A non-synonymous variant of C21R in the gene is significantly associated with brown eggshell color of Lueyang black-boned chicken.

Eggshell colors have a significant effect on sale of eggs. The aim of this study is to identify sequence variants associated with color variation of chicken brown eggs in the , a protoporphyrin transport-related gene. Three successive eggs were collected from each of 381 Lueyang black-boned hens at the 31 weeks old.

CoSe QDs/SnO PCNFs with high catalytic conversion kinetics towards high-efficiency Li-S batteries.

The redox reactions occurring at positive electrode of the lithium-sulfur (Li-S) batteries involve several key electrocatalytic processes that significantly impact the overall performance of the electrochemical energy storage system. This study presents a heterogeneous catalytic composite material composed of CoSe quantum dots (QDs) integrated with SnO nanosheets, which enhances the overall ionic conductivity and accessibility of active sites within the cathode. This controlled migration effectively traps polysulfides within the cathode, reducing their dissolution into the electrolyte and mitigating the shuttle effect.

Vertically Aligned Ultrathin CoNi-LDH@NiS@MXCF Core-Shell Heterostructure for Flexible Supercapacitor Electrodes and Oxygen Evolution Reaction.

A multilayer core-shell heterostructure with CoNi-LDH as the core and NiS nanosheets as the shell is deposited on MXene-coated carbon nanofibers by electrospinning and electrochemical deposition. This unique structure not only combines highly conductive and hydrophilic one-dimensional carbon nanofibers but also exposes abundant two-dimensional reactive sites and multiple ion diffusion channels to maximize material utilization, enhance electron transfer kinetics, accelerate Faraday reaction, high capacitance and strong stability. The CNNS@MXCF electrode exhibits outstanding electrochemical characteristics, including a capacity of 1441.

Porous VN nanosheet arrays on MXene carbon fibers for flexible supercapacitors.

VN usually has poor rate performance and cycle stability. In this work, porous VN nanosheet arrays were prepared on carbon nanofibers embedded with TiCT nanosheets by electrospinning and chemical vapor deposition. The 3D network accelerates the transfer of electrons and electrolyte ions, prevents the aggregation of VN and the self-stacking of MXene, and enhances cycle stability.

Cobalt-Nickel Layered Double Hydroxides on Electrospun MXene for Superior Asymmetric Supercapacitor Electrodes.

Flexible electrodes for energy storage and conversion require a micro-nanomorphology and stable structure. Herein, MXene fibers (MX-CNF) are fabricated by electrospinning, and Co-MOF nanoarrays are prepared on the fibers to form Co-MOF@MX-CNF. Hydrolysis and etching of Co-MOF@MX-CNF in the Ni solution produce cobalt-nickel layered double hydroxide (CoNi-LDH).

TiCT MXene-embedded MnO-based hydrophilic electrospun carbon nanofibers as a freestanding electrode for supercapacitors.

Herein, MnO nanoflowers are electrodeposited on a self-supported and electroconductive electrode in which 2D TiCT nanosheets are encased in carbon nanofibers (MnO@TiCT/CNFs). This improves the conductivity and hydrophilicity of the MnO composite electrode. The asymmetric supercapacitor shows a high energy density of 46.

Identifying the influencing factors and constructing incentive pattern of residents' waste classification behavior using PCA-logistic regression.

With the acceleration of urbanization, domestic waste has become one of the most inevitable factors threatening the environment and human health. Waste classification is of great significance and value for improving urban environmental quality and promoting human well-being. Based on the theory of planned behavior, we added external and socio-economic factors to systematically examine how they affect residents' waste classification behavior (WCB).

MXene nanofibers confining MnO nanoparticles: a flexible anode for high-speed lithium ion storage networks.

The electron and ion conductivities of anode materials such as MnO affect critically the properties of anodes in Li-ion batteries. Herein, a three-dimensional (3D) nanofiber network (MnO-MXene/CNFs) for high-speed electron and ion transport with a MnO surface anchored and embedded inside is designed electrospinning manganese ion-modified MXene nanosheets and subsequent carbonization. Ion transport analysis reveals improved Li transport on the MnO-MXene/CNF electrode and first-principles density functional theory (DFT) calculation elucidates the Li adsorption and storage mechanism.

MXene-encapsulated hollow FeO nanochains embedded in N-doped carbon nanofibers with dual electronic pathways as flexible anodes for high-performance Li-ion batteries.

Fe3O4 is one of the promising anode materials in Li-ion batteries and a potential alternative to graphite due to the high specific capacity, natural abundance, environmental benignity, non-flammability, and better safety. Nevertheless, the sluggish intrinsic reaction kinetics and huge volume variation severely limit the reversible capacity and cycling life. In order to overcome these hurdles and enhance the cycling life of Fe3O4, a one-dimensional (1D) nanochain structure composed of 2D Ti3C2-encapsulated hollow Fe3O4 nanospheres homogeneously embedded in N-doped carbon nanofibers (Fe3O4@MXene/CNFs) is designed and demonstrated as a high-performance anode in Li-ion batteries.

Inter-overlapped MoS/C composites with large-interlayer-spacing for high-performance sodium-ion batteries.

As a two-dimensional layered material with a structure analogous to that of graphene, molybdenum disulfide (MoS2) holds great promise in sodium-ion batteries (SIBs). However, recent research findings have revealed some disadvantages in two-dimensional (2D) materials such as poor interlayer conductivity and structural instability, resulting in poor rate performance and short cycle life for SIBs. Herein, we designed MoS2 nanoflowers with an ultra-wide spacing interlayer (W-MoS2/C) anchored on special double carbon tubes to construct three-dimensional (3D) nanostructures.

Ultra-thin NiS nanosheets as advanced electrode for high energy density supercapacitors.

Low energy density of supercapacitors is one of the major downsides for their practical applications. Here, a simple hydrothermal method was developed to synthesize NiS nanosheets on Ni foam. NiS nanosheets with a rough surface promise large electroactive surface area for energy storage, and show an ultra-high capacitance of 2587 F g at a scan rate of 0.

Self-limiting electrode with double-carbon layers as walls for efficient sodium storage performance.

As a promising energy storage device, sodium ion batteries (SIBs) have attracted more and more attention. Nevertheless, the radius of a sodium ion is much larger than that of a lithium ion, and it is still a significant challenge to solve the problem of volume expansion. In order to solve the problem of volume expansion, a rational nanostructure consisting of CNTs as a carbon matrix, and were sequentially coated with mesoporous SnO2 and N-doped porous carbon tube (NCT).

Adaptation mechanism and tolerance of Rhodopseudomonas palustris PSB-S under pyrazosulfuron-ethyl stress.

Background: Pyrazosulfuron-ethyl is a long lasting herbicide in the agro-ecosystem and its residue is toxic to crops and other non-target organisms. A better understanding of molecular basis in pyrazosulfuron-ethyl tolerant organisms will shed light on the adaptive mechanisms to this herbicide.

Results: Pyrazosulfuron-ethyl inhibited biomass production in Rhodopseudomonas palustris PSB-S, altered cell morphology, suppressed flagella formation, and reduced pigment biosynthesis through significant suppression of carotenoids biosynthesis.

Amorphous red phosphorus nanosheets anchored on graphene layers as high performance anodes for lithium ion batteries.

A facile solution-based method was developed to combine the advantage of amorphous nanoscale red P sheets and highly conductive graphene, forming a high-performance P/graphene composite anode for advanced lithium ion batteries. Graphene can be easily expanded into a 3D framework in solution with rich interior porosity and abundant adsorption points, which enables a large percentage of red P to be loaded and form a uniform P/graphene hybrid structure. The nanoscale and amorphous features of red P effectively reduce the volume expansion and mechanical stress within individual P sheets, thereby alleviating P pulverization during cycling.

Dinuclear zinc complex catalyzed asymmetric methylation and alkynylation of aromatic aldehydes.

A general AzePhenol dinuclear zinc catalytic system has been successfully developed and introduced into the asymmetric addition of dimethylzinc and alkynylzinc to aromatic aldehydes. In this system, an azetidine derived chiral ligand has proven to be an effective enantioselective promoter. Under the optimal reaction conditions, a series of chiral 1-hydroxyethyl (up to 99% ee) and secondary propargylic alcohols (up to 96% ee) were generated with good yields and enantioselectivities.

Urchin-like NiCoO nanoneedles grown on mesocarbon microbeads with synergistic electrochemical properties as electrodes for symmetric supercapacitors.

Here, we report a facile method to fabricate NiCoO nanoneedles on mesocarbon microbeads (MCMB) and form a unique urchin-like core-shell structure. In this composite, the MCMB not only provided high conductivity to benefit effective electron transfer, but also offered abundant adsorption points to load the NiCoO nanoneedles. The aggregation of the NiCoO nanoneedles was therefore alleviated and each NiCoO grain was unfolded to gain easy access to the electrolyte for efficient ion transfer.

Desilylation-Activated Propargylic Transformation: Enantioselective Copper-Catalyzed [3+2] Cycloaddition of Propargylic Esters with β-Naphthol or Phenol Derivatives.

A copper-catalyzed asymmetric [3+2] cycloaddition of 3-trimethylsilylpropargylic esters with either β-naphthols or electron-rich phenols has been realized and proceeds by a desilylation-activated process. Under the catalysis of Cu(OAc)2⋅H2O in combination with a structurally optimized ketimine P,N,N-ligand, a wide range of optically active 1,2-dihydronaphtho[2,1-b]furans or 2,3-dihydrobenzofurans were obtained in good yields and with high enantioselectivities (up to 96 % ee). This represents the first desilylation-activated catalytic asymmetric propargylic transformation.

Highly diastereo- and enantioselective copper-catalyzed propargylic alkylation of acyclic ketone enamines for the construction of two vicinal stereocenters.

The first highly diastereo- and enantioselective propargylic alkylation of acyclic ketone enamines to form vicinal tertiary stereocenters has been reported by employing copper catalysis in combination with a bulky and structurally rigid tridentate ketimine P,N,N-ligand.

Solution growth of NiO nanosheets supported on Ni foam as high-performance electrodes for supercapacitors.

Well-aligned nickel oxide (NiO) nanosheets with the thickness of a few nanometers supported on a flexible substrate (Ni foam) have been fabricated by a hydrothermal approach together with a post-annealing treatment. The three-dimensional NiO nanosheets were further used as electrode materials to fabricate supercapacitors, with high specific capacitance of 943.5, 791.

NiCo2O4 nanostructure materials: morphology control and electrochemical energy storage.

Three types of NiCo2O4 nanostructure, homogeneous NiCo2O4 nanoneedle arrays, heterogeneous NiCo2O4 nanoflake arrays and NiCo2O4 nanoneedle-assembled sisal-like microspheres are synthesized via facile solution methods in combination with thermal treatment. The NiCo2O4 nanoneedle arrays are evaluated as supercapacitor electrodes and demonstrate excellent electrochemical performances with a high specific capacitance (923 F g(-1) at 2 A g(-1)), good rate capability, and superior cycling stability. The superior capacitive performances are mainly due to the unique one dimensional porous nanoneedle architecture, which provides a faster ion/electron transfer rate, improved reactivity, and enhanced structural stability.

Enantioselective synthesis of highly functionalized dihydrofurans through copper-catalyzed asymmetric formal [3+2] cycloaddition of β-ketoesters with propargylic esters.

An enantioselective synthesis of highly functionalized dihydrofurans through a copper-catalyzed asymmetric [3+2] cycloaddition of β-ketoesters with propargylic esters has been developed. With a combination of Cu(OTf)2 and a chiral tridentate P,N,N ligand as the catalyst, a variety of 2,3-dihydrofurans bearing an exocyclic double bond at the 2 position were obtained in good chemical yields and with good to high enantioselectivities. The exocyclic double bond can be hydrogenated in a highly diastereoselective fashion to give unusual cis-2,3-dihydrofuran derivatives, thus further enhancing the scope of this transformation.

Hierarchical mesoporous nickel cobaltite nanoneedle/carbon cloth arrays as superior flexible electrodes for supercapacitors.

Hierarchical mesoporous NiCo2O4 nanoneedle arrays on carbon cloth have been fabricated by a simple hydrothermal approach combined with a post-annealing treatment. Such unique array nanoarchitectures exhibit remarkable electrochemical performance with high capacitance and desirable cycle life at high rates. When evaluated as an electrode material for supercapacitors, the NiCo2O4 nanoneedle arrays supported on carbon cloth was able to deliver high specific capacitance of 660 F g-1 at current densities of 2 A g-1 in 2 M KOH aqueous solution.

Enantioselective copper-catalyzed decarboxylative propargylic alkylation of propargyl β-ketoesters with a chiral ketimine P,N,N-ligand.

The first enantioselective copper-catalyzed decarboxylative propargylic alkylation has been developed. Treatment of propargyl β-ketoesters with a catalyst, prepared in situ from [Cu(CH3 CN)4 BF4 ] and a newly developed chiral tridentate ketimine P,N,N-ligand under mild reaction conditions, generates β-ethynyl ketones in good yields and with high enantioselectivities without requiring the pregeneration of ketone enolates. This new process provides facile access to a range of chiral β-ethynyl ketones in a highly enantioenriched form.