The synthesis of martensitic or shape-memory bulk metallic glass composites(BMGCs)via solidification of the glass-forming melts requires the meticulous selection of the chemical composition and the proper choice of th...The synthesis of martensitic or shape-memory bulk metallic glass composites(BMGCs)via solidification of the glass-forming melts requires the meticulous selection of the chemical composition and the proper choice of the processing parameters in order to ensure that the glassy matrix coexists with the desired amount of austenitic phase.Unfortunately,a relatively limited number of such systems,where austenite and glassy matrix coexist over a wide range of compositions,is available.Here,we study the effective-ness of powder metallurgy as an alternative to solidification for the synthesis of shape memory BMGCs.Zr_(48)Cu_(36)Al_(8)Ag_(8)matrix composites with different volume fractions of Ni_(50.6)Ti_(49.4)are fabricated using hot pressing and their microstructure,mechanical properties and deformation mechanism are investigated employing experiments and simulations.The results demonstrate that shape-memory BMGCs with tun-able microstructures and properties can be synthesized by hot pressing.The phase stability of the glass and austenitic components across a wide range of compositions allows us to examine fundamental as-pects in the field of shape memory BMGCs,including the effect of the confining stress on the martensitic transformation exerted by the glassy matrix,the contribution of each phase to the plasticity and the mechanism responsible for shear band formation.The present method gives a virtually infinite choice among the possible combinations of glassy matrices and shape memory phases,expanding the range of accessible shape memory BMGCs to systems where the glassy and austenitic phases do not form simul-taneously using the solidification route.展开更多
基金B.Bartusch,H.Merker,N.Geiβler and B.Opitz for technical support,and L.Deng,P.Zhao for stimulating discussions.T.He and X.Han acknowledge the financial support from the China Scholarship Council(CSC).We acknowledge DESY(Hamburg,Germany),a member of the Helmholtz Association HGF,for the provision of experimental facilities.Parts of this research were carried out at PETRA III and we would like to thank Dr.Z.Hegedues and Dr.U.Lienert for assistance in using beamline P21.2.Beamtime was allocated for proposal I-20200178.
文摘The synthesis of martensitic or shape-memory bulk metallic glass composites(BMGCs)via solidification of the glass-forming melts requires the meticulous selection of the chemical composition and the proper choice of the processing parameters in order to ensure that the glassy matrix coexists with the desired amount of austenitic phase.Unfortunately,a relatively limited number of such systems,where austenite and glassy matrix coexist over a wide range of compositions,is available.Here,we study the effective-ness of powder metallurgy as an alternative to solidification for the synthesis of shape memory BMGCs.Zr_(48)Cu_(36)Al_(8)Ag_(8)matrix composites with different volume fractions of Ni_(50.6)Ti_(49.4)are fabricated using hot pressing and their microstructure,mechanical properties and deformation mechanism are investigated employing experiments and simulations.The results demonstrate that shape-memory BMGCs with tun-able microstructures and properties can be synthesized by hot pressing.The phase stability of the glass and austenitic components across a wide range of compositions allows us to examine fundamental as-pects in the field of shape memory BMGCs,including the effect of the confining stress on the martensitic transformation exerted by the glassy matrix,the contribution of each phase to the plasticity and the mechanism responsible for shear band formation.The present method gives a virtually infinite choice among the possible combinations of glassy matrices and shape memory phases,expanding the range of accessible shape memory BMGCs to systems where the glassy and austenitic phases do not form simul-taneously using the solidification route.
