Huiming Ning

Dr. Huiming Ning

orcid

Research Focus & Metrics

Academic Career Length

16Years (2011-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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21 March 2021 in Advanced Functional Materials
Verified
Journal Article
Open access
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JWJie Wen
Jie Wen
JTJia Tang
Jia Tang
HNHuiming Ning
Huiming Ning
NHNing Hu
Ning Hu
YZYuanyuan Zhu
Yuanyuan Zhu
THTao Huang
Tao Huang
Conductive polymer hydrogels are receiving considerable attention in applications such as soft robots and human‐machine interfaces. Herein, a transparent and highly ionically conductive hydrogel that integrates sensing, UV‐filtering, water‐retaining, and anti‐freezing performances is achieved by the organic combination of tannic acid‐coated hydroxyapatite nanowires (TA@HAP NWs), polyvinyl alcohol (PVA) chains, ethylene glycol (EG), and metal ions. The highly ionic conductivity of the hydrogel enables tensile strain, pressure, and temperature sensing capabilities. In particular, in terms of the hydrogel strain sensors based on ionic conduction, it has high sensitivity (GF = 2.84) within a wide strain range (350%), high linearity (R2 = 0.99003), fast response (≈50 ms) and excellent cycle stability. In addition, the incorporated TA@HAP NWs act as a nano‐reinforced filler to improve the mechanical properties and confer a UV‐shielding ability upon the hydrogel due to its size effect and the characteristics of absorbing ultraviolet light waves, which can reflect and absorb short ultraviolet rays and transmit visible light. Meanwhile, owing to the water‐locking effect between EG and water molecules, the hydrogel exhibits freezing resistance at low temperatures and moisture retention at high temperatures. This biocompatible and multifunctional conductive hydrogel provides new ideas for the design of novel ionic skin devices.

1 January 2022 in Nanotechnology Reviews
Verified
Journal Article
Open access
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LWLiangke Wu
Liangke Wu
ZJZhaonan Jin
Zhaonan Jin
YLYaolu Liu
Yaolu Liu
HNHuiming Ning
Huiming Ning
XLXuyang Liu
Xuyang Liu
NHNing Hu
Ning Hu
In recent years, PVDF(polyvinylidene fluoride) and its copolymers have attracted great attention in the development of energy-harvesting devices because of their unique properties such as good flexibility, environmental friendliness, high halogen and acid resistance, lightweight and good biocompatibility. Compared to the most commonly used PZT (lead zirconate titanate), the piezoelectricity of PVDF and its copolymer-based materials is relatively low. To further expand the applications of PVDF, there is an urgent need for efficient methods to prepare high piezoelectric polymers or composites. In this work, the crystal phases are introduced first. Then, the preparation methods of PVDF and its copolymer-based materials are summarized, which are mainly focused on four determining factors of piezoelectricity. The mechanisms of piezoelectric β-phase formation and α- to β-phase transformation are introduced. The influence parameters of each process and their interactions are discussed in detail. In the last section, the progress of the preparation methods is summarized. This work will provide useful information to researchers working on piezoelectric composites.

1 October 2015 in Computational Materials Science
Verified
Journal Article
Closed access
FLFeng Liu
Feng Liu
NHNing Hu
Ning Hu
HNHuiming Ning
Huiming Ning
YLYaolu Liu
Yaolu Liu
YLYuan Li
Yuan Li
LWLiangke Wu
Liangke Wu

1 September 2015 in Carbon
Verified
Journal Article
Closed access
HNHuiming Ning
Huiming Ning
JLJinhua Li
Jinhua Li
NHNing Hu
Ning Hu
CYCheng Yan
Cheng Yan
YLYaolu Liu
Yaolu Liu
JZJianyu Zhang
Jianyu Zhang

3 October 2012 in Nanoscale
Verified
Journal Article
Closed access
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ALAlamusi
Alamusi
JXJun Min Xue
Jun Min Xue
LWLiangKe Wu
LiangKe Wu
NHNing Hu
Ning Hu
JQJianhui Qiu
Jianhui Qiu
YZYinghua Zhao
Yinghua Zhao
We improved the piezoelectric property of poly(vinylidene fluoride) (PVDF) by employing graphene. The reduced graphene oxide (rGO)–PVDF nanocomposites were prepared by a solution casting method and the rGO contents ranged from 0.0 wt% to 0.2 wt%. To induce the piezoelectric β-phase crystal structure, the nanocomposite films were drawn in a ratio of 4–5 and polarized by a step-wise poling method. To evaluate the piezoelectric property, the output voltages of the rGO–PVDF nanocomposite films were measured through extensive experimental vibration tests. The experimental results show that the rGO–PVDF nanocomposite film with 0.05 wt% rGO loading possesses the highest output voltage compared with other loadings, which is around 293% of that of the pure PVDF film. Moreover, it can be found that with the increase of the rGO content from 0 wt% to 0.2 wt%, the output voltage tends to have a peak at 0.05 wt%. The main reason for this phenomenon is that a more β-crystalline phase can be formed at those rGO loadings, as confirmed by XRD and FT-IR spectrum analyses.

15 February 2018 in Scientific Reports
Verified
Journal Article
Open access
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SWShayuan Weng
Shayuan Weng
HNHuiming Ning
Huiming Ning
TFTao Fu
Tao Fu
NHNing Hu
Ning Hu
YZYinbo Zhao
Yinbo Zhao
XPXianghe Peng
Xianghe Peng
Molecular dynamics simulations of nanolaminated graphene/Cu (NGCu) and pure Cu under compression are conducted to investigate the underlying strengthening mechanism of graphene and the effect of lamella thickness. It is found that the stress-strain curves of NGCu undergo 3 regimes i.e. the elastic regime I, plastic strengthening regime II and plastic flow regime III. Incorporating graphene monolayer is proved to simultaneously contribute to the strength and ductility of the composites and the lamella thickness has a great effect on the mechanical properties of NGCu composites. Different strengthening mechanisms play main role in different regimes, the transition of mechanisms is found to be related to the deformation behavior. Graphene affected zone is developed and integrated with rule of mixtures and confined layer slip model to describe the elastic properties of NGCu and the strengthening effect of the incorporated graphene.