High-performance perovskite photodetectors with self-driven characteristic usually need electron/hole transport layers to extract carriers. However, these devices with transport layer structure are prone to result in ...High-performance perovskite photodetectors with self-driven characteristic usually need electron/hole transport layers to extract carriers. However, these devices with transport layer structure are prone to result in a poor perovskite/transport layer interface, which restricts the performance and stability of the device. To solve this problem, this work reports a novel device structure in which perovskite nanowires are in-situ prepared on PbI_(2), which serves as both a reaction raw material and efficient carrier extraction layer. By optimizing the thickness of PbI_(2), nanowire growth time, and ion exchange time, a selfdriven photodetector with an ITO/PbI_(2)/CsPbBr_(3)/carbon structure is constructed. The optimized device achieves excellent performance with the responsivity of 0.33 A/W, the detectivity of as high as 3.52 × 10^(13) Jones. Furthermore, the device can detect the light with its optical power lowered to 0.1 nW/cm^(2). This research provides a new method for preparing perovskite nano/micro devices with simple structure but excellent performance.展开更多
Electrochemical reduction of carbon dioxide(CO_(2)RR)is a promising approach to complete the carbon cycle and potentially convert CO_(2)into valuable chemicals and fuels.Cu is unique among transition metals in its abi...Electrochemical reduction of carbon dioxide(CO_(2)RR)is a promising approach to complete the carbon cycle and potentially convert CO_(2)into valuable chemicals and fuels.Cu is unique among transition metals in its ability to catalyze the CO_(2)RR and produce multi-carbon products.However,achieving high selectivity for C2+products is challenging for copper-based catalysts,as C–C coupling reactions proceed slowly.Herein,a surface modification strategy involving grafting long alkyl chains onto copper nanowires(Cu NWs)has been proposed to regulate the electronic structure of Cu surface,which facilitates*CO-*CO coupling in the CO_(2)RR.The hydrophobicity of the catalysts increases greatly after the introduction of long alkyl chains,therefore the hydrogen evolution reaction(HER)has been inhibited effectively.Such surface modification approach proves to be highly efficient and universal,with the Faradaic efficiency(FE)of C_(2)H_(4) up to 53%for the optimized Cu–SH catalyst,representing a significant enhancement compared to the pristine Cu NWs(30%).In-situ characterizations and theoretical calculations demonstrate that the different terminal groups of the grafted octadecyl chains can effectively regulate the charge density of Cu NWs interface and change the adsorption configuration of*CO intermediate.The top-adsorbed*CO intermediates(*COtop)on Cu–SH catalytic interface endow Cu–SH with the highest charge density,which effectively lowers the reaction energy barrier for*CO-*CO coupling,promoting the formation of the*OCCO intermediate,thereby enhancing the selectivity towards C_(2)H_(4).This study provides a promising method for designing efficient Cu-based catalysts with high catalytic activity and selectivity towards C2H4.展开更多
We are deeply interested in the recent findings onβ-arrestin 2.Liu et al demonstrated thatβ-arrestin 2 knockout provides significant protection in diabetic nephropathy,underscoring its potential as a promising thera...We are deeply interested in the recent findings onβ-arrestin 2.Liu et al demonstrated thatβ-arrestin 2 knockout provides significant protection in diabetic nephropathy,underscoring its potential as a promising therapeutic target for diabetic nephropathy treatment.Furthermore,the role ofβ-arrestin 2 in metabolic regulation is equally critical,particularly in insulin signaling,hepatic glucose production,and adipose tissue function.Althoughβ-arrestin 2 plays a distinct role in metabolism and kidney protection,its tissue-specific regulation opens up valuable avenues for developing targeted therapeutic strategies centered onβ-arrestin 2.展开更多
Rechargeable lithium-carbon dioxide(Li-CO_(2))batteries have emerged as a highly promising approach to simultaneously address energy shortages and the greenhouse effect.However,certain limitations exist in Li-CO_(2)ba...Rechargeable lithium-carbon dioxide(Li-CO_(2))batteries have emerged as a highly promising approach to simultaneously address energy shortages and the greenhouse effect.However,certain limitations exist in Li-CO_(2)batteries like high charge overpotential and unstable Li metal interface,which adversely affect the energy efficiency and cycling life.The incorporation of soluble redox mediators(RMs)has proven effective in enhancing the charge transfer between lithium carbonate(Li_(2)CO_(3))and cathode,thereby substantially reducing the charge overpotential.Nevertheless,the severe shuttle effect of RMs results in the reactions with Li anode,not only exacerbating the corrosion of Li anode but also leading to the depletion of RMs and electrical energy efficiency.In this work,an organic compound containing large cation group,1-ethyl-3-methylimidazole bromide(EMIBr)is proposed as the defense donor RM for Li anode in Li-CO_(2)batteries to address the above problems simultaneously.During charging,Li_(2)CO_(3)oxidation kinetics can be accelerated by bromide anion pair(Br_(3)^(−)/Br^(−)).Meanwhile,the cations(EMI^(+))are preferentially adsorbed around the protruding tips of Li anode through electrostatic interaction driven by surface free energy,forming protective layers that effectively inhibit further Li deposition at these tips,which is verified by DFT calculations.Additionally,Li dendrites growth is inhibited by the electrostatic repulsion of polar groups in EMIBr,resulting in uniform Li deposition.Consequently,a lower overpotential(∼1.17 V)and a longer cycle life(∼200 cycles)have been obtained for Li-CO_(2)battery incorporating EMIBr.展开更多
Carbon dioxide(CO_(2))is the predominant greenhouse gas in the Earth’s atmosphere and plays a crucial role in global warming.Given the inherent limitations of monoethanolamine absorbents in current commercial large-s...Carbon dioxide(CO_(2))is the predominant greenhouse gas in the Earth’s atmosphere and plays a crucial role in global warming.Given the inherent limitations of monoethanolamine absorbents in current commercial large-scale CO_(2)capture applications,amino acid ionic liquids(AAILs)have garnered extensive interest in this field due to their adjustable structure,low volatility,high thermal stability,and significant absorption capacity.However,the number of comprehensive reviews recently published on the CO_(2)absorption by AAILs remains limited.In addition,researchers have differing opinions on the AAILs/CO_(2)reaction mechanisms.Therefore,this review provides a thorough overview of the reaction mechanisms and structure-activity relationships associated with AAILs for CO_(2)capture.Moreover,it outlines the research advancements in pure AAILs and their mixtures,including aqueous AAILs and AAIL-organic solvent mixtures.The effects of varying ionic structures and additives on the absorption properties of AAILs are examined in detail.In conclusion,although AAILs exhibit high CO_(2)absorption loading and possess numerous appealing characteristics,further research is essential to comprehensively evaluate their viability for large-scale CO_(2)capture from flue gas.展开更多
Herein,the effect of the Ru:Ni bimetallic composition in dual-function materials(DFMs)for the integrated CO_(2)capture and methanation process(ICCU-Methanation)is systematically evaluated and combined with a thorough ...Herein,the effect of the Ru:Ni bimetallic composition in dual-function materials(DFMs)for the integrated CO_(2)capture and methanation process(ICCU-Methanation)is systematically evaluated and combined with a thorough material characterization,as well as a mechanistic(in-situ diffuse reflectance infrared fourier-transform spectroscopy(in-situ DRIFTS))and computational(computational fluid dynamics(CFD)modelling)investigation,in order to improve the performance of Ni-based DFMs.The bimetallic DFMs are comprised of a main Ni active metallic phase(20 wt%)and are modified with low Ru loadings in the 0.1-1 wt%range(to keep the material cost low),supported on Na_(2)O/Al_(2)O_(3).It is shown that the addition of even a very low Ru loading(0.1-0.2 wt%)can drastically improve the material reducibility,exposing a significantly higher amount of surface-active metallic sites,with Ru being highly dispersed over the support and the Ni phase,while also forming some small Ru particles.This manifests in a significant enhancement in the CH_(4)yield and the CH_(4)production kinetics during ICCU-Methanation(which mainly proceeds via formate intermediates),with 0.2 wt%Ru addition leading to the best results.This bimetallic DFM also shows high stability and a relatively good performance under an oxidizing CO_(2)capture atmosphere.The formation rate of CH_(4)during hydrogenation is then further validated via CFD modelling and the developed model is subsequently applied in the prediction of the effect of other parameters,including the inlet H_(2)concentration,inlet flow rate,dual-fu nction material weight,and reactor internal diameter.展开更多
A meticulous design of the local environment at the interface between active species and the support,aimed at optimizing the adsorption of H_(2)O molecules and BH_(4)^(-)anion,offers an ideal strategy for enhancing hy...A meticulous design of the local environment at the interface between active species and the support,aimed at optimizing the adsorption of H_(2)O molecules and BH_(4)^(-)anion,offers an ideal strategy for enhancing hydrogen generation via Na BH4hydrolysis through dual activation pathways.Theoretical predictions based on d-band center analysis and electron transfer calculations suggest that introducing-OH functional groups induce charge redistribution,enhancing charge concentration on alk-Ti_(3)C_(2)and facilitating the adsorption and activation of dual active species,H2O molecules and BH4-anion.Inspired by these predictions,the optimized alk-Ti_(3)C_(2)/Ru Oxcatalyst demonstrates the highest catalytic activity,achieving a hydrogen generation rate(HGR)of 9468 m L min^(-1)gcat.^(-1).Both experimental data and theoretical analyses confirm that the-OH functional groups promote charge enrichment on alk-Ti_(3)C_(2),optimizing the adsorption of H_(2)O molecules and BH_(4)^(-)anion,and reducing the dissociation energy barrier of the*OH–H-TS intermediate.This dual activation pathways mechanism lowers the activation energy for Na BH4hydrolysis,significantly enhancing the HGR performance.These findings,guided by theoretical insights,establish alk-Ti_(3)C_(2)/Ru Oxas an efficient catalyst for Na BH4hydrolysis and provide a strong foundation for future hydrogen generation catalyst designs.展开更多
Amorphous bimetallic borides,as a new generation of catalytic nanomaterials with modifiable electronic properties,are of great importance in the design of high-efficiency catalysts for NaBH_(4) hydrolysis.This study s...Amorphous bimetallic borides,as a new generation of catalytic nanomaterials with modifiable electronic properties,are of great importance in the design of high-efficiency catalysts for NaBH_(4) hydrolysis.This study synthesizes an amorphous Co_(3)B-Mo_(2)B_(5) catalyst using a self-sacrificial template strategy and NaBH_(4) reduction for both NaBH_(4) hydrolysis and the reduction of 4-nitrophenol.The catalyst delivers an impressive hydrogen generation rate of 7690.5 mL min^(-1) g^(-1) at 25℃,coupled with a rapid reaction rate of 0.701 min^(-1) in the reduction of 4-nitrophenol.The enhanced catalytic performance is attributed to the unique amorphous structure and the electron rearrangement between Co_(3)B and Mo_(2)B_(5).Experimental and theoretical analyses suggest electron transfer from Co_(3)B to the Mo_(2)B_(5),with the electron-deficient Co_(3)B site favoring BH_(4)^(-) adsorption,while the electron-rich Mo_(2)B_(5) site favoring H_(2)O adsorption,Furthermore,Co_(3)B-Mo_(2)B_(5) demonstrated potential for energy applications,delivering a power output of 0.3 V in a hydrogen-air fuel cell.展开更多
目的探讨三酰甘油葡萄糖乘积(triglyceride-glucose index,TyG)指数和血浆致动脉粥样硬化指数(atherogenic index of plasma,AIP)与老年冠心病(coronary heart disease,CHD)合并2型糖尿病(type 2 diabetes mellitus,T2DM)患者冠状动脉...目的探讨三酰甘油葡萄糖乘积(triglyceride-glucose index,TyG)指数和血浆致动脉粥样硬化指数(atherogenic index of plasma,AIP)与老年冠心病(coronary heart disease,CHD)合并2型糖尿病(type 2 diabetes mellitus,T2DM)患者冠状动脉正性重构的关系。方法按照住院先后顺序选取2022年1月至2023年6月河南科技大学第一附属医院心血管内科收治的老年CHD合并T2DM患者120例,根据重构指数分为正性重构组47例和非正性重构组73例。比较2组临床资料;采用多因素logistic回归分析冠状动脉正性重构的危险因素;采用Spearman相关性分析TyG和AIP与冠状动脉正性重构的相关性;采用ROC曲线分析TyG和AIP对冠状动脉正性重构的预测价值。结果正性重构组吸烟、三酰甘油、糖化血红蛋白、TyG、AIP显著高于非正性重构组,高密度脂蛋白胆固醇、血钙水平显著低于非正性重构组(P<0.05,P<0.01)。单因素logistic回归分析显示,吸烟、三酰甘油、高密度脂蛋白胆固醇、糖化血红蛋白、血钙、TyG、AIP是老年CHD合并T2DM患者冠状动脉正性重构的危险因素(P<0.05,P<0.01)。多因素logistic回归分析显示,TyG(OR=7.253,95%CI:2.458~13.364,P=0.035)、AIP(OR=6.017,95%CI:2.205~12.025,P=0.030)是老年CHD合并T2DM患者冠状动脉正性重构的独立危险因素(P<0.05)。TyG、AIP预测老年CHD合并T2DM患者冠状动脉正性重构的曲线下面积分别为0.783、0.766,联合预测老年CHD合并T2DM患者冠状动脉正性重构的曲线下面积为0.868,显著优于单独预测(P<0.05)。结论TyG和AIP与老年CHD合并T2DM患者冠状动脉正性重构密切相关,可作为预测冠状动脉正性重构的有效指标,对临床早期识别高危患者及制定个体化干预策略具有重要意义。展开更多
基金financially supported by the National Natural Science Foundation of China (51972101)the Research platforms and projects of Guangdong Universities in 2022 (2022ZDZX1028)Guangdong Provincial Key Laboratory Project (2023KSYS003)。
文摘High-performance perovskite photodetectors with self-driven characteristic usually need electron/hole transport layers to extract carriers. However, these devices with transport layer structure are prone to result in a poor perovskite/transport layer interface, which restricts the performance and stability of the device. To solve this problem, this work reports a novel device structure in which perovskite nanowires are in-situ prepared on PbI_(2), which serves as both a reaction raw material and efficient carrier extraction layer. By optimizing the thickness of PbI_(2), nanowire growth time, and ion exchange time, a selfdriven photodetector with an ITO/PbI_(2)/CsPbBr_(3)/carbon structure is constructed. The optimized device achieves excellent performance with the responsivity of 0.33 A/W, the detectivity of as high as 3.52 × 10^(13) Jones. Furthermore, the device can detect the light with its optical power lowered to 0.1 nW/cm^(2). This research provides a new method for preparing perovskite nano/micro devices with simple structure but excellent performance.
文摘Electrochemical reduction of carbon dioxide(CO_(2)RR)is a promising approach to complete the carbon cycle and potentially convert CO_(2)into valuable chemicals and fuels.Cu is unique among transition metals in its ability to catalyze the CO_(2)RR and produce multi-carbon products.However,achieving high selectivity for C2+products is challenging for copper-based catalysts,as C–C coupling reactions proceed slowly.Herein,a surface modification strategy involving grafting long alkyl chains onto copper nanowires(Cu NWs)has been proposed to regulate the electronic structure of Cu surface,which facilitates*CO-*CO coupling in the CO_(2)RR.The hydrophobicity of the catalysts increases greatly after the introduction of long alkyl chains,therefore the hydrogen evolution reaction(HER)has been inhibited effectively.Such surface modification approach proves to be highly efficient and universal,with the Faradaic efficiency(FE)of C_(2)H_(4) up to 53%for the optimized Cu–SH catalyst,representing a significant enhancement compared to the pristine Cu NWs(30%).In-situ characterizations and theoretical calculations demonstrate that the different terminal groups of the grafted octadecyl chains can effectively regulate the charge density of Cu NWs interface and change the adsorption configuration of*CO intermediate.The top-adsorbed*CO intermediates(*COtop)on Cu–SH catalytic interface endow Cu–SH with the highest charge density,which effectively lowers the reaction energy barrier for*CO-*CO coupling,promoting the formation of the*OCCO intermediate,thereby enhancing the selectivity towards C_(2)H_(4).This study provides a promising method for designing efficient Cu-based catalysts with high catalytic activity and selectivity towards C2H4.
基金Supported by National Natural Science Foundation of China,No.82471616,No.82170418,and No.82271618Natural Science Foundation of Hubei Province,No.2022CFA015+2 种基金Central Guiding Local Science and Technology Development Project,No.2022BGE237Key Research and Development Program of Hubei Province,No.2022BCE001,and No.2023BCB139Hubei Provincial Health Commission Project,No.WJ2023M151。
文摘We are deeply interested in the recent findings onβ-arrestin 2.Liu et al demonstrated thatβ-arrestin 2 knockout provides significant protection in diabetic nephropathy,underscoring its potential as a promising therapeutic target for diabetic nephropathy treatment.Furthermore,the role ofβ-arrestin 2 in metabolic regulation is equally critical,particularly in insulin signaling,hepatic glucose production,and adipose tissue function.Althoughβ-arrestin 2 plays a distinct role in metabolism and kidney protection,its tissue-specific regulation opens up valuable avenues for developing targeted therapeutic strategies centered onβ-arrestin 2.
基金financially supported by National Natural Science Foundation of China(No.22075171).
文摘Rechargeable lithium-carbon dioxide(Li-CO_(2))batteries have emerged as a highly promising approach to simultaneously address energy shortages and the greenhouse effect.However,certain limitations exist in Li-CO_(2)batteries like high charge overpotential and unstable Li metal interface,which adversely affect the energy efficiency and cycling life.The incorporation of soluble redox mediators(RMs)has proven effective in enhancing the charge transfer between lithium carbonate(Li_(2)CO_(3))and cathode,thereby substantially reducing the charge overpotential.Nevertheless,the severe shuttle effect of RMs results in the reactions with Li anode,not only exacerbating the corrosion of Li anode but also leading to the depletion of RMs and electrical energy efficiency.In this work,an organic compound containing large cation group,1-ethyl-3-methylimidazole bromide(EMIBr)is proposed as the defense donor RM for Li anode in Li-CO_(2)batteries to address the above problems simultaneously.During charging,Li_(2)CO_(3)oxidation kinetics can be accelerated by bromide anion pair(Br_(3)^(−)/Br^(−)).Meanwhile,the cations(EMI^(+))are preferentially adsorbed around the protruding tips of Li anode through electrostatic interaction driven by surface free energy,forming protective layers that effectively inhibit further Li deposition at these tips,which is verified by DFT calculations.Additionally,Li dendrites growth is inhibited by the electrostatic repulsion of polar groups in EMIBr,resulting in uniform Li deposition.Consequently,a lower overpotential(∼1.17 V)and a longer cycle life(∼200 cycles)have been obtained for Li-CO_(2)battery incorporating EMIBr.
基金supported by the Natural Science Foundation of Shanghai(Grant No.24ZR1426200)the support from the Key Program of the National Natural Science Foundation of China(Grant No.52236004)。
文摘Carbon dioxide(CO_(2))is the predominant greenhouse gas in the Earth’s atmosphere and plays a crucial role in global warming.Given the inherent limitations of monoethanolamine absorbents in current commercial large-scale CO_(2)capture applications,amino acid ionic liquids(AAILs)have garnered extensive interest in this field due to their adjustable structure,low volatility,high thermal stability,and significant absorption capacity.However,the number of comprehensive reviews recently published on the CO_(2)absorption by AAILs remains limited.In addition,researchers have differing opinions on the AAILs/CO_(2)reaction mechanisms.Therefore,this review provides a thorough overview of the reaction mechanisms and structure-activity relationships associated with AAILs for CO_(2)capture.Moreover,it outlines the research advancements in pure AAILs and their mixtures,including aqueous AAILs and AAIL-organic solvent mixtures.The effects of varying ionic structures and additives on the absorption properties of AAILs are examined in detail.In conclusion,although AAILs exhibit high CO_(2)absorption loading and possess numerous appealing characteristics,further research is essential to comprehensively evaluate their viability for large-scale CO_(2)capture from flue gas.
基金support of this work by the project“Development of new innovative low carbon energy technologies to improve excellence in the Region of Western Macedonia”(MIS 5047197),which is implemented under the Action“Reinforcement of the Research and Innovation Infrastructure”funded by the Operational Program“Competitiveness,Entrepreneurship and Innovation”(NSRF 2014-2020)co-financed by Greece and the European Union(European Regional Development Fund)+4 种基金the Hellenic Foundation for Research and Innovation(HFRI)for supporting this research work under the 3~(rd)Call for HFRI PhD Fellowships(Fellowship Number:6033)the support of ELECMI-LMA nodeNanbiosis ICTSsfunded by the Swiss National Science Foundation(Grant:206021_189629)the Research Council of Norway(Grant:296087)。
文摘Herein,the effect of the Ru:Ni bimetallic composition in dual-function materials(DFMs)for the integrated CO_(2)capture and methanation process(ICCU-Methanation)is systematically evaluated and combined with a thorough material characterization,as well as a mechanistic(in-situ diffuse reflectance infrared fourier-transform spectroscopy(in-situ DRIFTS))and computational(computational fluid dynamics(CFD)modelling)investigation,in order to improve the performance of Ni-based DFMs.The bimetallic DFMs are comprised of a main Ni active metallic phase(20 wt%)and are modified with low Ru loadings in the 0.1-1 wt%range(to keep the material cost low),supported on Na_(2)O/Al_(2)O_(3).It is shown that the addition of even a very low Ru loading(0.1-0.2 wt%)can drastically improve the material reducibility,exposing a significantly higher amount of surface-active metallic sites,with Ru being highly dispersed over the support and the Ni phase,while also forming some small Ru particles.This manifests in a significant enhancement in the CH_(4)yield and the CH_(4)production kinetics during ICCU-Methanation(which mainly proceeds via formate intermediates),with 0.2 wt%Ru addition leading to the best results.This bimetallic DFM also shows high stability and a relatively good performance under an oxidizing CO_(2)capture atmosphere.The formation rate of CH_(4)during hydrogenation is then further validated via CFD modelling and the developed model is subsequently applied in the prediction of the effect of other parameters,including the inlet H_(2)concentration,inlet flow rate,dual-fu nction material weight,and reactor internal diameter.
基金supported by the Hebei province Natural Science Foundation(No.B2023108012)the Science Research Project of Hebei Education Department(No.BJK2024137)+2 种基金the S&T Program of Xingtai(No.2023ZZ096)the National Natural Science Foundation of China(No.62004143)the Key R&D Program of Hubei Province(No.2022BAA084)。
文摘A meticulous design of the local environment at the interface between active species and the support,aimed at optimizing the adsorption of H_(2)O molecules and BH_(4)^(-)anion,offers an ideal strategy for enhancing hydrogen generation via Na BH4hydrolysis through dual activation pathways.Theoretical predictions based on d-band center analysis and electron transfer calculations suggest that introducing-OH functional groups induce charge redistribution,enhancing charge concentration on alk-Ti_(3)C_(2)and facilitating the adsorption and activation of dual active species,H2O molecules and BH4-anion.Inspired by these predictions,the optimized alk-Ti_(3)C_(2)/Ru Oxcatalyst demonstrates the highest catalytic activity,achieving a hydrogen generation rate(HGR)of 9468 m L min^(-1)gcat.^(-1).Both experimental data and theoretical analyses confirm that the-OH functional groups promote charge enrichment on alk-Ti_(3)C_(2),optimizing the adsorption of H_(2)O molecules and BH_(4)^(-)anion,and reducing the dissociation energy barrier of the*OH–H-TS intermediate.This dual activation pathways mechanism lowers the activation energy for Na BH4hydrolysis,significantly enhancing the HGR performance.These findings,guided by theoretical insights,establish alk-Ti_(3)C_(2)/Ru Oxas an efficient catalyst for Na BH4hydrolysis and provide a strong foundation for future hydrogen generation catalyst designs.
基金supported by the National Natural Science Foundation of China(Nos.52363028,21965005)Natural Science Foundation of Guangxi(Nos.2021GXNSFAA076001,2018GXNSFAA294077)Guangxi Technology Base and Talent Subject(Nos.GUIKE AD23023004,GUIKE AD20297039)。
文摘Amorphous bimetallic borides,as a new generation of catalytic nanomaterials with modifiable electronic properties,are of great importance in the design of high-efficiency catalysts for NaBH_(4) hydrolysis.This study synthesizes an amorphous Co_(3)B-Mo_(2)B_(5) catalyst using a self-sacrificial template strategy and NaBH_(4) reduction for both NaBH_(4) hydrolysis and the reduction of 4-nitrophenol.The catalyst delivers an impressive hydrogen generation rate of 7690.5 mL min^(-1) g^(-1) at 25℃,coupled with a rapid reaction rate of 0.701 min^(-1) in the reduction of 4-nitrophenol.The enhanced catalytic performance is attributed to the unique amorphous structure and the electron rearrangement between Co_(3)B and Mo_(2)B_(5).Experimental and theoretical analyses suggest electron transfer from Co_(3)B to the Mo_(2)B_(5),with the electron-deficient Co_(3)B site favoring BH_(4)^(-) adsorption,while the electron-rich Mo_(2)B_(5) site favoring H_(2)O adsorption,Furthermore,Co_(3)B-Mo_(2)B_(5) demonstrated potential for energy applications,delivering a power output of 0.3 V in a hydrogen-air fuel cell.
文摘目的探讨三酰甘油葡萄糖乘积(triglyceride-glucose index,TyG)指数和血浆致动脉粥样硬化指数(atherogenic index of plasma,AIP)与老年冠心病(coronary heart disease,CHD)合并2型糖尿病(type 2 diabetes mellitus,T2DM)患者冠状动脉正性重构的关系。方法按照住院先后顺序选取2022年1月至2023年6月河南科技大学第一附属医院心血管内科收治的老年CHD合并T2DM患者120例,根据重构指数分为正性重构组47例和非正性重构组73例。比较2组临床资料;采用多因素logistic回归分析冠状动脉正性重构的危险因素;采用Spearman相关性分析TyG和AIP与冠状动脉正性重构的相关性;采用ROC曲线分析TyG和AIP对冠状动脉正性重构的预测价值。结果正性重构组吸烟、三酰甘油、糖化血红蛋白、TyG、AIP显著高于非正性重构组,高密度脂蛋白胆固醇、血钙水平显著低于非正性重构组(P<0.05,P<0.01)。单因素logistic回归分析显示,吸烟、三酰甘油、高密度脂蛋白胆固醇、糖化血红蛋白、血钙、TyG、AIP是老年CHD合并T2DM患者冠状动脉正性重构的危险因素(P<0.05,P<0.01)。多因素logistic回归分析显示,TyG(OR=7.253,95%CI:2.458~13.364,P=0.035)、AIP(OR=6.017,95%CI:2.205~12.025,P=0.030)是老年CHD合并T2DM患者冠状动脉正性重构的独立危险因素(P<0.05)。TyG、AIP预测老年CHD合并T2DM患者冠状动脉正性重构的曲线下面积分别为0.783、0.766,联合预测老年CHD合并T2DM患者冠状动脉正性重构的曲线下面积为0.868,显著优于单独预测(P<0.05)。结论TyG和AIP与老年CHD合并T2DM患者冠状动脉正性重构密切相关,可作为预测冠状动脉正性重构的有效指标,对临床早期识别高危患者及制定个体化干预策略具有重要意义。
