Sodium-ion batteries are considered as a promising candidate for lithium-ion batteries due to abundant sodium resources and similar intercalation chemistry.Hard carbon derived from biomass with the virtue of abundance...Sodium-ion batteries are considered as a promising candidate for lithium-ion batteries due to abundant sodium resources and similar intercalation chemistry.Hard carbon derived from biomass with the virtue of abundance and renewability is a cost-effective anode material.Herein,hard carbon is derived from renewable bagasse through a simple two-step method combining mechanical ball milling with carbonization.The hard carbon electrodes exhibit superior electrochemical performance with a high reversible capacity of 315 mA∙h/g.Furthermore,the initial capacity of the full cell,HC//NaMn0.4Ni0.4Ti0.1Mg0.1O2,is 253 mA∙h/g and its capacity retention rate is 77%after 80 cycles,which further verifies its practical application.The simple and low-cost preparation process,as well as excellent electrochemical properties,demonstrates that hard carbon derived from bagasse is a promising anode for sodium-ion batteries.展开更多
Pt monolayer-based core-shell catalysts have garnered significant interest for the application of low temperature fuel cell technology as their use may enable a decreased loading of Pt while still providing sufficient...Pt monolayer-based core-shell catalysts have garnered significant interest for the application of low temperature fuel cell technology as their use may enable a decreased loading of Pt while still providing sufficient current density to meet volumetric requirements. One promising candidate in this class of materials is a Pd@Pt core-shell catalyst, which shows enhanced activity toward oxygen reduction reaction(ORR). One concern with the use of Pd@Pt, however, is the durability of the core-shell structure as Pd atoms are thermodynamically favored to migrate to the surface. The pathway of the migration has not been systematically studied. The current study explores the stability of this structure to thermal annealing and probes the effect of this heat treatment on the catalyst surface structure and its oxygen reduction activity. It was found that surface alloying between Pd and Pt occurs at temperatures as low as 200 °C, and significantly alters the structure and ORR catalytic activity in the range of 200–300 °C. Our results shed lights on the thermal induced interatomic diffusion in all core-shell and thin film structures.展开更多
In order to optimize and select the appropriate binder to improve the electrochemical performance of aqueous zinc-manganese batteries,the influences of water-soluble binders and oil-based binders on the zinc storage p...In order to optimize and select the appropriate binder to improve the electrochemical performance of aqueous zinc-manganese batteries,the influences of water-soluble binders and oil-based binders on the zinc storage performance of manganese-based cathode materials were systematically investigated.The results show that the water-soluble binders with large numbers of hydroxyl and carboxyl groups are easily soluble in aqueous electrolytes,leading to poor electrochemical performance.Fortunately,the cathodes with polyvinylidene fluoride-hexafluoropropylene(PVDF-HFP)binder display high specific capacity of 264.9 mA·h/g and good capacity retention of 92%after 90 cycles at 100 mA/g.Meanwhile,PVDF-HFP binder with plenty of hydrophobic groups presents excellent ability in inhibiting cracks on the surface of electrode,reducing voltage polarization and charge transfer resistance,as well as maintaining electrode integrity.展开更多
The synthesis of Al2O3-coated and uncoated LiMn2O4 by solid-state method and fabrication of LiMn2O4/graphite battery were described. The structure and morphology of the powders were characterized by X-ray diffraction ...The synthesis of Al2O3-coated and uncoated LiMn2O4 by solid-state method and fabrication of LiMn2O4/graphite battery were described. The structure and morphology of the powders were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM), respectively. The electrochemical and overcharge performances of Al2O3-coated and uncoated LiMn2O4 batteries were investigated and compared. The uncoated LiMn2O4 battery shows capacity loss of 16.5% after 200 cycles, and the coated LiMn2O4 battery only shows 12.5% after 200 cycles. The uncoated LiMn2O4 battery explodes and creates carbon, MnO, and Li2CO3 after 3C/10 V overcharged test, while the coated LiMn2O4 battery passes the test. The steadier structure, polarization of electrode and modified layer are responsible for the safety performance.展开更多
Mesoporous TiO_2-B/anatase microparticles have been in-situ synthesized from K_2Ti_2O_5 without template.The TiO_2-B phase around the particle surface accelerates the diffusion of charges through the interface,while t...Mesoporous TiO_2-B/anatase microparticles have been in-situ synthesized from K_2Ti_2O_5 without template.The TiO_2-B phase around the particle surface accelerates the diffusion of charges through the interface,while the anatase phase in the core maintains the capacity stability.The heterojunction interface between the main polymorph of anatase and the trace of TiO_2-B exhibits promising lithium ion battery performance.This trace of 5%(by mass) TiO_2-B determined by Raman spectra brings the first discharge capacity of this material to 247 mA · h ·g^(-1),giving 20%improvement compared to the anatase counterpart Stability testing at 1 C reveals that the capacity maintains at 171 mA·h·^(-1),which is better than 162 mA·h·g^(-1) for single phase anatase or 159 mA·h·g^(-1) for TiO_2-B.The mesoporous TiO_2-B/anatase rnicroparticles also show superior rate performance with 100 mA·h·g^(-1) at 40 C,increased by nearly 25%as compared to pure anatase.This opens a possibility of a general design route,which can be applied to other metal oxide electrode materials for rechargeable batteries and supercapacitors.展开更多
High-temperature CO_(2)reduction reaction(HT-CO_(2)RR)in solid oxide electrochemical cells(SOECs)features near-unity selectivity,high energy efficiency,and industrial relevant current density for the production of CO,...High-temperature CO_(2)reduction reaction(HT-CO_(2)RR)in solid oxide electrochemical cells(SOECs)features near-unity selectivity,high energy efficiency,and industrial relevant current density for the production of CO,a widely-utilized“building block”in today’s chemical industry.Thus,it offers an intriguing and promising means to radically change the way of chemical manufacturing and achieve carbon neutrality using renewable energy sources,CO_(2),and water.Albeit with the great potential of HT-CO_(2)RR,this carbon utilization approach,unfortunately,has been suffering coke formation that is seriously detrimental to its energy efficiency and operating lifetime.In recent years,much effort has been added to understanding the mechanism of coke formation,managing reaction conditions to mitigate coke formation,and devising coke-formation-free electrode materials.These investigations have substantially advanced the HT-CO_(2)RR toward a practical industrial technology,but the resulting coke formation prevention strategies compromise activity and energy efficiency.Future research may target exploiting the control over both catalyst design and system design to gain selectivity,energy efficiency,and stability synchronously.Therefore,this perspective overviews the progress of research on coke formation in HT-CO_(2)RR,and elaborates on possible future directions that may accelerate its practical implementation at a large scale.展开更多
A flat thin TiO2 film was employed as the photo-electrode of a dye sensitized solar cell （DSSC）, on which only a geometrical mono-layer of dye was attached. The effect of sur- face protonation by HCI chemical treatm...A flat thin TiO2 film was employed as the photo-electrode of a dye sensitized solar cell （DSSC）, on which only a geometrical mono-layer of dye was attached. The effect of sur- face protonation by HCI chemical treatment on the performance of DSSCs was studied. The results showed that the short-circuit current Jsc increased significantly upon the HCI treatment, while the open-circuit voltage Voc decreased slightly. Compared to the untreated DSSC, the Jsc and energy conversion efficiency was increased by 31% and 25%, respectively, for the 1 mol/L HCI treated cell. TiO2 surface protonation improved electronic coupling between the chemisorbed dye and the TiO2 surface, resulting in an enhanced electron in- jection. The decreased open-circuit voltage after TiO2 surface protonation was mainly due to the TiO2 conduction band edge downshift and was partially caused by increased electron recombination with the electrolyte. In situ Raman degradation study showed that the dye stability was improved after the TiO2 surface protonation. The increased dye stability was contributed by the increased electron injection and electron back reaction with the electrolyte under the open-circuit condition.展开更多
NaxCoO2 is a commonly used cathode material for sodium ion batteries because of its easy synthesis, high reversible capacity and good cyclability. The structural and electrochemical properties of NaxCoO2 during sodium...NaxCoO2 is a commonly used cathode material for sodium ion batteries because of its easy synthesis, high reversible capacity and good cyclability. The structural and electrochemical properties of NaxCoO2 during sodium ion insertion/extraction process are studied based on first principles calculations. The calculation results of crystal structure parameters and average intercalation voltage are in good agreement with experiment data. Through calculation of the geometric structure and charge transfer in charging and discharging processes of NaxCoO2, it is found that the oxygen atom surrounding Co of the CoO6 octahedral screens the coulomb potential produced by sodium vacancy in NaxCoO2, and the charge is removed from the entire Co-O layer instead of the Co atom adjacent to sodium vacancy when sodium ions are extracted from the Na CoO2 lattice. Thus, during the insertion/extraction of sodium ion from Na CoO2, the CoO6 octahedral structure undergoes small lattice distortion, which makes the local structure quite stable and is beneficial to the cycling stability of the material for the application of sodium ion batteries.展开更多
Semiconducting silicon(Si)nanomaterials have great potential for the applications in electronics,physics,and energy storage fields.However,to date,it is still a challenge to realize the batch production of Si nanomate...Semiconducting silicon(Si)nanomaterials have great potential for the applications in electronics,physics,and energy storage fields.However,to date,it is still a challenge to realize the batch production of Si nanomaterials via efficient and low-cost approaches,owing to some long-standing shortcomings,e.g.,complex procedures and time and/or energy consumption.Herein,we report a green and inexpensive method to rapidly obtain two-dimensional(2D)free-standing Si/SiO_(x) nanosheets via the rapid thermal exfoliation of layered Zintl compound CaSi_(2).With the help of the rapid exfoliation reaction of CaSi_(2) in the atmosphere of greenhouse gas CO_(2),and the following mild sonication,2D free-standing Si/SiO_(x) nanosheets can be produced with very high yield.After applying the coating of a thin carbon outer layer,the electrodes of Si/SiO_(x)/C nanosheets serving as the anodes for lithium-ion batteries exhibit ultrahigh reversible capacity and outstanding electrochemical stability.We expect this study will provide new insights and inspirations for the convenient and batch production of nanostructural Si-based anode materials towards high-performance lithium-ion batteries.展开更多
The main drawbacks of vanadium oxide as a cathode material are its low conductivity, low practical capacity and poor cycling stability. Adding Cr can improve its conductivity and a metastable amorphous state may provi...The main drawbacks of vanadium oxide as a cathode material are its low conductivity, low practical capacity and poor cycling stability. Adding Cr can improve its conductivity and a metastable amorphous state may provide higher capacity and stability. In this work, metastable amorphous Cr-V-O nano- particles have been successfully prepared through a facile co-precipitation reaction followed by annealing treatment. As a cathode material for lithium batteries, the metastable amorphous Cr-V-O nanoparticles exhibit high capacity （260 mAh/g at 100 mA/g between 1.5-4 V）, low capacity loss （more than 80% was retained after 200 cycles at 100 mA/g） and high rate capability （up to 3 A/g）.展开更多
Aqueous organic flow batteries have attracted dramatic attention for stationary energy storage due to their resource sustainability and low cost. However, the current reported systems can normally be operated stably u...Aqueous organic flow batteries have attracted dramatic attention for stationary energy storage due to their resource sustainability and low cost. However, the current reported systems can normally be operated stably under a nitrogen or argon atmosphere due to their poor stability. Herein a stable airinsensitive biphenol derivative cathode, 3,30,5,50-tetramethylaminemethylene-4,40-biphenol(TABP), with high solubility(>1.5 mol L^(-1)) and redox potential(0.91 V vs. SHE) is designed and synthesized by a scalable one-step method. Paring with silicotungstic acid(SWO), an SWO/TABP flow battery shows a stable performance of zero capacity decay over 900 cycles under the air atmosphere. Further, an SWO/TABP flow battery manifests a high rate performance with an energy efficiency of 85% at a current density of60 m A cm^(-2) and a very high volumetric capacity of more than 47 Ah L^(-1). This work provides a new and practical option for next-generation practical large-scale energy storage.展开更多
The power conversion effciency(PCE)of flexible perovskite solar cells(PSCs)has increased rapidly,while the mechanical flexibility and environmental stability are still far from satisfactory.Previous studies show the e...The power conversion effciency(PCE)of flexible perovskite solar cells(PSCs)has increased rapidly,while the mechanical flexibility and environmental stability are still far from satisfactory.Previous studies show the environmental degradation and ductile cracks of perovskite films usually begin at the grain boundaries(GBs).Herein,sulfonated graphene oxide(s-GO)is employed to construct a cementitious GBs by interacting with the[Pb I6]4–at GBs.The resultant s-GO-[Pb I6]4–complex can effectively passivate the defects of vacant iodine,and the devices with s-GO exhibit remarkable waterproofness and flexibility due to the tough and water-insoluble GBs.The champion PCE of 20.56%(1.01 cm^(2))in a device treated with s-GO is achieved.This device retains 90%of its original PCE after 180 d stored in the ambient condition,as well as over 80%retention after 10,000 bending cycles at a curvature radius of 3 mm.展开更多
基金Projects(51661009,51761007)supported by the National Natural Science Foundation of China,Projects(2019GXNSFDA245014,2016GXNSFGA380001)supported by the Natural Science Foundation of Guangxi Province,China,Projects(2019AC20164,2019AC20053)supported by the Science and Technology Base and Talent Special Project of Guangxi Province,China。
文摘Sodium-ion batteries are considered as a promising candidate for lithium-ion batteries due to abundant sodium resources and similar intercalation chemistry.Hard carbon derived from biomass with the virtue of abundance and renewability is a cost-effective anode material.Herein,hard carbon is derived from renewable bagasse through a simple two-step method combining mechanical ball milling with carbonization.The hard carbon electrodes exhibit superior electrochemical performance with a high reversible capacity of 315 mA∙h/g.Furthermore,the initial capacity of the full cell,HC//NaMn0.4Ni0.4Ti0.1Mg0.1O2,is 253 mA∙h/g and its capacity retention rate is 77%after 80 cycles,which further verifies its practical application.The simple and low-cost preparation process,as well as excellent electrochemical properties,demonstrates that hard carbon derived from bagasse is a promising anode for sodium-ion batteries.
文摘Pt monolayer-based core-shell catalysts have garnered significant interest for the application of low temperature fuel cell technology as their use may enable a decreased loading of Pt while still providing sufficient current density to meet volumetric requirements. One promising candidate in this class of materials is a Pd@Pt core-shell catalyst, which shows enhanced activity toward oxygen reduction reaction(ORR). One concern with the use of Pd@Pt, however, is the durability of the core-shell structure as Pd atoms are thermodynamically favored to migrate to the surface. The pathway of the migration has not been systematically studied. The current study explores the stability of this structure to thermal annealing and probes the effect of this heat treatment on the catalyst surface structure and its oxygen reduction activity. It was found that surface alloying between Pd and Pt occurs at temperatures as low as 200 °C, and significantly alters the structure and ORR catalytic activity in the range of 200–300 °C. Our results shed lights on the thermal induced interatomic diffusion in all core-shell and thin film structures.
基金supported by the National Natural Science Foundation of China (Nos.51932011, 51972346)the Hunan Natural Science Fund for Distinguished Young Scholar, China (No. 2021JJ10064)+1 种基金the Program of Youth Talent Support for Hunan Province, China (No. 2020RC3011)the Innovation-Driven Project of Central South University, China (No. 2020CX024)
文摘In order to optimize and select the appropriate binder to improve the electrochemical performance of aqueous zinc-manganese batteries,the influences of water-soluble binders and oil-based binders on the zinc storage performance of manganese-based cathode materials were systematically investigated.The results show that the water-soluble binders with large numbers of hydroxyl and carboxyl groups are easily soluble in aqueous electrolytes,leading to poor electrochemical performance.Fortunately,the cathodes with polyvinylidene fluoride-hexafluoropropylene(PVDF-HFP)binder display high specific capacity of 264.9 mA·h/g and good capacity retention of 92%after 90 cycles at 100 mA/g.Meanwhile,PVDF-HFP binder with plenty of hydrophobic groups presents excellent ability in inhibiting cracks on the surface of electrode,reducing voltage polarization and charge transfer resistance,as well as maintaining electrode integrity.
基金Project(10JDG041) supported by the Advanced Person Fund of Jiangsu University, ChinaProject(2007CB613607) supported by the National Basic Research Program of China
文摘The synthesis of Al2O3-coated and uncoated LiMn2O4 by solid-state method and fabrication of LiMn2O4/graphite battery were described. The structure and morphology of the powders were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM), respectively. The electrochemical and overcharge performances of Al2O3-coated and uncoated LiMn2O4 batteries were investigated and compared. The uncoated LiMn2O4 battery shows capacity loss of 16.5% after 200 cycles, and the coated LiMn2O4 battery only shows 12.5% after 200 cycles. The uncoated LiMn2O4 battery explodes and creates carbon, MnO, and Li2CO3 after 3C/10 V overcharged test, while the coated LiMn2O4 battery passes the test. The steadier structure, polarization of electrode and modified layer are responsible for the safety performance.
基金Supported by the Program for Changjiang Scholars and Innovative Research Team in University(PCSIRT 0732)the National Natural Science Foundation of China(21136004,20736002,21176113,20876073)+2 种基金NSFC-RGC(20731160614)China Postdoctoral Science Foundation(20110491407)the National Basic Research Program of China(2009CB623407,2009CB219902 and 2009CB226103)
文摘Mesoporous TiO_2-B/anatase microparticles have been in-situ synthesized from K_2Ti_2O_5 without template.The TiO_2-B phase around the particle surface accelerates the diffusion of charges through the interface,while the anatase phase in the core maintains the capacity stability.The heterojunction interface between the main polymorph of anatase and the trace of TiO_2-B exhibits promising lithium ion battery performance.This trace of 5%(by mass) TiO_2-B determined by Raman spectra brings the first discharge capacity of this material to 247 mA · h ·g^(-1),giving 20%improvement compared to the anatase counterpart Stability testing at 1 C reveals that the capacity maintains at 171 mA·h·^(-1),which is better than 162 mA·h·g^(-1) for single phase anatase or 159 mA·h·g^(-1) for TiO_2-B.The mesoporous TiO_2-B/anatase rnicroparticles also show superior rate performance with 100 mA·h·g^(-1) at 40 C,increased by nearly 25%as compared to pure anatase.This opens a possibility of a general design route,which can be applied to other metal oxide electrode materials for rechargeable batteries and supercapacitors.
文摘High-temperature CO_(2)reduction reaction(HT-CO_(2)RR)in solid oxide electrochemical cells(SOECs)features near-unity selectivity,high energy efficiency,and industrial relevant current density for the production of CO,a widely-utilized“building block”in today’s chemical industry.Thus,it offers an intriguing and promising means to radically change the way of chemical manufacturing and achieve carbon neutrality using renewable energy sources,CO_(2),and water.Albeit with the great potential of HT-CO_(2)RR,this carbon utilization approach,unfortunately,has been suffering coke formation that is seriously detrimental to its energy efficiency and operating lifetime.In recent years,much effort has been added to understanding the mechanism of coke formation,managing reaction conditions to mitigate coke formation,and devising coke-formation-free electrode materials.These investigations have substantially advanced the HT-CO_(2)RR toward a practical industrial technology,but the resulting coke formation prevention strategies compromise activity and energy efficiency.Future research may target exploiting the control over both catalyst design and system design to gain selectivity,energy efficiency,and stability synchronously.Therefore,this perspective overviews the progress of research on coke formation in HT-CO_(2)RR,and elaborates on possible future directions that may accelerate its practical implementation at a large scale.
文摘A flat thin TiO2 film was employed as the photo-electrode of a dye sensitized solar cell （DSSC）, on which only a geometrical mono-layer of dye was attached. The effect of sur- face protonation by HCI chemical treatment on the performance of DSSCs was studied. The results showed that the short-circuit current Jsc increased significantly upon the HCI treatment, while the open-circuit voltage Voc decreased slightly. Compared to the untreated DSSC, the Jsc and energy conversion efficiency was increased by 31% and 25%, respectively, for the 1 mol/L HCI treated cell. TiO2 surface protonation improved electronic coupling between the chemisorbed dye and the TiO2 surface, resulting in an enhanced electron in- jection. The decreased open-circuit voltage after TiO2 surface protonation was mainly due to the TiO2 conduction band edge downshift and was partially caused by increased electron recombination with the electrolyte. In situ Raman degradation study showed that the dye stability was improved after the TiO2 surface protonation. The increased dye stability was contributed by the increased electron injection and electron back reaction with the electrolyte under the open-circuit condition.
基金Project(51472211)supported by the National Natural Science Foundation of ChinaProject(2012CK1006)supported by Scientific and Technical Achievement Transformation Fund of Hunan Province,China
文摘NaxCoO2 is a commonly used cathode material for sodium ion batteries because of its easy synthesis, high reversible capacity and good cyclability. The structural and electrochemical properties of NaxCoO2 during sodium ion insertion/extraction process are studied based on first principles calculations. The calculation results of crystal structure parameters and average intercalation voltage are in good agreement with experiment data. Through calculation of the geometric structure and charge transfer in charging and discharging processes of NaxCoO2, it is found that the oxygen atom surrounding Co of the CoO6 octahedral screens the coulomb potential produced by sodium vacancy in NaxCoO2, and the charge is removed from the entire Co-O layer instead of the Co atom adjacent to sodium vacancy when sodium ions are extracted from the Na CoO2 lattice. Thus, during the insertion/extraction of sodium ion from Na CoO2, the CoO6 octahedral structure undergoes small lattice distortion, which makes the local structure quite stable and is beneficial to the cycling stability of the material for the application of sodium ion batteries.
基金financially supported by the National Key Research and Development Program of China(2017YFA0208200 and 2016YFB0700600)the Fundamental Research Funds for the Central Universities of China(0205-14380219)+3 种基金the Projects of National Natural Science Foundation of China(22022505,21872069 and 51761135104)the Natural Science Foundation of Jiangsu Province(BK20181056,BK20180008 and BK20191042)Jiangsu Postdoctoral Science Fundation(2020Z258)the Funding for School-level Research Projects of Yancheng Institute of Technology(xjr2019006).
文摘Semiconducting silicon(Si)nanomaterials have great potential for the applications in electronics,physics,and energy storage fields.However,to date,it is still a challenge to realize the batch production of Si nanomaterials via efficient and low-cost approaches,owing to some long-standing shortcomings,e.g.,complex procedures and time and/or energy consumption.Herein,we report a green and inexpensive method to rapidly obtain two-dimensional(2D)free-standing Si/SiO_(x) nanosheets via the rapid thermal exfoliation of layered Zintl compound CaSi_(2).With the help of the rapid exfoliation reaction of CaSi_(2) in the atmosphere of greenhouse gas CO_(2),and the following mild sonication,2D free-standing Si/SiO_(x) nanosheets can be produced with very high yield.After applying the coating of a thin carbon outer layer,the electrodes of Si/SiO_(x)/C nanosheets serving as the anodes for lithium-ion batteries exhibit ultrahigh reversible capacity and outstanding electrochemical stability.We expect this study will provide new insights and inspirations for the convenient and batch production of nanostructural Si-based anode materials towards high-performance lithium-ion batteries.
文摘The main drawbacks of vanadium oxide as a cathode material are its low conductivity, low practical capacity and poor cycling stability. Adding Cr can improve its conductivity and a metastable amorphous state may provide higher capacity and stability. In this work, metastable amorphous Cr-V-O nano- particles have been successfully prepared through a facile co-precipitation reaction followed by annealing treatment. As a cathode material for lithium batteries, the metastable amorphous Cr-V-O nanoparticles exhibit high capacity （260 mAh/g at 100 mA/g between 1.5-4 V）, low capacity loss （more than 80% was retained after 200 cycles at 100 mA/g） and high rate capability （up to 3 A/g）.
基金The authors acknowledge financial support from the National Natural Science Foundation of China(21925804,21935003)CASDOE Collaborative Project(121421KYSB20170032)+1 种基金CAS Engineering Laboratory for Electrochemical Energy Storage,Liaoning Revitalization Talents Program(XLYC1802050)China and DICP funding,China(ZZBS201707)。
文摘Aqueous organic flow batteries have attracted dramatic attention for stationary energy storage due to their resource sustainability and low cost. However, the current reported systems can normally be operated stably under a nitrogen or argon atmosphere due to their poor stability. Herein a stable airinsensitive biphenol derivative cathode, 3,30,5,50-tetramethylaminemethylene-4,40-biphenol(TABP), with high solubility(>1.5 mol L^(-1)) and redox potential(0.91 V vs. SHE) is designed and synthesized by a scalable one-step method. Paring with silicotungstic acid(SWO), an SWO/TABP flow battery shows a stable performance of zero capacity decay over 900 cycles under the air atmosphere. Further, an SWO/TABP flow battery manifests a high rate performance with an energy efficiency of 85% at a current density of60 m A cm^(-2) and a very high volumetric capacity of more than 47 Ah L^(-1). This work provides a new and practical option for next-generation practical large-scale energy storage.
基金support from the National Natural Science Foundation of China(NSFC)(51673091,51833004,and 51425304)NSFC-Guangdong Joint funding(U1801256)+2 种基金support from the National Key R&D Program of China(2018YFA0208501)the National Natural Science Foundation of China(51803217,91963212,51961145102,and 51773206)K.C.Wong Education Foundation。
文摘The power conversion effciency(PCE)of flexible perovskite solar cells(PSCs)has increased rapidly,while the mechanical flexibility and environmental stability are still far from satisfactory.Previous studies show the environmental degradation and ductile cracks of perovskite films usually begin at the grain boundaries(GBs).Herein,sulfonated graphene oxide(s-GO)is employed to construct a cementitious GBs by interacting with the[Pb I6]4–at GBs.The resultant s-GO-[Pb I6]4–complex can effectively passivate the defects of vacant iodine,and the devices with s-GO exhibit remarkable waterproofness and flexibility due to the tough and water-insoluble GBs.The champion PCE of 20.56%(1.01 cm^(2))in a device treated with s-GO is achieved.This device retains 90%of its original PCE after 180 d stored in the ambient condition,as well as over 80%retention after 10,000 bending cycles at a curvature radius of 3 mm.
