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Guo, Yuanhang

Publications and source records attributed to Guo, Yuanhang.

Property enhancement of CoCrNi medium-entropy alloy by introducing nano-scale features

CoCrNi -medium-entropy alloy (MEA) has been widely investigated due to its superior mechanical properties that overcome strength-ductility tradeoff. Here we show further property enhancement of CoCrNi MEA by introducing nano-scale features. Both CoCrNi and oxide dispersion strengthened (ODS) CoCrNi are fabricated by mechanical alloying and spark plasma sintering. Microstructural characterization and mechanical testing of these nanostructured MEAs revealed that the nano-scale features significantly improves the strength of the alloys. In ODS-CoCrNi MEA, Y 2 Ti 2 O 7 oxides with an average diameter of 7.3 ± 3.2 nm are incoherent with the matrix, and a specific orientation relationship exists between Y 2 Ti 2 O 7 and the matrix, which is [011] Y 2 Ti 2 O 7 //[011]Matrix, (400) Y 2 Ti 2 O 7 //(200)Matrix and ($22\bar2$) Y 2 Ti 2 O 7 //($11\bar1$)Matrix. The recrystallization and grain growth processes are effectively suppressed by the introduction of Y 2 Ti 2 O 7 nanoparticles. Strengthening mechanism analyses indicate that the strength improvement of ODS-CoCrNi is mainly ascribed to the precipitation strengthening of Y 2 Ti 2 O 7 .

36 MATERIALS SCIENCE↗

Microstructure and mechanical properties of oxide dispersion strengthened FeCoNi concentrated solid solution alloys

Microstructure and mechanical properties of two kinds of oxide dispersion strengthened concentrated solid solution alloys (CSAs), FeCoNi-1.5Y 2 O 3 (FCNY) and FeCoNi-1.2Ti-1.5Y 2 O 3 (FCNTY), are studied through a comparing investigation with FeCoNi (FCN) CSAs. All these alloys are fabricated by mechanical alloying, spark plasma sintering, hot rolling and annealing treatment. For three kinds of alloys, both the as-milled powders and bulk materials are of single face-centered cubic structure. Electron backscattered diffraction results reveal that the texture transformation is suppressed during the hot rolling process because the movement of grain boundaries is hindered by the oxide particles. Compared with FCN CSAs, grains are refined by 43% and 47% for FCNY and FCNTY CSAs, respectively. Nano-sized Y 2 O 3 (monoclinic structure) and Y 2 Ti 2 O 7 (pyrochlore structure) particles are uniformly distributed in FCNY and FCNTY CSAs, respectively. Both Y2O3 and Y2Ti2O7 particles show a semi-coherent relationship with the matrix. Yield strength of FCN, FCNY and FCNTY CSAs is 559, 981 and 1050 MPa, respectively. Theoretical calculations illustrate that high strength of FCNY and FCNTY CSAs comes from refined grains and high-density nano-sized oxide particles.

36 MATERIALS SCIENCE↗

Decoding Liquid Crystal Oligomer Phase Transitions: Toward Molecularly Engineered Shape Changing Materials

This work details an integrated investigation of liquid crystal (LC) oligomers that combines experiments and molecular dynamics simulations to obtain a detailed understanding of the molecular structure of LC oligomers and the mechanism underlying their phase transition temperatures. We synthesized and characterized a series of LC oligomers prepared from different lengths of methylene spacers in the reactive LC monomers and n-alkylamine chain extenders via the aza -Michael addition reaction. In parallel, we performed isothermal–isobaric ( NPT ) ensemble coarse-grained molecular dynamics (CG-MD) simulation of analogue mesogens that are connected to flexible spacers and extenders at varying temperatures, spacer lengths, and extender lengths. This approach allowed the effect of length in the flexible spacer as well as in the chain extender on the nematic–isotropic transition temperature ( T ni ) to be determined. The results showed that increasing the length of the extender decreases T ni for LC oligomers and amplifies the decrease of T ni in LC oligomers when the spacer length is short. We infer that the combination of spacer and extender changes the shape anisotropy of LC oligomers, changing the packing behavior of constituent mesogens, thus affecting their ability to transition from the isotropic to the nematic phase. Here, the detailed molecular structure–property relationships formulated enable prescribing design rules for LC oligomers geared toward molecularly engineered shape changing materials.

36 MATERIALS SCIENCE↗