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Dive into the research topics where Wanqiang Liu is active.

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Featured researches published by Wanqiang Liu.


Philosophical Magazine | 2011

Preparation and wear resistance of Ti–Zr–Ni quasicrystal and polyamide composite materials

X. D. Wang; Xuesong Li; Zhenjiang Zhang; Shanshan Zhang; Wanqiang Liu; Limin Wang

Ti–Zr–Ni icosahedral quasicrystal powders (Ti-QC), prepared by mechanical alloying and then annealing in a vacuum furnace, were used as a novel filler material in polyamide 12 (PA12). The melt processability of the composite was studied using a Haake torque rheometer. This indicates that PA12/Ti-QC composites can be melt-processed into a wear-resistant material. Further, these composites, fabricated by compression molding, were tested in sliding wear against a polished bearing steel counterface. The results from wear testing show that the addition of Ti-QC filler to PA12 enhances wear resistance and reduces volume loss by half compared with neat PA12. Furthermore, it is found that the hardness of the composite increases with increasing content of Ti-QC filler. In addition, PA12/Ti-QC composites exhibit a slightly higher crystallization temperature and better thermal stability than PA12. These combined results demonstrate that Ti-QC filler may be a desirable alternative when attempting to increase the wear resistance of PA12.


Journal of Applied Physics | 2016

Responsivity enhancement of ZnO/Pt/MgZnO/SiO2 and MgZnO/Pt/ZnO/SiO2 structured ultraviolet detectors by surface plasmons in Pt nanoparticles

Long Sun; Dayong Jiang; Guoyu Zhang; Rusheng Liu; Qian Duan; Jieming Qin; Qingcheng Liang; Shang Gao; Janhua Hou; Jianxun Zhao; Wanqiang Liu; Xiande Shen

The structured (ZnO/Pt/MgZnO/SiO2) ultraviolet detector was fabricated and demonstrated to investigate how metallic nanoparticles localized surface plasmons contribute when the two different dielectrics surrounded simultaneously. After sandwiching the Pt nanoparticles between the double layers of MgZnO and ZnO, the extinction was increased largely. Meanwhile, by examining the dependence of MgZnO and ZnO peak responsivity enhancement ratio, we found that MgZnO was significantly larger than ZnO. The interpretation by considering is that the localized surface plasmons of energy match with MgZnO which is superior to ZnO. In order to validate this conclusion and make it more accurate, we also fabricated the MgZnO/Pt/ZnO/SiO2 structure. Our work suggests that rational integration of double-layer and metal nanoparticles is a viable approach to perceive localized surface plasmons with double-layer ultraviolet detectors, which may help to advance optoelectronic devices.


New Journal of Chemistry | 2015

Exploring the geometrical structures of X©BnHnm [(X, m) = (B, +1), (C, +2) for n = 5; (X, m) = (Be, 0), (B, +1) for n = 6] by an electronic method

Jianhua Hou; Ying Chen; Qian Duan; Qingcheng Liang; Dayong Jiang; Wanqiang Liu; Bing Yan; Zhi-Ru Li; Fenglong Gu; Qian-shu Li

A series of singlet and triplet wheel-type clusters obtained through an electronic method, i.e., adding two and four electrons into X©BnHnm [(X, m) = (B, +1), (C, +2) for n = 5; (X, m) = (Be, 0), (B, +1) for n = 6], have been studied theoretically. With the increase of the number of electrons, the sizes of peripheral boron rings tend to decrease due to the increase of negative charges on the boron rings. The results of the kinetic stability and the electronic stability suggest that the triplet C©B5H5 and singlet Be©B6H6 are stable and may be detected experimentally. Nucleus-independent chemical shift and molecular orbital analysis reveal that some wheel-type clusters with the planar ring possess aromaticity properties that are attributed to the delocalized π electrons conforming to the Huckel rule, i.e. 4n + 2 for singlets or 4n for triplets. These findings from this work are significant for designing novel wheel-type clusters.


Transactions of Nonferrous Metals Society of China | 2012

Influence of heat treatment on electrochemical properties of Ti1.4V0.6Ni alloy electrode containing icosahedral quasicrystalline phase

Wanqiang Liu; Shanshan Zhang; Limin Wang

Abstract The structures and electrochemical properties of the Ti 1.4 V 0.6 Ni ribbon before and after heat treatment are investigated systematically. The structure of the sample is characterized by X-ray powder diffraction analysis. Electrochemical properties including the discharge capacity, the cyclic stability and the high-rate discharge ability are tested. X-ray powder diffraction analysis shows that after heat treatment at 590 °C for 30 min, all samples mainly consist of the icosahedral quasicrystal phase (I-phase), Ti 2 Ni phase (FCC), V-based solid solution phase (BCC) and C14 Laves phase (hexagonal). Electrochemical measurements show that the maximum discharge capacity of the alloy electrode after heat treatment is 330.9 mA·h/g under the conditions that the discharge current density is 30 mA/g and the temperature is 30 °C. The result indicates that the cyclic stability and the high-rate discharge ability are all improved. In addition, the electrochemical kinetics of the alloy electrode is also studied by electrochemical impedance spectroscopy (EIS) and hydrogen diffusion coefficient ( D ).


Journal of Applied Physics | 2015

Controlled response wavelength shifting in ultraviolet photodetectors based on double-layer films

Rusheng Liu; Dayong Jiang; Qian Duan; Long Sun; Zexuan Guo; Jianan Pei; Jieming Qin; Jianxun Zhao; Jianhua Hou; Shang Gao; Qingcheng Liang; Wanqiang Liu

By integrating ZnO and MgZnO films onto a quartz substrate (both films with the same growth time), the ultraviolet photodetectors (Au/ZnO/MgZnO/SiO2 and Au/MgZnO/ZnO/SiO2 structured photodetectors) have been fabricated. The responsivity peaks blue-shift from 380 to 370u2009nm (380 to 375u2009nm) by increasing the bias voltage in 1.0u2009h (1.5u2009h) photodetectors, which is denoted by the growth time of one layer of the films. More interestingly, the Au/MgZnO/ZnO/SiO2 photodetectors shift the same response wavelength range at smaller bias voltages than the Au/ZnO/MgZnO/SiO2 photodetectors. The results are well-rationalized in term of the role played by the double-layer structure.


International Journal of Nanotechnology | 2013

Electrochemical hydrogen storage characteristics of TiVNi–quasicrystalline composite materials

Wanqiang Liu; Shanshan Zhang; Wen Hu; Limin Wang

The Ti1.4V0.6Ni ribbon alloy and VTZN (V5Ti9Zr26.7Ni38Cr5Mn16Sn0.3) alloy ingot are prepared by melt–spinning technique and induction levitation melting technique, respectively. The Ti1.4V0.6Ni + 20 wt.% VTZN mixture powders are synthesised by ball–milling the above prepared alloy ingots, and their structures and the electrochemical hydrogen storage properties are investigated. It is found that the icosahedral quasicrystal, FCC and BCC structural solid solution phase are all presented in the composite material. The maximum electrochemical discharge capacity of the composite electrode is 308.2 mAh/g at the discharge current density of 30 mA/g and 303 K. In addition, the electrode made of Ti1.4V0.6Ni and AB3 composite holds better high–rate discharge ability than that of Ti1.4V0.6Ni.


International Journal of Hydrogen Energy | 2011

Electrochemical performance of TiVNi-Quasicrystal and AB3-Type hydrogen storage alloy composite materials

Wanqiang Liu; X. D. Wang; Wen Hu; Yoshiteru Kawabe; Masaharu Watada; Limin Wang


International Journal of Hydrogen Energy | 2014

Hydrogen storage properties of Ti1.4V0.6Ni + x Mg (x = 1–3, wt.%) alloys

Jing Lin; Fei Liang; Yaoming Wu; Wanqiang Liu; Limin Wang


Materials Letters | 2012

Ti1.4V0.6Ni quasicrystal and its composites with xV18Ti15Zr18Ni29Cr5Co7Mn alloy used as negative electrode materials for the nickel–metal hydride (Ni–MH) secondary batteries

Wanqiang Liu; Shanshan Zhang; Limin Wang


Journal of Non-crystalline Solids | 2012

Electrochemical properties of Ti-based Quasicrystal and ZrV2 Laves phase alloy composite materials as negative electrode for Ni-MH secondly batteries

Wanqiang Liu; Fei Liang; Shanshan Zhang; Jing Lin; X. D. Wang; Limin Wang

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Limin Wang

Chinese Academy of Sciences

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Dayong Jiang

Changchun University of Science and Technology

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Jianxun Zhao

Changchun University of Science and Technology

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Fei Liang

Chinese Academy of Sciences

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Shanshan Zhang

Changchun University of Science and Technology

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Cheng Xing

Changchun University of Science and Technology

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Shang Gao

Changchun University of Science and Technology

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X. D. Wang

Chinese Academy of Sciences

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