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Verified CAS / Academic Author2 Decoded Studies

Prof. Yue Yunfei

National United Engineering Laboratory for Advanced Bearing Tribology, Henan University of Science and Technology

Co-Affiliations:Key Laboratory of Interface Science and Engineering in Advanced Materials Ministry of Education, Taiyuan University of Technology, Taiyuan 030024, Shanxi, China

Research Publications & English Decoded Briefs

Showing 2 publications
Surface Technology (表面技术)2026DOI: 10.16490/j.cnki.issn.1001-3660.2026.11.003

Effect of Ni Content on the Microstructure and Tribological Properties of NiTi Alloy Coatings

Plasma arc cladding was employed to fabricate NiTi coatings with varying Ni contents (60, 63, 65, 67, and 70 wt.%) on TC4 titanium alloy to enhance surface wear resistance. Microstructural characterization via SEM, OM, and XRD revealed that coatings with 60–67 wt.% Ni were dense and defect-free, whereas the 70 wt.% Ni coating exhibited through-thickness cracks. All coatings exceeded 1.2 mm in thickness and comprised a NiTi toughening phase and Ti2Ni strengthening phase. Increased dilution ratio with higher Ni content reduced actual Ni in the coating, maximizing Ti2Ni fraction (78.6%) in the 67NiTi coating, which achieved a peak hardness of 677.41 HV0.2 (2.05 times that of the TC4 substrate). Tribological testing under 5–20 N loads showed that the average wear rate of all coatings decreased significantly, following a V-shaped trend with Ni content. The 67NiTi coating exhibited the lowest wear rate (2.74×10⁻⁴ mm³/(N·m)) at 20 N, a 65% improvement over the substrate, with wear mechanisms dominated by mild abrasive and adhesive wear. These findings demonstrate that optimized Ni content in plasma-clad NiTi coatings effectively mitigates the poor wear resistance of titanium alloys, offering a viable surface engineering solution for load-bearing applications.

New Carbon Materials (新型炭材料)2025DOI: 10.1016/S1872-5805(NCM2026-41-03-10)

Electrochemically activated NiOOH/NiFeV-LDH@CC for a highly efficient oxygen evolution reaction

The surface reconstruction of NiFe-based layered double hydroxide (LDH) electrocatalysts has been widely studied. The reconstructed NiOOH phase plays a critical role in improving the oxygen evolution reaction (OER) performance of NiFe-based LDHs, but observing the NiOOH phase is difficult because of its instability and exploring the functional mechanism of NiOOH in NiFe-based LDHs remains a great challenge. A simple electrochemical activation was used to synthesize a NiOOH/NiFeV-LDH@CC catalyst consisting of an array of V-doped NiFe-LDH nanosheets on carbon cloth (CC), in which the reconstructed NiOOH phase is the active species. During electrochemical activation, the release of doped V leads to the formation of abundant vanadium vacancy (VV) and oxygen vacancy (VO) species, and thus the surface of the NiFe-LDH nanosheets is reconstructed to form NiOOH. Because of the improved intrinsic activity from the NiOOH active phase, and the increased electrical conductivity produced by the abundant VO, NiOOH/NiFeV-LDH@CC has an excellent OER performance in an alkaline solution, with low overpotentials of 209 mV and 241 mV at 20 mA cm−2 and 100 mA cm−2, respectively. It also has a long-term stability of 80,000 s at a constant current density of 10 mA cm−2. Using NiOOH/NiFeV-LDH@CC as the anode, an assembled over water splitting (OWS) battery can drive a current density of 20 mA cm−2 (without iR compensation) at a much lower voltage of 1.597 V. At the same time, the electrolytic cell can deliver a current density of 10 mA cm−2 at ~1.55V for more than 80,000 s without significant loss. This electrochemical activation method can be used in future designs of electrocatalysts for OER.