Microstructure and room temperature mechanical properties of NiAl-Cr(Mo)-(Hf,Dy) hypoeutectic alloy prepared by injection casting

The NiA1 Cr（Mo） （Hf, Dy） hypoeutectic alloys were prepared by conventional casting and injection casting techniques respectively, and their microstructure and room temperature mechanical properties were investigated. The results reveal that with the addition of Hf and Dy, the Ni2AIHf Heusler phase and NisDy phase form along the NiAI/Cr（Mo） phase boundaries in intercellular region. By the injection casting method, some Ni2AIHf Heusler phase and NisDy phase transform into Hf and Dy solid solutions, respectively. Moreover, the microstructure of the alloy gets good optimization, which can be characterized by the fine interlamellar spacing, high proportion of eutectic cell area and homogeneously distributed fine Ni2AIHf, NisDy, Hf solid solution and Dy solid solutions. Compared with conventional-cast alloy, the room temperature mechanical properties of injection-cast alloy are improved obviously.

Effect of Dy addition on microstructure and mechanical properties of Mg-4Y-3Nd-0.4Zr alloy

Minor Dy element was added into a Mg?4Y?3Nd?0.4Zr alloy,and its effects on the microstructure and the mechanicalproperties at elevated temperatures were investigated.Scanning electron microscope(SEM)and transmission electron microscope(TEM)were used to observe the microstructures.The results indicated that the as-cast eutectic and isolated cuboid-shaped Mg?REphases were Mg5RE and Mg3RE17,respectively,and distributed mainly along grain boundaries.After a solution treatment,theeutectic Mg5RE phases were dissolved into the matrix,whereas the Mg3RE17compound still remained.After peak aging,fineMg?RE phases were precipitated homogeneously within the matrix of the alloys containing Dy.Dy addition can result in asignificant improvement in the tensile strength at both room and elevated temperatures,and a slight decrease in the elongation.

Dissolution-regrowth of hierarchical Fe-Dy oxide modulates the electronic structure of nickel-organic frameworks as highly active and stable water splitting electrocatalysts

As the kinetically sluggish oxygen evolution reaction(OER)is considered to be a bottleneck in overall water splitting,it is necessary to develop a highly active and stable electrocatalyst to overcome this issue.Herein,we successfully fabricated a three-dimensional iron-dysprosium oxide co-regulated in-situ formed MOF-Ni arrays on carbon cloth(FeDy@MOF-Ni/CC)through a facile two-step hydrothermal method.Electrochemical studies demonstrate that the designed FeDy@MOF-Ni/CC catalyst requires an overpotential of only 251 mV to reach 10 mA cm-2 with a small Tafel slope of 52.1 mV dec-1.Additionally,the stability declined by only 5.5%after 80 h of continuous testing in 1.0 M KOH.Furthermore,a cell voltage of only 1.57 V in the overall water splitting system is sufficient to achieve 10 mA cm-2;this value is far better than that of most previously reported catalysts.The excellent catalytic performance originates from the unique 3D rhombus-like structure,as well as coupling synergies of Fe-Dy-Ni species.The combination of lanthanide and transition metal species in the synthesis strategy may open entirely new possibilities with promising potential in the design of highly active OER electrocatalysts.