Deformable Catalytic Material Derived from Mechanical Flexibility for Hydrogen Evolution Reaction

Deformable catalytic material with excellent flexible structure is a new type of catalyst that has been applied in various chemical reactions,especially electrocatalytic hydrogen evolution reaction(HER).In recent years,deformable catalysts for HER have made great progress and would become a research hotspot.The catalytic activities of deformable catalysts could be adjustable by the strain engineering and surface reconfiguration.The surface curvature of flexible catalytic materials is closely related to the electrocatalytic HER properties.Here,firstly,we systematically summarized self-adaptive catalytic performance of deformable catalysts and various micro–nanostructures evolution in catalytic HER process.Secondly,a series of strategies to design highly active catalysts based on the mechanical flexibility of lowdimensional nanomaterials were summarized.Last but not least,we presented the challenges and prospects of the study of flexible and deformable micro–nanostructures of electrocatalysts,which would further deepen the understanding of catalytic mechanisms of deformable HER catalyst.

Anti-aging performance improvement and enhanced combustion efficiency of boron via the coating of PDA

Boron is an ambitious fuel in energetic materials since its high heat release values,but its application is prohibited by low combustion efficiency and oxidization during storage.The polydopamine(PDA)was introduced into boron particles,investigating the impact of PDA content on the energetic behavior of boron.The results indicated that the PDA coating formed a fishing net structure on the surface of boron particles.The heat release results showed that the combustion calorific value of B@PDA was higher than that of the raw boron.Specifically,the actual combustion heat of boron powder in B@10%PDA increased by 38.08%.Meanwhile,the DSC peak temperature decreased by 100.65℃under similar oxidation rate compared to raw boron.Simultaneously,the B@PDA@AP and B@AP composites were prepared,and their combustion properties were evaluated.It was demonstrated that B@10%PDA@AP exhibited superior performance in terms of peak pressure and burning time,respectively.The peak pressure is 12.43 kPa more than B@AP and burning time is 2.22 times higher than B@AP.Therefore,the coating of PDA effectively inhibits the oxidization of boron during storage and enhances the energetic behavior of boron and corresponding composites.

Combination of iTRAQ proteomics and RNA-seq transcriptomics reveals multiple levels of regulation in phytoplasma-infected Ziziphus jujuba Mill

Jujube witches’broom(JWB)is caused by infection with a phytoplasma.A multi-omics approach was taken during graft infection of jujube by JWB-infected scion through the analysis of the plant transcriptome,proteome and phytohormone levels.A high number of differentially expressed genes(DEGs)were identified 37 weeks after grafting(WAG),followed by observation of typical symptoms of JWB at 48 WAG.At 37 WAG,the majority of the upregulated DEGs and differentially expressed proteins(DEPs)were related to flavonoid biosynthesis,phenylalanine metabolism and phenylpropanoid biosynthesis.Two of the four upregulated proteins were similar to jasmonate-induced protein-like.Among the downregulated genes,the two most populated GO terms were plant–pathogen interaction and plant hormone signal transduction(mainly for tryptophan metabolism).Moreover,phytoplasma infection resulted in reduced auxin content and increased jasmonate content,indicating that auxin and jasmonic acid have important roles in regulating jujube responses during the first and second stages of phytoplasma infection.At 48 WAG,the two largest groups of upregulated genes were involved in phenylpropanoid biosynthesis and flavonoid biosynthesis.Both genes and proteins involved in carbon metabolism and carbon fixation in photosynthetic organisms were downregulated,indicating that photosynthesis was affected by the third stage of phytoplasma infection.

Effect of lens-to-sample distance on spatial uniformity and emission spectrum of flat-top laser-induced plasma

The optimal spectral excitation and acquisition scheme is explored by studying the effect of the lensto-sample distance(LTSD)on the spatial homogeneity and emission spectra of flat-top laser converging spot induced plasma.The energy distribution characteristics before and after the convergence of the laser beam with quasi flat-top intensity profile used in this study are theoretically simulated and experimentally measured.For an aspheric converging mirror with a focal length of100 mm,the LTSD(106 mm≥LTSD≥96 mm)was changed by raising the stainless-steel sample height.The plasma images acquired by ICCD show that there is air breakdown when the sample is below the focal point,and a ring-like plasma is produced when the sample is above the focal point.When the sample is located near the focal point,the plasma shape resembles a hemisphere.Since the spectral acquisition region is confined to the plasma core and the image contains all the optical information of the plasma,it has a lower relative standard deviation(RSD)than the spectral lines.When the sample surface is slightly higher than the focal plane of the lens,the converging spot has a quasi flat-top distribution,the spatial distribution of the plasma is more uniform,and the spectral signal is more stable.Simultaneously,there is little difference between the RSD of the plasma image and the laser energy.In order to further improve the stability of the spectral signal,it is necessary to expand the spectral acquisition area.

钌基单原子和团簇催化剂在电催化反应中的竞争和协同效应

单原子和团簇催化剂在电催化领域,尤其是可持续能源存储和转化领域的重要性,得到越来越多地认可.单原子催化剂具有低金属负载和高原子利用效率的优点,但由于其表面自由能常常使得单个原子不稳定而发生聚集.团簇催化剂则因为其高原子利用率以及多样的活性位点,能够克服单原子催化剂在中间体吸附和活化等方面的局限性.钌基催化剂在电催化中有着十分重要的应用前景.然而,准确设计钌基单原子和团簇催化剂的几何和电子结构,并揭示它们之间的结构-性质关系,仍然面临着巨大的挑战.因此,我们对钌基催化剂进行了分类和比较(同源/异源),重点总结了钌基单原子和团簇在电催化领域的竞争和协同效应.近年来,钌基催化剂在析氢反应(HER)方面取得了显著进展,因此着重介绍钌基催化剂在HER中的应用,并涵盖了其他电催化反应、双功能反应(HER/OER、HER/HOR)和电化学有机反应.此外,本文还探讨了钌基单原子和团簇在HER过程中的催化机理.最后,我们指出了在复杂钌基催化剂的工业应用开发策略中所面临的挑战和前景.

Molecular surface functionalization of In_(2)O_(3) to tune interfacial microenvironment for enhanced catalytic performance of CO_(2) electroreduction

Indium-based materials(e.g.,In_(2)O_(3))are a class of promising non-noble metal-based catalysts for electroreduction of carbon dioxide(CO_(2)).However,competitive hydrogen reduction reaction(HER)on indium-based catalysts hampers CO_(2) reduction reaction(CO_(2)RR)process.We herein tune the interfacial microenvironment of In_(2)O_(3) through chemical graft of alkyl phosphoric acid molecules using a facile solution-processed strategy for the first time,which is distinguished from other researches that tailor intrinsic activity of In_(2)O_(3) themselves.The surface functionalization of alkyl phosphoric acids over In_(2)O_(3) is demonstrated to remarkably boost CO_(2) conversion.For example,octadecylphosphonic acid modified In_(2)O_(3) exhibits Faraday efficiency for H_(2) H_(2) H_(2)(FE)of as low as 6.6%and FEHCOOH of 86.5%at-0.67 V vs.RHE,which are far superior to parent In_(2)O_(3) counterparts(FE of 24.0%and FEHCOOH of 63.1%).Moreover,the enhancing effect of alkyl phosphoric acid functionalization is found to be closely related to the length of alkyl chains.By virtue of comprehensive experimental characterizations and molecular dynamics simulations,it is revealed that the modification of alkyl phosphoric acids significantly alters the interface microenvironment of the electrocatalyst,which changes the electrocatalyst surface from hydrophilic and aerophobic to hydrophobic and aerophilic.In this case,the water molecules are pushed away and more CO_(2) molecules are trapped,increasing local CO_(2) concentration at In_(2)O_(3) active sites,thus leading to the significantly enhanced CO_(2)RR and suppressed HER.This work highlights the importance of regulating the interfacial microenvironment of inorganic catalysts by molecular surface functionalization as a means for promoting the electrochemical performance in electrosynthesis and beyond.

“Treat-all”Strategy for Patients with Chronic Hepatitis B Virus Infection in China:Are We There Yet?

Chronic hepatitis B remains the primary cause of liver-related events in China.The World Health Organization set a goal to eliminate viral hepatitis as a public health threat by 2030.However,achieving this goal appears challenging due to the current low rates of diagnosis and treatment.The“Treat-all”strategy,which proposes treating all patients with detectable hepatitis B virus(HBV)DNA or even all patients with positive HBsAg,has been suggested to simplify anti-HBV treatment.In 2022,the Chinese Society of Hepatology and the Chinese Society of Infectious Diseases updated the guidelines for the prevention and treatment of chronic hepatitis B in China,expanding antiviral indications and simplifying the treatment algorithm.According to this latest guideline,nearly 95%of patients with detectable HBV DNA are eligible for antiviral treatment.This review aimed to provide a detailed interpretation of the treatment indications outlined in the Chinese Guidelines for the Prevention and Treatment of Chronic Hepatitis B(version 2022)and to identify gaps in achieving the“Treat-all”strategy in China.

Recent advances on liquid intercalation and exfoliation of transition metal dichalcogenides: From fundamentals to applications

The weak van der Waals gap endows two dimensional transition metal dichalcogenides(2D TMDs)with the potential to realize guest intercalation and host exfoliation.Intriguingly,the liquid intercalation and exfoliation is a facile,low-cost,versatile and scalable strategy to modulate the structure and physiochemical property of TMDs via introducing foreign species into interlayer.In this review,firstly,we briefly introduce the resultant hybrid superlattice and disperse nanosheets with tailored properties fabricated via liquid intercalation and exfoliation.Subsequently,we systematically analyze the intercalation phenomenon and limitations of various intercalants in chemical or electrochemical methods.Afterwards,we intensely discuss diverse functionalities of resultant materials,focusing on their potential applications in energy conversion,energy storage,water purification,electronics,thermoelectrics and superconductor.Finally,we highlight the challenges and outlooks for precise and mass production of 2D TMDs-based materials via liquid intercalation and exfoliation.This review enriches the overview of liquid intercalation and exfoliation strategy,and paves the path for relevant high-performance devices.

Advanced emerging ambient energy harvesting technologies enabled by transition metal dichalcogenides: Opportunity and challenge

Environmental pollution and global warming caused by fossil fuels have become increasingly serious issues. Therefore, it is urgent to explore novel strategies to obtain sustainable, renewable and clean energy. Fortunately, ambient energy harvesting technologies, which are receiving increasing attention, provide an optimal solution. Additionally, the investigation of two-dimensional (2D) materials represented by transition metal dichalcogenides (TMDs) significantly facilitates the advancement of ambient energy harvesting technologies due to their unique properties, enabling the application of ambient energy harvesting. Herein, we summarized recent advances in the application of TMDs in thermal energy harvesting, osmotic energy harvesting, mechanical energy harvesting, water energy harvesting and radiofrequency energy harvesting respectively. In the meanwhile, we listed some representative structure and device optimization strategies for enhancing the energy conversion performance of these ambient energy harvesters, aiming to provide valuable insights for future investigations towards further optimization. Finally, we highlight the pressing issues currently faced in the application of the TMDs ambient energy harvesting technologies and propose some potential solutions to these challenges. We aimed to provide a comprehensive review in the applications of the energy harvesting technologies, in order to provide innovative insights for optimizing existing TMDs-based technologies.

Raman imaging analysis of intracellular biothiols independent of the aggregation of sensing substrates

The content of biothiols in cells is highly associated with the occurrence and development of several diseases.However,due to their active chemical properties,thiol-contained molecules are normally volatile during the detection process,rendering precise analysis of intracellular biothiols challenging.In this study,5,5’-dithiobis-(2-nitrobenzoic acid)(DTNB)is covalently modified on the surface of gold nanorods(AuNRs),constructing sensing substrates for in situ Raman imaging analysis of biothiols in cells.Au NRs are able to serve as ideal surface-enhanced Raman scattering substrates,and thus Raman signals of DTNB are greatly amplified by AuNRs.Meanwhile,the disulfide bond of DTNB can be broken by thiols,thereby releasing part of DTNB from the surface of AuNRs.As a result,three kinds of main biothiols are sensitively quantified with DTNB-modified AuNRs according to the variation of Raman signals,and DTNB-modified Au NRs exhibit far better analytical performance than a commercial probe.In addition,the sensing substrates can be readily delivered to cytoplasm with the transmembrane of Au NRs,and are capable of responding to biothiols in cells.Notably,the Raman approach is established by the breaking of chemical bonds rather than the aggregation of substrates,which is more inclined to analyze intracellular biothiols with a desirable spatial resolution.Therefore,fluctuation of biothiols in glioma cells is evidently observed via Raman imaging.Overall,this work provides an alternative strategy for designing Raman sensors to visualize active molecules in cells.

A self-powered gas sensor based on PDMS/Ppy triboelectric-gas-sensing arrays for the real-time monitoring of automotive exhaust gas at room temperature

A new self-powered active gas sensor for realtime monitoring of automotive exhaust gas was devised.The pipe-shaped device was fabricated from polydimethylsiloxane/polypyrrole(PDMS/Ppy)triboelectric gas-sensing unit arrays.The gas-sensing units can actively convert the mechanical energy of gas flow into a triboelectric current.The output current signal depends on the species and concentrations of the target chemical gases(CO,NH3,NO)in the gas flow,and thus can be used as a sensing signal.The device consists of seven gas-sensing units with different Ppy derivatives.As the different sensing units respond to the gases in different ways,the device can differentiate between gas species.The working mechanism is attributed to the coupling effect between the triboelectric effect of PDMS/Ppy and the gas-sensing properties of Ppy.The device can be installed in the tailpipe of an automobile,and can thus analyze the exhaust gas in real time without the need for any external electrical power.The results of the present study spur a new research direction for the development of automotive exhaust gas monitoring systems,thus playing an important role in the detection of air pollution.