Metal-organic frameworks（MOFs） are a unique class of porous crystalline materials that have shown promise for a wide range of applications. MOFs have been explored as a new type of heterogeneous catalytic materials,...Metal-organic frameworks（MOFs） are a unique class of porous crystalline materials that have shown promise for a wide range of applications. MOFs have been explored as a new type of heterogeneous catalytic materials, because of their high surface area, uniform and tunable pores, facile functionalization and incorporation of catalytic active sites. The use of multi-functional sites MOF materials as catalysts for synergistic catalysis and tandem reactions has attracted increasing attention. In this review, we aim to introduce the construction of bi-or multi-functional MOF catalysts with cooperative or cascade functions via post-synthetic modification（PSM）.展开更多
Gallium nitride(GaN)single crystal with prominent electron mobility and heat resistance have great potential in the high temperature integrate electric power systems.However,the sluggish charge storage kinetics and in...Gallium nitride(GaN)single crystal with prominent electron mobility and heat resistance have great potential in the high temperature integrate electric power systems.However,the sluggish charge storage kinetics and inadequate energy densities are bottlenecks to its practical application.Herein,the self-supported GaN/Mn_(3)O_(4) integrated electrode is developed for both energy harvesting and storage under the high temperature environment.The experimental and theoretical calculations results reveal that such integrated structures with Mn-N heterointerface bring abundant active sites and reconstruct low-energy barrier channels for efficient charge transferring,reasonably optimizing the ions adsorption ability and strengthening the structural stability.Consequently,the assembled GaN based supercapacitors deliver the power density of 34.0 mW cm^(-2) with capacitance retention of 81.3%after 10000 cycles at 130℃.This work innovatively correlates the centimeter scale GaN single crystal with ideal theoretical capacity Mn_(3)O_(4) and provides an effective avenue for the follow-up energy storage applications of the wide bandgap semiconductor.展开更多
The CO_(2)-assisted oxidative dehydrogenation of ethane(CO_(2)-ODHE)provides a promising way to produce ethylene and utilize CO_(2).Simultaneous upgrading of ethane into the high value-added chemical products and the ...The CO_(2)-assisted oxidative dehydrogenation of ethane(CO_(2)-ODHE)provides a promising way to produce ethylene and utilize CO_(2).Simultaneous upgrading of ethane into the high value-added chemical products and the reduction of greenhouse gas CO_(2)emissions could be achieved.However,the targeted breaking of the C-C/C-H bonds of ethane is still a challenge for the designed catalysts.In this paper,ZnO-doped ZrO_(2)bifunctional catalysts(Zn_(x)ZrO)with different Zn/Zr molar ratios were prepared by the deposition-precipitation method,and the functions of various sites for CO_(2)-ODHE reaction were revealed by in situ characterizations and ethane pulse experiment:the medium-strength acidic Zn-O-Zr sites are responsible for the purposefully cracking of ethane C-H bonds to ethylene,while the more oxygen vacancies(OV)created by the introduction of Zn^(2+)are responsible for the efficient activation C=O bonds of CO_(2),thus promoting the RWGS reaction.In addition,the Zn0.2ZrO catalyst demonstrated excellent catalytic performances,with C_(2)H_(6)conversion,C_(2)H_(4)yield,and CO_(2)conversion about 19.1%,10.5%,and 10.6%within 5 h,respectively(600℃,GHSV=3000 mL/(g·h)).Especially,the initial ethylene space-time yield of 355.5μmol/(min·g)was obtained under 6000 mL/(g·h);Finally,the tandem reaction mechanism of ethane dehydrogenation and RWGS was revealed.展开更多
Cu/ZnO-based catalysts are widely employed for methanol synthesis via CO_(2) hydrogenation.The preparation procedure is sensitive to the particle size and interfacial structure,which are considered as potential active...Cu/ZnO-based catalysts are widely employed for methanol synthesis via CO_(2) hydrogenation.The preparation procedure is sensitive to the particle size and interfacial structure,which are considered as potential active centers influencing the rate of both methanol and CO formation.The particle size and the interaction between Cu and the support materials are influenced by the coprecipitation conditions,let alone that the mechanistic divergence remains unclear.In this work,a series of Cu/ZnO/ZrO_(2) catalysts were prepared via co-precipitation at different pH value and systematically characterized.The structure has been correlated with kinetic results to establish the structure-performance relationship.Kinetic analysis demonstrates that methanol synthesis follows a single-site Langmuir-Hinshelwood(L-H)mechanism,i.e.,Cu serves as the active site where CO_(2) and H_(2) competitively adsorb and react to form methanol.In contrast,CO formation proceeds via a dual-site L-H mechanism,where CO_(2) adsorbs onto ZnO and H_(2) onto Cu,with the reaction occurring at the Cu/ZnO interface.Therefore,for the direct formation of methanol,solely reducing the particle size of Cu would not be beneficial.展开更多
Two protected sites located on the outskirts of the Sena Oura National Park (PNSO) in West Mayo-Kebbi cover an area of 1800 m2 is pattern choose in pastoral enclave in both village. This study was undertaken to highli...Two protected sites located on the outskirts of the Sena Oura National Park (PNSO) in West Mayo-Kebbi cover an area of 1800 m2 is pattern choose in pastoral enclave in both village. This study was undertaken to highlight the floristic diversity of the herbaceous and woody vegetation on these sites in the offing to know the ability of charge into UBT that most support the park peripheral. It took place on two experimental sites on a natural course in two villages: Wazetelan and Massang. The approach used for the study was a survey using the systematic sampling method and a 30 m × 30 m plot. The survey consisted in listing all the taxa in a floristically homogeneous plot, each assigned the Braun-Blanquet dominance abundance coefficient. These surveys revealed a floristic richness of 73 species, 58 genera, including 46 herbaceous and 26 woody species. The Shannon result gives H1' = 0.12 bit for herbaceous species and H2' = 0.44 bit for woody species, meaning that the herbaceous and woody populations of all the surveys have a very low species diversity, as H' < 3 according to the Shannon index assessment threshold. Herbaceous species are divided into 13 families and 33 genera. The most represented families are Fabaceae (27.3%) and Poaceae (21.9%). Most of the other families (1.3%) have only one species, if any. Herbaceous species are divided into 33 genera grouped into 13 families. The most represented families are Fabaces (16 species), 34%, and Poaceae (12 species), 26%. The 26 woody species, most of which come from itinerant surveys, are distributed across 24 genera and 12 families, the most important of which is Fabaceae with 09 species (34.6%). This floristic assessment, in terms of quantity and quality, has enabled us to estimate the carrying capacity of the two pastoral enclaves in Dari and Goumadji cantons, and to guide the government’s actions with regard to rangeland management.展开更多
Objective N6-methyladenosine(m6A),the most prevalent epigenetic modification in eukaryotic RNA,plays a pivotal role in regulating cellular differentiation and developmental processes,with its dysregulation implicated ...Objective N6-methyladenosine(m6A),the most prevalent epigenetic modification in eukaryotic RNA,plays a pivotal role in regulating cellular differentiation and developmental processes,with its dysregulation implicated in diverse pathological conditions.Accurate prediction of m6A sites is critical for elucidating their regulatory mechanisms and informing drug development.However,traditional experimental methods are time-consuming and costly.Although various computational approaches have been proposed,challenges remain in feature learning,predictive accuracy,and generalization.Here,we present m6A-PSRA,a dual-branch residual-network-based predictor that fully exploits RNA sequence information to enhance prediction performance and model generalization.Methods m6A-PSRA adopts a parallel dual-branch network architecture to comprehensively extract RNA sequence features via two independent pathways.The first branch applies one-hot encoding to transform the RNA sequence into a numerical matrix while strictly preserving positional information and sequence continuity.This ensures that the biological context conveyed by nucleotide order is retained.A bidirectional long short-term memory network(BiLSTM)then processes the encoded matrix,capturing both forward and backward dependencies between bases to resolve contextual correlations.The second branch employs a k-mer tokenization strategy(k=3),decomposing the sequence into overlapping 3-mer subsequences to capture local sequence patterns.A pre-trained Doc2vec model maps these subsequences into fixeddimensional vectors,reducing feature dimensionality while extracting latent global semantic information via context learning.Both branches integrate residual networks(ResNet)and a self-attention mechanism:ResNet mitigates vanishing gradients through skip connections,preserving feature integrity,while self-attention adaptively assigns weights to focus on sequence regions most relevant to methylation prediction.This synergy enhances both feature learning and generalization capability.Results Across 11 tissues from humans,mice,and rats,m6A-PSRA consistently outperformed existing methods in accuracy(ACC)and area under the curve(AUC),achieving>90%ACC and>95%AUC in every tissue tested,indicating strong cross-species and cross-tissue adaptability.Validation on independent datasets—including three human cell lines(MOLM1,HEK293,A549)and a long-sequence dataset(m6A_IND,1001 nt)—confirmed stable performance across varied biological contexts and sequence lengths.Ablation studies demonstrated that the dual-branch architecture,residual network,and self-attention mechanism each contribute critically to performance,with their combination reducing interference between pathways.Motif analysis revealed an enrichment of m6A sites in guanine(G)and cytosine(C),consistent with known regulatory patterns,supporting the model’s biological plausibility.Conclusion m6A-PSRA effectively captures RNA sequence features,achieving high prediction accuracy and robust generalization across tissues and species,providing an efficient computational tool for m6A methylation site prediction.展开更多
Single atom catalysts supported by two-dimensional(2D)materials,including graphene,g-C_(3)N_(4),and graphdiyne,ex-hibit promising electrocatalytic nitrogen reduction reaction(NRR)activity.Nevertheless,sometimes theore...Single atom catalysts supported by two-dimensional(2D)materials,including graphene,g-C_(3)N_(4),and graphdiyne,ex-hibit promising electrocatalytic nitrogen reduction reaction(NRR)activity.Nevertheless,sometimes theoretical works failed to predict the high activity of NRR of single atom cat-alysts,especially for Fe,Co,Mn,Cu,Ru.In this work,based on DFT calculations,it is suggested that dual-atom sites on N doped graphene(M_(2)@N-graphene)rather than single-atom sites are more likely to be the active sites for NRR.Notably,Fe_(2)@N_(3),Co_(2)@N_(2),Mn_(2)@N_(2),Cu_(2)@N_(1),and Ru_(2)@N_(3)endow the best catalytic activity with corresponding limiting potentials of-0.26,-0.18,-0.17,-0.39,and-0.30 V,re-spectively.Furthermore,on g-C_(3)N_(4)and graphdiyne,triple-atom sites(TAS,M_(3))such as Ru_(3)(Co_(3))@g-C_(3)N_(4)and Ru_(3)(Rh_(3))@graphdiyne are expected to exhibit higher stability and NRR catalytic performance than single-atom sites(SAS)and dual-atom sites(DAS),with corresponding limiting potentials of-0.28,-0.48,-0.24,and-0.23 V.The calculated results with the corresponding experimental potentials indicate that the origin of superior NRR ac-tivity observed in experiments may be contributed by M_(2)or M_(3)on 2D materials.This study provides an in-depth investigation into real active NRR sites of metal atoms supported on 2D materials and contributes to the design of effective NRR catalysts.展开更多
The naturally fermented Inner Mongolian cheese’s flavor and nutritional value make it a popular choice among customers.In this work,to create multi-functional peptides that have taste and biological activity,peptidom...The naturally fermented Inner Mongolian cheese’s flavor and nutritional value make it a popular choice among customers.In this work,to create multi-functional peptides that have taste and biological activity,peptidomics and bioinformatics were used to screen flavor peptides from Inner Mongolian cheese and further assess their antioxidant and angiotensin I-converting enzyme(ACE)inhibitory properties.According to sensory data,YH8 and IL7 had detectable bitter tastes with low thresholds of 0.03 and 0.06 mmol/L,respectively.With an umami threshold range of 0.24‒0.81 mmol/L,VQ6,FK13,HP13 and QT14 exhibited a range of flavors dominated by umami,including sweet,bitter,salty,sour and kokumi.Antioxidant activity wise,YH8,VQ6,HP13 and QT14 were well represented.The above-mentioned peptides all had some ACE inhibitory effect.The bitter peptide IL7(IC_(50)=0.08 mmol/L)had the highest level of ACE inhibitory activity,followed by YH8(IC_(50)=0.33 mmol/L).These multi-functional peptides,which have been assessed for bioactive and taste features in Inner Mongolian cheese,may have positive impacts on health and harmonize the cheese’s overall flavor.These results suggest that some flavor peptides produced in fermented foods might be with bioactivities while providing a basis for the exploration and application of multi-functional peptides.展开更多
Figure 6(a)in the paper[Chin.Phys.B 33074203(2024)]was incorrect due to editorial oversight.The correct figure is provided.This modification does not affect the result presented in the paper.
Molecular recognition of bioreceptors and enzymes relies on orthogonal interactions with small molecules within their cavity. To date, Chinese scientists have developed three types of strategies for introducing active...Molecular recognition of bioreceptors and enzymes relies on orthogonal interactions with small molecules within their cavity. To date, Chinese scientists have developed three types of strategies for introducing active sites inside the cavity of macrocyclic arenes to better mimic molecular recognition of bioreceptors and enzymes.The editorial aims to enlighten scientists in this field when they develop novel macrocycles for molecular recognition, supramolecular assembly, and applications.展开更多
The kidney is essential for maintaining fluid,electrolyte,and metabolite homeostasis,and for regulating blood pressure.The pig serves as a valuable biomedical model for human renal physiology,offering insights across ...The kidney is essential for maintaining fluid,electrolyte,and metabolite homeostasis,and for regulating blood pressure.The pig serves as a valuable biomedical model for human renal physiology,offering insights across different physiological states.In this study,single-cell RNA sequencing was used to profile 138469 cells from 12 pig kidney samples collected during the embryonic(E),fattening(F),and pregnancy(P)periods,identifying 29 cell types.Proximal tubule(PT)cells exhibited elevated expression of metabolism-related transcription factors(TFs),including GPD1,ACAA1,and AGMAT,with validation across multiple individuals,periods,and species.Fluorescence homologous double-labeling of paraffin sections further confirmed the expression of ACAA1 and AGMAT in PT cells.Comparative analysis of pig and human kidneys revealed a high degree of similarity among corresponding cell types.Analysis of cell-type heterogeneity highlighted the diversity of thick ascending limb(TAL)cells,identifying a TAL subpopulation related to immune function.Additionally,the functional heterogeneity of kidney-resident macrophages(KRM)was explored across different anatomical sites.In the renal medulla,KRM were implicated in phagocytosis and leukocyte activation,whereas in the renal pelvis,they functioned as ligands,recruiting neutrophils with bactericidal activity to the renal pelvis to combat urinary tract infections.展开更多
Disrupting the symmetric electron distribution of porphyrin-like Fe singleatom catalysts has been considered as an effective way to harvest high intrinsic activity.Understanding the catalytic performance governed by g...Disrupting the symmetric electron distribution of porphyrin-like Fe singleatom catalysts has been considered as an effective way to harvest high intrinsic activity.Understanding the catalytic performance governed by geometric microstrains is highly desirable for further optimization of such efficient sites.Here,we decipher the crucial role of local microstrain in boosting intrinsic activity and durability of asymmetric Fe single-atom catalysts(Fe-N_(3)S_(1))by replacing one N atom with S atom.The high-curvature hollow carbon nanosphere substrate introduces 1.3%local compressive strain to Fe-N bonds and 1.5%tensile strain to Fe-S bonds,downshifting the d-band center and accelerating the kinetics of*OH reduction.Consequently,highly curved Fe-N_(3)S_(1)sites anchored on hollow carbon nanosphere(FeNS-HNS-20)exhibit negligible current loss,a high half-wave potential of 0.922 V vs.RHE and turnover frequency of 6.2 e^(−1)s^(−1)site−1,which are 53 mV more positive and 1.7 times that of flat Fe-N-S counterpart,respectively.More importantly,multiple operando spectroscopies monitored the dynamic optimization of strained Fe-N_(3)S_(1)sites into Fe-N_(3)sites,further mitigating the overadsorption of*OH intermediates.This work not only sheds new light on local microstrain-induced catalytic enhancement,but also provides a plausible direction for optimizing efficient asymmetric sites via geometric configurations.展开更多
Enhancing the catalytic hydrolysis efficiency of microcystins(MCs)at ambient temperature has been a persistent challenge in water treatment.We employed N_(2)/low-temperature plasma technology to modify the surface of ...Enhancing the catalytic hydrolysis efficiency of microcystins(MCs)at ambient temperature has been a persistent challenge in water treatment.We employed N_(2)/low-temperature plasma technology to modify the surface of natural pyrites(NP),and the resulting nitrogenmodified pyrites(NPN)with a nanorod structure and new Fe-Nx sites are more efficient for the hydrolysis of microcystins-LR(MC-LR).Kinetic experiments revealed that NPN exhibited significantly higher hydrolysis activity(k_(obs)=0.1471 h^(-1))than NP(0.0914 h^(-1)).Liquid chromatography-mass spectrometry(LC/MS)for the intermediates produced by hydrolyzing MC-LR,in situ attenuated total reflectance Fourier transform infrared spectroscopy(in situ ATR-FTIR)and X-ray photoelectron spectroscopy(XPS)analysis unfolded that the Fe and N atoms of Fe-Nx sites on the surface act of NPN as Lewis acid and Bronsted basic respectively,selectively breaking amide bond on MC-LR molecule.This study demonstrates the effectiveness of plasma technology in modifying mineral materials to enhance their catalytic activity,providing a new method for eliminating MCs in practical water treatment.展开更多
Atomic hydrogen(H∗)plays a crucial role in electrochemical reduction technology towards various environmental and energy applications,but suffers from low utilization efficiency arisen from the undesirable H-H dimeriz...Atomic hydrogen(H∗)plays a crucial role in electrochemical reduction technology towards various environmental and energy applications,but suffers from low utilization efficiency arisen from the undesirable H-H dimerization and the competitive adsorption between water molecule with reactants on the traditional adjacent catalytic sites.Herein,we anchored Pd single atoms on the naturally formed titanium oxide of titanium foam to construct Pd_(1)-O-Ti dual-site electrocatalyst with spatially isolated water dissociation and H∗utilization site,which synchronously inhibits the H-H dimerization and the competitive adsorption of water molecule and targeted reactants.Experiments and theoretical calculations revealed that the Ti-O sites could synergistically dissociate water to H∗,which overflowed to nearby Pd single-atom sites for designed reduction reactions and utilization benefiting from the hydrogen spillover ability of titanium oxide substrate.These Pd_(1)-O-Ti dual sites delivered almost 100%bromate reduction efficiency with a rate constant of 1.57 h^(-1),far superior to those of Pdn-O-Ti with adjacent Pd sites(0.52 h^(-1)),Pd_(1)-N-C with single sites(0.04 h^(-1))and commercial Pd/C(0.18 h^(-1)),respectively.This study sheds light on the importance of integrating synergistic active sites for complicated electrochemical reactions,and provide new insights in improving H∗ utilization for environmental remediation.展开更多
Objective To explore the risk management of the changes of sponsors and/or production sites during drug clinical trials based on the theories of quality management,risk management,and change management.Methods The met...Objective To explore the risk management of the changes of sponsors and/or production sites during drug clinical trials based on the theories of quality management,risk management,and change management.Methods The method of failure modes and effect analysis(FMEA)was used to identify risks through literature research,expert consultation,comparative research,and comprehensive analysis.Besides,risk priority number(RPN)was used to evaluate the risks.Results and Conclusion A FMEA of the changes of sponsors and/or production sites in clinical trials was constructed and RPN values of every failure mode and causes were obtained.Based on the RPN values,the core risk control points for different combination modes of sponsors and/or production sites after their changes were identified.It is recommended that China should strengthen the construction of the sponsor responsibility system.In addition,the changes of sponsors and/or production sites during the clinical trial period should be allowed in an orderly manner under the premise of ensuring the quality of clinical trials and subject protection.展开更多
Photocatalytic CO_(2)reduction reaction(CO_(2)RR)is one of the promising strategies for sustainably producing solar fuels.The precise identification of catalytic sites and the enhancement of photocatalytic CO_(2)conve...Photocatalytic CO_(2)reduction reaction(CO_(2)RR)is one of the promising strategies for sustainably producing solar fuels.The precise identification of catalytic sites and the enhancement of photocatalytic CO_(2)conversion is imperative yet quite challenging.This critical review summarizes recent advances in porous photo-responsive polymers,including covalent organic frameworks(COFs),covalent triazine frameworks(CTFs),and conjugated microporous polymers(CMPs),those can be rationally designed from the molecular level for visible-light-driven photocatalytic CO_(2)reduction.Additionally,special emphasis is placed on how the well-defined active sites on these polymers can influence their properties and photocatalytic performance.The precise regulation and control of microenvironments and electronic properties of metal active centers are crucial for boosting catalytic efficiency and selectivity,as well as for the design of better photocatalysts for CO_(2)reduction.展开更多
Ground response analysis and determination of site-specific ground motion parameters are necessary for evaluating seismic loads to enable sustainable design of aboveground and underground structures,particularly in de...Ground response analysis and determination of site-specific ground motion parameters are necessary for evaluating seismic loads to enable sustainable design of aboveground and underground structures,particularly in deep overburden sites.This study investigates the influence of bedrock interface conditions and depth of soil deposits on obtained site-specific ground motion parameters.Employing the one-dimensional seismic response analysis program SOILQUAKE,the ground responses of five representative soil profiles and 1050 case studies are calculated considering three different site models of seismic input interfaces.The analysis employs the actual bedrock interface with a shear wave velocity of 760 m/s as the reference input bedrock interface.The results illustrate that the selection of the bedrock interface condition significantly affects the seismic response on the ground surface of deep overburden sites.Specifically,the ground surface acceleration response spectra at longer periods are notably smaller compared to those at the actual bedrock site.This may present a challenge for designing long-period high-rise buildings situated in deep overburden sites.It is recommended to select a seismic input bedrock interface closely approximating the actual bedrock depth when conducting seismic response analyses for deep overburden sites.展开更多
The utilization of nuclear power will persist as a prominent energy source in the foreseeable future.However,it presents substantial challenges concerning waste disposal and the potential emission of untreated radioac...The utilization of nuclear power will persist as a prominent energy source in the foreseeable future.However,it presents substantial challenges concerning waste disposal and the potential emission of untreated radioactive substances,such as radioactive 129I and 131I.The transportation of radioactive iodine poses a significant threat to both the environment and human health.Nevertheless,effectively,rapidly removing iodine ion from water using porous adsorbents remains a crucial challenge.In this work,three kinds of multiple sites porous organic polymers(POPs,POP-1,POP-2,and POP-3)have been developed using a monomer pre-modification strategy for highly efficient and fast I_(3) absorption from water.It is found that the POPs exhibited exceptional performance in terms of I3 adsorption,achieving a top-performing adsorption capacity of 5.25 g g^(-1) and the fastest average adsorption rate(K_(80%)=4.25 g g^(-1) h^(-1))with POP-1.Moreover,POP-1 exhibited exceptional capacity for the removal of I3 fromflowing aqueous solutions,with 95%removal efficiency observed even at 0.0005 mol L^(-1).Such results indicate that this material has the potential to be utilized for the emergency preparation of potable water in areas contaminated with radioactive iodine.The adsorption process can be effectively characterized by the Freundlich model and the pseudo-second-order model.The exceptional I_(3) absorption capacity is primarily attributed to the incorporation of a substantial number of active adsorption sites,including bromine,carbonyl,and amide groups.展开更多
Here,we present a regulation strategy involving heteroatom doping and structural construction to adjust zincophilic sites and electric field distribution,achieving a robust and dendrite-free Zn host anode.Theoretical ...Here,we present a regulation strategy involving heteroatom doping and structural construction to adjust zincophilic sites and electric field distribution,achieving a robust and dendrite-free Zn host anode.Theoretical calculations and experimental results confirm that sulfur atoms can provide moderate zincophilicity,while graphene-like nanosheets can even the electric field distribution,imparting the sulfurdoped graphene-like network(S-GP) with a longer lifespan(exceeding 500 h) and acceptable coulombic efficiency.Importantly,the S-GP host is used as the substrate for flexible Zn-ion batteries,exhibiting impressive electrochemical performance and great mechanical flexibility,indicating a broad application prospect in portable and wearable electronic devices.展开更多
Lead(Pb)-zinc(Zn)slags contain large amounts of Pb,causing irreversible damage to the environment.Therefore,developing an effective strategy to extract Pb from Pb-Zn slags and convert them into a renewable high-value ...Lead(Pb)-zinc(Zn)slags contain large amounts of Pb,causing irreversible damage to the environment.Therefore,developing an effective strategy to extract Pb from Pb-Zn slags and convert them into a renewable high-value catalyst not only solves the energy crisis but also reduces environmental pollution.Herein,we present a viable strategy to recycle Pb and iron(Fe)from Pb-Zn slags for the fabrication of efficient methylammonium lead tri-iodide(r-MAPbI_(3))piezocatalysts with single-atom Fe-N_(4) sites.Intriguingly,atomically dispersed Fe sites from Pb-Zn slags,which coordinated with N in the neighboring four CH3NH3 to form the FeN_(4) configuration,were detected in the as-obtained r-MAPbI_(3) by synchrotron X-ray absorption spectroscopy.The introduction of Fe single atoms amplified the polarization of MAPbI_(3) and upshifted the d-band center of MAPbI_(3).This not only enhanced the piezoelectric response of MAPbI_(3) but also promoted the proton transfer during the hydrogen evolution process.Due to the decoration of Fe single atoms,r-MAPbI_(3) showed a pronounced H2 yield of 322.4μmol g^(−1) h^(−1),which was 2.52 times that of MAPbI_(3) synthesized using commercially available reagents.This simple yet robust strategy to manufactureMAPbI_(3) piezocatalysts paves a novel way to the large-scale and value-added consumption of Pb-containing waste residues.展开更多
基金supported by the National Natural Science Foundation of China (Nos. 21371069 and 21621001)
文摘Metal-organic frameworks（MOFs） are a unique class of porous crystalline materials that have shown promise for a wide range of applications. MOFs have been explored as a new type of heterogeneous catalytic materials, because of their high surface area, uniform and tunable pores, facile functionalization and incorporation of catalytic active sites. The use of multi-functional sites MOF materials as catalysts for synergistic catalysis and tandem reactions has attracted increasing attention. In this review, we aim to introduce the construction of bi-or multi-functional MOF catalysts with cooperative or cascade functions via post-synthetic modification（PSM）.
基金supported by NSFC(Grant No.52202265,52302004,52472010,62434010)the Taishan Scholars Program of Shandong Province(tsqn202306330)+1 种基金Shenzhen Science and Technology Program(JCYJ20230807094009018)Xiaomi Young Talents Program(2023XM06).
文摘Gallium nitride(GaN)single crystal with prominent electron mobility and heat resistance have great potential in the high temperature integrate electric power systems.However,the sluggish charge storage kinetics and inadequate energy densities are bottlenecks to its practical application.Herein,the self-supported GaN/Mn_(3)O_(4) integrated electrode is developed for both energy harvesting and storage under the high temperature environment.The experimental and theoretical calculations results reveal that such integrated structures with Mn-N heterointerface bring abundant active sites and reconstruct low-energy barrier channels for efficient charge transferring,reasonably optimizing the ions adsorption ability and strengthening the structural stability.Consequently,the assembled GaN based supercapacitors deliver the power density of 34.0 mW cm^(-2) with capacitance retention of 81.3%after 10000 cycles at 130℃.This work innovatively correlates the centimeter scale GaN single crystal with ideal theoretical capacity Mn_(3)O_(4) and provides an effective avenue for the follow-up energy storage applications of the wide bandgap semiconductor.
文摘The CO_(2)-assisted oxidative dehydrogenation of ethane(CO_(2)-ODHE)provides a promising way to produce ethylene and utilize CO_(2).Simultaneous upgrading of ethane into the high value-added chemical products and the reduction of greenhouse gas CO_(2)emissions could be achieved.However,the targeted breaking of the C-C/C-H bonds of ethane is still a challenge for the designed catalysts.In this paper,ZnO-doped ZrO_(2)bifunctional catalysts(Zn_(x)ZrO)with different Zn/Zr molar ratios were prepared by the deposition-precipitation method,and the functions of various sites for CO_(2)-ODHE reaction were revealed by in situ characterizations and ethane pulse experiment:the medium-strength acidic Zn-O-Zr sites are responsible for the purposefully cracking of ethane C-H bonds to ethylene,while the more oxygen vacancies(OV)created by the introduction of Zn^(2+)are responsible for the efficient activation C=O bonds of CO_(2),thus promoting the RWGS reaction.In addition,the Zn0.2ZrO catalyst demonstrated excellent catalytic performances,with C_(2)H_(6)conversion,C_(2)H_(4)yield,and CO_(2)conversion about 19.1%,10.5%,and 10.6%within 5 h,respectively(600℃,GHSV=3000 mL/(g·h)).Especially,the initial ethylene space-time yield of 355.5μmol/(min·g)was obtained under 6000 mL/(g·h);Finally,the tandem reaction mechanism of ethane dehydrogenation and RWGS was revealed.
基金supported by Research Grant from China Petroleum and Chemical Corp。
文摘Cu/ZnO-based catalysts are widely employed for methanol synthesis via CO_(2) hydrogenation.The preparation procedure is sensitive to the particle size and interfacial structure,which are considered as potential active centers influencing the rate of both methanol and CO formation.The particle size and the interaction between Cu and the support materials are influenced by the coprecipitation conditions,let alone that the mechanistic divergence remains unclear.In this work,a series of Cu/ZnO/ZrO_(2) catalysts were prepared via co-precipitation at different pH value and systematically characterized.The structure has been correlated with kinetic results to establish the structure-performance relationship.Kinetic analysis demonstrates that methanol synthesis follows a single-site Langmuir-Hinshelwood(L-H)mechanism,i.e.,Cu serves as the active site where CO_(2) and H_(2) competitively adsorb and react to form methanol.In contrast,CO formation proceeds via a dual-site L-H mechanism,where CO_(2) adsorbs onto ZnO and H_(2) onto Cu,with the reaction occurring at the Cu/ZnO interface.Therefore,for the direct formation of methanol,solely reducing the particle size of Cu would not be beneficial.
文摘Two protected sites located on the outskirts of the Sena Oura National Park (PNSO) in West Mayo-Kebbi cover an area of 1800 m2 is pattern choose in pastoral enclave in both village. This study was undertaken to highlight the floristic diversity of the herbaceous and woody vegetation on these sites in the offing to know the ability of charge into UBT that most support the park peripheral. It took place on two experimental sites on a natural course in two villages: Wazetelan and Massang. The approach used for the study was a survey using the systematic sampling method and a 30 m × 30 m plot. The survey consisted in listing all the taxa in a floristically homogeneous plot, each assigned the Braun-Blanquet dominance abundance coefficient. These surveys revealed a floristic richness of 73 species, 58 genera, including 46 herbaceous and 26 woody species. The Shannon result gives H1' = 0.12 bit for herbaceous species and H2' = 0.44 bit for woody species, meaning that the herbaceous and woody populations of all the surveys have a very low species diversity, as H' < 3 according to the Shannon index assessment threshold. Herbaceous species are divided into 13 families and 33 genera. The most represented families are Fabaceae (27.3%) and Poaceae (21.9%). Most of the other families (1.3%) have only one species, if any. Herbaceous species are divided into 33 genera grouped into 13 families. The most represented families are Fabaces (16 species), 34%, and Poaceae (12 species), 26%. The 26 woody species, most of which come from itinerant surveys, are distributed across 24 genera and 12 families, the most important of which is Fabaceae with 09 species (34.6%). This floristic assessment, in terms of quantity and quality, has enabled us to estimate the carrying capacity of the two pastoral enclaves in Dari and Goumadji cantons, and to guide the government’s actions with regard to rangeland management.
基金supported by grants from The National Natural Science Foundation of China(12361104)Yunnan Fundamental Research Projects(202301AT070016,202401AT070036)+2 种基金the Youth Talent Program of Xingdian Talent Support Plan(XDYC-QNRC-2022-0514)the Yunnan Province International Joint Laboratory for Intelligent Integration and Application of Ethnic Multilingualism(202403AP140014)the Open Research Fund of Yunnan Key Laboratory of Statistical Modeling and Data Analysis,Yunnan University(SMDAYB2023004)。
文摘Objective N6-methyladenosine(m6A),the most prevalent epigenetic modification in eukaryotic RNA,plays a pivotal role in regulating cellular differentiation and developmental processes,with its dysregulation implicated in diverse pathological conditions.Accurate prediction of m6A sites is critical for elucidating their regulatory mechanisms and informing drug development.However,traditional experimental methods are time-consuming and costly.Although various computational approaches have been proposed,challenges remain in feature learning,predictive accuracy,and generalization.Here,we present m6A-PSRA,a dual-branch residual-network-based predictor that fully exploits RNA sequence information to enhance prediction performance and model generalization.Methods m6A-PSRA adopts a parallel dual-branch network architecture to comprehensively extract RNA sequence features via two independent pathways.The first branch applies one-hot encoding to transform the RNA sequence into a numerical matrix while strictly preserving positional information and sequence continuity.This ensures that the biological context conveyed by nucleotide order is retained.A bidirectional long short-term memory network(BiLSTM)then processes the encoded matrix,capturing both forward and backward dependencies between bases to resolve contextual correlations.The second branch employs a k-mer tokenization strategy(k=3),decomposing the sequence into overlapping 3-mer subsequences to capture local sequence patterns.A pre-trained Doc2vec model maps these subsequences into fixeddimensional vectors,reducing feature dimensionality while extracting latent global semantic information via context learning.Both branches integrate residual networks(ResNet)and a self-attention mechanism:ResNet mitigates vanishing gradients through skip connections,preserving feature integrity,while self-attention adaptively assigns weights to focus on sequence regions most relevant to methylation prediction.This synergy enhances both feature learning and generalization capability.Results Across 11 tissues from humans,mice,and rats,m6A-PSRA consistently outperformed existing methods in accuracy(ACC)and area under the curve(AUC),achieving>90%ACC and>95%AUC in every tissue tested,indicating strong cross-species and cross-tissue adaptability.Validation on independent datasets—including three human cell lines(MOLM1,HEK293,A549)and a long-sequence dataset(m6A_IND,1001 nt)—confirmed stable performance across varied biological contexts and sequence lengths.Ablation studies demonstrated that the dual-branch architecture,residual network,and self-attention mechanism each contribute critically to performance,with their combination reducing interference between pathways.Motif analysis revealed an enrichment of m6A sites in guanine(G)and cytosine(C),consistent with known regulatory patterns,supporting the model’s biological plausibility.Conclusion m6A-PSRA effectively captures RNA sequence features,achieving high prediction accuracy and robust generalization across tissues and species,providing an efficient computational tool for m6A methylation site prediction.
基金partially supported by the National Natural Science Foundation of China(Nos.22373092,22288201)CAS Project for Young Scientists in Basic Research(YSBR-051)+1 种基金Innovation Program for Quantum Science and Technology(2021ZD0303306)supported by University of Science and Technology of China Tang Scholarship and State Scholarship Fund(202206345005)。
文摘Single atom catalysts supported by two-dimensional(2D)materials,including graphene,g-C_(3)N_(4),and graphdiyne,ex-hibit promising electrocatalytic nitrogen reduction reaction(NRR)activity.Nevertheless,sometimes theoretical works failed to predict the high activity of NRR of single atom cat-alysts,especially for Fe,Co,Mn,Cu,Ru.In this work,based on DFT calculations,it is suggested that dual-atom sites on N doped graphene(M_(2)@N-graphene)rather than single-atom sites are more likely to be the active sites for NRR.Notably,Fe_(2)@N_(3),Co_(2)@N_(2),Mn_(2)@N_(2),Cu_(2)@N_(1),and Ru_(2)@N_(3)endow the best catalytic activity with corresponding limiting potentials of-0.26,-0.18,-0.17,-0.39,and-0.30 V,re-spectively.Furthermore,on g-C_(3)N_(4)and graphdiyne,triple-atom sites(TAS,M_(3))such as Ru_(3)(Co_(3))@g-C_(3)N_(4)and Ru_(3)(Rh_(3))@graphdiyne are expected to exhibit higher stability and NRR catalytic performance than single-atom sites(SAS)and dual-atom sites(DAS),with corresponding limiting potentials of-0.28,-0.48,-0.24,and-0.23 V.The calculated results with the corresponding experimental potentials indicate that the origin of superior NRR ac-tivity observed in experiments may be contributed by M_(2)or M_(3)on 2D materials.This study provides an in-depth investigation into real active NRR sites of metal atoms supported on 2D materials and contributes to the design of effective NRR catalysts.
基金supported by the central government and guides local funds for science and technology development(2022ZY0109).
文摘The naturally fermented Inner Mongolian cheese’s flavor and nutritional value make it a popular choice among customers.In this work,to create multi-functional peptides that have taste and biological activity,peptidomics and bioinformatics were used to screen flavor peptides from Inner Mongolian cheese and further assess their antioxidant and angiotensin I-converting enzyme(ACE)inhibitory properties.According to sensory data,YH8 and IL7 had detectable bitter tastes with low thresholds of 0.03 and 0.06 mmol/L,respectively.With an umami threshold range of 0.24‒0.81 mmol/L,VQ6,FK13,HP13 and QT14 exhibited a range of flavors dominated by umami,including sweet,bitter,salty,sour and kokumi.Antioxidant activity wise,YH8,VQ6,HP13 and QT14 were well represented.The above-mentioned peptides all had some ACE inhibitory effect.The bitter peptide IL7(IC_(50)=0.08 mmol/L)had the highest level of ACE inhibitory activity,followed by YH8(IC_(50)=0.33 mmol/L).These multi-functional peptides,which have been assessed for bioactive and taste features in Inner Mongolian cheese,may have positive impacts on health and harmonize the cheese’s overall flavor.These results suggest that some flavor peptides produced in fermented foods might be with bioactivities while providing a basis for the exploration and application of multi-functional peptides.
文摘Figure 6(a)in the paper[Chin.Phys.B 33074203(2024)]was incorrect due to editorial oversight.The correct figure is provided.This modification does not affect the result presented in the paper.
文摘Molecular recognition of bioreceptors and enzymes relies on orthogonal interactions with small molecules within their cavity. To date, Chinese scientists have developed three types of strategies for introducing active sites inside the cavity of macrocyclic arenes to better mimic molecular recognition of bioreceptors and enzymes.The editorial aims to enlighten scientists in this field when they develop novel macrocycles for molecular recognition, supramolecular assembly, and applications.
基金supported by the International Cooperation and Exchange Program of the National Natural Science Foundation of China(32261133531)。
文摘The kidney is essential for maintaining fluid,electrolyte,and metabolite homeostasis,and for regulating blood pressure.The pig serves as a valuable biomedical model for human renal physiology,offering insights across different physiological states.In this study,single-cell RNA sequencing was used to profile 138469 cells from 12 pig kidney samples collected during the embryonic(E),fattening(F),and pregnancy(P)periods,identifying 29 cell types.Proximal tubule(PT)cells exhibited elevated expression of metabolism-related transcription factors(TFs),including GPD1,ACAA1,and AGMAT,with validation across multiple individuals,periods,and species.Fluorescence homologous double-labeling of paraffin sections further confirmed the expression of ACAA1 and AGMAT in PT cells.Comparative analysis of pig and human kidneys revealed a high degree of similarity among corresponding cell types.Analysis of cell-type heterogeneity highlighted the diversity of thick ascending limb(TAL)cells,identifying a TAL subpopulation related to immune function.Additionally,the functional heterogeneity of kidney-resident macrophages(KRM)was explored across different anatomical sites.In the renal medulla,KRM were implicated in phagocytosis and leukocyte activation,whereas in the renal pelvis,they functioned as ligands,recruiting neutrophils with bactericidal activity to the renal pelvis to combat urinary tract infections.
基金supported by the Natural Science Foundation of Shandong Province (ZR2024JQ004)the National Natural Science Foundation of China (22108306, 22478432)Taishan Scholars Program of Shandong Province
文摘Disrupting the symmetric electron distribution of porphyrin-like Fe singleatom catalysts has been considered as an effective way to harvest high intrinsic activity.Understanding the catalytic performance governed by geometric microstrains is highly desirable for further optimization of such efficient sites.Here,we decipher the crucial role of local microstrain in boosting intrinsic activity and durability of asymmetric Fe single-atom catalysts(Fe-N_(3)S_(1))by replacing one N atom with S atom.The high-curvature hollow carbon nanosphere substrate introduces 1.3%local compressive strain to Fe-N bonds and 1.5%tensile strain to Fe-S bonds,downshifting the d-band center and accelerating the kinetics of*OH reduction.Consequently,highly curved Fe-N_(3)S_(1)sites anchored on hollow carbon nanosphere(FeNS-HNS-20)exhibit negligible current loss,a high half-wave potential of 0.922 V vs.RHE and turnover frequency of 6.2 e^(−1)s^(−1)site−1,which are 53 mV more positive and 1.7 times that of flat Fe-N-S counterpart,respectively.More importantly,multiple operando spectroscopies monitored the dynamic optimization of strained Fe-N_(3)S_(1)sites into Fe-N_(3)sites,further mitigating the overadsorption of*OH intermediates.This work not only sheds new light on local microstrain-induced catalytic enhancement,but also provides a plausible direction for optimizing efficient asymmetric sites via geometric configurations.
基金supported by the National Natural Science Foundation of China(Nos.22076098,22376118 and 21577078)the Outstanding Youth Project of the Natural Science Foundation of Hubei Province(2023AFA054)the 111 Project of China(No.D20015).
文摘Enhancing the catalytic hydrolysis efficiency of microcystins(MCs)at ambient temperature has been a persistent challenge in water treatment.We employed N_(2)/low-temperature plasma technology to modify the surface of natural pyrites(NP),and the resulting nitrogenmodified pyrites(NPN)with a nanorod structure and new Fe-Nx sites are more efficient for the hydrolysis of microcystins-LR(MC-LR).Kinetic experiments revealed that NPN exhibited significantly higher hydrolysis activity(k_(obs)=0.1471 h^(-1))than NP(0.0914 h^(-1)).Liquid chromatography-mass spectrometry(LC/MS)for the intermediates produced by hydrolyzing MC-LR,in situ attenuated total reflectance Fourier transform infrared spectroscopy(in situ ATR-FTIR)and X-ray photoelectron spectroscopy(XPS)analysis unfolded that the Fe and N atoms of Fe-Nx sites on the surface act of NPN as Lewis acid and Bronsted basic respectively,selectively breaking amide bond on MC-LR molecule.This study demonstrates the effectiveness of plasma technology in modifying mineral materials to enhance their catalytic activity,providing a new method for eliminating MCs in practical water treatment.
基金supported by the National Natural Science Foundation of China(Nos.U22A20402,U21A20286,and 22102100)the Key Program of Shenzhen Science and Technology Commission(No.JCYJ20220818095601002)the Natural Science Foundation of Shanghai(No.22ZR1431700).
文摘Atomic hydrogen(H∗)plays a crucial role in electrochemical reduction technology towards various environmental and energy applications,but suffers from low utilization efficiency arisen from the undesirable H-H dimerization and the competitive adsorption between water molecule with reactants on the traditional adjacent catalytic sites.Herein,we anchored Pd single atoms on the naturally formed titanium oxide of titanium foam to construct Pd_(1)-O-Ti dual-site electrocatalyst with spatially isolated water dissociation and H∗utilization site,which synchronously inhibits the H-H dimerization and the competitive adsorption of water molecule and targeted reactants.Experiments and theoretical calculations revealed that the Ti-O sites could synergistically dissociate water to H∗,which overflowed to nearby Pd single-atom sites for designed reduction reactions and utilization benefiting from the hydrogen spillover ability of titanium oxide substrate.These Pd_(1)-O-Ti dual sites delivered almost 100%bromate reduction efficiency with a rate constant of 1.57 h^(-1),far superior to those of Pdn-O-Ti with adjacent Pd sites(0.52 h^(-1)),Pd_(1)-N-C with single sites(0.04 h^(-1))and commercial Pd/C(0.18 h^(-1)),respectively.This study sheds light on the importance of integrating synergistic active sites for complicated electrochemical reactions,and provide new insights in improving H∗ utilization for environmental remediation.
文摘Objective To explore the risk management of the changes of sponsors and/or production sites during drug clinical trials based on the theories of quality management,risk management,and change management.Methods The method of failure modes and effect analysis(FMEA)was used to identify risks through literature research,expert consultation,comparative research,and comprehensive analysis.Besides,risk priority number(RPN)was used to evaluate the risks.Results and Conclusion A FMEA of the changes of sponsors and/or production sites in clinical trials was constructed and RPN values of every failure mode and causes were obtained.Based on the RPN values,the core risk control points for different combination modes of sponsors and/or production sites after their changes were identified.It is recommended that China should strengthen the construction of the sponsor responsibility system.In addition,the changes of sponsors and/or production sites during the clinical trial period should be allowed in an orderly manner under the premise of ensuring the quality of clinical trials and subject protection.
基金National Natural Science Foundation of China(No.22005154)for financial support。
文摘Photocatalytic CO_(2)reduction reaction(CO_(2)RR)is one of the promising strategies for sustainably producing solar fuels.The precise identification of catalytic sites and the enhancement of photocatalytic CO_(2)conversion is imperative yet quite challenging.This critical review summarizes recent advances in porous photo-responsive polymers,including covalent organic frameworks(COFs),covalent triazine frameworks(CTFs),and conjugated microporous polymers(CMPs),those can be rationally designed from the molecular level for visible-light-driven photocatalytic CO_(2)reduction.Additionally,special emphasis is placed on how the well-defined active sites on these polymers can influence their properties and photocatalytic performance.The precise regulation and control of microenvironments and electronic properties of metal active centers are crucial for boosting catalytic efficiency and selectivity,as well as for the design of better photocatalysts for CO_(2)reduction.
基金supported by the National Natural Science Foundation of China(Nos.52408435,52278384)。
文摘Ground response analysis and determination of site-specific ground motion parameters are necessary for evaluating seismic loads to enable sustainable design of aboveground and underground structures,particularly in deep overburden sites.This study investigates the influence of bedrock interface conditions and depth of soil deposits on obtained site-specific ground motion parameters.Employing the one-dimensional seismic response analysis program SOILQUAKE,the ground responses of five representative soil profiles and 1050 case studies are calculated considering three different site models of seismic input interfaces.The analysis employs the actual bedrock interface with a shear wave velocity of 760 m/s as the reference input bedrock interface.The results illustrate that the selection of the bedrock interface condition significantly affects the seismic response on the ground surface of deep overburden sites.Specifically,the ground surface acceleration response spectra at longer periods are notably smaller compared to those at the actual bedrock site.This may present a challenge for designing long-period high-rise buildings situated in deep overburden sites.It is recommended to select a seismic input bedrock interface closely approximating the actual bedrock depth when conducting seismic response analyses for deep overburden sites.
基金support from the National Natural Science Foundation of China(No.22273016,22273017,22233006)Plan for Henan Province University Science and Technology Innovation Team(No.25IRTSTHN002)+1 种基金Young Backbone Teacher Training Program of Henan Province(2023GGJS036)the 111 project(No.D17007).
文摘The utilization of nuclear power will persist as a prominent energy source in the foreseeable future.However,it presents substantial challenges concerning waste disposal and the potential emission of untreated radioactive substances,such as radioactive 129I and 131I.The transportation of radioactive iodine poses a significant threat to both the environment and human health.Nevertheless,effectively,rapidly removing iodine ion from water using porous adsorbents remains a crucial challenge.In this work,three kinds of multiple sites porous organic polymers(POPs,POP-1,POP-2,and POP-3)have been developed using a monomer pre-modification strategy for highly efficient and fast I_(3) absorption from water.It is found that the POPs exhibited exceptional performance in terms of I3 adsorption,achieving a top-performing adsorption capacity of 5.25 g g^(-1) and the fastest average adsorption rate(K_(80%)=4.25 g g^(-1) h^(-1))with POP-1.Moreover,POP-1 exhibited exceptional capacity for the removal of I3 fromflowing aqueous solutions,with 95%removal efficiency observed even at 0.0005 mol L^(-1).Such results indicate that this material has the potential to be utilized for the emergency preparation of potable water in areas contaminated with radioactive iodine.The adsorption process can be effectively characterized by the Freundlich model and the pseudo-second-order model.The exceptional I_(3) absorption capacity is primarily attributed to the incorporation of a substantial number of active adsorption sites,including bromine,carbonyl,and amide groups.
文摘Here,we present a regulation strategy involving heteroatom doping and structural construction to adjust zincophilic sites and electric field distribution,achieving a robust and dendrite-free Zn host anode.Theoretical calculations and experimental results confirm that sulfur atoms can provide moderate zincophilicity,while graphene-like nanosheets can even the electric field distribution,imparting the sulfurdoped graphene-like network(S-GP) with a longer lifespan(exceeding 500 h) and acceptable coulombic efficiency.Importantly,the S-GP host is used as the substrate for flexible Zn-ion batteries,exhibiting impressive electrochemical performance and great mechanical flexibility,indicating a broad application prospect in portable and wearable electronic devices.
基金supported by the Foundation for Innovative Research Groups of the National Natural Science Foundation of China(No.52121004,U23B20166)Guangdong Basic and Applied Basic Research Foundation(2024A1515030039,2025A1515010312).
文摘Lead(Pb)-zinc(Zn)slags contain large amounts of Pb,causing irreversible damage to the environment.Therefore,developing an effective strategy to extract Pb from Pb-Zn slags and convert them into a renewable high-value catalyst not only solves the energy crisis but also reduces environmental pollution.Herein,we present a viable strategy to recycle Pb and iron(Fe)from Pb-Zn slags for the fabrication of efficient methylammonium lead tri-iodide(r-MAPbI_(3))piezocatalysts with single-atom Fe-N_(4) sites.Intriguingly,atomically dispersed Fe sites from Pb-Zn slags,which coordinated with N in the neighboring four CH3NH3 to form the FeN_(4) configuration,were detected in the as-obtained r-MAPbI_(3) by synchrotron X-ray absorption spectroscopy.The introduction of Fe single atoms amplified the polarization of MAPbI_(3) and upshifted the d-band center of MAPbI_(3).This not only enhanced the piezoelectric response of MAPbI_(3) but also promoted the proton transfer during the hydrogen evolution process.Due to the decoration of Fe single atoms,r-MAPbI_(3) showed a pronounced H2 yield of 322.4μmol g^(−1) h^(−1),which was 2.52 times that of MAPbI_(3) synthesized using commercially available reagents.This simple yet robust strategy to manufactureMAPbI_(3) piezocatalysts paves a novel way to the large-scale and value-added consumption of Pb-containing waste residues.
