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Duanwei He

Publications and source records attributed to Duanwei He.

4 recordsLinked to original sources

Observation of Iron Oxide to Nitride Conversion via Liquid Liquid Phase Separation in High pressure Borate Melt

High pressure chemistry provides a powerful route to materials that are inaccessible or difficult to synthesize under ambient conditions. However, high pressure chemical reaction processes and mechanisms remain largely unexplored because of the challenges associated with in situ characterization under high pressure and high temperature, particularly within the deeply enclosed sample environment of a large volume press. Here, we employ the state of the art real time synchrotron X ray radiography to image a high pressure chemical reaction at 5.4 GPa and 1700 K within a large volume press. Using Fe2O3 and BN as precursors, we capture the complete dynamic metal oxide to nitride conversion and show that it differs fundamentally from conventional solid state diffusion controlled nitridation. Synchrotron X ray radiography clearly revealed that this conversion involves a two stage liquid liquid separation process (LLPS), including fluid nitrogen and fluid Fe N alloy. On the basis of these observations, we propose a nitrogen driven mechanism for LLPS in borate melts. Specifically, nitrogen reduces metal cations in the borate network, altering their coordination environments and triggering a substantial reorganization of the melt structure. This coordination induced restructuring destabilizes the borate melt and promotes the LLPS of fluid Fe N alloy. Our in-situ observations suggest a general pathway for high pressure metal oxide to nitride conversion. This study provides a direct visualization of a pres-sure-enabled chemical reaction that is inaccessible under ambient conditions, offering fundamental in-sight into how high pressure reshapes chemical reaction pathways and enables the synthesis of metal nitrides.

physics.chem-ph

Three-Dimensional Continuous Multi-Walled Carbon Nanotubes Network-Toughened Diamond Composite

Enhancing the fracture toughness of diamond while preserving its hardness is a significant challenge. Traditional toughening strategies have primarily focused on modulating the internal microstructural units of diamonds, including adjustments to stacking sequences, faults, nanotwinning, and the incorporation of amorphous phases, collectively referred to as intrinsic toughening. Here, we introduce an extrinsic toughening strategy to develop an unparalleled tough diamond composite with complex and abundant sp2-sp3 bonding interfaces, by incorporating highly dispersed multi-walled carbon nanotubes (MWCNTs) into the gaps of diamond grains to create a three-dimensional (3D) continuous MWCTNs network-toughen heterogeneous structure. The resultant composite exhibits a hardness of approximately 91.6 GPa and a fracture toughness of roughly 36.4 MPa.m1/2, which is six times higher than that of synthetic diamond and even surpasses that of tungsten alloys, surpassing the benefits achievable through intrinsic toughening alone. The remarkable toughening behavior can be attributed to the formation of numerous mixed sp2-sp3 bonding interactions at the 3D continuous network MWCNTs/diamond interfaces, which facilitate efficient energy dissipation. Our 3D continuous network heterogeneous structure design provides an effective approach for enhancing the fracture toughness of superhard materials, offering a new paradigm for the advanced composite ceramics.

cond-mat.other

Origin of the phase change from pyrochlore to perovskite-like layered structure and a new lead free ferroelectric

Materials with formula of A2B2O7 is a famous family with more than 300 compounds, and have abundant properties, like ferroelectric, multiferroic, and photocatalyst properties, etc. Generally, two structures dominate this family, which are pyrochlore and perovskite-like layered (PL) structure. Previously, the structure and properties design of these materials are usually complex, and solid solutions, which complicates the manufacture, as well as introducing complexity in the study of the microscopic origins of the properties. Here, we report that the pyrochlore-PL structure change happened in pure Eu2Ti2O7 under high pressure and temperature, and the formed PL structure will transfer back by heating. These results reveal that the PL structure formed in PL-pyrochlore solid solutions, is due to tuning of the high-pressure formed PL structure in pure pyrochlore compounds to ambient pressure. These results indicate the high pressure and high temperature can be used to manipulate the crystal structures from pyrochlore to PL structure, or vice versa. Furthermore, the PL Eu2Ti2O7 was confirmed as a lead free ferroelectric material for the first time.

cond-mat.mtrl-sci

Polycrystalline γ-boron: As hard as polycrystalline cubic boron nitride

The Vickers hardness of polycrystalline γ-B was measured using a diamond indentation method. The elastic properties of polycrystalline γ-B (B=213.9 GPa, G=227.2 GPa, and E=503.3 GPa) were determined using ultrasonic measurement at ambient condition. Under the loading force up to 20 N, our test gave an average Vickers hardness in the asymptotic-hardness region of 30.3 GPa. The average fracture toughness was measured as 4.1MPa m1/2. Additionally, We also measured the hardness and elastic properties of polycrystalline β-B and PcBN for comparison. The hardness and elastic properties for polycrystalline γ-B was found to be very close to that of PcBN. Our results suggest that the polycrystalline γ-B could be a superhard polycrystalline material for industrial applications.

cond-mat.mtrl-sci