Combining the first-principles calculations and structural enumeration with recognition,the delithiation process of LiNiO_(2)is investigated,where various supercell shapes are considered in order to obtain the formati...Combining the first-principles calculations and structural enumeration with recognition,the delithiation process of LiNiO_(2)is investigated,where various supercell shapes are considered in order to obtain the formation energy of Li_(x)NiO_(2).Meanwhile,the voltage profile is simulated and the ordered phases of lithium vacancies corresponding to concentrations of 1/4,2/5,3/7,1/2,2/3,3/4,5/6,and 6/7 are predicted.To understand the capacity decay in the experiment during the charge/discharge cycles,deoxygenation and Li/Ni antisite defects are calculated,revealing that the chains of oxygen vacancies will be energetically preferrable.It can be inferred that in the absence of oxygen atom in high delithiate state,the diffusion of Ni atoms is facilitated and the formation of Li/Ni antisite is induced.展开更多
High temperature vaccum evaporation is a recycling technology that includes a selective material recovering process. The fundamental research on a process of disassembling and recovering selected materials from Ni Cd ...High temperature vaccum evaporation is a recycling technology that includes a selective material recovering process. The fundamental research on a process of disassembling and recovering selected materials from Ni Cd batteries was conducted using self designed experimental apparatus. An effective recycling technology based on the evaporation phenomenon of batteries and the elements of cadmium under the laboratory condition was studied. The results show that: (1)Ni/Cd can be effectively recovered by vacuum distillation at appropriate temperature, pressure and time, and high purity cadmium (>99%) can be obtained through the process; (2)the effective distillatory temperature should be at the range of 5731 173 K; (3)the higher the evaporation temperature, the lower the purity of cadmium in condensate展开更多
To separate the cadmium and nickel resources in waste Ni-Cd batteries, aself-designed vacuum distillation recycling system was studied under laboratory conditions. Theeffects of system temperature, operating pressure,...To separate the cadmium and nickel resources in waste Ni-Cd batteries, aself-designed vacuum distillation recycling system was studied under laboratory conditions. Theeffects of system temperature, operating pressure, and time on the separation of Ni and Cd werestudied respectively. The mechanism of vacuum thermal recycling was also discussed. Results showthat vacuum distillation is a very effective separation method for waste Ni-Cd batteries. At aconstant pressure, the increase of temperature can improve the separating efficiency of Cd. When thetemperature is 1 173 K, cadmium can evaporate completely from the samples during 3 h at 10 Pa. Thereduction of pressure in a certain range is effective to the separating of Cd from Ni-Cd batteriesby vacuum distillation.展开更多
Recovery of Ni-Cd batteries was studied by a self-designed vacuum-aided recovering system under laboratory conditions. The fundamental research on a process of disassembling and recovering selected materials from Ni-C...Recovery of Ni-Cd batteries was studied by a self-designed vacuum-aided recovering system under laboratory conditions. The fundamental research on a process of disassembling and recovering selected materials from Ni-Cd batterieswas conducted. The impacts of temperature, pressure and time were studied respectively. The mechanism of vacuum thermal recovering was also discussed. The results show that: Ni-Cd batteries can be recovered effectively byvacuum-aided recovering system at 573~1173 K. At constant pressure, the increase of temperature can improve theseparating efficiency of cadmium. When the temperature is 1173 K, the cadmium can evaporate completely fromthe residue during 3 h at 10 Pa. The reduction of pressure in the certain range is effective to separate cadmium byvacuum distillation. Distillation time is a very important factor affecting separation of cadmium.展开更多
In this work,we synthesized LaFeO_3–xwt%Ni(x=0,5,10,15)composites via a solid-state reaction method by adding Ni to the reactants,La_2O_3 and Fe_2O_3.Field-emission scanning electron microscopy(FE-SEM)and energy-disp...In this work,we synthesized LaFeO_3–xwt%Ni(x=0,5,10,15)composites via a solid-state reaction method by adding Ni to the reactants,La_2O_3 and Fe_2O_3.Field-emission scanning electron microscopy(FE-SEM)and energy-dispersive X-ray spectroscopy(EDS)results revealed that Ni powders evenly dispersed among the LaFeO_3 particles and apparently reduced their aggregation,which imparted the composites with a loose structure.Moreover,the Ni formed a conductive network,thus improving the conductivity of the composites.The maximum discharge capacity of the LaFeO_3 electrodes remarkably increased from 266.8 mAh·g^(–1)(x=0)to 339.7 mAh·g^(–1)(x=10).In particular,the high-rate dischargeability of the LaFeO_3–10wt%Ni electrode at a discharge current density of 1500 mA·g^(-1) reached 54.6%,which was approximately 1.5 times higher than that of the pure LaFeO_3.Such a Ni-modified loose structure not only increased the charge transfer rate on the surface of the LaFeO_3 particles but also enhanced the hydrogen diffusion rate in the bulk LaFeO_3.展开更多
A binder-free Ni3S2 electrode was prepared directly on a graphene-coated Ni foam （G/Ni） substrate through surface sulfiding of substrate using thiourea as the sulfur source in this work. The Ni3S2 showed a flower-li...A binder-free Ni3S2 electrode was prepared directly on a graphene-coated Ni foam （G/Ni） substrate through surface sulfiding of substrate using thiourea as the sulfur source in this work. The Ni3S2 showed a flower-like morphology and was uniformly distributed on the G/Ni surface. The flower-like Ni3S2 was composed of cross-arrayed nanoflakes with a diameter and a thickness of 1-2 μm and -50 nm, re- spectively. The free space in the flowers and the thin feature of Ni3S2 buffered the volume changes and relieved mechanical strain during re- peated cycling. The intimate contact with the Ni substrate and the fixing effect of graphene maintained the structural stability of the Ni3S2 electrode during cycling. The G/Ni-supported Ni3S2 maintained a reversible capacity of 250 mAh·g^-1 after 100 cycles at 50 mA·g^-1, demon- strating the good cycling stability as a result of the unique microstructure of this electrode material.展开更多
One approach to accelerate the stagnant kinetics of both the oxygen reduction and evolution reactions(ORR/OER)is to develop a rationally designed multiphase nanocomposite,where the functions arising from each of the c...One approach to accelerate the stagnant kinetics of both the oxygen reduction and evolution reactions(ORR/OER)is to develop a rationally designed multiphase nanocomposite,where the functions arising from each of the constituent phases,their interfaces,and the overall structure are properly controlled.Herein,we successfully synthesized an oxygen electrocatalyst consisting of Ni nanoparticles purposely interpenetrated into mesoporous NiO nanosheets(porous Ni/NiO).Benefiting from the contributions of the Ni and NiO phases,the well-established pore channels for charge transport at the interface between the phases,and the enhanced conductivity due to oxygen-deficiency at the pore edges,the porous Ni/NiO nanosheets show a potential of 1.49 V(10 mA cm^-2)for the OER and a half-wave potential of 0.76 V for the ORR,outperforming their noble metal counterparts.More significantly,a Zn-air battery employing the porous Ni/NiO nanosheets exhibits an initial charging-discharging voltage gap of 0.83 V(2 mA cm^-2),specific capacity of 853 mAh gZn^-1 at 20 mA cm^-2,and long-time cycling stability(120 h).In addition,the porous Ni/NiO-based solid-like Zn-air battery shows excellent electrochemical performance and flexibility,illustrating its great potential as a next-generation rechargeable power source for flexible electronics.展开更多
Cylindrical nickel metal hydride （Ni-MH） battery with high specific volume capacity was prepared by using the oxyhydroxide Ni（OH）2 and AB5 type hydrogen storage alloy and adjusting the designing parameters of posi...Cylindrical nickel metal hydride （Ni-MH） battery with high specific volume capacity was prepared by using the oxyhydroxide Ni（OH）2 and AB5 type hydrogen storage alloy and adjusting the designing parameters of positive and negative electrodes. The oxyhydroxide Ni（OH）2 was synthesized by oxidizing spherical β-Ni（OH）2 with chemical method. The X-ray diffraction （XRD） patterns and the Fourier transform infrared （PT-IR） spectra indicated that 7-NiOOH was formed on the oxyhydroxide Ni（OH）2 powders, and some H2O molecules were inserted into their crystal lattice spacing. The battery capacity could not be improved when the oxyhydroxide Ni（OH）2 sample was directly used as the positive active materials. However, based on the conductance and residual capacity of the oxyhydroxide Ni（OH）2 powders, AA size Ni-MH battery with 2560 mA.h capacity and 407 W·h·L^-1 specific volume energy at 0.2C was obtained by using the commercial spherical β-Ni（OH）2 and AB5-type hydrogen-storage alloy powders as the active materials when 10% mass amount of the oxyhydroxide Ni（OH）2 with 2.50 valence was added to the positive active materials and subsequently the battery designing parameters were adjusted as well. The as-prepared battery showed 70% initial capacity after 80 cycles at 0.5C. The possibility for adjusting the capacity ratio of positive and negative electrodes from 1 ： 1.35 to 1 ： 1.22 was demonstrated preliminarily. It is considered the as-prepared battery can meet the requirement of some special portable electrical instruments.展开更多
The CoO/CoVO/Ni nanocomposites were rationally designed and prepared by a two-step hydrothermal synthesis and subsequent annealing treatment. The one-dimensional（1D） CoOnanowire arrays directly grew on Ni foam, wher...The CoO/CoVO/Ni nanocomposites were rationally designed and prepared by a two-step hydrothermal synthesis and subsequent annealing treatment. The one-dimensional（1D） CoOnanowire arrays directly grew on Ni foam, whereas the 1D CoVOnanowires adhered to parts of CoOnanowires.Most of the hybrid nanowires were inlayed with each other, forming a 3D hybrid nanowires network.As a result, the discharge capacity of CoO/CoVO/Ni nanocomposites could reach 1201.8 mAh/g after100 cycles at 100 mA/g. After 600 cycles at 1 A/g, the discharge capacity was maintained at 828.1 mAh/g.Moreover, even though the charge/discharge rates were increased to 10 A/g, it rendered reversible capacity of 491.2 mAh/g. The superior electrochemical properties of nanocomposites were probably ascribed to their unique 3D architecture and the synergistic effects of two active materials. Therefore, such CoO/CoVO/Ni nanocomposites could potentially be used as anode materials for high-performance Li-ion batteries.展开更多
Cobalt-free cathode materials are attractive for their high capacity and low cost,yet they still encounter issues with structural and surface instability.AlPO_(4),in particular,has garnered attention as an effective s...Cobalt-free cathode materials are attractive for their high capacity and low cost,yet they still encounter issues with structural and surface instability.AlPO_(4),in particular,has garnered attention as an effective stabilizer for bulk and surface.However,the impact of interfacial reactions and elemental interdiffusion between AlPO_(4) and LiNi_(0.95)Mn_(0.05)O_(2) upon sintering on the bulk and surface remains elusive.In this study,we demonstrate that during the heat treatment process,AlPO_(4) decomposes,resulting in Al doping into the bulk of the cathode through elemental interdiffusion.Simultaneously,PO_(4)^(3-)reacts with the surface Li of material to form a Li_3PO_(4) coating,inducing lithium deficiency,thereby increasing Li/Ni mixing.The suitable Li/Ni mixing,previously overlooked in AlPO_(4) modification,plays a pivotal role in stabilizing the bulk and surface,exceeding the synergy of Al doping and Li_3PO_(4) coating.The presence of Ni^(2+)ions in the lithium layers contributes to the stabilization of the delithiated structure via a structural pillar effect.Moreover,suitable Li/Ni mixing can stabilize the lattice oxygen and electrode-electrolyte interface by increasing oxygen removal energy and reducing the overlap between the Ni^(3+/4+)e_g and O^(2-)2p orbitals.These findings offer new perspectives for the design of stable cobalt-free cathode materials.展开更多
The Li-rich layered oxides show a higher discharge capacity over 250 mAh/g and have been developed into a promising positive material for lithium ion batteries. A rare earth metal oxyfluoride YOF-coated Li[Lio.2Mno.54...The Li-rich layered oxides show a higher discharge capacity over 250 mAh/g and have been developed into a promising positive material for lithium ion batteries. A rare earth metal oxyfluoride YOF-coated Li[Lio.2Mno.54Ni0.13Co0.13]O2 composites have been synthesized by a simple wet chem- ical method. Crystal structure, micro-morphology and element valence of the pristine and YOF-coated Li[Li0.2Mn0.54Ni0.13Co0.13]O2 materials are characterized by XRD, SEM, TEM, and XPS. The results indicate that all materials exhibit a typical layered structure, and are made up of small and homogenous parti- cles ranging from 100 nm to 200 nm. In addition, YOF layer with a thickness of approximately 3-8 nm is precisely coated on the surface of the Li[Li0.2Mn0.54Ni0.13Co0.13]02. Constant current charge/discharge tests at various current densities show that the electrochemical performance of 2 wt% YOF-coated Li[Li0.2Mn0.54Ni0.13Co0.13]O2 has been improved significantly. 2 wt% YOF-coated Li[Li0.2Mn0.54Ni0.13Co0.13]O2 delivers the highest discharge capacity of 250.4 mAh/g at 20 mA/g among all the samples, and capacity retention of 87% after 100 charge/discharge cycles at 200 mA/g while that of the pristine one is only 81.6%. The superior electrochemical performance of 2wt% YOF-coated sample is ascribed to YOF coating layer, which could not only reduce side reactions between the electrode and liquid electrolyte, but also promote lithium ion migration.展开更多
Traditional carbon layer enwrapping active materials cannot easily realize perfect cladding.Therefore,it still cannot prevent the pulverization of active materials during the course of charging/discharging.In this pa...Traditional carbon layer enwrapping active materials cannot easily realize perfect cladding.Therefore,it still cannot prevent the pulverization of active materials during the course of charging/discharging.In this paper,we utilize natural bacteria to absorb nickel acetate,the active materials Ni3P nanoparticles are well enwrapped,as a natural organisms surviving for billions of years,their cell walls have a perfect carbon structure,and the cell walls become carbon layer through high annealing temperature.Based on this,the yolk-shell Ni3P–carbon@reduced graphene oxides paper is prepared,through a proper annealing temperature,the Ni3P particles disperse in the inner surface or both ends,so the active materials were prevented from dissolving into the electrolyte,so it may keep from invalidity during charging/discharging.The electrochemical performances display that it has stable and high capacities as Li-ion batteries(LIBs)anode.Its capacity can keep 200 cycles without any decrease,and especially its rate performance exhibits an excellent peculiarity,with the current density increasing from 400 to 1000 mA g^(−1) every 200 mA g^(−1),its capacities decrease only 9.8%,2.9%and 6.4%,and its can recover the same capacity when the current density comes back to 200 mA g^(−1).It may be a fine choice for LIBs.展开更多
The structure and electrochemical properties of nanocrystalline LaNi_5-type alloys were studied. These materials were prepared by mechanical alloying (MA) followed by annealing. The properties of hydrogen host materia...The structure and electrochemical properties of nanocrystalline LaNi_5-type alloys were studied. These materials were prepared by mechanical alloying (MA) followed by annealing. The properties of hydrogen host materials can be modified substantially by alloying to obtain the desired storage characteristics. It was found that the partial substitution of Ni by Al or Mn in LaNi_(5-x)M_x alloy leads to an increase in discharge capacity. The alloying elements such as Al, Mn and Co greatly improved the cycle life of LaNi_5 material. For example, in the nanocrystalline LaNi_(3.75)Mn_(0.75)Al_(0.25)Co_(0.25) powder, discharge capacity up to 258 mAh·g^(-1) was measured (at 40 mA·g^(-1) discharge current). Furthermore, the effect of the graphite coating on the structure of some nanocrystalline alloys and the electrodes characteristics were investigated. The mechanical coating with graphite effectively reduced the degradation rate of the studied electrode materials. The combination of a nanocrystalline LaNi_5-type hydride electrodes and a nickel positive electrode to form a Ni-MH battery, was successful.展开更多
The effects of low-Co AB_5 type hydrogen storage alloys prepared by quenchingand annealing on the performances of MH-Ni batteries were investigated, and the characteristics ofthe low-Co AB_5 type hydrogen storage allo...The effects of low-Co AB_5 type hydrogen storage alloys prepared by quenchingand annealing on the performances of MH-Ni batteries were investigated, and the characteristics ofthe low-Co AB_5 type hydrogen storage alloys were compared with those of the high-Co AB_5 typehydrogen storage alloy as well. The results showed that the faster the cooling of the low-Cohydrogen storage alloy is, the better homogeneity of the chemical composition for the alloy and thelonger cycle life of the battery are, but the electrochemical discharge capacity and high-ratedischarge ability are reduced. The high-rate discharge ability and charge retention of MH-Nibatteries for the conventional as-cast annealed low-Co hydrogen storage alloy were superior to thosefor the rapidly quenched low-Co hydrogen storage alloy and the high-Co hydrogen storage alloy, buta little inferior in the cycle life.展开更多
Spherical Ni(OH)2 powder coated with Co(OH)2 as raw material was mixed with LiOH to synthesize cathode material for lithium ion battery by using solid-state reaction. After sintered at temperature above 600 ℃, a soli...Spherical Ni(OH)2 powder coated with Co(OH)2 as raw material was mixed with LiOH to synthesize cathode material for lithium ion battery by using solid-state reaction. After sintered at temperature above 600 ℃, a solid solution with layer structure was formed. The result of XPS shows that it is a concentration gradient material with higher cobalt content at the surface, and the gradient decreases with increasing sintering temperature from 650 to 750 ℃. This new gradient material, called as Co-coated LiNiO2, exhibits excellent electrochemical performances for the cathode of Li-ion batteries in comparison with LiNiO2 and Co-doping LiNiO2. The discharge capacity of Co-coated LiNiO2 is over 180 mA·h/g and capacity decay per cycle is less than 0.07% when Co-coated LiNiO2 consisting of 92% nickel and 8% cobalt was sintered at the temperatures between 650-670 ℃. Though initial discharge capacity could be increased with higher sintering temperature, the cycle life would be reduced.展开更多
In order to confirm the optimal Li content of Li-rich Mn-based cathode materials(a fixed mole ratio of Mn to Ni to Co is0.6:0.2:0.2),Li1+x(Mn0.6Ni0.2Co0.2)1-xO2(x=0,0.1,0.2,0.3)composites were obtained,which had a typ...In order to confirm the optimal Li content of Li-rich Mn-based cathode materials(a fixed mole ratio of Mn to Ni to Co is0.6:0.2:0.2),Li1+x(Mn0.6Ni0.2Co0.2)1-xO2(x=0,0.1,0.2,0.3)composites were obtained,which had a typical layered structure with R3m and C2/m space group observed from X-ray powder diffraction(XRD).Electron microscopy micrograph(SEM)reveals that the particle sizes in the range of0.4-1.1μm increase with an increase of x value.Li1.2(Mn0.6Ni0.2Co0.2)0.8O2sample delivers a larger initial discharge capacity of275.7mA·h/g at the current density of20mA/g in the potential range of2.0-4.8V,while Li1.1(Mn0.6Ni0.2Co0.2)0.9O2shows a better cycle performance with a capacity retention of93.8%at0.2C after50cycles,showing better reaction kinetics of lithium ion insertion and extraction.展开更多
基金Project supported by the Science Fund of the Guangdong Major Project of Basic and Applied Basic Research,China(Grant No.2019B030302011)the Fund of the Science and Technology Program of Guangzhou,China(Grant No.202201010090)。
文摘Combining the first-principles calculations and structural enumeration with recognition,the delithiation process of LiNiO_(2)is investigated,where various supercell shapes are considered in order to obtain the formation energy of Li_(x)NiO_(2).Meanwhile,the voltage profile is simulated and the ordered phases of lithium vacancies corresponding to concentrations of 1/4,2/5,3/7,1/2,2/3,3/4,5/6,and 6/7 are predicted.To understand the capacity decay in the experiment during the charge/discharge cycles,deoxygenation and Li/Ni antisite defects are calculated,revealing that the chains of oxygen vacancies will be energetically preferrable.It can be inferred that in the absence of oxygen atom in high delithiate state,the diffusion of Ni atoms is facilitated and the formation of Li/Ni antisite is induced.
文摘High temperature vaccum evaporation is a recycling technology that includes a selective material recovering process. The fundamental research on a process of disassembling and recovering selected materials from Ni Cd batteries was conducted using self designed experimental apparatus. An effective recycling technology based on the evaporation phenomenon of batteries and the elements of cadmium under the laboratory condition was studied. The results show that: (1)Ni/Cd can be effectively recovered by vacuum distillation at appropriate temperature, pressure and time, and high purity cadmium (>99%) can be obtained through the process; (2)the effective distillatory temperature should be at the range of 5731 173 K; (3)the higher the evaporation temperature, the lower the purity of cadmium in condensate
文摘To separate the cadmium and nickel resources in waste Ni-Cd batteries, aself-designed vacuum distillation recycling system was studied under laboratory conditions. Theeffects of system temperature, operating pressure, and time on the separation of Ni and Cd werestudied respectively. The mechanism of vacuum thermal recycling was also discussed. Results showthat vacuum distillation is a very effective separation method for waste Ni-Cd batteries. At aconstant pressure, the increase of temperature can improve the separating efficiency of Cd. When thetemperature is 1 173 K, cadmium can evaporate completely from the samples during 3 h at 10 Pa. Thereduction of pressure in a certain range is effective to the separating of Cd from Ni-Cd batteriesby vacuum distillation.
文摘Recovery of Ni-Cd batteries was studied by a self-designed vacuum-aided recovering system under laboratory conditions. The fundamental research on a process of disassembling and recovering selected materials from Ni-Cd batterieswas conducted. The impacts of temperature, pressure and time were studied respectively. The mechanism of vacuum thermal recovering was also discussed. The results show that: Ni-Cd batteries can be recovered effectively byvacuum-aided recovering system at 573~1173 K. At constant pressure, the increase of temperature can improve theseparating efficiency of cadmium. When the temperature is 1173 K, the cadmium can evaporate completely fromthe residue during 3 h at 10 Pa. The reduction of pressure in the certain range is effective to separate cadmium byvacuum distillation. Distillation time is a very important factor affecting separation of cadmium.
基金financially supported by the National Natural Science Foundation of China(Nos.51771164,51571173,and 51701175)the National Postdoctoral Program for Innovative Talents of China(No.BX201700204)the Innovation Fund for the Graduate Students of Hebei Province(No.CXZZBS2017057)
文摘In this work,we synthesized LaFeO_3–xwt%Ni(x=0,5,10,15)composites via a solid-state reaction method by adding Ni to the reactants,La_2O_3 and Fe_2O_3.Field-emission scanning electron microscopy(FE-SEM)and energy-dispersive X-ray spectroscopy(EDS)results revealed that Ni powders evenly dispersed among the LaFeO_3 particles and apparently reduced their aggregation,which imparted the composites with a loose structure.Moreover,the Ni formed a conductive network,thus improving the conductivity of the composites.The maximum discharge capacity of the LaFeO_3 electrodes remarkably increased from 266.8 mAh·g^(–1)(x=0)to 339.7 mAh·g^(–1)(x=10).In particular,the high-rate dischargeability of the LaFeO_3–10wt%Ni electrode at a discharge current density of 1500 mA·g^(-1) reached 54.6%,which was approximately 1.5 times higher than that of the pure LaFeO_3.Such a Ni-modified loose structure not only increased the charge transfer rate on the surface of the LaFeO_3 particles but also enhanced the hydrogen diffusion rate in the bulk LaFeO_3.
基金financially supported by the Scientific and Technological Project of State Grid Corporation of China
文摘A binder-free Ni3S2 electrode was prepared directly on a graphene-coated Ni foam （G/Ni） substrate through surface sulfiding of substrate using thiourea as the sulfur source in this work. The Ni3S2 showed a flower-like morphology and was uniformly distributed on the G/Ni surface. The flower-like Ni3S2 was composed of cross-arrayed nanoflakes with a diameter and a thickness of 1-2 μm and -50 nm, re- spectively. The free space in the flowers and the thin feature of Ni3S2 buffered the volume changes and relieved mechanical strain during re- peated cycling. The intimate contact with the Ni substrate and the fixing effect of graphene maintained the structural stability of the Ni3S2 electrode during cycling. The G/Ni-supported Ni3S2 maintained a reversible capacity of 250 mAh·g^-1 after 100 cycles at 50 mA·g^-1, demon- strating the good cycling stability as a result of the unique microstructure of this electrode material.
基金the National Natural Science Foundation of China(Grant Nos.11474137,11674143)the Fundamental Research Funds for the Central Universities(Grant No.Lzujbky-2019-cd02).
文摘One approach to accelerate the stagnant kinetics of both the oxygen reduction and evolution reactions(ORR/OER)is to develop a rationally designed multiphase nanocomposite,where the functions arising from each of the constituent phases,their interfaces,and the overall structure are properly controlled.Herein,we successfully synthesized an oxygen electrocatalyst consisting of Ni nanoparticles purposely interpenetrated into mesoporous NiO nanosheets(porous Ni/NiO).Benefiting from the contributions of the Ni and NiO phases,the well-established pore channels for charge transport at the interface between the phases,and the enhanced conductivity due to oxygen-deficiency at the pore edges,the porous Ni/NiO nanosheets show a potential of 1.49 V(10 mA cm^-2)for the OER and a half-wave potential of 0.76 V for the ORR,outperforming their noble metal counterparts.More significantly,a Zn-air battery employing the porous Ni/NiO nanosheets exhibits an initial charging-discharging voltage gap of 0.83 V(2 mA cm^-2),specific capacity of 853 mAh gZn^-1 at 20 mA cm^-2,and long-time cycling stability(120 h).In addition,the porous Ni/NiO-based solid-like Zn-air battery shows excellent electrochemical performance and flexibility,illustrating its great potential as a next-generation rechargeable power source for flexible electronics.
基金Supported by the Natural Science Foundation of Department of Education （05Z008） and the Science and Technology Projects of Guangdong Province （2007B030101007）.
文摘Cylindrical nickel metal hydride （Ni-MH） battery with high specific volume capacity was prepared by using the oxyhydroxide Ni（OH）2 and AB5 type hydrogen storage alloy and adjusting the designing parameters of positive and negative electrodes. The oxyhydroxide Ni（OH）2 was synthesized by oxidizing spherical β-Ni（OH）2 with chemical method. The X-ray diffraction （XRD） patterns and the Fourier transform infrared （PT-IR） spectra indicated that 7-NiOOH was formed on the oxyhydroxide Ni（OH）2 powders, and some H2O molecules were inserted into their crystal lattice spacing. The battery capacity could not be improved when the oxyhydroxide Ni（OH）2 sample was directly used as the positive active materials. However, based on the conductance and residual capacity of the oxyhydroxide Ni（OH）2 powders, AA size Ni-MH battery with 2560 mA.h capacity and 407 W·h·L^-1 specific volume energy at 0.2C was obtained by using the commercial spherical β-Ni（OH）2 and AB5-type hydrogen-storage alloy powders as the active materials when 10% mass amount of the oxyhydroxide Ni（OH）2 with 2.50 valence was added to the positive active materials and subsequently the battery designing parameters were adjusted as well. The as-prepared battery showed 70% initial capacity after 80 cycles at 0.5C. The possibility for adjusting the capacity ratio of positive and negative electrodes from 1 ： 1.35 to 1 ： 1.22 was demonstrated preliminarily. It is considered the as-prepared battery can meet the requirement of some special portable electrical instruments.
基金supported by the National Natural Science Foundation of China(no.51362018)the Foundation for Innovation Groups of Basic Research in Gansu Province(no.1606RJIA322)
文摘The CoO/CoVO/Ni nanocomposites were rationally designed and prepared by a two-step hydrothermal synthesis and subsequent annealing treatment. The one-dimensional（1D） CoOnanowire arrays directly grew on Ni foam, whereas the 1D CoVOnanowires adhered to parts of CoOnanowires.Most of the hybrid nanowires were inlayed with each other, forming a 3D hybrid nanowires network.As a result, the discharge capacity of CoO/CoVO/Ni nanocomposites could reach 1201.8 mAh/g after100 cycles at 100 mA/g. After 600 cycles at 1 A/g, the discharge capacity was maintained at 828.1 mAh/g.Moreover, even though the charge/discharge rates were increased to 10 A/g, it rendered reversible capacity of 491.2 mAh/g. The superior electrochemical properties of nanocomposites were probably ascribed to their unique 3D architecture and the synergistic effects of two active materials. Therefore, such CoO/CoVO/Ni nanocomposites could potentially be used as anode materials for high-performance Li-ion batteries.
基金financial support from the Natural Science Foundation of Shandong Province (ZR2022QB140)the PhD Initiation Program of Liaocheng University (318052138)the Natural Science Foundation of Shandong Province (ZR2023MB002 and ZR2021MB114)。
文摘Cobalt-free cathode materials are attractive for their high capacity and low cost,yet they still encounter issues with structural and surface instability.AlPO_(4),in particular,has garnered attention as an effective stabilizer for bulk and surface.However,the impact of interfacial reactions and elemental interdiffusion between AlPO_(4) and LiNi_(0.95)Mn_(0.05)O_(2) upon sintering on the bulk and surface remains elusive.In this study,we demonstrate that during the heat treatment process,AlPO_(4) decomposes,resulting in Al doping into the bulk of the cathode through elemental interdiffusion.Simultaneously,PO_(4)^(3-)reacts with the surface Li of material to form a Li_3PO_(4) coating,inducing lithium deficiency,thereby increasing Li/Ni mixing.The suitable Li/Ni mixing,previously overlooked in AlPO_(4) modification,plays a pivotal role in stabilizing the bulk and surface,exceeding the synergy of Al doping and Li_3PO_(4) coating.The presence of Ni^(2+)ions in the lithium layers contributes to the stabilization of the delithiated structure via a structural pillar effect.Moreover,suitable Li/Ni mixing can stabilize the lattice oxygen and electrode-electrolyte interface by increasing oxygen removal energy and reducing the overlap between the Ni^(3+/4+)e_g and O^(2-)2p orbitals.These findings offer new perspectives for the design of stable cobalt-free cathode materials.
基金financially supported by the National Basic Research Program of China(Grant no.2015CB251100)
文摘The Li-rich layered oxides show a higher discharge capacity over 250 mAh/g and have been developed into a promising positive material for lithium ion batteries. A rare earth metal oxyfluoride YOF-coated Li[Lio.2Mno.54Ni0.13Co0.13]O2 composites have been synthesized by a simple wet chem- ical method. Crystal structure, micro-morphology and element valence of the pristine and YOF-coated Li[Li0.2Mn0.54Ni0.13Co0.13]O2 materials are characterized by XRD, SEM, TEM, and XPS. The results indicate that all materials exhibit a typical layered structure, and are made up of small and homogenous parti- cles ranging from 100 nm to 200 nm. In addition, YOF layer with a thickness of approximately 3-8 nm is precisely coated on the surface of the Li[Li0.2Mn0.54Ni0.13Co0.13]02. Constant current charge/discharge tests at various current densities show that the electrochemical performance of 2 wt% YOF-coated Li[Li0.2Mn0.54Ni0.13Co0.13]O2 has been improved significantly. 2 wt% YOF-coated Li[Li0.2Mn0.54Ni0.13Co0.13]O2 delivers the highest discharge capacity of 250.4 mAh/g at 20 mA/g among all the samples, and capacity retention of 87% after 100 charge/discharge cycles at 200 mA/g while that of the pristine one is only 81.6%. The superior electrochemical performance of 2wt% YOF-coated sample is ascribed to YOF coating layer, which could not only reduce side reactions between the electrode and liquid electrolyte, but also promote lithium ion migration.
基金This work was financially supported by Jiangxi Provincial Natural Science Foundation(No.20202BABL204049)Education Department of Jiangxi Province(No.GJJ170898)+3 种基金Science and technology project of Yichun University(No.2017DF001)Doctor yang received his funding from Jiangxi Provincial Natural Science Foundation(No.20202BABL204049)Doctor Jun Zhou received his funding from Education Department of Jiangxi Province(No.GJJ170898)Science and technology project of Yichun University(No.2017DF001).
文摘Traditional carbon layer enwrapping active materials cannot easily realize perfect cladding.Therefore,it still cannot prevent the pulverization of active materials during the course of charging/discharging.In this paper,we utilize natural bacteria to absorb nickel acetate,the active materials Ni3P nanoparticles are well enwrapped,as a natural organisms surviving for billions of years,their cell walls have a perfect carbon structure,and the cell walls become carbon layer through high annealing temperature.Based on this,the yolk-shell Ni3P–carbon@reduced graphene oxides paper is prepared,through a proper annealing temperature,the Ni3P particles disperse in the inner surface or both ends,so the active materials were prevented from dissolving into the electrolyte,so it may keep from invalidity during charging/discharging.The electrochemical performances display that it has stable and high capacities as Li-ion batteries(LIBs)anode.Its capacity can keep 200 cycles without any decrease,and especially its rate performance exhibits an excellent peculiarity,with the current density increasing from 400 to 1000 mA g^(−1) every 200 mA g^(−1),its capacities decrease only 9.8%,2.9%and 6.4%,and its can recover the same capacity when the current density comes back to 200 mA g^(−1).It may be a fine choice for LIBs.
文摘The structure and electrochemical properties of nanocrystalline LaNi_5-type alloys were studied. These materials were prepared by mechanical alloying (MA) followed by annealing. The properties of hydrogen host materials can be modified substantially by alloying to obtain the desired storage characteristics. It was found that the partial substitution of Ni by Al or Mn in LaNi_(5-x)M_x alloy leads to an increase in discharge capacity. The alloying elements such as Al, Mn and Co greatly improved the cycle life of LaNi_5 material. For example, in the nanocrystalline LaNi_(3.75)Mn_(0.75)Al_(0.25)Co_(0.25) powder, discharge capacity up to 258 mAh·g^(-1) was measured (at 40 mA·g^(-1) discharge current). Furthermore, the effect of the graphite coating on the structure of some nanocrystalline alloys and the electrodes characteristics were investigated. The mechanical coating with graphite effectively reduced the degradation rate of the studied electrode materials. The combination of a nanocrystalline LaNi_5-type hydride electrodes and a nickel positive electrode to form a Ni-MH battery, was successful.
文摘The effects of low-Co AB_5 type hydrogen storage alloys prepared by quenchingand annealing on the performances of MH-Ni batteries were investigated, and the characteristics ofthe low-Co AB_5 type hydrogen storage alloys were compared with those of the high-Co AB_5 typehydrogen storage alloy as well. The results showed that the faster the cooling of the low-Cohydrogen storage alloy is, the better homogeneity of the chemical composition for the alloy and thelonger cycle life of the battery are, but the electrochemical discharge capacity and high-ratedischarge ability are reduced. The high-rate discharge ability and charge retention of MH-Nibatteries for the conventional as-cast annealed low-Co hydrogen storage alloy were superior to thosefor the rapidly quenched low-Co hydrogen storage alloy and the high-Co hydrogen storage alloy, buta little inferior in the cycle life.
文摘Spherical Ni(OH)2 powder coated with Co(OH)2 as raw material was mixed with LiOH to synthesize cathode material for lithium ion battery by using solid-state reaction. After sintered at temperature above 600 ℃, a solid solution with layer structure was formed. The result of XPS shows that it is a concentration gradient material with higher cobalt content at the surface, and the gradient decreases with increasing sintering temperature from 650 to 750 ℃. This new gradient material, called as Co-coated LiNiO2, exhibits excellent electrochemical performances for the cathode of Li-ion batteries in comparison with LiNiO2 and Co-doping LiNiO2. The discharge capacity of Co-coated LiNiO2 is over 180 mA·h/g and capacity decay per cycle is less than 0.07% when Co-coated LiNiO2 consisting of 92% nickel and 8% cobalt was sintered at the temperatures between 650-670 ℃. Though initial discharge capacity could be increased with higher sintering temperature, the cycle life would be reduced.
基金Project(21473258) supported by the National Natural Science Foundation of ChinaProject(13JJ1004) supported by Distinguished Young Scientists of Hunan Province,ChinaProject(NCET-11-0513) supported by Program for the New Century Excellent Talents in University,China
文摘In order to confirm the optimal Li content of Li-rich Mn-based cathode materials(a fixed mole ratio of Mn to Ni to Co is0.6:0.2:0.2),Li1+x(Mn0.6Ni0.2Co0.2)1-xO2(x=0,0.1,0.2,0.3)composites were obtained,which had a typical layered structure with R3m and C2/m space group observed from X-ray powder diffraction(XRD).Electron microscopy micrograph(SEM)reveals that the particle sizes in the range of0.4-1.1μm increase with an increase of x value.Li1.2(Mn0.6Ni0.2Co0.2)0.8O2sample delivers a larger initial discharge capacity of275.7mA·h/g at the current density of20mA/g in the potential range of2.0-4.8V,while Li1.1(Mn0.6Ni0.2Co0.2)0.9O2shows a better cycle performance with a capacity retention of93.8%at0.2C after50cycles,showing better reaction kinetics of lithium ion insertion and extraction.
