In the context of the global energy low-carbon transition,phase change energy storage technology becomes a key technology to solve the problem of intermittent renewable energy.Oriented phase change composites(OCPCMs)r...In the context of the global energy low-carbon transition,phase change energy storage technology becomes a key technology to solve the problem of intermittent renewable energy.Oriented phase change composites(OCPCMs)receive widespread attention in practical energy storage applications due to their unique oriented thermally conductive structure,which achieves significant thermal conductivity enhancement in specific directions while retaining the high energy storage capacity of the phase change components.This review systematically summarizes the overall analysis of OCPCMs from synthesis and preparation to application scenarios in recent years.Herein,we introduce the analysis of the heat transfer mechanism of the materials and explore the advantages of the oriented structure in OCPCMs in the heat transfer behavior from a bionic perspective.We then focus on summarizing and generalizing the methods for preparing OCPCMs,giving suggestions for suitable methods according to different scenarios.Besides,we discuss the application of finite element simulation methods to the monitoring of the thermal management behavior of OCPCMs,and look into the potential future application areas of such materials.Finally,it is hoped that this review will provide guidance for the academic community in developing high-performance OCPCMs.展开更多
T_(1)'phase in Al-2.6Li-1.3Cu alloy was studied systematically by selected area clectron diffraction,serial rotation and matrix analysis of electron diffraction pattern.The results show that the crystalline struct...T_(1)'phase in Al-2.6Li-1.3Cu alloy was studied systematically by selected area clectron diffraction,serial rotation and matrix analysis of electron diffraction pattern.The results show that the crystalline structure of T,’phase is orthohombic.The lattice parameters are a=0.2876nm,b=0.86nm,c=0.406nm,and orientation relationship with the matrix is(010)://(110)。,[001]T_(1)'//[100]。.展开更多
We present a controlled fabrication of selective ultrathin metal-organic framework(MOF)nanosheets as preassembling platforms,yolk-shell structured with a few-layered N-doped carbon(NC)shell-encapsulated Ni_(0.85)Se co...We present a controlled fabrication of selective ultrathin metal-organic framework(MOF)nanosheets as preassembling platforms,yolk-shell structured with a few-layered N-doped carbon(NC)shell-encapsulated Ni_(0.85)Se core(denoted as Ni_(0.85)Se@NC)via an oriented phase modulation(OPM)strategy.The ultrathin nature of the MOF nanosheets gave rise to the modification of structure at the electronic level with abundant Se-vacancies and effective electronic coupling via an Ni-N_(x) coordination at the interface between the Ni0.85Se core and NC shell.The Ni0.85Se@NC obtained exhibited low overpotentials for both oxygen evolution reaction(OER;300 mV)and hydrogen evolution reaction(HER;157 mV)at 10 mA·cm^(−2) under an alkaline condition,outperforming their corresponding bulk MOF-derived counterparts.By exploiting Ni_(0.85)Se@NC as anode and cathode catalysts,a low cell voltage of 1.61 V was achieved by performing alkaline water electrolysis.Remarkably,it also reached a high activity in natural seawater(pH=7.98)and simulated seawater(pH=7.86)electrolytes,even surpassing integrated Pt/C-RuO_(2)/CC electrodes.Density functional theory(DFT)studies illustrated that abundant Se-vacancies effectively regulated the electronic structure of Ni_(0.85)Se@NC by accelerating electron transfer from Ni to N atoms at the interface,and thus,enabling the Ni_(0.85)Se@NC to attain a near-optimal electronic configuration that stimulated ideal adsorption-free energy toward key reaction intermediates.展开更多
基金financially supported by the Fundamental Research Funds for the Central Universities(No.FRF-KST-25-001)the Beijing Natural Science Foundation(No.L253029)。
文摘In the context of the global energy low-carbon transition,phase change energy storage technology becomes a key technology to solve the problem of intermittent renewable energy.Oriented phase change composites(OCPCMs)receive widespread attention in practical energy storage applications due to their unique oriented thermally conductive structure,which achieves significant thermal conductivity enhancement in specific directions while retaining the high energy storage capacity of the phase change components.This review systematically summarizes the overall analysis of OCPCMs from synthesis and preparation to application scenarios in recent years.Herein,we introduce the analysis of the heat transfer mechanism of the materials and explore the advantages of the oriented structure in OCPCMs in the heat transfer behavior from a bionic perspective.We then focus on summarizing and generalizing the methods for preparing OCPCMs,giving suggestions for suitable methods according to different scenarios.Besides,we discuss the application of finite element simulation methods to the monitoring of the thermal management behavior of OCPCMs,and look into the potential future application areas of such materials.Finally,it is hoped that this review will provide guidance for the academic community in developing high-performance OCPCMs.
文摘T_(1)'phase in Al-2.6Li-1.3Cu alloy was studied systematically by selected area clectron diffraction,serial rotation and matrix analysis of electron diffraction pattern.The results show that the crystalline structure of T,’phase is orthohombic.The lattice parameters are a=0.2876nm,b=0.86nm,c=0.406nm,and orientation relationship with the matrix is(010)://(110)。,[001]T_(1)'//[100]。.
基金supported by the National Natural Science Foundation of China(grant nos.21875285,21771191,and 22001265)the Taishan Scholar Foundation(grant no.ts201511019)+1 种基金Key Research and Development Projects of Shandong Province(grant no.2019JZZY010331)the Fundamental Research Funds for the Central Universities(grant no.19CX05001A).
文摘We present a controlled fabrication of selective ultrathin metal-organic framework(MOF)nanosheets as preassembling platforms,yolk-shell structured with a few-layered N-doped carbon(NC)shell-encapsulated Ni_(0.85)Se core(denoted as Ni_(0.85)Se@NC)via an oriented phase modulation(OPM)strategy.The ultrathin nature of the MOF nanosheets gave rise to the modification of structure at the electronic level with abundant Se-vacancies and effective electronic coupling via an Ni-N_(x) coordination at the interface between the Ni0.85Se core and NC shell.The Ni0.85Se@NC obtained exhibited low overpotentials for both oxygen evolution reaction(OER;300 mV)and hydrogen evolution reaction(HER;157 mV)at 10 mA·cm^(−2) under an alkaline condition,outperforming their corresponding bulk MOF-derived counterparts.By exploiting Ni_(0.85)Se@NC as anode and cathode catalysts,a low cell voltage of 1.61 V was achieved by performing alkaline water electrolysis.Remarkably,it also reached a high activity in natural seawater(pH=7.98)and simulated seawater(pH=7.86)electrolytes,even surpassing integrated Pt/C-RuO_(2)/CC electrodes.Density functional theory(DFT)studies illustrated that abundant Se-vacancies effectively regulated the electronic structure of Ni_(0.85)Se@NC by accelerating electron transfer from Ni to N atoms at the interface,and thus,enabling the Ni_(0.85)Se@NC to attain a near-optimal electronic configuration that stimulated ideal adsorption-free energy toward key reaction intermediates.
