Heteroatom dopant strategy triggered high-potential plateau to non-graphitized carbon with highly disordered microstructure for high-performance sodium ion storage

Non-graphitized carbon(NGC)has been extensively utilized as carbonaceous anode in sodium-ion batteries(SIBs).However,more optimization to achieve competitive capacity and stability is still challenging for SIBs.In the study,the dopant strategy is utilized to construct nitrogen/sulfur-doped non-graphitized carbon(N-NGC or S-NGC)shell decorated on three-dimensional graphene foam(GF)as a self-support electrode.The highly disordered microstructures of heteroatom doped carbons are produced by applying a low-temperature pyrolysis treatment to precursors containing nitrogen and sulfur.The DFT calculations of Na-ion adsorption energies at diverse heteroatom sites show marginal-S,pyrrolic N and pyridinic N with more intensive Na-ion adsorption ability than middle-S,C=O and pristine carbon.The N-NGC with dominant small graphitic regions delivers adsorption ability to Na-ion,while the S-NGC with significant single carbon lattice stripes demonstrates redox reaction with Na-ion.Evidently,in comparison with only adsorption-driven slope regions at high potential for N-NGC,the redox reaction-generated potentialplateau enables non-graphitized S-NGC superior discharge/charge capacity and cycle-stability in the slope region.This work could provide deep insight into the rational design of non-graphitized carbon with rich microstructure and composition.

Corrosion engineering on AlCoCrFeNi high-entropy alloys toward highly efficient electrocatalysts for the oxygen evolution of alkaline seawater

Seawater splitting is a prospective approach to yield renewable and sustainable hydrogen energy.Complex preparation processes and poor repeatability are currently considered to be an insuperable impediment to the promotion of the large-scale production and application of electrocatalysts.Avoiding the use of intricate instruments,corrosion engineering is an intriguing strategy to reduce the cost and presents considerable potential for electrodes with catalytic performance.An anode comprising quinary AlCoCrFeNi layered double hydroxides uniformly decorated on an AlCoCrFeNi high-entropy alloy is proposed in this paper via a one-step corrosion engineering method,which directly serves as a remarkably active catalyst for boosting the oxygen evolution reaction(OER)in alkaline seawater.Notably,the best-performing catalyst exhibited oxygen evolution reaction activity with overpotential values of 272.3 and 332 mV to achieve the current densities of 10 and100 mA·cm^(-2),respectively.The failure mechanism of the obtained catalyst was identified for advancing the development of multicomponent catalysts.

Electrically Tunable Wafer-Sized Three-Dimensional Topological Insulator Thin Films Grown by Magnetron Sputtering

Three-dimensional(3 D)topological insulators(TIs)are candidate materials for various electronic and spintronic devices due to their strong spin-orbit coupling and unique surface electronic structure.Rapid,low-cost preparation of large-area TI thin films compatible with conventional semiconductor technology is the key to the practical applications of TIs.Here we show that wafer-sized Bi2Te3 family TI and magnetic TI films with decent quality and well-controlled composition and properties can be prepared on amorphous SiO2/Si substrates by magnetron cosputtering.The SiO2/Si substrates enable us to electrically tune(Bi1-xSbx)2Te3 and Cr-doped(Bi1-xSbx)2 Te3 TI films between p-type and n-type behavior and thus study the phenomena associated with topological surface states,such as the quantum anomalous Hall effect(QAHE).This work significantly facilitates the fabrication of TI-based devices for electronic and spintronic applications.

In situ optical spectroscopic understanding of electrochemical passivation mechanism on sol–gel processed WO_(3) photoanodes

A prevailing understanding on electrochemical activation of photoelectrodes is that electrochemical treatment leads to increased charge carrier densities thereby improved photoelectrode performances.Contrary to this understanding,in this study enhanced photoactivity of WO_(3) photoanode upon electrochemical treatment is ascribed to an extraordinary mechanism of surface trap passivation.The associated mechanism is analyzed by in situ optical spectroscopy,using which the optical property changes of WO_(3) electrode during electrochemical treatment are monitored.The results suggest surface W^(5+)species,the origin of surface traps on WO_(3) photoanodes,are converted to W^(6+) ions by electrochemical treatment.This study demonstrates the particular ability of the electrochemical strategy to passivate surface traps of photoanodes,and also shows the advantages of in situ optical spectroscopy to investigate the real-time electronic structure variations of electrodes during electrochemical treatment.

A Bulk‑Heterostructure Nanocomposite Electrolyte of Ce_(0.8)Sm_(0.2)O_(2‑δ)-SrTiO_(3) for Low‑Temperature Solid Oxide Fuel Cells

Since colossal ionic conductivity was detected in the planar heterostructures consisting of fluorite and perovskite,heterostructures have drawn great research interest as potential electrolytes for solid oxide fuel cells(SOFCs).However,so far,the practical uses of such promising material have failed to materialize in SOFCs due to the short circuit risk caused by SrTiO3.In this study,a series of fluorite/perovskite heterostructures made of Sm-doped CeO2 and SrTiO3(SDC–STO)are developed in a new bulk-heterostructure form and evaluated as electrolytes.The prepared cells exhibit a peak power density of 892 mW cm−2 along with open circuit voltage of 1.1 V at 550°C for the optimal composition of 4SDC–6STO.Further electrical studies reveal a high ionic conductivity of 0.05–0.14 S cm^−1 at 450–550°C,which shows remarkable enhancement compared to that of simplex SDC.Via AC impedance analysis,it has been shown that the small grain-boundary and electrode polarization resistances play the major roles in resulting in the superior performance.Furthermore,a Schottky junction effect is proposed by considering the work functions and electronic affinities to interpret the avoidance of short circuit in the SDC–STO cell.Our findings thus indicate a new insight to design electrolytes for low-temperature SOFCs.

Unravelling the genetic basis for skeletal muscle mitochondrial DNA copy number variations in pigs

Dear Editor,Mitochondria are the center of cellular energy generation and free radical metabolism,with important functions in regulating intracellular calcium levels,cell apoptosis,cell cycle and epigenetic modifications.Mitochondrial DNA copy number(mtDNA-CN)is an indicator of mitochondrial biogenesis and has been associated with several diseases,such as cardiovascular disease,depression,chronic kidney disease and aging in humans(Clyde,2022).

Improving sulfur transformation of lean electrolyte lithium-sulfur battery using nickel nanoparticles encapsulated in N-doped carbon nanotubes

Efficient redox reactions of lean electrolyte lithium-sulfur(Li-S)batteries highly rely on rational catalyst design.Herein,we report an electrocatalyst based on N-doped carbon nanotubes(CNT)-encapsulated Ni nanoparticles(Ni@NCNT)as kinetics regulators for Li-S batteries to propel the polysulfide-involving multiphase transformation.Moreover,such a CNT-encapsulation strategy greatly prevents the aggregation of Ni nanoparticles and enables the extraordinary structural stability of the hybrid electrocatalyst,which guarantees its persistent catalytic activity on sulfur redox reactions.When used as a modified layer on a commercial separator,the Ni@NCNT interlayer contributes to stabilizing S cathode and Li anode by significantly retarding the shuttle effect.The corresponding batteries with a 3.5 mg cm^(−2)sulfur loading achieve the promising cycle stability with~85%capacity retention at the electrolyte/sulfur ratios of 5 and 3μL mg^(−1).Even at a high loading of 12.2 mg cm^(−2),the battery affords an areal capacity of 7.5 mA h cm^(−2).

An atlas of expression quantitative trait loci of microRNAs in longissimus muscle of eight-way crossbred pigs

MicroRNAs(miRNAs)are key regulators of myocyte development and traits,yet insight into the genetic basis of variation in miRNA expression is still limited.Here,we present a systematic analysis of expression quantitative trait loci(eQTL)for miRNA profiling in longissimus muscle of pigs from an eight-breed crossed heterogeneous population.By integrating the whole-genome sequencing and miRNAomics data,we map 54 cis-and 292 trans-e QTLs at high resolution that are associated with the expression of 54 and 92miRNAs,respectively.Twenty-three trans-acting loci are identified to affect the expression of nine myomi Rs(known muscle-specific miRNAs).MiRNAs in mammalian conserved miRNA clusters are found to be subjected to regulation by shared cis-e QTLs,while the expression of mature miRNA-5p/-3p counterparts is more likely to be regulated by different cis-e QTLs.Fine mapping and bioinformatics analyses pinpoint the peak cis-e SNP of mi R-4331-5p,rs344650810,which is located in its seed region,as a causal variant for the changes in expression and function of this miRNA.Additionally,rs344650810 is significantly(P<0.01)correlated with the density and percentage of type I muscle fibers.Altogether,this study provides a comprehensive atlas of miRNA-e QTLs in porcine skeletal muscle and new insights into regulatory mechanisms of miRNA expression.

Nonlinear optical absorption of few-layer molybdenum diselenide （MoSe2） for passively mode-locked soliton fiber laser [Invited]

In this paper,both nonlinear saturable absorption and two-photon absorption（TPA） of few-layer molybdenum diselenide（MoSe2） were observed at 1.56 μm wavelength and further applied to mode-locked ultrafast fiber laser for the first time to our knowledge.Few-layer MoSe2 nanosheets were prepared by liquid-phase exfoliation method and characterized by x ray diffractometer,Raman spectroscopy,and atomic force microscopy.The obtained fewlayer MoSe2 dispersion is further composited with a polymer material for convenient fabrication of MoSe2 thin films.Then,we investigated the nonlinear optical（NLO） absorption property of the few-layer MoSe2 film using a balanced twin-detector measurement technique.Both the saturable absorption and TPA effects of the few-layer MoSe2 film were found by increasing the input optical intensity.The saturable absorption shows a modulation depth of 0.63% and a low nonsaturable loss of 3.5%,corresponding to the relative modulation depth of 18%.The TPA effect occurred when the input optical intensity exceeds 260 MW∕cm2.Furthermore,we experimentally exploit the saturable absorption of few-layer MoSe2 film to mode lock an all-fiber erbium-doped fiber laser.Stable soliton mode locking at 1558 nm center wavelength is achieved with pulse duration of 1.45 ps.It was also observed that the TPA process suppresses the mode-locking operation in the case of higher optical intensity.Our results indicate that layered MoSe2,as another two-dimensional nanomaterial,can provide excellent NLO properties（e.g.,saturable absorption and TPA） for potential applications in ultrashort pulse generation and optical limiting.

Chip-scale broadband spectroscopic chemical sensing using an integrated supercontinuum source in a chalcogenide glass waveguide

On-chip spectroscopic sensors have attracted increasing attention for portable and field-deployable chemical detection applications. So far, these sensors largely rely on benchtop tunable lasers for spectroscopic interrogation. Large footprint and mechanical fragility of the sources, however, preclude compact sensing system integration. In this paper, we address the challenge through demonstrating, for the first time to our knowledge, a supercontinuum source integrated on-chip spectroscopic sensor, where we leverage nonlinear Ge_(22)Sb_(18)Se_(60) chalcogenide glass waveguides as a unified platform for both broadband supercontinuum generation and chemical detection. A home-built, palm-sized femtosecond laser centering at 1560 nm wavelength was used as the pumping source. Sensing capability of the system was validated through quantifying the optical absorption of chloroform solutions at 1695 nm. This work represents an important step towards realizing a miniaturized spectroscopic sensing system based on photonic chips.

Significant enhancement of UV emission in ZnO nanorods subject to Ga＋ ion beam irradiation

在光电子的 ZnO nanomaterials 的应用仍然由于他们的不够的光致发光效率被限制。以便优化 ZnO nanorods 的光致发光性质，在与在不同离子精力(0.5 keV16 keV ) 的 Ga + 离子照耀的关联，在 Si 底层上种的垂直地排列的 ZnO nanorods 的紫外排放在现在的学习被调查。我们发现紫外紧张与增加 Ga + 离子精力很快增加了，直到它在 2 keV，在点，紧张比由成长得当的 ZnO nanorods 生产了那高约 50 倍附近的最大值。低精力的 Ga + 离子的轻轻的轰炸把缺点从 ZnO nanorod 表面移开。在另一方面， Ga + 离子植入进 nanorods，导致压缩紧张。在表面缺点和压缩紧张的介绍的移动之上的水晶格子的完美的安排是贡献紫外轻产生的重要改进的二个因素，这被相信。

Cobalt tungsten phosphide with tunable W-doping as highly efficient electrocatalysts for hydrogen evolution reaction

It has been of interest in seeking electrocatalysts that could exercise equally high-efficient and durable hydrogen evolution upon nonselective electrolytes in both acidic and alkaline environments. Herein, we report a facile strategy to fabricate cobalt tungsten phosphides (CoxW2−xP2/C) hollow polyhedrons with tunable composition based on metal-organic frameworks (MOFs) template method. By the deliberate control of W doping, the synthesized catalyst with the composition of Co0.9W1.1P2/C is found to be able to achieve a current density of 10 mA·cm^(−2) at overpotentials of 35 and 54 mV in acidic and alkaline media, respectively. This combined electrochemical property stands atop the state-of-the-art electrocatalyst counterparts. To unveil the peculiar behavior of the structure, density functional theory (DFT) calculation was implemented and reveals that the surface W-doping facilitates the optimization of hydrogen absorption free energy (ΔGH*) as well as the thermodynamic and kinetics barriers for water dissociation, which is coupled with the hollow structure of Co-W phosphides, leading to the prominent HER catalytic performance.

212-kHz-linewidth,transform-limited pulses from a single-frequency Q-switched fiber laser based on a few-layer Bi_2Se_3 saturable absorber

Conventional Q-switched fiber lasers operating at multi-longitudinal-mode oscillation usually suffer from selfmode-locking-induced temporal instability, relatively strong noise, and low coherence. Here, we address the challenge through demonstrating, for the first time, to the best of our knowledge, a single-longitudinal-mode(SLM)Er-doped fiber(EDF) laser passively Q-switched by a few-layer Bi_2Se_3 saturable absorber(SA). The Bi_2Se_3 SA prepared by the liquid-phase exfoliation method shows a modulation depth of ～5% and saturation optical intensity of 1.8 MW∕cm^2. A section of 1-m unpumped EDF together with a 0.06-nm-bandwidth fiber Bragg grating is used as an ultra-narrow autotracking filter to realize SLM oscillation. Stable SLM Q-switching operation at 1.55 μm is successfully achieved with the spectral linewidth as narrow as 212 kHz and the pulse duration of2.54 μs, manifesting near-transform-limited pulses with a time-bandwidth product of 0.53. In particular, we found that the SLM Q-switching possesses the higher signal-to-noise ratios of 62 dB(optical) and 48 dB(radio frequency), exhibiting its advantages of low noise and high stability. Such an SLM Q-switched fiber laser could gain great interest for some applications in coherent detection, coherent optical communications, and high-sensitivity optical sensing.

Flexible Au micro-array electrode with atomic-scale Au thin film for enhanced ethanol oxidation reaction

The catalysis of Au thin film could be improved by fabrication of array structures in large area.In this work,nanoimprint lithography has been developed tofabricate flexible Au micro-array(MA)electrodes with~100%coverage.Advanced electron microscopy characterisations have directly visualised the atomic-scale three-dimensional(3D)nanostructures with a maximum depth of 6 atomic layers.In-situ observation unveils the crystal growth in the form of twinning.High double layer capacitance brings about large number of active sites on the Au thin film and has a logarithmic relationship with mesh grade.Electrochemistry testing shows that the Au MAs perform much better ethanol oxidation reaction than the planar sample;MAs with higher mesh grade have a greater active site utilisation ratio(ASUR),which is important to build electrochemical double layer for efficient charge transfer.Further improvement on ASUR is expected for greater electrocatalytic performance and potential application in direct ethanol fuel cell.

Electrochemical behaviors of hierarchical copper nano- dendrites in alkaline media

In this study, hierarchical copper nano-dendrites （CuNDs） are fabricated via the electrodeposition method. The electrochemical behaviors of the as-obtained hierarchical CuNDs in 0.1 M NaOH aqueous solution are subsequently studied. The CuNDs experience a non-equilibritrm oxidation process when subjected to cyclic voltammetry （CV） measurements. The first oxidation peak O1 in CV is attributed to the formation of an epitaxial Cu20 layer over the surface of the hierarchical CuNDs. However, the second oxidation peak 02 in CV appears unusually broad across a wide potential range. In this region, the reaction process starts with the nucleation and growth of Cu（OH）2 nanoneedles, followed by the oxidation of Cu20. Upon the increase of potential Cu20 is gradually transformed to CuO and Cu（OH）2, forming a dual-layer structure with high productivity of Cu（OH）2 nanoneedles.