Distributed energy resources have been proven to be an effective and promising solution to enhance power system resilience and improve household-level reliability.In this paper,we propose a method to evaluate the reli...Distributed energy resources have been proven to be an effective and promising solution to enhance power system resilience and improve household-level reliability.In this paper,we propose a method to evaluate the reliability value of a photovoltaic(PV)energy system with a battery storage system(BSS)by considering the probability of grid outages causing household blackouts.Considering this reliability value,which is the economic profit and capital cost of PV+BSS,a simple formula is derived to calculate the optimal planning strategy.This strategy can provide household-level customers with a simple and straightforward expression for invested PV+BSS capacity.Case studies on 600 households located in eight zones of the US for the period of 2006 to 2015 demonstrate that adding the reliability value to economic profit allows households to invest in a larger PV+BSS and avoid loss of load caused by blackouts.Owing to the differences in blackout hours,households from the 8 zones express distinct willingness to install PV+BSS.The greater the probability of blackout,the greater revenue that household can get from the PV+BSS.The simulation example shows that the planning strategy obtained by proposed model has good economy in the actual operation and able to reduce the economic risk of power failure of the household users.This model can provide household with an easy and straightforward investment strategy of PV+BSS capacity.展开更多
Focusing on sustainability of water resources and ecology in the complex karst critical zone, we illustrated functions of the hydro-geochemical analysis on hydrology from the aspects of connection and interaction amon...Focusing on sustainability of water resources and ecology in the complex karst critical zone, we illustrated functions of the hydro-geochemical analysis on hydrology from the aspects of connection and interaction among hydrology–vegetation–soils/rock fractures along the karst subsurface profile. We reviewed isotopic and geochemical interpretations on tracing water sources for plant uptake, quantifying watershed outlet flow composition and residence times, and evaluating long-term evolution among climate–landscape–hydrology in the karst critical zone. In this paper, the application of the hydro-geochemical analysis on the above aspects in the karst areas of southwest China was summarized.展开更多
While enol-keto tautomerism has attracted great interest in Schiff bases and related compounds in solution and crystal states,the self-assembly of energy-unfavored keto form were scarcely investigated.Here,we report a...While enol-keto tautomerism has attracted great interest in Schiff bases and related compounds in solution and crystal states,the self-assembly of energy-unfavored keto form were scarcely investigated.Here,we report a keto-form directed self-assembly of a naphthalene-attached enantiomeric N-salicylideneanil analog L/DGG-Nap accompanied with a significantly amplified circularly polarized luminescence(CPL).It was found that LGG-Nap exists as a mixture of enol and keto form in monomer at a diluted toluene solution.The increment of the concentrations leads to the formation of predominated keto form,which subsequently triggers the self-assembly.Cryo-transmission electron microscopy(Cryo-TEM)revealed that a hierarchical assembly process happened upon increasing the concentration of LGG-Nap in toluene.Individual nanofibers formed at 1×10-4 mol/L and transferred into helical nanofiber bundles in 5×10-3 mol/L.Interestingly,while these is nearly no circular dichroism(CD)or CPL in the monomeric solution,the assembly showed strong CD and CPL.Remarkably,the dissymmetry factor(glum)was significantly amplified from zero in solution through the 0.005 in individual nanofiber to 0.1 in nanofiber bundles.This work demonstrates that the enol-keto tautomerism can be broken and trigger the self-assembly upon increasing the concentration,which can subsequently direct the chiral self-assembly and significantly amplify the dissymmetry factor of assembled CPL materials.展开更多
Temperature plays a crucial role in regulating polymorphism in supramolecular polymers.Understanding the mechanism behind temperature-dependent supramolecular polymorphism is crucial as it provides an opportunity to t...Temperature plays a crucial role in regulating polymorphism in supramolecular polymers.Understanding the mechanism behind temperature-dependent supramolecular polymorphism is crucial as it provides an opportunity to tailor polymorphs for specific properties and applications.In this study,we present our findings on a naphthalimide-substituted benzene-1,3,5-tricarboxamide derivative,R-Nap-1,which exhibits two distinct polymerization pathways at varying temperatures.At 313 K,polymerization results in the formation of an M-chiral polymorph,whereas at 253 K,a P-chiral polymorph is formed.Both polymorphs are notably stable,remaining unchanged for over six months under ambient conditions.Theoretical calculations and experimental investigations allowed us to elucidate the mechanisms underlying these polymorphic transformations.The formation of the M-chiral polymorph at 313 K is attributed to the nucleation and growth of R-Nap-1 monomers once their concentration surpasses a critical threshold.Conversely,at lower temperatures(e.g.,253 K),the monomers undergo facile transformation into dimers due to a lower energy barrier and reduced Gibbs energy compared to the monomeric state.Subsequently,these dimers undergo nucleation-elongation to form the P-chiral polymorph when their concentration exceeds the critical polymerization concentration.The stability and lack of interconversion between the two polymorphs can be attributed to their close thermodynamic stabilities,as evidenced by variable-temperature CD spectra and DFT calculations.These findings highlight the importance of accurate temperature control in supramolecular polymerization processes,making a significant contribution to the understanding of supramolecular polymorphism,thus advancing the field of supramolecular chemistry.展开更多
Construction of iridium(Ir)based active sites on certain acid stable supports now is a general strategy for the development of low-Ir OER catalysts.Atomically doped Ir in the lattice of acid stableγ-MnO_(2) has been ...Construction of iridium(Ir)based active sites on certain acid stable supports now is a general strategy for the development of low-Ir OER catalysts.Atomically doped Ir in the lattice of acid stableγ-MnO_(2) has been recently achieved,which shows high activity and stability though Ir usage was reduced more than 95%than that in current commercial proton exchange membrane water electrolyzer(PEMWE).However,the activity and stability enhancement by Ir doping inγ-MnO_(2) still remains elusive.Herein,high dispersion of iridium(up to 1.37 atom%)doping in the lattice ofγ-MnO_(2) has been achieved by optimizing the thermal decomposition of the iridium precursors.Benefiting from atomic dispersive doping of Ir,the optimized Ir-MnO_(2) catalyst shows high OER activity,as it has turnover frequency of 0.655 s^(–1) at an overpotential of 300 mV in 0.5 mol L^(-1) H_(2)SO_(4).The catalyst also shows high stability,as it can sustainably work at 100 mA cm^(-2) for 24 h.Experimental and theoretical studies reveal that Ir is preferentially doped intoβphase rather than R phase,and the Ir site is the active site for OER.The OER active site is postulated to be Ir^(5+)-O(H)-Mn^(3+)unit structure on the surface.Furthermore,Ir doping changes the potential determining step from the formation of O*to the formation of*OOH,emphasizing the promoting effect toward OER derived from Ir sites.This work not only demonstrates the possibility of achieving atomic-level doping of Ir on the surface of a support to dramatically reduce Ir usage,but also,more importantly,reveals the mechanism behind accounting for the stability and activity enhancement by Ir doping.These important findings may serve as valuable guidance for further development of more efficient,stable and cost-effective low Ir-based OER catalysts for PEMWE.展开更多
The coordination polymer poly（nickel-ethylenetetrathiolate） （poly（Ni-ett））, formed by nickel（Ⅱ） and 1,1,2,2-ethenetetrathiolate （ett）, is the most promising N-type organic thermoelectric material ever repor...The coordination polymer poly（nickel-ethylenetetrathiolate） （poly（Ni-ett））, formed by nickel（Ⅱ） and 1,1,2,2-ethenetetrathiolate （ett）, is the most promising N-type organic thermoelectric material ever reported; it is synthesized via potentiostatic deposition, and the effect of different applied potentials on the optimal performance of the polymers is investigated. The optimal thermoelectric property ofpoly（Ni-ett） synthesized at 0.6 V is remarkably greater than that of the polymers synthesized at 1 and 1.6 V, exhibiting a maximum power factor of up to 131.6μW/mK2 at 360 K. Furthermore, the structure-property correlation ofpoly（Ni-ett） is also extensively investigated. X-ray diffraction （XRD） and X-ray photoelectron spectroscopy （XPS） analyses revealed that the larger size of crystalline domains and the higher oxidation state of poly（Ni-ett） synthesized at 0.6 V possibly results in the higher bulk mobility and carrier concentration in the polymer chains, respectively, accounting for the enhanced power factor.展开更多
Glycyrrhizic acid(GA),as a traditional herbal,can self-assemble into helical nanofiber in the water.The formed helical nanostructures can be employed as scaffolds for asymmetric Diels-Alder reaction.Through co-assembl...Glycyrrhizic acid(GA),as a traditional herbal,can self-assemble into helical nanofiber in the water.The formed helical nanostructures can be employed as scaffolds for asymmetric Diels-Alder reaction.Through co-assembling with a series of achiral copper-ligands,the chirality of GA helical nanostructures can be transferred to catalytic site,and resulted assemblies showed moderated enantioselectivity toward catalysis of Diels-Alder reaction.展开更多
Thermoelectric(TE)materials can realize mutual energy conversion between heat and electricity and are applied broadly in energy harvesting,local cooling or heating,and thermal sensing[1].TE devices are crucial to solv...Thermoelectric(TE)materials can realize mutual energy conversion between heat and electricity and are applied broadly in energy harvesting,local cooling or heating,and thermal sensing[1].TE devices are crucial to solve the global energy crisis with renewable energy resources.Currently,most of the research works are focused on inorganic TE materials because of their superior performance.Very recently,due to the growing demands展开更多
Z-classified topological phases lead to a larger-than-unity number of topological states.However,these multiple topological states are only localized at the corners in nonlocal systems.Here,first,we rigorously prove t...Z-classified topological phases lead to a larger-than-unity number of topological states.However,these multiple topological states are only localized at the corners in nonlocal systems.Here,first,we rigorously prove that the multiple topological states of nonlocal Su–Schrieffer–Heeger(SSH)chains can be inherited and realized by local aperiodic chains with only the nearest couplings.Then,we report a new class of higher-order topological insulators constructed with the local aperiodic chains,which can have any integer number of 0D topological states localized at arbitrary positions in the whole domain of the insulators,including within the bulk.The 0D topological states are protected by the local topological marker in each direction,instead of the bulk multipole chiral numbers in existing work.We experimentally demonstrate these multimode topological states in designed acoustic coupled-resonators systems.Our work enables multiple combinations of localized corner-bulk topological states,which leads to programmable lasers and sasers by selecting the excitation sites without altering the structure,and thus opens a new avenue to signal enhancement for computing and sensing.展开更多
基金supported by National Natural Science Foundation of China(Project 51907064)in part by China State Key Lab.of Power System(SKLD19KM09)in part by State Grid Corporation of China(1400202024222A-0-0-00)
文摘Distributed energy resources have been proven to be an effective and promising solution to enhance power system resilience and improve household-level reliability.In this paper,we propose a method to evaluate the reliability value of a photovoltaic(PV)energy system with a battery storage system(BSS)by considering the probability of grid outages causing household blackouts.Considering this reliability value,which is the economic profit and capital cost of PV+BSS,a simple formula is derived to calculate the optimal planning strategy.This strategy can provide household-level customers with a simple and straightforward expression for invested PV+BSS capacity.Case studies on 600 households located in eight zones of the US for the period of 2006 to 2015 demonstrate that adding the reliability value to economic profit allows households to invest in a larger PV+BSS and avoid loss of load caused by blackouts.Owing to the differences in blackout hours,households from the 8 zones express distinct willingness to install PV+BSS.The greater the probability of blackout,the greater revenue that household can get from the PV+BSS.The simulation example shows that the planning strategy obtained by proposed model has good economy in the actual operation and able to reduce the economic risk of power failure of the household users.This model can provide household with an easy and straightforward investment strategy of PV+BSS capacity.
基金supported by the National Natural Scientific Foundation of China(No.41571130071)
文摘Focusing on sustainability of water resources and ecology in the complex karst critical zone, we illustrated functions of the hydro-geochemical analysis on hydrology from the aspects of connection and interaction among hydrology–vegetation–soils/rock fractures along the karst subsurface profile. We reviewed isotopic and geochemical interpretations on tracing water sources for plant uptake, quantifying watershed outlet flow composition and residence times, and evaluating long-term evolution among climate–landscape–hydrology in the karst critical zone. In this paper, the application of the hydro-geochemical analysis on the above aspects in the karst areas of southwest China was summarized.
基金National Natural Science foundation of China(Nos.21861132002,21773043,21973020 and 21890734).
文摘While enol-keto tautomerism has attracted great interest in Schiff bases and related compounds in solution and crystal states,the self-assembly of energy-unfavored keto form were scarcely investigated.Here,we report a keto-form directed self-assembly of a naphthalene-attached enantiomeric N-salicylideneanil analog L/DGG-Nap accompanied with a significantly amplified circularly polarized luminescence(CPL).It was found that LGG-Nap exists as a mixture of enol and keto form in monomer at a diluted toluene solution.The increment of the concentrations leads to the formation of predominated keto form,which subsequently triggers the self-assembly.Cryo-transmission electron microscopy(Cryo-TEM)revealed that a hierarchical assembly process happened upon increasing the concentration of LGG-Nap in toluene.Individual nanofibers formed at 1×10-4 mol/L and transferred into helical nanofiber bundles in 5×10-3 mol/L.Interestingly,while these is nearly no circular dichroism(CD)or CPL in the monomeric solution,the assembly showed strong CD and CPL.Remarkably,the dissymmetry factor(glum)was significantly amplified from zero in solution through the 0.005 in individual nanofiber to 0.1 in nanofiber bundles.This work demonstrates that the enol-keto tautomerism can be broken and trigger the self-assembly upon increasing the concentration,which can subsequently direct the chiral self-assembly and significantly amplify the dissymmetry factor of assembled CPL materials.
基金supported by the Chinese Academy of Sciences CAS Project for Young Scientists in Basic Research(No.YSBR-027)。
文摘Temperature plays a crucial role in regulating polymorphism in supramolecular polymers.Understanding the mechanism behind temperature-dependent supramolecular polymorphism is crucial as it provides an opportunity to tailor polymorphs for specific properties and applications.In this study,we present our findings on a naphthalimide-substituted benzene-1,3,5-tricarboxamide derivative,R-Nap-1,which exhibits two distinct polymerization pathways at varying temperatures.At 313 K,polymerization results in the formation of an M-chiral polymorph,whereas at 253 K,a P-chiral polymorph is formed.Both polymorphs are notably stable,remaining unchanged for over six months under ambient conditions.Theoretical calculations and experimental investigations allowed us to elucidate the mechanisms underlying these polymorphic transformations.The formation of the M-chiral polymorph at 313 K is attributed to the nucleation and growth of R-Nap-1 monomers once their concentration surpasses a critical threshold.Conversely,at lower temperatures(e.g.,253 K),the monomers undergo facile transformation into dimers due to a lower energy barrier and reduced Gibbs energy compared to the monomeric state.Subsequently,these dimers undergo nucleation-elongation to form the P-chiral polymorph when their concentration exceeds the critical polymerization concentration.The stability and lack of interconversion between the two polymorphs can be attributed to their close thermodynamic stabilities,as evidenced by variable-temperature CD spectra and DFT calculations.These findings highlight the importance of accurate temperature control in supramolecular polymerization processes,making a significant contribution to the understanding of supramolecular polymorphism,thus advancing the field of supramolecular chemistry.
文摘Construction of iridium(Ir)based active sites on certain acid stable supports now is a general strategy for the development of low-Ir OER catalysts.Atomically doped Ir in the lattice of acid stableγ-MnO_(2) has been recently achieved,which shows high activity and stability though Ir usage was reduced more than 95%than that in current commercial proton exchange membrane water electrolyzer(PEMWE).However,the activity and stability enhancement by Ir doping inγ-MnO_(2) still remains elusive.Herein,high dispersion of iridium(up to 1.37 atom%)doping in the lattice ofγ-MnO_(2) has been achieved by optimizing the thermal decomposition of the iridium precursors.Benefiting from atomic dispersive doping of Ir,the optimized Ir-MnO_(2) catalyst shows high OER activity,as it has turnover frequency of 0.655 s^(–1) at an overpotential of 300 mV in 0.5 mol L^(-1) H_(2)SO_(4).The catalyst also shows high stability,as it can sustainably work at 100 mA cm^(-2) for 24 h.Experimental and theoretical studies reveal that Ir is preferentially doped intoβphase rather than R phase,and the Ir site is the active site for OER.The OER active site is postulated to be Ir^(5+)-O(H)-Mn^(3+)unit structure on the surface.Furthermore,Ir doping changes the potential determining step from the formation of O*to the formation of*OOH,emphasizing the promoting effect toward OER derived from Ir sites.This work not only demonstrates the possibility of achieving atomic-level doping of Ir on the surface of a support to dramatically reduce Ir usage,but also,more importantly,reveals the mechanism behind accounting for the stability and activity enhancement by Ir doping.These important findings may serve as valuable guidance for further development of more efficient,stable and cost-effective low Ir-based OER catalysts for PEMWE.
基金supported by the National Basic Research Program of China (2013CB632506)the Strategic Priority Research Program of the Chinese Academy of Sciences (XDB12000000)+1 种基金Key Project of National Natural Science Foundation of China (51336009)National Natural Science Foundation of China (21290191, 21333011)
文摘The coordination polymer poly（nickel-ethylenetetrathiolate） （poly（Ni-ett））, formed by nickel（Ⅱ） and 1,1,2,2-ethenetetrathiolate （ett）, is the most promising N-type organic thermoelectric material ever reported; it is synthesized via potentiostatic deposition, and the effect of different applied potentials on the optimal performance of the polymers is investigated. The optimal thermoelectric property ofpoly（Ni-ett） synthesized at 0.6 V is remarkably greater than that of the polymers synthesized at 1 and 1.6 V, exhibiting a maximum power factor of up to 131.6μW/mK2 at 360 K. Furthermore, the structure-property correlation ofpoly（Ni-ett） is also extensively investigated. X-ray diffraction （XRD） and X-ray photoelectron spectroscopy （XPS） analyses revealed that the larger size of crystalline domains and the higher oxidation state of poly（Ni-ett） synthesized at 0.6 V possibly results in the higher bulk mobility and carrier concentration in the polymer chains, respectively, accounting for the enhanced power factor.
基金the National Natural Science Foundation of China(Nos.21861132002,21773043)Chinese Academy of Sciences(Nos.XDB12020200,QYZDJ-SSW-SLH044)for the financial support
文摘Glycyrrhizic acid(GA),as a traditional herbal,can self-assemble into helical nanofiber in the water.The formed helical nanostructures can be employed as scaffolds for asymmetric Diels-Alder reaction.Through co-assembling with a series of achiral copper-ligands,the chirality of GA helical nanostructures can be transferred to catalytic site,and resulted assemblies showed moderated enantioselectivity toward catalysis of Diels-Alder reaction.
基金supported by the National Basic Research Program of China(2013CB632506)the Strategic Priority Research Program of the Chinese Academy of Sciences(XDB12000000)+1 种基金the National Natural Science Foundation of China(21333011)Chinese Academy of Sciences(QYZDY-SSW-SLH024)
文摘Thermoelectric(TE)materials can realize mutual energy conversion between heat and electricity and are applied broadly in energy harvesting,local cooling or heating,and thermal sensing[1].TE devices are crucial to solve the global energy crisis with renewable energy resources.Currently,most of the research works are focused on inorganic TE materials because of their superior performance.Very recently,due to the growing demands
基金National Natural Science Foundation of China(11991033,11890681,and 12232001).
文摘Z-classified topological phases lead to a larger-than-unity number of topological states.However,these multiple topological states are only localized at the corners in nonlocal systems.Here,first,we rigorously prove that the multiple topological states of nonlocal Su–Schrieffer–Heeger(SSH)chains can be inherited and realized by local aperiodic chains with only the nearest couplings.Then,we report a new class of higher-order topological insulators constructed with the local aperiodic chains,which can have any integer number of 0D topological states localized at arbitrary positions in the whole domain of the insulators,including within the bulk.The 0D topological states are protected by the local topological marker in each direction,instead of the bulk multipole chiral numbers in existing work.We experimentally demonstrate these multimode topological states in designed acoustic coupled-resonators systems.Our work enables multiple combinations of localized corner-bulk topological states,which leads to programmable lasers and sasers by selecting the excitation sites without altering the structure,and thus opens a new avenue to signal enhancement for computing and sensing.
