000°C for the emission on the BS. The crystallizing proceeding in annealing on the BS can be used to explain the above annealing effect. It is interesting that the emission band becomes intensive and broader on the BS prepared in oxygen atmosphere than that prepared in vacuum in the analysis of photoluminescence spectra, where the electronic states localized at the defects from D1 to D4 doped with oxygen play an important role in the emission with the broader band which are obviously enhanced in the room temperature.

Floating Bimetallic Catalysts for Growing 30 cm-Long Carbon Nanotube Arrays with High Yields and Uniformity.

Ultralong carbon nanotubes (CNTs) are considered as promising candidates for many cutting-edge applications. However, restricted by the extremely low yields of ultralong CNTs, their practical applications can hardly be realized. Therefore, new methodologies shall be developed to boost the growth efficiency of ultralong CNTs and alleviate their areal density decay at the macroscale level. Herein, a facile, universal, and controllable method for the in situ synthesis of floating bimetallic catalysts (FBCs) is proposed to grow ultralong CNT arrays with high yields and uniformity. Ferrocene and metal acetylacetonates serve as catalyst precursors, affording the successful synthesis of a series of FBCs with controllable compositions. Among these FBCs, the optimized FeCu catalyst increases the areal density of ultralong CNT arrays to a record-breaking value of ≈8100 CNTs mm-1 and exhibits a lifetime 3.40 times longer than that of Fe, thus achieving both high yields and uniformity. A 30-centimeters-long and high-density ultralong CNT array is also successfully grown with the assistance of FeCu catalysts. As evidenced by this kinetic model and molecular dynamics simulations, the introduction of Cu into Fe can simultaneously improve the catalyst fluidity and decrease carbon solubility, and an optimal catalytic performance will be achieved by balancing this tradeoff.

A dual-selective thermal emitter with enhanced subambient radiative cooling performance.

Radiative cooling is a zero-energy technology that enables subambient cooling by emitting heat into outer space (~3 K) through the atmospheric transparent windows. However, existing designs typically focus only on the main atmospheric transparent window (8-13 µm) and ignore another window (16-25 µm), under-exploiting their cooling potential. Here, we show a dual-selective radiative cooling design based on a scalable thermal emitter, which exhibits selective emission in both atmospheric transparent windows and reflection in the remaining mid-infrared and solar wavebands. As a result, the dual-selective thermal emitter exhibits an ultrahigh subambient cooling capacity (~9 °C) under strong sunlight, surpassing existing typical thermal emitters (≥3 °C cooler) and commercial counterparts (as building materials). Furthermore, the dual-selective sample also exhibits high weather resistance and color compatibility, indicating a high practicality. This work provides a scalable and practical radiative cooling design for sustainable thermal management.

Scalable Structural Coloration of Carbon Nanotube Fibers via a Facile Silica Photonic Crystal Self-Assembly Strategy.

The coloration of carbon nanotube (CNT) fibers (CNTFs) is a long-lasting challenge because of the intrinsic black color and chemically inert surfaces of CNTs, which cannot satisfy the aesthetic and fashion requirements and thus significantly restrict their performance in many cutting-edge fields. Recently, a structural coloration method of CNTFs was developed by our group using atomic layer deposition (ALD) technology. However, the ALD-based structural coloration method of CNTFs is expensive, time-consuming, and not suitable for the large-scale production of colorful CNTFs. Herein, we developed a very simple and scalable liquid-phase method to realize the structural coloration of CNTFs. A SiO2/ethanol dispersion containing SiO2 nanospheres with controllable sizes was synthesized. The SiO2 nanospheres could self-assemble into photonic crystal layers on the surface of CNTFs and exhibited brilliant colors. The colors of SiO2 nanoparticle-coated CNTFs could be easily changed by tuning the sizes of SiO2 nanospheres. This method provides a simple, effective, and promising way for the large-scale production of colorful CNTFs.

Fast In-Situ Optical Visualization of Carbon Nanotubes Assisted by Smoke.

The fast visualization and manipulation of individual carbon nanotubes (CNTs) has always been a significant technology for their fundamental research. Here, a fast and facile approach is proposed to realize the optical observation of individual suspended CNTs and CNT networks under conventional optical microscopes with the assistance of tar nanodroplets from smoke. The nanodroplets deposited on CNTs render them with strong light scattering to visible light, thus making the CNTs visible under optical microscopes. This visualization method is controllable, environmentally friendly, low-cost, and can be completed in just a few seconds in ambient conditions. Besides, the tar nanodroplets can be easily removed from the CNTs by laser irradiation. More importantly, the smoke sources are widely available and there are no strict requirements for operating conditions. This smoke-assisted visualization method shows great potential in the fundamental research of CNTs.

Ultrasensitive Airflow Sensors Based on Suspended Carbon Nanotube Networks.

High-performance airflow sensors are in great demand in numerous fields but still face many challenges, such as slow response speed, low sensitivity, large detection threshold, and narrow sensing range. Carbon nanotubes (CNTs) exhibit many advantages in fabricating airflow sensors due to their nanoscale diameters, excellent mechanical and electrical properties, and so on. However, the intrinsic extraordinary properties of CNTs are not fully exhibited in previously reported CNT-based airflow sensors due to the mixed structures of macroscale CNT assemblies. Herein, this article presents suspended CNT networks (SCNTNs) as high-performance airflow sensors, which are self-assembled by ultralong CNTs and short CNTs in a one-step floating catalyst chemical vapor deposition process. The SCNTN-based airflow sensors achieved a record-breaking short response time of 0.021 s, a high sensitivity of 0.0124 s m-1 , a small detection threshold of 0.11 m s-1 , and a wide detection range of ≈0.11-5.51 m s-1 , superior to most of the state-of-the-art airflow sensors. To reveal the sensing mechanism, an acoustic response testing system and a mathematical model are developed. It is found that the airflow-caused intertube stress change resulted in the resistance variation of SCNTNs.

Superdurable and fire-retardant structural coloration of carbon nanotubes.

Carbon nanotubes (CNTs) are promising candidates for numerous cutting-edge fields because of their excellent properties. However, the inherent black color of CNTs cannot satisfy the aesthetic/fashion requirement, and the flammability of CNTs severely restricts their application in high-temperature environments with oxygen. Here, we realized a structural coloration of CNTs by coating them with amorphous TiO2 layers. By tuning the TiO2 coating thickness, both CNT fibers and membranes exhibited controllable and brilliant colors, which exhibited remarkable superdurability that could endure 2000 cycles of laundering tests and more than 10 months of high-intensity ultraviolet irradiation. The TiO2-coated CNTs exhibited a notable fire-retardant performance and could endure 8 hours of fire burning. The structural coloration of CNTs with excellent fire retardance substantially improves their performance and broadens their applications.

Metabolite profiling of chondrosarcoma cells: A robust GC-MS method for the analysis of endogenous metabolome.

Chondrosarcoma is the 2nd most frequent bone sarcoma. In this study, the metabolic profiling of human chondrosarcoma SW-1353 cell line was investigated for the first time. To obtain more precise information about the metabolites from chondrosarcoma cells, pretreatment methods including washing steps/solvents, harvesting conditions, and extraction protocols for chondrosarcoma SW-1353 cells were evaluated in the context of metabolite profiling by GC-MS technique. In addition, a total of 32 representative metabolites (related to amino acid metabolism, TCA cycle, glycolysis, and fatty acid metabolism) were quantitatively determined. We found that a fast water rinse step before metabolic quenching, may reduce the contaminants and improve sensitivity. Trypsin/ethylene diamine tetraacetic acid treatment led to a large amount of metabolite leakage, which was not suitable for metabolomics research. Methanol was selected as a more suitable extraction solvent among four extraction approaches applied to SW-1353 cells. The final protocol can provide a simple, robust, and reproducible method to obtain precise information about the metabolites from chondrosarcoma cells, which is helpful to further understand the chondrosarcoma cell physiology and the mechanism of drug resistance in this disease, from the perspective of metabolomics.

Solvent-free microwave synthesis of ultra-small Ru-Mo2C@CNT with strong metal-support interaction for industrial hydrogen evolution.

Exploring a simple, fast, solvent-free synthetic method for large-scale preparation of cheap, highly active electrocatalysts for industrial hydrogen evolution reaction is one of the most promising work today. In this work, a simple, fast and solvent-free microwave pyrolysis method is used to synthesize ultra-small (3.5 nm) Ru-Mo2C@CNT catalyst with heterogeneous structure and strong metal-support interaction in one step. The Ru-Mo2C@CNT catalyst only exhibits an overpotential of 15 mV at a current density of 10 mA cm-2, and exhibits a large turnover frequency value up to 21.9 s-1 under an overpotential of 100 mV in 1.0 M KOH. In addition, this catalyst can reach high current densities of 500 mA cm-2 and 1000 mA cm-2 at low overpotentials of 56 mV and 78 mV respectively, and it displays high stability of 1000 h. This work provides a feasible way for the reasonable design of other large-scale production catalysts.

Bio-inspired structural colors and their applications.

Structural colors, generated by the interaction of interference, diffraction, and scattering between incident light and periodic nanostructured surfaces with features of the same scale with incident visible light wavelengths, have recently attracted intense interest in a wide range of research fields, due to their advantages such as various brilliant colors, long-term stability and environmental friendliness, low energy consumption, and mysterious biological functions. Tremendous effort has been made to design structural colors and considerable progress has been achieved in the past few decades. However, there are still significant challenges and obstacles, such as durability, portability, compatibility, recyclability, mass production of structural-color materials, etc., that need to be solved by rational structural design and novel manufacturing strategies. In this review, we summarize the recent progress of bio-inspired structural colors and their applications. First, we introduce several typical natural structural colors displayed by living organisms from fundamental optical phenomena, including interference, diffraction grating, scattering, photonic crystals effects, the combination of different phenomena, etc. Subsequently, we review recent progress in bio-inspired artificial structural colors generated from advanced micro/nanoscale manufacturing strategies to relevant biomimetic approaches, including self-assembly, template methods, phase conversion, magnetron sputtering, atomic layer deposition, etc. Besides, we also present the current and potential applications of structural colors in various fields, such as displays, anti-counterfeiting, wearable electronics, stealth, printing, etc. Finally, we discuss the challenges and future development directions of structural colors, aiming to push forward the research and applications of structural-color materials.

An ultrasensitive ratiometric fluorescent thermometer based on frustrated static excimers in the physiological temperature range.

A ratiometric fluorescent thermometer (RFT) based on the frustrated static excimers (FSEs) of DEH-PDI (N,N'-di(2-ethylhexyl)-3,4,9,10-perylenetetracarboxylic diimide) was designed and synthesized. The RFT exhibited ultrahigh sensitivities, which far exceed the existing RFTs in the physiological temperature range. The RFT also showed outstanding precisions, stability, and an obvious thermochromism in the temperature range.

Bifunctional Gold Nanobipyramids for Photothermal Therapy and Temperature Monitoring.

To realize a real-time thermal feedback, monitoring the temperature of the treated tissue is critical for photothermal therapy (PTT). The poor spatial resolution and low accuracy of current methods for the detection of tissue temperature limits the application of PTT. Herein, by assembling the temperature-responsive DNA stem-loop marked with Texas red (TR) onto the surface of gold nanobipyramids (AuNBPs), a bifunctional reagent (AuNBPs-DNA-TR) was fabricated for PTT and synchronously monitoring the temperature. In this configuration, the AuNBPs not only have a high efficiency for photothermal conversion but also could be quenchers to inhibit the fluorescence of TR. During PTT, the significant photothermal effect of the AuNBPs could elevate the temperature. Meanwhile, the increase of the temperature could open the DNA stem-loop assembled on the AuNBPs and as a result enlarge the distance between the TR and AuNBPs. As a result, the TR fluorescence quenched by the AuNBPs was sensitively recovered. The fluorescence intensity (FI) of the TR could be utilized to monitor the temperature during PTT. It was found that irradiating the cancer cells cultured with the AuNBPs-DNA-TR with an 808 nm laser could distinctly increase the system temperature, while the cells could be inactivated due to the remarkable photothermal effect of the AuNBPs-DNA-TR. Meanwhile, the fluorescence of the AuNBPs-DNA-TR for the measurement of the temperature was significantly enhanced. The results indicated that the variation of the fluorescence from the AuNBPs-DNA-TR could be used as thermal feedback to monitor the effect of PTT.

Advanced Ultrathin RuPdM (M = Ni, Co, Fe) Nanosheets Electrocatalyst Boosts Hydrogen Evolution.

The hydrogen evolution reaction (HER) is one of the most significant reactions in the electrolysis water process, and electrocatalysts which possess high mass activity and excellent stability are the most important driving factors to improve the efficiency of HER. As for the efficient commercially electrocatalyst, Pt/C is limited in development because of its high cost. Therefore, the study of non-Pt high-efficiency catalysts is particularly important at this moment. Here, we creatively report for the first time a kind of RuPdM (M= Ni, Co, Fe) ultrathin nanosheets (NSs), which exhibit extraordinary electrochemical properties for HER under alkaline conditions. The overpotential of optimized trimetallic Ru38Pd34Ni28 ultrathin NSs is only 20 mV (10 mA cm-2), and the mass activity reaches 6.15 A mg-1 noble metal at -0.07 V vs RHE. It can be compared to Pt-based electrocatalysts, which have the highest mass activity currently reported. The durability tests also prove that the stability of the electrocatalyst is outstanding. DFT calculations disclose that the flexible modulation of electronic structures of RuPd ultrathin NSs is achieved by utilizing the additional 3d transition metals Fe, Co, and Ni. In particular, the Ni-3d bands act as the continuous electron-supply center for Ru to ensure an efficient electron transfer toward the adsorbates. Meanwhile, the stable Pd sites are critical for coupling the O-2pπ orbital in the initial H2O splitting with a facile barrier. This work will open up a new era of non-Pt materials for alkaline hydrogen evolution toward practical application.

Retraction Note: Enhanced Emission of Quantum System in Si-Ge Nanolayer Structure.

RETRACTION NOTE: The Editor has retracted this article [1] due to significant overlap in text and figures with a previous article published in another journal [2]. The authors do not agree with the retraction.

Localized states and quantum effect of photo-generated carriers in photovoltaic system.

We have fabricated the multiple nanolayers impuritied on silicon pillars for Si solar cells to pick up photons in ultraviolet and infrared region of solar spectra, in which the localized states originated from nanosilicon doped with oxygen are built to avoid Auger recombination, and some interesting quantum phenomena in the localized states have been observed. The quantum effect of photo-generated carriers has been observed in I-V curve measurement on the photovoltaic sample prepared in oxygen by using nanosecond pulsed laser. More interesting, the twin states of quantum vibration are measured in the localized states originated from the impuritied nanosilicon, which provides a stable reservoir for electrons in the photovaltaic system. It should be noted that the amplitude change of the quantum vibration occurs under magnetic field with 0.33T on the sample prepared in oxygen, owing to the electron spin in the localized states. The photoluminescence (PL) spectra measured from 300 nm to 1700 nm exhibit the localized states in various regions in the photovoltaic system, in which the electrons can stand in the localized states with longer lifetime to be uneasy into Auger recombination.