Machine-learning-assisted omnidirectional bending sensor based on a cascaded asymmetric dual-core PCF sensor.

An omnidirectional bending sensor comprising cascaded asymmetric dual-core photonic crystal fibers (ADCPCFs) is designed and demonstrated experimentally. Upon cascading and splicing two ADCPCFs at a lateral rotation angle, the transmission spectrum of the sensor becomes highly dependent on the bending direction. Machine learning (ML) is employed to predict the curvature and bending orientation of the bending sensor for the first time, to the best of our knowledge. The experimental results demonstrate that the ADCPCF sensor used in combination with machine learning can predict the curvature and omnidirectional bending orientation within 360° without requiring any post-processing fabrication steps. The prediction accuracy is 99.85% with a mean absolute error (MAE) of 2.7° for bending direction measurement and 98.08% with an MAE of 0.03 m-1 for the curvature measurement. This promising strategy utilizes the global features (full spectra) in combination with machine learning to overcome the dependence of the sensor on high-quality transmission spectra, the wavelength range, and a special wavelength dip in the conventional dip tracking method. This excellent omnidirectional bending sensor has large potential for structural health monitoring, robotic arms, medical instruments, and wearable devices.

Porous Ionic Network/CNT Composite Separator as a Polysulfide Snaring Shield for High Performance Lithium-Sulfur Battery.

Lithium-sulfur (Li-S) battery features a high theoretical energy density, but the shuttle of soluble polysulfides between the two electrodes often results in a rapid capacity decay. Herein, a straightforward electrostatic adsorption strategy based on a cross-linked polyimidazolium separator as a snaring shield of polysulfides is reported, which suppresses the undesirable migration of polysulfides to the anode. The porous ionic network (PIN)-modified carbon nanotubes (CNTs) are successfully prepared and coated onto a commercial porous polypropylene membrane in a vacuum-filtration step. The favorable affinity of the imidazolium ring toward polysulfide via the polar interaction and the electrostatic effect of ions mitigates the undesirable shuttle of polysulfides in the electrolyte, improving the Li─S battery in terms of rate performance and cycling life. Compared to the reference PIN-free CNT-coated separator, the PIN/CNT-coated one has an increased initial capacity of 1.3 folds (up to 1394.8 mAh g-1 for PIN/CNT/PP-3) at 0.1 C.

N, S-Coordinated Co Single Atomic Catalyst Boosting Adsorption and Conversion of Lithium Polysulfides for Lithium-Sulfur Batteries.

Boosting reversible solid-liquid phase transformation from lithium polysulfides to Li2 S and suppressing the shuttling of lithium polysulfides from the cathode to the lithium anode are critical challenges in lithium-sulfur batteries. Here, sulfiphilic single atomic cobalt implanted in lithiophilic heteroatoms-dopped carbon (SACo@HC) matrix with a CoN3 S structure for high-performance lithium-sulfur batteries is reported. Density functional theory calculation and in situ experiments demonstrate that the optimal CoN3 S structure in SACo@HC can effectively improve the adsorption and redox conversion efficiency of lithium polysulfides. Consequently, the S-SACo@HC composite with sulfur loading of 80 wt% delivers a high capacity of 1425.1 mAh g-1 at 0.05 C and outstanding rate performance with 745.9 mAh g-1 at 4 C. Furthermore, a capacity of 680.8 mAh g-1 at 0.5 C with a low electrolyte/sulfur ratio (6 µL mg-1 ) can be achieved even after 300 cycles. With the harsh conditions of lean electrolyte (E/S = 4 µL mg-1 ) and high sulfur loading (5.4 mg cm-2 ), a superior area capacity of 5.8 mAh cm-2 can be obtained. This work contributes to building a profound understanding of the adsorption and interface engineering of lithium polysulfides and provides ideas to tackle the long-standing polysulfide shuttle problem of lithium-sulfur batteries.

Single-ring hollow-core anti-resonant fiber with a record low loss (4.3†dB/km) for high-power laser delivery at 1†µm.

We report a 7-tube single-ring hollow-core anti-resonant fiber (SR-ARF) with a record low transmission loss of 4.3 dB/km @1080 nm, which is almost half of the current lowest loss record of an SR-ARF (7.7 dB/km @750 nm). The 7-tube SR-ARF has a large core diameter of 43 µm and a wide low-loss transmission window exceeding 270 nm for the 3-dB bandwidth. Moreover, it exhibits an excellent beam quality with an M2 factor of 1.05 after 10-m-long transmission. The robust single-mode operation, ultralow loss, and wide bandwidth make the fiber an ideal candidate for short-distance Yb and Nd:YAG high-power laser delivery.

Large-mode-area all-solid anti-resonant fiber with single-mode operation for high-power fiber lasers.

We investigate the feasibility of applying an anti-resonant guiding mechanism in an all-solid anti-resonant fiber (AS-ARF) to achieve a large mode area (LMA) and single mode for high-power fiber laser applications. A novel, to the best of our knowledge, AS-ARF with nonuniform rods is proposed to enhance the single-mode property and enlarge the mode area. The numerical results show that the core diameter can expand to 57, 80, and 100 µm at the wavelengths of 1.064, 1.55, and 2 µm, respectively. The loss ratio of the lowest loss of higher-order modes to the loss of the fundamental mode can exceed 1000, 550, and 860 at the wavelength of 1.064, 1.55, and 2 µm; thus, robust single-mode operation can be ensured. Besides, the fiber can also be adapted to bent condition under certain heat load. These indicate that the proposed AS-ARF with nonuniform rods is a great candidate as an LMA fiber for high-power fiber lasers.

Tunable Redox Chemistry and Stability of Radical Intermediates in 2D Covalent Organic Frameworks for High Performance Sodium Ion Batteries.

Radicals are inevitable intermediates during the charging and discharging of organic redox electrodes. The increase of the reactivity of the radical intermediates is desirable to maximize the capacity and enhance the rate capability but is detrimental to cycling stability. Therefore, it is a great challenge to controllably balance the redox reactivity and stability of radical intermediates to optimize the electrochemical properties with a good combination of high specific capacity, excellent rate capability, and long-term cycle life. Herein, we reported the redox and tunable stability of radical intermediates in covalent organic frameworks (COFs) considered as high capacity and stable anode for sodium-ion batteries. The comprehensive characterizations combined with theoretical simulation confirmed that the redox of C-O· and α-C radical intermediates play an important role in the sodiation/desodiation process. Specifically, the stacking behavior could be feasibly tuned by the thickness of 2D COFs, essentially determining the redox reactivity and stability of the α-C radical intermediates and their contributive capacity. The modulation of reversible redox chemistry and stabilization mechanism of radical intermediates in COFs offers a novel entry to design novel high performance organic electrode materials for energy storage and conversion.

Nanopurification of silicon from 84% to 99.999% purity with a simple and scalable process.

Silicon, with its great abundance and mature infrastructure, is a foundational material for a range of applications, such as electronics, sensors, solar cells, batteries, and thermoelectrics. These applications rely on the purification of Si to different levels. Recently, it has been shown that nanosized silicon can offer additional advantages, such as enhanced mechanical properties, significant absorption enhancement, and reduced thermal conductivity. However, current processes to produce and purify Si are complex, expensive, and energy-intensive. Here, we show a nanopurification process, which involves only simple and scalable ball milling and acid etching, to increase Si purity drastically [up to 99.999% (wt %)] directly from low-grade and low-cost ferrosilicon [84% (wt %) Si; ∼$1/kg]. It is found that the impurity-rich regions are mechanically weak as breaking points during ball milling and thus, exposed on the surface, and they can be conveniently and effectively removed by chemical etching. We discovered that the purity goes up with the size of Si particles going down, resulting in high purity at the sub-100-nm scale. The produced Si nanoparticles with high purity and small size exhibit high performance as Li ion battery anodes, with high reversible capacity (1,755 mAh g(-1)) and long cycle life (73% capacity retention over 500 cycles). This nanopurification process provides a complimentary route to produce Si, with finely controlled size and purity, in a diverse set of applications.

Nodeless hollow-core fiber for the visible spectral range.

We report on a hollow-core fiber (HCF) whose fundamental transmission band covers almost the whole visible spectral window, starting at 440 nm. This HCF, in the form of a nodeless structure (NL-HCF), exhibits unprecedented optical performance in terms of low transmission attenuation of 80 dB/km at 532 nm, a broad transmission bandwidth from 440 to 1200 nm, a low bending loss of 0.2 dB/m at 532 nm under 8 cm bending radius, and single-mode profile. When launched to high-power picosecond laser systems at 532 nm, the fiber, exposed to ambient air, could easily deliver an 80 ps, 58 MHz, 32 W average power laser pulse with no damage and a 20 ps, 1 kHz high-energy laser pulse with a damage threshold in excess of 144 µJ at a fiber output. A proof-of-concept experiment on Raman spectroscopy in ambient air shows the significance of this broadband visible guiding HCF for interdisciplinary applications in nonlinear optics, ultrafast optics, lasers, spectroscopy, biophotonics, material processing, etc.

Direct Conversion of Perovskite Thin Films into Nanowires with Kinetic Control for Flexible Optoelectronic Devices.

With significant progress in the past decade, semiconductor nanowires have demonstrated unique features compared to their thin film counterparts, such as enhanced light absorption, mechanical integrity and reduced therma conductivity, etc. However, technologies of semiconductor thin film still serve as foundations of several major industries, such as electronics, displays, energy, etc. A direct path to convert thin film to nanowires can build a bridge between these two and therefore facilitate the large-scale applications of nanowires. Here, we demonstrate that methylammonium lead iodide (CH3NH3PbI3) nanowires can be synthesized directly from perovskite film by a scalable conversion process. In addition, with fine kinetic control, morphologies, and diameters of these nanowires can be well-controlled. Based on these perovskite nanowires with excellent optical trapping and mechanical properties, flexible photodetectors with good sensitivity are demonstrated.

The role of the internal molecular free volume in defining organic porous copolymer properties: tunable porosity and highly selective CO2 adsorption.

A series of novel azo-functionalized copolymerized networks (simply known as NOP-34 series) with tunable permanent microporosity and highly selective carbon dioxide capture are disclosed. The synthesis was accomplished by Zn-induced reductive cross-coupling copolymerization of two nitrobenzene-like building blocks with different 'internal molecular free volumes' (IMFVs), i.e., 2,7,14-trinitrotriptycene and 2,2',7,7'-tetranitro-9,9'-spirobifluorene, with different molar ratios. Increasing the content of spirobifluorene (SBF) segments with a smaller IMFV relative to that of triptycene leads to an unconventional rise-fall pattern in porosity. Unlike most reported porous copolymers whose surface area lies between the corresponding homopolymers, the copolymer NOP-34@7030 with 30% SBF segments unprecedentedly shows the largest Brunauer-Emmett-Teller specific surface area (up to 823 m(2) g(-1)) as well as promoted CO2 uptake abilities (from 2.31 to 3.22 mmol g(-1), at 273 K/1.0 bar). The 100% triptycene(TPC)-derived homopolymer (NOP-34@1000) with a moderate surface area shows the highest CO2/N2 IAST selectivity of 109 (273 K) among the five samples, surpassing most known nanoporous organic polymers. This may contribute significantly to our understanding of the relationship of IMFVs with the properties of copolymerized materials.

Metal Microporous Aromatic Polymers with Improved Performance for Small Gas Storage.

A novel metal-doping strategy was developed for the construction of iron-decorated microporous aromatic polymers with high small-gas-uptake capacities. Cost-effective ferrocene-functionalized microporous aromatic polymers (FMAPs) were constructed by a one-step Friedel-Crafts reaction of ferrocene and s-triazine monomers. The introduction of ferrocene endows the microporous polymers with a regular and homogenous dispersion of iron, which avoids the slow reunion that is usually encountered in previously reported metal-doping procedures, permitting a strong interaction between the porous solid and guest gases. Compared to ferrocene-free analogues, FMAP-1, which has a moderate BET surface area, shows good gas-adsorption capabilities for H2 (1.75 wt % at 77 K/1.0 bar), CH4 (5.5 wt % at 298 K/25.0 bar), and CO2 (16.9 wt % at 273 K/1.0 bar), as well as a remarkably high ideal adsorbed solution theory CO2 /N2 selectivity (107 v/v at 273 K/(0-1.0) bar), and high isosteric heats of adsorption of H2 (16.9 kJ mol(-1) ) and CO2 (41.6 kJ mol(-1) ).

A Luminescent Hypercrosslinked Conjugated Microporous Polymer for Efficient Removal and Detection of Mercury Ions.

A hypercrosslinked conjugated microporous polymer (HCMP-1) with a robustly efficient absorption and highly specific sensitivity to mercury ions (Hg(2+)) is synthesized in a one-step Friedel-Crafts alkylation of cost-effective 2,4,6-trichloro-1,3,5-triazine and dibenzofuran in 1,2-dichloroethane. HCMP-1 has a moderate Brunauer-Emmett-Teller specific surface (432 m(2) g(-1)), but it displays a high adsorption affinity (604 mg g(-1)) and excellent trace efficiency for Hg(2+). The π-π* electronic transition among the aromatic heterocyclic rings endows HCMP-1 a strong fluorescent property and the fluorescence is obviously weakened after Hg(2+) uptake, which makes the hypercrosslinked conjugated microporous polymer a promising fluorescent probe for Hg(2+) detection, owning a super-high sensitivity (detection limit 5 × 10(-8) mol L(-1)).

Alternative respiration and fumaric acid production of Rhizopus oryzae.

Under the conditions of fumaric acid fermentation, Rhizopus oryzae ME-F14 possessed at least two respiratory systems. The respiration of mycelia was partially inhibited by the cytochrome respiration inhibitor antimycin A or the alternative respiration inhibitor salicylhydroxamic acid and was completely inhibited in the presence of both antimycin A and salicylhydroxamic acid. During fumaric acid fermentation process, the activity of alternative respiration had a great correlation with fumaric acid productivity; both of them reached peak at the same time. The alternative oxidase gene, which encoded the mitochondrial alternative oxidase responsible for alternative respiration in R. oryzae ME-F14, was cloned and characterized in Escherichia coli. The activity of alternative respiration, the alternative oxidase gene transcription level, as well as the fumaric acid titer were measured under different carbon sources and different carbon-nitrogen ratios. The activity of alternative respiration was found to be comparable to the transcription level of the alternative oxidase gene and the fumaric acid titer. These results indicated that the activity of the alternative oxidase was regulated at the transcription stage under the conditions tested for R. oryzae ME-F14.

Regeneration of NCM622 from end-of-life lithium-ion battery cathode materials.

The boom of the electric vehicle industry significantly aggravates the demand for lithium-ion batteries (LIBs), especially the ternary cathode materials, however, the majority of end-of-life (EOL) LIBs on the market are batteries utilized in customer electronics. Here, we utilized the mixed EOL LIBs from cell phones and laptops to manufacture the LiNi0.6Co0.2Mn0.2O2 (NCM622) cathode material. A feasible, high efficiency (99.98% Co, 99.98% Ni, 99.99% Mn, and 99.99% Li), and ultra-fast leaching of EOL LIB cathodes was achieved. Thermodynamic calculations suggested that the coordination number, coordination species concentrations, and fractions have significant effects on the apparent activation energy and the equilibrium of the leaching reactions. The remanufactured NCM622 cathode material demonstrated a well-ordered layered hexagonal structure with a low Li+/Ni2+ mixing ratio, which facilitated reliable reversible capacity, low polarization, high rate capabilities (163.8 mA h g-1), and capacity retention ratio (94.3%).

Modulation of Radical Intermediates in Rechargeable Organic Batteries.

Organic materials have been considered as promising electrodes for next-generation rechargeable batteries in view of their sustainability, structural flexibility, and potential recyclability. The radical intermediates generated during the redox process of organic electrodes have profound effect on the reversible capacity, operation voltage, rate performance, and cycling stability. However, the radicals are highly reactive and have very short lifetime during the redox of organic materials. Great efforts have been devoted to capturing and investigating the radical intermediates in organic electrodes. Herein, this review summarizes the importance, history, structures, and working principles of organic radicals in rechargeable batteries. More importantly, challenges and strategies to track and regulate the radicals in organic batteries are highlighted. Finally, further perspectives of organic radicals are proposed for the development of next-generation high-performance rechargeable organic batteries.

Post-crotonylation oxidation by a monooxygenase promotes acetyl-CoA synthetase degradation in Streptomyces roseosporus.

Protein post-translational modifications (PTMs) with various acyl groups play central roles in Streptomyces. But whether these acyl groups can be further modified, and the influences of these potential modifications on bacterial physiology have not been addressed. Here in Streptomyces roseosporus with rich crotonylation, a luciferase monooxygenase LimB is identified to elaborately regulate the crotonylation level, morphological development and antibiotic production by oxidation on the crotonyl groups of an acetyl-CoA synthetase Acs. This chemical modification on crotonylation leads to Acs degradation via the protease ClpP1/2 pathway and lowered intracellular crotonyl-CoA pool. Thus, we show that acyl groups after PTMs can be further modified, herein named post-PTM modification (PPM), and LimB is a PTM modifier to control the substrate protein turnover for cell development of Streptomyces. These findings expand our understanding of the complexity of chemical modifications on proteins for physiological regulation, and also suggest that PPM would be widespread.

Precisely manipulated π-π stacking of catalytic exfoliated iron polyphthalocyanine/reduced graphene oxide hybrid via pyrolysis-free path.

Metal macrocycles with well-defined molecular structures are ideal platforms for the in-depth study of electrochemical oxygen reduction reaction (ORR). Structural integrity of metal macrocycles is vital but remain challenging since the commonly used high-temperature pyrolysis would cause severe structure damage and unidentifiable active sites. Herein, we propose a pyrolysis-free strategy to precisely manipulate the exfoliated 2D iron polyphthalocyanine (FePPc) anchored on reduced graphene oxide (rGO) via π-π stacking using facile high-energy ball milling. A delocalized electron shift caused by π-π interaction is firstly found to be the mechanism of facilitating the remarkable ORR activity of this hybrid catalyst. The optimal FePPc@rGO-HE achieves superior half-wave potential (0.90 V) than 20 % Pt/C. This study offers a new insight in designing stable and high-performance metal macrocycle catalysts with well-defined active sites.

Ultrafast Strategy to Fabricate Sulfur Cathodes for High-Performance Lithium-Sulfur Batteries.

Based on the different dielectric properties of materials and the selective heating property of microwaves, the ultrafast (30 s) preparation of S-NiS2@SP@Bitu as a cathode material for lithium-sulfur batteries was achieved using bitumen, sulfur, Super P, and nickel naphthenate as raw materials for the first time, under microwave treatment. NiS2@SP@Bitu forms Li-N, Li-O, Li-S, and Ni-S bonds with polysulfide, which contributes to promoting the adsorption of polysulfide, reducing the precipitation and decomposition energy barrier of Li2S, and accelerating the catalytic conversion of polysulfide, as result of inhibiting the "shuttle effect" and improving the electrochemical performance. S-NiS2@SP@Bitu as the sulfur cathode material demonstrates outstanding rate performance (518.6 mAh g-1 at 4C), and stable cycling performance. The lithium-sulfur battery with a sulfur loading of 4.8 mg cm-2 shows an areal capacity of 4.6 mAh cm-2. Based on the advantages of microwave selective and rapid heating, this method creatively realized that the sulfur carrier material was prepared and sulfur was fixed in it at the same time. Therefore, this method would have implications for the preparation of sulfur cathode materials.

Deciphering Electrolyte Dominated Na+ Storage Mechanisms in Hard Carbon Anodes for Sodium-Ion Batteries.

Although hard carbon (HC) demonstrates superior initial Coulombic efficiency, cycling durability, and rate capability in ether-based electrolytes compared to ester-based electrolytes for sodium-ion batteries (SIBs), the underlying mechanisms responsible for these disparities remain largely unexplored. Herein, ex situ electron paramagnetic resonance (EPR) spectra and in situ Raman spectroscopy are combined to investigate the Na storage mechanism of HC under different electrolytes. Through deconvolving the EPR signals of Na in HC, quasi-metallic-Na is successfully differentiated from adsorbed-Na. By monitoring the evolution of different Na species during the charging/discharging process, it is found that the initial adsorbed-Na in HC with ether-based electrolytes can be effectively transformed into intercalated-Na in the plateau region. However, this transformation is obstructed in ester-based electrolytes, leading to the predominant storage of Na in HC as adsorbed-Na and pore-filled-Na. Furthermore, the intercalated-Na in HC within the ether-based electrolytes contributes to the formation of a uniform, dense, and stable solid-electrolyte interphase (SEI) film and eventually enhances the electrochemical performance of HC. This work successfully deciphers the electrolyte-dominated Na+ storage mechanisms in HC and provides fundamental insights into the industrialization of HC in SIBs.

Animal- and Human-Inspired Nanostructures as Supercapacitor Electrode Materials: A Review.

Human civilization has been relentlessly inspired by the nurturing lessons; nature is teaching us. From birds to airplanes and bullet trains, nature gave us a lot of perspective in aiding the progress and development of countless industries, inventions, transportation, and many more. Not only that nature inspired us in such technological advances but also, nature stimulated the advancement of micro- and nanostructures. Nature-inspired nanoarchitectures have been considered a favorable structure in electrode materials for a wide range of applications. It offers various positive attributes, especially in energy storage applications, such as the formation of hierarchical two-dimensional and three-dimensional interconnected networked structures that benefit the electrodes in terms of high surface area, high porosity and rich surface textural features, and eventually, delivering high capacity and outstanding overall material stability. In this review, we comprehensively assessed and compiled the recent advances in various nature-inspired based on animal- and human-inspired nanostructures used for supercapacitors. This comprehensive review will help researchers to accommodate nature-inspired nanostructures in industrializing energy storage and many other applications.