Electrochemical reduction of air-abundant molecules(e.g.,CO_(2),N_(2),and O_(2))offers a sustainable solution to address global energy and environmental challenges,where high current density and energy efficiency are ...Electrochemical reduction of air-abundant molecules(e.g.,CO_(2),N_(2),and O_(2))offers a sustainable solution to address global energy and environmental challenges,where high current density and energy efficiency are highly desirable.However,commercially-relevant current density will cause dramatic change of cation,solvent,p H,and reactant molecular distribution near electrode,resulting in severe concentration polarization and sluggish reaction kinetics.In this case,mass transfer such as molecule migration pathway in electrolytes,electrodes,and devices need to be rationally designed and systematically optimized.Here this review will present a systematical introduction on regulating mass transfer on electrochemical fixation of air-abundant molecules.We firstly discuss the fundamental mass transport from bulk electrolyte to catalyst surface and within electric double layer(EDL)and review the recent advances in regulating mass transport behaviors and optimizing strategy of mass transfer on the catalytic surface.Then we compare the mass transport differences among different cell architectures combining with innovative prospect for transfer pathway towards breaking natural limitation of gas solubility over electroactive interfaces.It is expected that this review can inspire research on comprehensive understanding of fundamental mass transport mechanism at catalyst/electrolyte interface and shed light on optimizing the catalytical device towards practical application for electrochemical fixation of air-abundant molecules.展开更多
Efficient surface passivation is critical for achieving high-performance perovskite solar cells(PSCs),yet the discovery of optimal passivators remains a time-consuming,trial-and-error process.Here,we report a synergis...Efficient surface passivation is critical for achieving high-performance perovskite solar cells(PSCs),yet the discovery of optimal passivators remains a time-consuming,trial-and-error process.Here,we report a synergistic machine learning(ML)and density functional theory(DFT)approach that enables predictive and rapid identification of effective passivation materials.By training an XGBoost model(91.3%accuracy)with DFT-derived molecular descriptors and activity calculations,we identify 2-(4-aminophenyl)-3H-benzimidazol-5-amine(APBIA)as a promising passivator.Experimental validation demonstrates that APBIA effectively removes surface impurities and passivates defects within perovskite films,leading to a significant increase in power conversion efficiency(PCE)from 22.48%to 25.55%(certified as 25.02%).This ML-DFT framework provides a generalizable pathway for accelerating the development of advanced functional materials for photovoltaic applications.展开更多
Monocrystal LiMn_(0. 6)Fe_(0. 4)PO_4 cathode material was obtained via hydrothermal method at 180℃ for 10 h without any surfactant. The effects of hydrothermal time on the phase and morphology of the material were di...Monocrystal LiMn_(0. 6)Fe_(0. 4)PO_4 cathode material was obtained via hydrothermal method at 180℃ for 10 h without any surfactant. The effects of hydrothermal time on the phase and morphology of the material were discussed.By controlling the reaction solutions, the rodlike, flowerlike,and strawlike LiMn_(0.6)Fe_(0.4)PO_4 cathode materials were synthesized. Electrochemical performances show that the rodlike LiMn_(0. 6)Fe_(0. 4)PO_4 has the best electrochemical properties. The initial discharge capacity of the rodlike structure is 106.4 mAh·g^(-1), which is higher than those of flowerlike and strawlike materials.展开更多
Three types of carbon nano-onions（CNOs） including Ni@CNOs.Fe3C@CNOs and Fe0.64Ni0.36@CNOs nanoparticles have been synthesized by catalytic decomposition of methane at 850 ℃ using nickel,iron and iron-nickel alloy c...Three types of carbon nano-onions（CNOs） including Ni@CNOs.Fe3C@CNOs and Fe0.64Ni0.36@CNOs nanoparticles have been synthesized by catalytic decomposition of methane at 850 ℃ using nickel,iron and iron-nickel alloy catalysts.Comparative and systematic studies have been carried out on the morphology,structural characteristics and graphitic crystallinity of these CNOs products.Furthermore,the electrochemical hydrogen storage properties of three types of CNOs have been investigated.Measurements show that the Ni@CNOs have the highest discharge capacity of 387.2 mAh/g,coiTesponding to a hydrogen storage of 1.42%.This comparison study shows the advantages of each catalyst in the growth of CNOs.enabling the controllable synthesis and tuning the properties of CNOs by mediating different metals and their alloy for using in the fuel cell system.展开更多
The centralized treatment method is a widely used form of wastewater treatment that tends to be less effective at removing toxic substances. Therefore, a detailed analysis of the composition of wastewater can provide ...The centralized treatment method is a widely used form of wastewater treatment that tends to be less effective at removing toxic substances. Therefore, a detailed analysis of the composition of wastewater can provide important information for the design of an effective wastewater treatment process. The objective of this paper was to investigate particle size distribution(PSD), biodegradability, and the chemical composition of the petrochemical wastewater discharges. For this purpose, this project selected the petrochemical wastewater and treated wastewater of China National Offshore Oil Corporation Zhongjie Petrochemical Co, Ltd. as the analysis objects.The step-by-step filtration method, along with a molecular weight classification method, was selected to build the chemical oxygen demand(COD) and biochemical oxygen demand(BOD) fingerprints of petrochemical wastewater and treated wastewater. The results showed that the main pollutants were settleable particles in petrochemical wastewater, which contributed to over 54.85% of the total COD. The colloidal particles with particle sizes in the range of 450–1000 nm had the highest COD value in the treated wastewater, which contributed34.17% of the total COD of treated wastewater. The results of the BOD analysis showed that the soluble fractions were the main reason that treated wastewaters did not meet the treatment standards. Tests on the organic compounds in petrochemical wastewater found that there were mainly linear paraffins, branched paraffins, benzene series compounds, and some plasticizers in the influent of the petrochemical wastewater. The most abundant pollutants in treated petrochemical wastewater were the adjacent diisobutyl phthalate and the linear alkanes.Fourier transform infrared(FTIR) transmission spectroscopy analysis showed that the settleable particles of petrochemical wastewater and membrane bioreactor(MBR)-treated wastewater contained multiple types of organic substances. The results also indicated that removing the oil-settleable substances, the colloidal particles(450–1000 nm), and the soluble organics will be necessary for the treatment of petrochemical wastewater.展开更多
Alkali and alkaline‐earth metals from fly ash have a significant deactivation effect on catalysts used for selective catalytic reduction of NOx by NH3(NH3‐SCR).Bromides are considered effective additives to improve ...Alkali and alkaline‐earth metals from fly ash have a significant deactivation effect on catalysts used for selective catalytic reduction of NOx by NH3(NH3‐SCR).Bromides are considered effective additives to improve Hg0 oxidation on SCR catalysts.In this work,the effects of different bromides(NH4Br,NaBr,KBr,and CaBr2)on a commercial V2O5‐WO3/TiO2 catalyst were studied.NOx conversion decreased significantly over the KBr‐poisoned catalyst(denoted as L‐KBr),while that over NaBr‐and CaBr2‐poisoned catalysts(denoted as L‐NaBr and L‐CaBr,respectivity)decreased to a lesser extent compared with the fresh sample.Poor N2 selectivity was observed over L‐NaBr,L‐KBr and L‐CaBr catalysts.The decrease in the ratio of chemisorbed oxygen to total surface oxygen(Oα/(Oα+Oβ+Ow)),reducibility and surface acidity might contribute to the poor activity and N2 selectivity over L‐KBr catalyst.The increased Oαratio was conducive to the enhanced reducibility of L‐CaBr.Combined with enhanced surface acidity,this might offset the negative effect of the loss of active sites by CaBr2 covering.The overoxidation of NH3 and poor N2 selectivity in NH3 oxidation should retard the SCR activity at high temperatures over L‐CaBr catalyst.The increased basicity might contribute to increased NOx adsorption on L‐KBr and L‐CaBr catalysts.A correlation between the acid‐basic and redox properties of bromide‐poisoned catalysts and their catalytic properties is established.展开更多
The need for the separation of azeotropic mixtures for the production of high-end chemicals and resource recovery has spurred significant research into the development of new separation methods in the chemical industr...The need for the separation of azeotropic mixtures for the production of high-end chemicals and resource recovery has spurred significant research into the development of new separation methods in the chemical industry.In this paper,a green and sustainable method for azeotrope separation is proposed based on a chemical-looping concept with the help of reversible-reaction-assisted distillation.The central concept in the chemical-looping separation(CLS)method is the selection of a reactant that can react with the azeotrope components and can also be recycled by the reverse reaction to close the loop and achieve cyclic azeotrope separation.This paper aims to provide an informative perspective on the fundamental theory and applications of the CLS method based on the separation principle,reactant selection,and case analysis,for example,the separation of alkenes,alkane,aromatics,and polyol products.In summary,we provide guidance and references for chemical separation process intensification in product refining and separation from azeotropic systems for the development of a more sustainable chemical industry.展开更多
Developing a suitable catalyst for the elimination of highly toxic carbonyl sulfide(COS)and hydrogen sulfide(H_(2)S) is of great significance in terms of industrial safety and environmental protection.We demonstrate h...Developing a suitable catalyst for the elimination of highly toxic carbonyl sulfide(COS)and hydrogen sulfide(H_(2)S) is of great significance in terms of industrial safety and environmental protection.We demonstrate here the facile synthesis of graphitized 2D micro-meso-macroporous carbons by one-step carbonization of a mixture of urea and glucose at 700–900℃.The as-synthesized graphitized catalysts,designated as 2DNHPC-x(x=urea/glucose mass ratio),are endowed with an ultra-high concentration(12.9–20.2 wt%)of stable and versatile nitrogen sites(e.g.pyrrole and pyridine)which are anchored on the surface via stable covalent bonding.As a result,the 2D-NHPC-x are active in catalytic hydrolysis of COS on pyrrolic N to H_(2)S,and the H_(2)S can be subsequently captured on pyridinic N and converted to elemental sulfur at ambient conditions over the same materials.Among the prepared catalysts,2D-NHPC-x can catalytically hydrolysize 91%of COS to H_(2)S at 30℃,whereas the conversion ratio over the common catalysts g-C_(3)N_(4)and Fe_(2)O_(3)are below 6.0%.Furthermore,these catalysts also exhibit H_(2)S conversion and sulfur selectivity of nearly 100%at 180℃with long-time durability,which is higher than those of the most reported carbonbased catalysts.In contrast,the H_(2)S capacities of activated carbon,ordered mesoporous carbons(OMC)and N-doped OMC are 3.9,1.5 and2.39 mmol g^(-1),respectively.Both the experimental and theoretical results are disclosed that 2D-NHPC-x are superior to the nitrogen-doped porous materials ever applied in simultaneous catalytic elimination of both COS and H_(2)S.展开更多
As one of the most common cathode materials for aqueous zinc-ion batteries(AZIBs),manganese oxides have the advantages of abundant reserves,low cost,and low toxicity.However,the electrochemical mechanism at the cathod...As one of the most common cathode materials for aqueous zinc-ion batteries(AZIBs),manganese oxides have the advantages of abundant reserves,low cost,and low toxicity.However,the electrochemical mechanism at the cathode of aqueous zinc-manganese batteries(AZMBs) is complicated due to different electrode materials,electrolytes and working conditions.These complicated mechanisms severely limit the research progress of AZMBs system and the design of cells with better performance.Hence,the mechanism of AZMBs currently recognized by most researchers according to the classification of the main ions involved in the faradaic reaction is introduced in the review.Then a series of reasons that affect the electrochemical behavior of the battery are summarized.Finally,the failure mechanisms of AZMBs over prolonged cycling are discussed,and the current insufficient research areas of the system are explained,along with the direction of further research being prospected.展开更多
When the actual installation center distance between a pair of spur gears is greater than the theoretical center distance,backlash increases,leading to increased vibration and noise.The structural parameters of an int...When the actual installation center distance between a pair of spur gears is greater than the theoretical center distance,backlash increases,leading to increased vibration and noise.The structural parameters of an integral squeeze film damper(ISFD)were designed with the stiffness of rigid support as reference to investigate the effect of an ISFD on the dynamic characteristics of a spur gear transmission system with center-distance installation error.A spur gear test bench with center distance-error was built to investigate the vibration and noise reduction characteristics of ISFD.The experimental results indicate that,compared with a rigid support,the ISFD can reduce vibration by approximately 40%and noise by approximately 5 d B.ISFD can effectively absorb the impact energy caused by an increase of in backlash,which is conducive to the stable operation of the spur gear transmission system.展开更多
Hydrogen is an indispensable energy carrier for the sustainable development of human society.Nevertheless,its storage,transportation,and in situ generation still face significant challenges.Methanol can be used as an ...Hydrogen is an indispensable energy carrier for the sustainable development of human society.Nevertheless,its storage,transportation,and in situ generation still face significant challenges.Methanol can be used as an intermediate carrier for hydrogen supplies,providing hydrogen energy through instant methanol conversion.In this study,a sorption-enhanced,chemical-looping,oxidative steam methanol-reforming(SECLOSRM)process is proposed using CuO–MgO for the on-board hydrogen supply,which could be a promising method for safe and efficient hydrogen production.Aspen Plus software was used for feasibility verification and parameter optimization of the SECL-OSRM process.The effects of CuO/CH_(3)OH,MgO/CH_(3)OH,and H_(2)O/CH_(3)OH mole ratios and of temperature on H_(2)production rate,H utilization efficiency,CH_(3)OH conversion,CO concentration,and system heat balance are discussed thoroughly.The results indicate that the system can be operated in autothermal conditions with high-purity hydrogen(99.50 vol%)and ultra-low-concentration CO(<50 ppm)generation,which confirms the possibility of integrating low-temperature proton-exchange membrane fuel cells(LT-PEFMCs)with the SECL-OSRM process.The simulation results indicate that the CO can be modulated in a lower concentration by reducing the temperature and by improving the H_(2)O/CH_(3)OH and MgO/CH_(3)OH mole ratios.展开更多
The low catalytic efficiency of redox-active cofactor photoregeneration severely limits the performance of photoenzymatic hybrid systems. Herein, we synthesized thiophene-conjugated porous C3N4 nanosheets(CN-ATCN) exh...The low catalytic efficiency of redox-active cofactor photoregeneration severely limits the performance of photoenzymatic hybrid systems. Herein, we synthesized thiophene-conjugated porous C3N4 nanosheets(CN-ATCN) exhibiting boosted photoregeneration activity of nicotinamide cofactors(NADH and NADPH), which are the most common redox cofactors of oxidoreductases, with regeneration rates of 59.00 μM/min for NADH and 40.99 μM/min for NADPH, ~ 84.3 and 24.7 times higher than those of bulk g-C3N4, respectively. The thin nanosheet structure of CN-ATCN facilitates the exposure of active sites to reactants and favors the diff usion of reactants and products. Upon conjugation of a thiophene moiety into the carbon nitride framework, the optical and photoelectric properties of CN-ATCN were considerably enhanced by an extended π-conjugation system in the frameworks and molecular type II heterojunctions formed between the incorporated and nonincorporated portions of CN-ATCN. Upon coupling NAD(P)H photoregeneration reaction by CN-ATCN with NAD(P)H-dependent enzymatic systems, sustainable synthesis of L-tert-leucine and styrene oxide was achieved with rates of 964 and 14.9 μM/h, respectively.展开更多
Hexafluoropropylene oxide（HFPO） oligomers are toxic,bioaccumulative,and persistent organic pollutants（POPs）.Consuming the harmful chemicals to prevent them from releasing to nature is of serious significance as fa...Hexafluoropropylene oxide（HFPO） oligomers are toxic,bioaccumulative,and persistent organic pollutants（POPs）.Consuming the harmful chemicals to prevent them from releasing to nature is of serious significance as far as both natural environments and human health are concerned.In this study,investigation on degradation of HFPO oligomers to pentafluoropropionyl fluoride（PPF）,a valuable industrial chemical,is reported.Different combinations of alkali metal fluoride in either diglyme or tetraglyme under both flask and batch autoclave conditions were examined.Under the optimal reaction conditions,HFPO oligomers（n = 2-10） were completely degraded to PPF in over 90%yield.Reactions on200 g scale were tested and no deduction of efficiency was observed,which indicates the potential for practical industrial application of this chemistry.展开更多
This study aimed determine the activity of aqueous and ethanolic extracts of Origanum vulgare against some viruses of veterinary importance (bovine viral diarrhea virus (BVDV), equine arteritis virus (EAV), equine inf...This study aimed determine the activity of aqueous and ethanolic extracts of Origanum vulgare against some viruses of veterinary importance (bovine viral diarrhea virus (BVDV), equine arteritis virus (EAV), equine influenza virus (EIV), feline calicivirus (FCV), canine distemper virus (CDV), canine adenovirus (CAV), and canine cororavirus (CCoV) by evaluating the possibility of inhibition of viral particles production. The aqueous extract from 1600 μg/mL did not show cytotoxicity for all cellular lineages evaluated, Madin Darby bovine kidney cells (MDBK), Rabbit kidney cells (RK 13), Madin Darby canine kidney cells (MDCK) and Crandell feline kidney cells (CRFK), and the ethanolic extract of Origanum vulgare was not toxic at 600 μg/mL. The addition of aqueous extract of Origanum vulgare in media resulted in a significant reduction of the EAV titer from 105.42 infecting dose for cellular culture at 50% (TCID50) to 102.09 TCID50/100 μL while in the presence of the ethanolic extract of Origanum vulgare in media resulted in a significant reduction of the EAV titer from 105.42 TCID50 to 100.79 TCID50/100 μL. To CDV the addition of aqueous extract resulted in a reduction from 102.00 TCID50 to 100.00 TCID50/100 μL while in the presence of the ethanolic extract titers were reduced from 102.00 TCID50 to 101.50 TCID50/100 μL. No significant differences in titers regarding the others analyzed viruses were detected. With respect to chemical analysis of the extracts of Origanum vulgare, were identified in the ethanol extract phenolics rosmarinic acid, caffeic acid, carnosol, p-coumaric acid, carnosic acid, luteolin, apigenin, kaempferol and quercetin. In aqueous extracts of Origanum vulgare were detected rosmarinic acid, p-coumaric acid carnosic acid, luteolin, apigenin, kaempferol and quercetin. The data obtained stimulate other biological assays in order to determine which compounds are responsible for the antiviral activity as well as which are the mechanisms involved. The results presented and the considerations we were able to draw from them allowed us to conclude that the ethanolic extract of Origanum vulgare demonstrated lower cell viability than the aqueous extract and has significant antiviral activity against EAV and the both aqueous and ethanolic extracts have antiviral action against CDV.展开更多
This study aimed to identify the chemical composition of essential oil from fruits(EOAF)and the hexanic crude extract from aerial parts(At-Hex)of atemoya(Annona cherimola x Annona squamosa),a hybrid belonging to the A...This study aimed to identify the chemical composition of essential oil from fruits(EOAF)and the hexanic crude extract from aerial parts(At-Hex)of atemoya(Annona cherimola x Annona squamosa),a hybrid belonging to the Annonaceae family.Cytotoxic and antimicrobial activity was also evaluated.OEAF was obtained by hydrodistillation using a Clevenger apparatus,and their composition was analyzed by gas chromatography-mass spectrometry(GC-MS)analyses.Cytotoxicity was tested against human tumor cell lines HCT-116(colon carcinoma),SF-295(glioblastoma),OVCAR-8(ovarian carcinoma)and HL60(leukemia)using 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide(MTT)assay,while antimicrobial activity was conducted by bioauthography method against eleven microorganisms strains.Twenty-four compounds were identified in the EOAF and twenty-nine in At-Hex.The monoterpenes linalool(25.70%),α-pinene(10.38%),β-pinene(9.12%),transocimene(7.43%),and the sesquiterpene bicyclogermacrene(12.58%)were the major constituents of EOAF,whereas the sesquiterpene spathulenol(13.91%)was the main compound of At-Hex.At-Hex showed a high cytotoxicity against SF-295(glioblastoma).These findings show an important chemotaxonomic contribution for the Annonaceae family,mainly for the Annona genus.Atemoya proved to be a promising source of substances with potential cytotoxic activity.展开更多
Zwitterions(ZIs)are considered as an ideal,novel ionic conductive medium due to their high dipole moment and good solubility of lithium salts.However,the strong interactions between ZIs and Li^(+)severely hinder Li^(+...Zwitterions(ZIs)are considered as an ideal,novel ionic conductive medium due to their high dipole moment and good solubility of lithium salts.However,the strong interactions between ZIs and Li^(+)severely hinder Li^(+)migration.Herein,a quasi-solid electrolyte(MSQSE-2Na)was fabricated by adding sodium bis(fluorosulfonyl)imide(NaFSI)to sulfobetaine methacrylate(SBMA,a ZI)based polymerization system.Na^(+)occupies the–SO_(3)^(-)site in SBMA prior to Li^(+),which weakens the self-crosslinking of SBMA and frees the Li^(+)bound to the polymer segments.Thus,the polymer conformation of MSQSE-2Na changes to a relaxed,homogeneous"sea-island"type.Meanwhile,Na^(+),due to its electron-withdrawing effect,decreases the electron cloud density of the polymer segments,building a weakly coordinated environment in MSQSE-2Na.Consequently,MSQSE-2Na exhibits excellent ionic conductivity of 7.38×10^(-4)S cm^(-1)and a high Li^(+)transference number of 0.632 at 25℃.The(-)Li|MSQSE-2Na|Li(+)cells exhibit super stability,sustaining operation for over 6182h.The(-)Li|MSQSE-2Na|LiFePO_(4)(+)cells demonstrate outstanding charge/discharge reversibility with a Coulombic efficiency exceeding 99.9%over 270 cycles(≈4500 h),with a capacity retention of 70.0%.This work proposes a new design concept for regulating the polymer conformation and charge characteristics through competitive coordination,thereby advancing the application of ZI-based polymer electrolytes in lithium metal batteries.展开更多
CO_(2) hydrogenation to methanol is a critical technology for hydrogen energy conversion and a promising approach to mitigate the energy crisis and greenhouse effect.However,developing highly selective catalysts remai...CO_(2) hydrogenation to methanol is a critical technology for hydrogen energy conversion and a promising approach to mitigate the energy crisis and greenhouse effect.However,developing highly selective catalysts remains a major challenge for its practical application.Herein,we synthesize an efficient CoCuInO-r catalyst with Cu_(11)In_(9) and Co^(0) dual sites on In_(2)O_(3) via a sol-gel method.The Cu_(11)In_(9) intermetallic compound enhances H_(2) adsorption capacity and strength,and increases oxygen vacancy concentration on the catalyst surface,thereby improving CO_(2) activation and hydrogenation efficiency.Meanwhile,Co^(0) suppresses the desorption of the*CO species,facilitating its further hydrogenation to methanol.In-situ DRIFTS experiments indicate that the CO_(2) hydrogenation to methanol over CoCuInO-r follows the formate pathway.Compared with CuInO-r(containing Cu_(11)In_(9) on In_(2)O_(3)),CoCuInO-r exhibits a~20%increase in methanol selectivity and a 2-fold higher methanol space-time yield,reaching 7.68 mmol·g^(-1)·h^(-1) at 300℃ and 4 MPa.展开更多
Osteoarthritis(OA)is the most prevalent joint disease and icariin is a promising drug for its treatment.However,the clinical use of icariin is hindered by poor water solubility,low bioavailability,and nonspecific rele...Osteoarthritis(OA)is the most prevalent joint disease and icariin is a promising drug for its treatment.However,the clinical use of icariin is hindered by poor water solubility,low bioavailability,and nonspecific release and biological distribution.Herein,sulfonated azocalix[4]arene(SAC4A)with enhanced water solubility,recognition capacity,and designed responsiveness was used to improve the efficiency of icariin for OA therapy.SAC4A,a macrocycle with well-defined molecular weight and structure,could encapsulate and enhance water solubility of various drugs.In addition,SAC4A enables hypoxia-responsive release of loaded drug.Compared with icariin treatment,supramolecular complex icariin@SAC4A significantly relieved OA symptoms of rats,including more regular bone morphology and structure,and lower degree of cartilage damage.Moreover,the supramolecular formulation demonstrated various advantages,including easy preparation,hypoxia-triggered release,and small size that conducive to drug penetration.展开更多
The tensile strain in inorganic perovskite films induced by thermal annealing is one of the primary factors contributing to the inefficiency and instability of inorganic perovskite solar cells(IPSCs),which reduces the...The tensile strain in inorganic perovskite films induced by thermal annealing is one of the primary factors contributing to the inefficiency and instability of inorganic perovskite solar cells(IPSCs),which reduces the defect formation energy.Here,a flexible molecule 5-maleimidovaleric acid(5-MVA)was introduced as a strain buffer to release the residual strain of CsPbI_(2.85)Br_(0.15)perovskite.Maleic anhydride and carboxyl groups in 5-MVA interact strongly with the uncoordinated Pb^(2+)through Lewis acid-base reaction,thus tightly“pull”the perovskite lattice.The in-between soft carbon chain increased the structural flexibility of CsPbI_(2.85)Br_(0.15)perovskite materials,which effectively relieved the intrinsic internal strain of CsPbI_(2.85)Br_(0.15),resisted the corrosion of external strain,and also reduced the formation of defects such as VIand Pb0.In addition,the introduction of 5-MVA improved crystal quality,passivated residual defects,and narrowed energy level barriers.Eventually,power conversion efficiency(PCE)of NiOxbased inverted IPSCs increased from 19.25%to 20.82%with the open-circuit voltage enhanced from 1.164 V to 1.230 V.The release of strain also improved the stability of CsPbI_(2.85)Br_(0.15)perovskite films and devices.展开更多
基金the support from the National Natural Science Foundation of China(Nos.22375103,22105107)Ministry of Science and Technology of China(No.2021YFA1201900)the Fundamental Research Funds for the Central Universities。
文摘Electrochemical reduction of air-abundant molecules(e.g.,CO_(2),N_(2),and O_(2))offers a sustainable solution to address global energy and environmental challenges,where high current density and energy efficiency are highly desirable.However,commercially-relevant current density will cause dramatic change of cation,solvent,p H,and reactant molecular distribution near electrode,resulting in severe concentration polarization and sluggish reaction kinetics.In this case,mass transfer such as molecule migration pathway in electrolytes,electrodes,and devices need to be rationally designed and systematically optimized.Here this review will present a systematical introduction on regulating mass transfer on electrochemical fixation of air-abundant molecules.We firstly discuss the fundamental mass transport from bulk electrolyte to catalyst surface and within electric double layer(EDL)and review the recent advances in regulating mass transport behaviors and optimizing strategy of mass transfer on the catalytic surface.Then we compare the mass transport differences among different cell architectures combining with innovative prospect for transfer pathway towards breaking natural limitation of gas solubility over electroactive interfaces.It is expected that this review can inspire research on comprehensive understanding of fundamental mass transport mechanism at catalyst/electrolyte interface and shed light on optimizing the catalytical device towards practical application for electrochemical fixation of air-abundant molecules.
基金supported by the National Key Research and Development Program of China (Grant No. 2024YFB4205101)the National Natural Science Foundation of China (No. 62274098 and No. 62074084)+2 种基金the Natural Science Foundation of Tianjin (No.22JCYBJC01300, No. 23JCYBJC01620 and No. 21JCYBJC00270)the Overseas Expertise Introduction Project for Discipline Innovation of Higher Edu cation of China (Grant No. B16027)the Fundamental Research Funds for the Central Universities,Nankai University (No. 63241568)
文摘Efficient surface passivation is critical for achieving high-performance perovskite solar cells(PSCs),yet the discovery of optimal passivators remains a time-consuming,trial-and-error process.Here,we report a synergistic machine learning(ML)and density functional theory(DFT)approach that enables predictive and rapid identification of effective passivation materials.By training an XGBoost model(91.3%accuracy)with DFT-derived molecular descriptors and activity calculations,we identify 2-(4-aminophenyl)-3H-benzimidazol-5-amine(APBIA)as a promising passivator.Experimental validation demonstrates that APBIA effectively removes surface impurities and passivates defects within perovskite films,leading to a significant increase in power conversion efficiency(PCE)from 22.48%to 25.55%(certified as 25.02%).This ML-DFT framework provides a generalizable pathway for accelerating the development of advanced functional materials for photovoltaic applications.
基金financially supported by the National Natural Science Foundation of China (Nos. 21231005 and 51071087)the Major State Basic Research Development Program of China(Nos. 2011CB935900 and 2010CB631303)+2 种基金the Discipline Innovative Engineering Plan (B12015)the Research Fund for the Doctoral Program of Higher Education of China (No.20120031110001)the Tianjin Science & Technology Project (No. 10SYSYJC27600)
文摘Monocrystal LiMn_(0. 6)Fe_(0. 4)PO_4 cathode material was obtained via hydrothermal method at 180℃ for 10 h without any surfactant. The effects of hydrothermal time on the phase and morphology of the material were discussed.By controlling the reaction solutions, the rodlike, flowerlike,and strawlike LiMn_(0.6)Fe_(0.4)PO_4 cathode materials were synthesized. Electrochemical performances show that the rodlike LiMn_(0. 6)Fe_(0. 4)PO_4 has the best electrochemical properties. The initial discharge capacity of the rodlike structure is 106.4 mAh·g^(-1), which is higher than those of flowerlike and strawlike materials.
基金supported by the National Natural Science Foundation of China(51272173,51002188)the National Basic Research Program of China(2010CB934703)Tianjin Municipal Science and Technology Commission(12ZCZDGX00800)
文摘Three types of carbon nano-onions（CNOs） including Ni@CNOs.Fe3C@CNOs and Fe0.64Ni0.36@CNOs nanoparticles have been synthesized by catalytic decomposition of methane at 850 ℃ using nickel,iron and iron-nickel alloy catalysts.Comparative and systematic studies have been carried out on the morphology,structural characteristics and graphitic crystallinity of these CNOs products.Furthermore,the electrochemical hydrogen storage properties of three types of CNOs have been investigated.Measurements show that the Ni@CNOs have the highest discharge capacity of 387.2 mAh/g,coiTesponding to a hydrogen storage of 1.42%.This comparison study shows the advantages of each catalyst in the growth of CNOs.enabling the controllable synthesis and tuning the properties of CNOs by mediating different metals and their alloy for using in the fuel cell system.
基金Supported by the National Basic Research Program of China(2014CB745100)the National Natural Science Foundation of China(21576197)the Tianjin Key Research&Development Program(16YFXTSF00460)
文摘The centralized treatment method is a widely used form of wastewater treatment that tends to be less effective at removing toxic substances. Therefore, a detailed analysis of the composition of wastewater can provide important information for the design of an effective wastewater treatment process. The objective of this paper was to investigate particle size distribution(PSD), biodegradability, and the chemical composition of the petrochemical wastewater discharges. For this purpose, this project selected the petrochemical wastewater and treated wastewater of China National Offshore Oil Corporation Zhongjie Petrochemical Co, Ltd. as the analysis objects.The step-by-step filtration method, along with a molecular weight classification method, was selected to build the chemical oxygen demand(COD) and biochemical oxygen demand(BOD) fingerprints of petrochemical wastewater and treated wastewater. The results showed that the main pollutants were settleable particles in petrochemical wastewater, which contributed to over 54.85% of the total COD. The colloidal particles with particle sizes in the range of 450–1000 nm had the highest COD value in the treated wastewater, which contributed34.17% of the total COD of treated wastewater. The results of the BOD analysis showed that the soluble fractions were the main reason that treated wastewaters did not meet the treatment standards. Tests on the organic compounds in petrochemical wastewater found that there were mainly linear paraffins, branched paraffins, benzene series compounds, and some plasticizers in the influent of the petrochemical wastewater. The most abundant pollutants in treated petrochemical wastewater were the adjacent diisobutyl phthalate and the linear alkanes.Fourier transform infrared(FTIR) transmission spectroscopy analysis showed that the settleable particles of petrochemical wastewater and membrane bioreactor(MBR)-treated wastewater contained multiple types of organic substances. The results also indicated that removing the oil-settleable substances, the colloidal particles(450–1000 nm), and the soluble organics will be necessary for the treatment of petrochemical wastewater.
基金supported by the National Key R&D Program of China(2016YFC0203900,2016YFC0203901)National Natural Science Foundation of China(51778619,21577173)~~
文摘Alkali and alkaline‐earth metals from fly ash have a significant deactivation effect on catalysts used for selective catalytic reduction of NOx by NH3(NH3‐SCR).Bromides are considered effective additives to improve Hg0 oxidation on SCR catalysts.In this work,the effects of different bromides(NH4Br,NaBr,KBr,and CaBr2)on a commercial V2O5‐WO3/TiO2 catalyst were studied.NOx conversion decreased significantly over the KBr‐poisoned catalyst(denoted as L‐KBr),while that over NaBr‐and CaBr2‐poisoned catalysts(denoted as L‐NaBr and L‐CaBr,respectivity)decreased to a lesser extent compared with the fresh sample.Poor N2 selectivity was observed over L‐NaBr,L‐KBr and L‐CaBr catalysts.The decrease in the ratio of chemisorbed oxygen to total surface oxygen(Oα/(Oα+Oβ+Ow)),reducibility and surface acidity might contribute to the poor activity and N2 selectivity over L‐KBr catalyst.The increased Oαratio was conducive to the enhanced reducibility of L‐CaBr.Combined with enhanced surface acidity,this might offset the negative effect of the loss of active sites by CaBr2 covering.The overoxidation of NH3 and poor N2 selectivity in NH3 oxidation should retard the SCR activity at high temperatures over L‐CaBr catalyst.The increased basicity might contribute to increased NOx adsorption on L‐KBr and L‐CaBr catalysts.A correlation between the acid‐basic and redox properties of bromide‐poisoned catalysts and their catalytic properties is established.
基金The authors acknowledge financial support from the National Key Research and Development Program of China(2018YFB0604900)the National Natural Science Foundation of China(21690084 and 21878219).
文摘The need for the separation of azeotropic mixtures for the production of high-end chemicals and resource recovery has spurred significant research into the development of new separation methods in the chemical industry.In this paper,a green and sustainable method for azeotrope separation is proposed based on a chemical-looping concept with the help of reversible-reaction-assisted distillation.The central concept in the chemical-looping separation(CLS)method is the selection of a reactant that can react with the azeotrope components and can also be recycled by the reverse reaction to close the loop and achieve cyclic azeotrope separation.This paper aims to provide an informative perspective on the fundamental theory and applications of the CLS method based on the separation principle,reactant selection,and case analysis,for example,the separation of alkenes,alkane,aromatics,and polyol products.In summary,we provide guidance and references for chemical separation process intensification in product refining and separation from azeotropic systems for the development of a more sustainable chemical industry.
基金supported by the National Natural Science Foundation of China(22022804,21978052)the Natural Science Foundation for the Distinguished Young Scholar of Fujian Province(2020J06037)the National Key Research and Development Program of China(2018YFA0209304)。
文摘Developing a suitable catalyst for the elimination of highly toxic carbonyl sulfide(COS)and hydrogen sulfide(H_(2)S) is of great significance in terms of industrial safety and environmental protection.We demonstrate here the facile synthesis of graphitized 2D micro-meso-macroporous carbons by one-step carbonization of a mixture of urea and glucose at 700–900℃.The as-synthesized graphitized catalysts,designated as 2DNHPC-x(x=urea/glucose mass ratio),are endowed with an ultra-high concentration(12.9–20.2 wt%)of stable and versatile nitrogen sites(e.g.pyrrole and pyridine)which are anchored on the surface via stable covalent bonding.As a result,the 2D-NHPC-x are active in catalytic hydrolysis of COS on pyrrolic N to H_(2)S,and the H_(2)S can be subsequently captured on pyridinic N and converted to elemental sulfur at ambient conditions over the same materials.Among the prepared catalysts,2D-NHPC-x can catalytically hydrolysize 91%of COS to H_(2)S at 30℃,whereas the conversion ratio over the common catalysts g-C_(3)N_(4)and Fe_(2)O_(3)are below 6.0%.Furthermore,these catalysts also exhibit H_(2)S conversion and sulfur selectivity of nearly 100%at 180℃with long-time durability,which is higher than those of the most reported carbonbased catalysts.In contrast,the H_(2)S capacities of activated carbon,ordered mesoporous carbons(OMC)and N-doped OMC are 3.9,1.5 and2.39 mmol g^(-1),respectively.Both the experimental and theoretical results are disclosed that 2D-NHPC-x are superior to the nitrogen-doped porous materials ever applied in simultaneous catalytic elimination of both COS and H_(2)S.
基金supported by the National Natural Science Foundation of China (No. 21878226, No. U20A20153)the Chemistry and Chemical Engineering Guangdong Laboratory (Grant No. 1912011)。
文摘As one of the most common cathode materials for aqueous zinc-ion batteries(AZIBs),manganese oxides have the advantages of abundant reserves,low cost,and low toxicity.However,the electrochemical mechanism at the cathode of aqueous zinc-manganese batteries(AZMBs) is complicated due to different electrode materials,electrolytes and working conditions.These complicated mechanisms severely limit the research progress of AZMBs system and the design of cells with better performance.Hence,the mechanism of AZMBs currently recognized by most researchers according to the classification of the main ions involved in the faradaic reaction is introduced in the review.Then a series of reasons that affect the electrochemical behavior of the battery are summarized.Finally,the failure mechanisms of AZMBs over prolonged cycling are discussed,and the current insufficient research areas of the system are explained,along with the direction of further research being prospected.
基金Supported by the National Science and Technology Major Project(No.2017-IV-0010-0047)China Postdoctoral Science Foundation FundedProject(No.2020M670113)Fundamental Research Funds for the Central Universities(No.JY2105)。
文摘When the actual installation center distance between a pair of spur gears is greater than the theoretical center distance,backlash increases,leading to increased vibration and noise.The structural parameters of an integral squeeze film damper(ISFD)were designed with the stiffness of rigid support as reference to investigate the effect of an ISFD on the dynamic characteristics of a spur gear transmission system with center-distance installation error.A spur gear test bench with center distance-error was built to investigate the vibration and noise reduction characteristics of ISFD.The experimental results indicate that,compared with a rigid support,the ISFD can reduce vibration by approximately 40%and noise by approximately 5 d B.ISFD can effectively absorb the impact energy caused by an increase of in backlash,which is conducive to the stable operation of the spur gear transmission system.
基金supported by the National Key R&D Program of China(2018YFE0111100)National Natural Science Foundation of China(52106193,21908162)+2 种基金the Natural Science Foundation of Hunan Province(2021JJ40756)the Science and Technology Innovation Program of Hunan Province(2020GK2070)the Innovation-Driven Project of Central South University(2020CX008)
文摘Hydrogen is an indispensable energy carrier for the sustainable development of human society.Nevertheless,its storage,transportation,and in situ generation still face significant challenges.Methanol can be used as an intermediate carrier for hydrogen supplies,providing hydrogen energy through instant methanol conversion.In this study,a sorption-enhanced,chemical-looping,oxidative steam methanol-reforming(SECLOSRM)process is proposed using CuO–MgO for the on-board hydrogen supply,which could be a promising method for safe and efficient hydrogen production.Aspen Plus software was used for feasibility verification and parameter optimization of the SECL-OSRM process.The effects of CuO/CH_(3)OH,MgO/CH_(3)OH,and H_(2)O/CH_(3)OH mole ratios and of temperature on H_(2)production rate,H utilization efficiency,CH_(3)OH conversion,CO concentration,and system heat balance are discussed thoroughly.The results indicate that the system can be operated in autothermal conditions with high-purity hydrogen(99.50 vol%)and ultra-low-concentration CO(<50 ppm)generation,which confirms the possibility of integrating low-temperature proton-exchange membrane fuel cells(LT-PEFMCs)with the SECL-OSRM process.The simulation results indicate that the CO can be modulated in a lower concentration by reducing the temperature and by improving the H_(2)O/CH_(3)OH and MgO/CH_(3)OH mole ratios.
基金supported by the National Key Research and Development Program of China(No.2018YFA0901300)the National Natural Science Foundation of China(No.NSFC 21621004)。
文摘The low catalytic efficiency of redox-active cofactor photoregeneration severely limits the performance of photoenzymatic hybrid systems. Herein, we synthesized thiophene-conjugated porous C3N4 nanosheets(CN-ATCN) exhibiting boosted photoregeneration activity of nicotinamide cofactors(NADH and NADPH), which are the most common redox cofactors of oxidoreductases, with regeneration rates of 59.00 μM/min for NADH and 40.99 μM/min for NADPH, ~ 84.3 and 24.7 times higher than those of bulk g-C3N4, respectively. The thin nanosheet structure of CN-ATCN facilitates the exposure of active sites to reactants and favors the diff usion of reactants and products. Upon conjugation of a thiophene moiety into the carbon nitride framework, the optical and photoelectric properties of CN-ATCN were considerably enhanced by an extended π-conjugation system in the frameworks and molecular type II heterojunctions formed between the incorporated and nonincorporated portions of CN-ATCN. Upon coupling NAD(P)H photoregeneration reaction by CN-ATCN with NAD(P)H-dependent enzymatic systems, sustainable synthesis of L-tert-leucine and styrene oxide was achieved with rates of 964 and 14.9 μM/h, respectively.
基金the National Natural Science Foundation of China (Nos. 21372127, 21572104)Program for New Century Excellent Talents in UniversityChanglu Engineering Research Center of New Chemical Materials for financial support
文摘Hexafluoropropylene oxide（HFPO） oligomers are toxic,bioaccumulative,and persistent organic pollutants（POPs）.Consuming the harmful chemicals to prevent them from releasing to nature is of serious significance as far as both natural environments and human health are concerned.In this study,investigation on degradation of HFPO oligomers to pentafluoropropionyl fluoride（PPF）,a valuable industrial chemical,is reported.Different combinations of alkali metal fluoride in either diglyme or tetraglyme under both flask and batch autoclave conditions were examined.Under the optimal reaction conditions,HFPO oligomers（n = 2-10） were completely degraded to PPF in over 90%yield.Reactions on200 g scale were tested and no deduction of efficiency was observed,which indicates the potential for practical industrial application of this chemistry.
文摘This study aimed determine the activity of aqueous and ethanolic extracts of Origanum vulgare against some viruses of veterinary importance (bovine viral diarrhea virus (BVDV), equine arteritis virus (EAV), equine influenza virus (EIV), feline calicivirus (FCV), canine distemper virus (CDV), canine adenovirus (CAV), and canine cororavirus (CCoV) by evaluating the possibility of inhibition of viral particles production. The aqueous extract from 1600 μg/mL did not show cytotoxicity for all cellular lineages evaluated, Madin Darby bovine kidney cells (MDBK), Rabbit kidney cells (RK 13), Madin Darby canine kidney cells (MDCK) and Crandell feline kidney cells (CRFK), and the ethanolic extract of Origanum vulgare was not toxic at 600 μg/mL. The addition of aqueous extract of Origanum vulgare in media resulted in a significant reduction of the EAV titer from 105.42 infecting dose for cellular culture at 50% (TCID50) to 102.09 TCID50/100 μL while in the presence of the ethanolic extract of Origanum vulgare in media resulted in a significant reduction of the EAV titer from 105.42 TCID50 to 100.79 TCID50/100 μL. To CDV the addition of aqueous extract resulted in a reduction from 102.00 TCID50 to 100.00 TCID50/100 μL while in the presence of the ethanolic extract titers were reduced from 102.00 TCID50 to 101.50 TCID50/100 μL. No significant differences in titers regarding the others analyzed viruses were detected. With respect to chemical analysis of the extracts of Origanum vulgare, were identified in the ethanol extract phenolics rosmarinic acid, caffeic acid, carnosol, p-coumaric acid, carnosic acid, luteolin, apigenin, kaempferol and quercetin. In aqueous extracts of Origanum vulgare were detected rosmarinic acid, p-coumaric acid carnosic acid, luteolin, apigenin, kaempferol and quercetin. The data obtained stimulate other biological assays in order to determine which compounds are responsible for the antiviral activity as well as which are the mechanisms involved. The results presented and the considerations we were able to draw from them allowed us to conclude that the ethanolic extract of Origanum vulgare demonstrated lower cell viability than the aqueous extract and has significant antiviral activity against EAV and the both aqueous and ethanolic extracts have antiviral action against CDV.
基金This work was supported by grants from Brazilian agency CNPq(Process 470594/2013-6).
文摘This study aimed to identify the chemical composition of essential oil from fruits(EOAF)and the hexanic crude extract from aerial parts(At-Hex)of atemoya(Annona cherimola x Annona squamosa),a hybrid belonging to the Annonaceae family.Cytotoxic and antimicrobial activity was also evaluated.OEAF was obtained by hydrodistillation using a Clevenger apparatus,and their composition was analyzed by gas chromatography-mass spectrometry(GC-MS)analyses.Cytotoxicity was tested against human tumor cell lines HCT-116(colon carcinoma),SF-295(glioblastoma),OVCAR-8(ovarian carcinoma)and HL60(leukemia)using 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide(MTT)assay,while antimicrobial activity was conducted by bioauthography method against eleven microorganisms strains.Twenty-four compounds were identified in the EOAF and twenty-nine in At-Hex.The monoterpenes linalool(25.70%),α-pinene(10.38%),β-pinene(9.12%),transocimene(7.43%),and the sesquiterpene bicyclogermacrene(12.58%)were the major constituents of EOAF,whereas the sesquiterpene spathulenol(13.91%)was the main compound of At-Hex.At-Hex showed a high cytotoxicity against SF-295(glioblastoma).These findings show an important chemotaxonomic contribution for the Annonaceae family,mainly for the Annona genus.Atemoya proved to be a promising source of substances with potential cytotoxic activity.
基金supported by the National Natural Science Foundation of China(22078228)。
文摘Zwitterions(ZIs)are considered as an ideal,novel ionic conductive medium due to their high dipole moment and good solubility of lithium salts.However,the strong interactions between ZIs and Li^(+)severely hinder Li^(+)migration.Herein,a quasi-solid electrolyte(MSQSE-2Na)was fabricated by adding sodium bis(fluorosulfonyl)imide(NaFSI)to sulfobetaine methacrylate(SBMA,a ZI)based polymerization system.Na^(+)occupies the–SO_(3)^(-)site in SBMA prior to Li^(+),which weakens the self-crosslinking of SBMA and frees the Li^(+)bound to the polymer segments.Thus,the polymer conformation of MSQSE-2Na changes to a relaxed,homogeneous"sea-island"type.Meanwhile,Na^(+),due to its electron-withdrawing effect,decreases the electron cloud density of the polymer segments,building a weakly coordinated environment in MSQSE-2Na.Consequently,MSQSE-2Na exhibits excellent ionic conductivity of 7.38×10^(-4)S cm^(-1)and a high Li^(+)transference number of 0.632 at 25℃.The(-)Li|MSQSE-2Na|Li(+)cells exhibit super stability,sustaining operation for over 6182h.The(-)Li|MSQSE-2Na|LiFePO_(4)(+)cells demonstrate outstanding charge/discharge reversibility with a Coulombic efficiency exceeding 99.9%over 270 cycles(≈4500 h),with a capacity retention of 70.0%.This work proposes a new design concept for regulating the polymer conformation and charge characteristics through competitive coordination,thereby advancing the application of ZI-based polymer electrolytes in lithium metal batteries.
基金financial support from the National Key Research and Development Program of China(2022YFB4101800)National Natural Science Foundation of China(22278298)the Key Research&Development Program of Shandong Province,China(2024CXGC010410).
文摘CO_(2) hydrogenation to methanol is a critical technology for hydrogen energy conversion and a promising approach to mitigate the energy crisis and greenhouse effect.However,developing highly selective catalysts remains a major challenge for its practical application.Herein,we synthesize an efficient CoCuInO-r catalyst with Cu_(11)In_(9) and Co^(0) dual sites on In_(2)O_(3) via a sol-gel method.The Cu_(11)In_(9) intermetallic compound enhances H_(2) adsorption capacity and strength,and increases oxygen vacancy concentration on the catalyst surface,thereby improving CO_(2) activation and hydrogenation efficiency.Meanwhile,Co^(0) suppresses the desorption of the*CO species,facilitating its further hydrogenation to methanol.In-situ DRIFTS experiments indicate that the CO_(2) hydrogenation to methanol over CoCuInO-r follows the formate pathway.Compared with CuInO-r(containing Cu_(11)In_(9) on In_(2)O_(3)),CoCuInO-r exhibits a~20%increase in methanol selectivity and a 2-fold higher methanol space-time yield,reaching 7.68 mmol·g^(-1)·h^(-1) at 300℃ and 4 MPa.
基金supported by grants from the National Natural Science Foundation of China(Nos.82374489,U20A20259 and 22201299)the Scientific Research Program of the Tianjin Municipal Education Commission(No.2021ZD013)。
文摘Osteoarthritis(OA)is the most prevalent joint disease and icariin is a promising drug for its treatment.However,the clinical use of icariin is hindered by poor water solubility,low bioavailability,and nonspecific release and biological distribution.Herein,sulfonated azocalix[4]arene(SAC4A)with enhanced water solubility,recognition capacity,and designed responsiveness was used to improve the efficiency of icariin for OA therapy.SAC4A,a macrocycle with well-defined molecular weight and structure,could encapsulate and enhance water solubility of various drugs.In addition,SAC4A enables hypoxia-responsive release of loaded drug.Compared with icariin treatment,supramolecular complex icariin@SAC4A significantly relieved OA symptoms of rats,including more regular bone morphology and structure,and lower degree of cartilage damage.Moreover,the supramolecular formulation demonstrated various advantages,including easy preparation,hypoxia-triggered release,and small size that conducive to drug penetration.
基金financial support of National Key Research and Development Program of China(Grant No.2022YFB04200302)joint funds of National Natural Science Foundation of China(Grant No.62104115)+5 种基金National Natural Science Foundation of China(Grant No.U21A2072)Overseas Expertise Introduction Project for Discipline Innovation of Higher Education of China(Grant No.B16027)Key R&D Program of Hebei Province(No.19214301D)Yunnan Provincial Science and Technology Project at Southwest United Graduate School(No.202302A0370009)Haihe Laboratory of Sustainable Chemical TransformationsFundamental Research Funds for the Central Universities,Nankai University。
文摘The tensile strain in inorganic perovskite films induced by thermal annealing is one of the primary factors contributing to the inefficiency and instability of inorganic perovskite solar cells(IPSCs),which reduces the defect formation energy.Here,a flexible molecule 5-maleimidovaleric acid(5-MVA)was introduced as a strain buffer to release the residual strain of CsPbI_(2.85)Br_(0.15)perovskite.Maleic anhydride and carboxyl groups in 5-MVA interact strongly with the uncoordinated Pb^(2+)through Lewis acid-base reaction,thus tightly“pull”the perovskite lattice.The in-between soft carbon chain increased the structural flexibility of CsPbI_(2.85)Br_(0.15)perovskite materials,which effectively relieved the intrinsic internal strain of CsPbI_(2.85)Br_(0.15),resisted the corrosion of external strain,and also reduced the formation of defects such as VIand Pb0.In addition,the introduction of 5-MVA improved crystal quality,passivated residual defects,and narrowed energy level barriers.Eventually,power conversion efficiency(PCE)of NiOxbased inverted IPSCs increased from 19.25%to 20.82%with the open-circuit voltage enhanced from 1.164 V to 1.230 V.The release of strain also improved the stability of CsPbI_(2.85)Br_(0.15)perovskite films and devices.
