Na_(3)V_(2)(PO_(4))_(2)F_(3)(NVPF) is shown to be an attractive cathode material for sodium storage due to its high theoretical capacity and suitable working voltage.However,its low electronic conductivity and poor cy...Na_(3)V_(2)(PO_(4))_(2)F_(3)(NVPF) is shown to be an attractive cathode material for sodium storage due to its high theoretical capacity and suitable working voltage.However,its low electronic conductivity and poor cycling stability have to be addressed in order for enhanced high-rate performance and cycle life.Herein,we have prepared a 3D reduced graphene oxide (rGO) host-supported NVPF nanocuboids.We discover that polyvinyl alcohol (PVA) serves as an important structural directing agent that bridges between NVPF and rGO through the hydrogen bonding,and thus regulates the formation of the 3D r GO framework with NVPF nanocuboids embedded inside (NVPF@C@rGO).With such a unique construction,NVPF@C@rGO exhibits excellent cycling stability and rate performance for sodium storage,showing high reversible capacities of 121 m Ah/g and 113 mAh/g at 1C and 10C,respectively,and 103 mAh/g after 700cycles at 50C with 98.3%retention.Even at an extremely high current of 100C,it also delivers a reversible capacity of 64 mAh/g,surpassing the performance of many recently reported NVPF-based electrodes.Cyclic voltammetry (CV) and galvanostatic intermittent titration technique (GITT) data confirm the much better kinetic properties of NVPF@C@rGO electrode than the control samples of NVPF@rGO and pure NVPF.In-situ XRD results reveal that the 3D rGO housing can effectively suppress the lattice variation of NVPF,with a maximum volume change of only 1.84%during cycling.Moreover,the in-situ temperature sensing reveals the more stable working temperature of NVPF@C@rGO compared to phase-pure NVPF,suggesting a higher temperature safety of the electrode.Using NVPF@C@rGO as the positive electrode and commercial hard carbon as the negative electrode,a sodium-ion full battery has been assembled with about 110 m Ah/g at 1C for 300 cycles,corresponding to an energy density of 291 Wh kg^(-1).The construction of 3D r GO housing as a conductive support offers an effective strategy for high-rate,long cycle life and high safety sodium-ion battery cathodes.展开更多
To mitigate interference on celledge users and improve fairness of the whole system, dynamic inter-cell interference coordination(ICIC) is one of the promising solutions. However, traditional dynamic ICIC is considere...To mitigate interference on celledge users and improve fairness of the whole system, dynamic inter-cell interference coordination(ICIC) is one of the promising solutions. However, traditional dynamic ICIC is considered as an NP-hard problem and power variability further adds another dimension to this joint optimization issue, making it even more difficult to quickly reach a near-optimal solution. Therefore, we theoretically obtain the closed-form expression of the near-optimal power allocation ratio for users in adjacent cells paired in the same resource block and interfere each other, so that the total utility corresponding to α-fairness is maximized. Dynamic ICIC using this closed-form solution could improve user fairness without causing an increment of the computational complexity. Numerical results show that, compared with the schemes using identical power for different users, our method does not obviously degrade the system's average spectral efficiency.展开更多
Amber can emit room temperature phosphorescence(RTP)under the well-known 365 nm fluorescence ultraviolet light.This paper is devoted to the phosphorescence study of 20 pieces of amber materials from the Dominican Repu...Amber can emit room temperature phosphorescence(RTP)under the well-known 365 nm fluorescence ultraviolet light.This paper is devoted to the phosphorescence study of 20 pieces of amber materials from the Dominican Republic,Mexico,Baltic sea,Myanmar,and Fushun,China.The results show that amber from the same geographic origin has similar shape in phosphorescence spectra.However,the shape of the amber phosphorescence spectra varies depending on their different localities.Burmite(amber from Myanmar)and Fushun amber have a bright yellow phosphorescence with a long lifetime,while the Dominican and Mexican ones are weaker and last shorter.The irradiation of Baltic amber becomes faint or even inert.Phosphorescence spectral Gaussian fitting results suggest an emission maximum near 550 nm in most amber samples.Their phosphorescence lifetime,analyzed through the exponential function fitting,is up to 1 second in Burmite and Fushun samples,shorter in the Dominican and Mexican ones,about 0.230 s,and the shortest in Baltic amber,close to 0.151 s.These variations of phosphorescence lifetime and intensity are related to the relative geological ages of these amber.It indicated that the phosphorescence agent was probably formed during the long geological time.While the anomaly occurred in Baltic amber,the only one found in a sea secondary deposit form,it demonstrated that the terrestrial geological environment these amber preserved has prevented the phosphorescence agent to be deactivated.展开更多
基金financially supported by the National Natural Science Foundation of China (No. 52372176)Guangdong Basic and Applied Basic Research Foundation (No. 2024A1515011517)。
文摘Na_(3)V_(2)(PO_(4))_(2)F_(3)(NVPF) is shown to be an attractive cathode material for sodium storage due to its high theoretical capacity and suitable working voltage.However,its low electronic conductivity and poor cycling stability have to be addressed in order for enhanced high-rate performance and cycle life.Herein,we have prepared a 3D reduced graphene oxide (rGO) host-supported NVPF nanocuboids.We discover that polyvinyl alcohol (PVA) serves as an important structural directing agent that bridges between NVPF and rGO through the hydrogen bonding,and thus regulates the formation of the 3D r GO framework with NVPF nanocuboids embedded inside (NVPF@C@rGO).With such a unique construction,NVPF@C@rGO exhibits excellent cycling stability and rate performance for sodium storage,showing high reversible capacities of 121 m Ah/g and 113 mAh/g at 1C and 10C,respectively,and 103 mAh/g after 700cycles at 50C with 98.3%retention.Even at an extremely high current of 100C,it also delivers a reversible capacity of 64 mAh/g,surpassing the performance of many recently reported NVPF-based electrodes.Cyclic voltammetry (CV) and galvanostatic intermittent titration technique (GITT) data confirm the much better kinetic properties of NVPF@C@rGO electrode than the control samples of NVPF@rGO and pure NVPF.In-situ XRD results reveal that the 3D rGO housing can effectively suppress the lattice variation of NVPF,with a maximum volume change of only 1.84%during cycling.Moreover,the in-situ temperature sensing reveals the more stable working temperature of NVPF@C@rGO compared to phase-pure NVPF,suggesting a higher temperature safety of the electrode.Using NVPF@C@rGO as the positive electrode and commercial hard carbon as the negative electrode,a sodium-ion full battery has been assembled with about 110 m Ah/g at 1C for 300 cycles,corresponding to an energy density of 291 Wh kg^(-1).The construction of 3D r GO housing as a conductive support offers an effective strategy for high-rate,long cycle life and high safety sodium-ion battery cathodes.
基金supported by the National Natural Science Foundation of China under Grant No. 61501160supported by the Fundamental Research Funds for the Central Universities of China under Grant No. 2015HGCH0013
文摘To mitigate interference on celledge users and improve fairness of the whole system, dynamic inter-cell interference coordination(ICIC) is one of the promising solutions. However, traditional dynamic ICIC is considered as an NP-hard problem and power variability further adds another dimension to this joint optimization issue, making it even more difficult to quickly reach a near-optimal solution. Therefore, we theoretically obtain the closed-form expression of the near-optimal power allocation ratio for users in adjacent cells paired in the same resource block and interfere each other, so that the total utility corresponding to α-fairness is maximized. Dynamic ICIC using this closed-form solution could improve user fairness without causing an increment of the computational complexity. Numerical results show that, compared with the schemes using identical power for different users, our method does not obviously degrade the system's average spectral efficiency.
基金the financial support from the National Key R&D Program of China(2018YFF0215400)grants from the Gemmological Institute of the China University of Geosciences in Wuhan。
文摘Amber can emit room temperature phosphorescence(RTP)under the well-known 365 nm fluorescence ultraviolet light.This paper is devoted to the phosphorescence study of 20 pieces of amber materials from the Dominican Republic,Mexico,Baltic sea,Myanmar,and Fushun,China.The results show that amber from the same geographic origin has similar shape in phosphorescence spectra.However,the shape of the amber phosphorescence spectra varies depending on their different localities.Burmite(amber from Myanmar)and Fushun amber have a bright yellow phosphorescence with a long lifetime,while the Dominican and Mexican ones are weaker and last shorter.The irradiation of Baltic amber becomes faint or even inert.Phosphorescence spectral Gaussian fitting results suggest an emission maximum near 550 nm in most amber samples.Their phosphorescence lifetime,analyzed through the exponential function fitting,is up to 1 second in Burmite and Fushun samples,shorter in the Dominican and Mexican ones,about 0.230 s,and the shortest in Baltic amber,close to 0.151 s.These variations of phosphorescence lifetime and intensity are related to the relative geological ages of these amber.It indicated that the phosphorescence agent was probably formed during the long geological time.While the anomaly occurred in Baltic amber,the only one found in a sea secondary deposit form,it demonstrated that the terrestrial geological environment these amber preserved has prevented the phosphorescence agent to be deactivated.
