Loading direction dependence of asymmetric response of pyramidal slip in rolled AZ31 magnesium alloy

Textured magnesium alloys usually exhibit anisotropic mechanical behavior due to the asymmetric activation of different twinning and slipping modes.This work focuses on the pyramidal slip responses of rolled AZ31 magnesium alloy under two loading conditions,compressive and tensile loading along the normal direction.Under the condition where the compressive loading direction is closely parallel to the c-axis of the unit cell,tensile twinning and basal slips are prohibited, dislocations then active and tend to accumulate at grain boundaries and form dislocation walls.Meanwhile,these dislocations exhibit zigzag morphologies,which result from the cross-slip from {10■1} first-order pyramidal plane to {11■2} second-order pyramidal plane,then back to {10■1} first-order pyramidal plane.Under the condition where tensile twins are prevalent,{10■1} first-order and {11■2} second-order pyramidal dislocations are favorable to be activated.Both types of dislocations behave climb-like dissociations onto the basal plane,forming zigzag dislocations.

Quasi in-situ EBSD analysis of twinning-detwinning and slip behaviors in textured AZ31 magnesium alloy subjected to compressive-tensile loading

Twinning and detwinning behavior,together with slip behavior,are studied in a textured AZ31 magnesium alloy under compressive and tensile strains along the rolling direction(RD)after each interrupted mechanical test via quasi in-situ electron backscattered diffraction technique.The results show that twinning firstly takes place under the compressive strain along the RD.With the increasing compressive strain,{1012}tensile twins firstly nucleate,then propagate,and finally thicken.While under a reversed tensile strain along the RD,detwinning occurs.No nucleation happens during detwinning.Thus,tensile twins can detwin at lower tensile strain,followed by thinning,shortening,and vanishing.Slips are also activated to accommodate the plastic deformation.In the matrix,prismatic slip can only dominate at relatively high strains.Otherwise,basal slip dominates.While in the twins,prismatic slip can activate at lower strains,which is ascribed to the texture reorientation.

Heterostructure engineering in electrode materials for sodium-ion batteries:Recent progress and perspectives

Sodium-ion batteries(SIBs)have stepped into the spotlight as a promising alternative to lithium-ion batteries for large-scale energy storage systems.However,SIB electrode materials,in general,have inferior performance than their lithium counterparts because Nat is larger and heavier than Lit.Heterostructure engineering is a promising strategy to overcome this intrinsic limitation and achieve practical SIBs.We provide a brief review of recent progress in heterostructure engineering of electrode materials and research on how the phase interface influences Nat storage and transport properties.Efficient strategies for the design and fabrication of heterostructures(in situ methods)are discussed,with a focus on the heterostructure formation mechanism.The heterostructure's influence on Nat storage and transport properties arises primarily from local distortions of the structure and chemomechanical coupling at the phase interface,which may accelerate ion/electron diffusion,create additional active sites,and bolster structural stability.Finally,we offer our perspectives on the existing challenges,knowledge gaps,and opportunities for the advancement of heterostructure engineering as a means to develop practical,highperformance sodium-ion batteries.