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Author

Hong Liu

Other affiliations: Shanghai University, Guangzhou University, University of Jinan  ...read more
Bio: Hong Liu is an academic researcher from Shandong University. The author has contributed to research in topics: Medicine & Materials science. The author has an hindex of 100, co-authored 1905 publications receiving 57561 citations. Previous affiliations of Hong Liu include Shanghai University & Guangzhou University.


Papers
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TL;DR: In this paper, the influence of Nb2O5 doping on the phase structure, microstructure, and energy storage properties of lead-free electroceramics was investigated.
Abstract: Lead-free (1 − x)Bi0.5Na0.5TiO3–xSrTiO3 + ywt%Nb2O5 electroceramics were synthesized using the conventional method to investigate the influences of SrTiO3 content and Nb2O5 doping on the material’s phase structure, microstructure, and energy storage properties. All the investigated compositions possessed a single perovskite phase structure of pseudocubic symmetry. The introduction of SrTiO3 and Nb2O5 led to a weakened relaxor characteristic and a decrease of Tm. The microstructure was refined by Nb2O5 doping, and the average grain size of the 0.6Bi0.5Na0.5TiO3–0.4SrTiO3 sample decreased drastically from ~ 10 to ~ 1 µm when 2.5 wt% Nb2O5 was added. Enhanced electrical breakdown and polarization were achieved for the samples with the refined microstructure. Among the various Bi0.5Na0.5TiO3-based ceramics, 0.6Bi0.5Na0.5TiO3–0.4SrTiO3 + 2.5 wt%Nb2O5 ceramic exhibited excellent energy-storage properties with thermal stability, in which large recoverable energy-storage density Wrec ~ 1.82 J/cc and efficiency η ~ 81% were both achieved. Our results indicate that this ceramic is a promising material for lead-free energy storage applications.

25 citations

Journal ArticleDOI
TL;DR: In this article, a new perovskite family with the formula of La0.8 Sr0.2 Mn1-x Px O3-δ (x=0, 0.02, 0., 0.05, and 0.1, respectively) was proposed.
Abstract: Because of their structural and compositional flexibility, perovskite oxides represent an attractive alternative electrocatalyst class to precious metals for the oxygen reduction reaction (ORR); an important reaction in fuel cells and metal-air batteries. Partial replacement of the original metal cation with another cation, namely, doping, can be used to tailor the ORR activity of perovskite, for which a metal has been exclusively used as the dopant component in the past. Herein, phosphorus is proposed as a non-metal dopant for the cation site to develop a new perovskite family with the formula of La0.8 Sr0.2 Mn1-x Px O3-δ (x=0, 0.02, 0.05, and 0.1; denoted as LSM, LSMP0.02, LSMP0.05, and LSMP0.1, respectively). Powder XRD patterns reveal that the solubility of phosphorus in the perovskite structure is around 0.05. Rotating ring-disk electrode experiments in the form of linear-sweep voltammetry scans demonstrated the best ORR performance for LSMP0.05, and also revealed close to a four-electron ORR pathway for all four compositions. A chronoamperometric test (9000 s) and 500 cycle accelerated durability test demonstrated higher durability for LSMP0.05 relative to that of LSM and the commercial 20 wt % Pt/C catalyst. The higher ORR activity for LSMP0.05 is attributed to the optimised average valence of Mn, as evidenced by combined X-ray photoelectron spectroscopy and soft X-ray absorption spectroscopy data. Doping phosphorus into perovskites is an effective way to develop high-performance electrocatalysts for ORR.

25 citations

Journal ArticleDOI
TL;DR: It is demonstrated that high‐dose MK treatment initiates TIF by activating HIF‐1α‐KLF5‐TGF‐β1 signaling activation, which is the potential mechanism of high-dose MK‐induced TIF, as knockdown of KLF5 reduced TIF in vivo.
Abstract: The discovery of hypoxia-inducible factor (HIF)-prolyl hydroxylase inhibitor (PHI) has revolutionized the treatment strategy for renal anemia. However, the presence of multiple transcription targets of HIF raises safety concerns regarding HIF-PHI. Here, we explored the dose-dependent effect of MK-8617 (MK), a kind of HIF-PHI, on renal fibrosis. MK was administered by oral gavage to mice for 12 wk at doses of 1.5, 5, and 12.5 mg/kg. In vitro, the human proximal tubule epithelial cell line HK-2 was treated with increasing doses of MK administration. Transcriptome profiling was performed, and fibrogenesis was evaluated. The dose-dependent biphasic effects of MK on tubulointerstitial fibrosis (TIF) were observed in chronic kidney disease mice. Accordingly, high-dose MK treatment could significantly enhance TIF. Using RNA-sequencing, combined with in vivo and in vitro experiments, we found that Kruppel-like factor 5 (KLF5) expression level was significantly increased in the proximal tubular cells, which could be transcriptionally regulated by HIF-1α with high-dose MK treatment but not low-dose MK. Furthermore, our study clarified that HIF-1α-KLF5-TGF-β1 signaling activation is the potential mechanism of high-dose MK-induced TIF, as knockdown of KLF5 reduced TIF in vivo. Collectively, our study demonstrates that high-dose MK treatment initiates TIF by activating HIF-1α-KLF5-TGF-β1 signaling. These findings provide novel insights into TIF induction by high-dose MK (HIF-PHI), suggesting that the safety dosage window needs to be emphasized in future clinical applications.-Li, Z.-L., Lv, L.-L., Wang, B., Tang, T.-T., Feng, Y., Cao, J.-Y., Jiang, L.-Q., Sun, Y.-B., Liu, H., Zhang, X.-L., Ma, K.-L., Tang, R.-N., Liu, B.-C. The profibrotic effects of MK-8617 on tubulointerstitial fibrosis mediated by the KLF5 regulating pathway.

25 citations

Journal ArticleDOI
TL;DR: In this article, a time-adaptive loosely coupled analysis of aerothermostructural response is proposed for the fluid thermal-structural coupling of hypersonic vehicles under high thermal and mechanical loads due to severe aeroheating.

25 citations

Journal ArticleDOI
TL;DR: The electronic structure of WS2 was further modified with N doping to deliver an addressable surface for the reaction species involved in the electrocatalytic hydrogen evolution reaction (HER), and the resultant N-WS2 exhibited enhanced HER activity compared with the original WS2.
Abstract: The precise control over the geometric and electronic structures of active materials on flexible substrates is of great importance to address the current challenges in optimizing and developing high-performance flexible devices for energy conversion and storage. In this work, an addressable surface was demonstrated to engineer structurally controllable active nanomaterials for electrocatalytic hydrogen evolution. The nanostructures of WS2/MOF/metal hydroxide/oxide with different formation energy barriers electrodes could be tuned by modifying the ratio of O/C and the concentration of carbon defects at the surface of carbon cloth. The morphological structure of the vertical WS2 nanosheets that are favorable to electrocatalysis was found to be highly related to the addressable surface of carbon cloth though heterogeneous nucleation and the interactions between the monomers and surface functional groups. Moreover, the electronic structure of WS2 was further modified with N doping (N-WS2) to deliver an addressable surface for the reaction species involved in the electrocatalytic hydrogen evolution reaction (HER), and the resultant N-WS2 exhibited enhanced HER activity compared with the original WS2. The systematic experimental research and electronic-structure density functional theory (DFT) calculations demonstrated the interesting features of the N dopant: (i) the strong hybridization of the p orbital of dopant N with d orbital of W and p orbital of S atoms (W d-S p-N p hybridization) close to the Fermi level can disperse the conducting charges, thus leading to an improved conductivity across the basal plane of WS2 nanosheets; (ii) the local electron transfer from W to N atoms provides the local charge, thus promoting the H adsorption process in the HER for N-WS2. Our research can be expected to offer new perspectives in the precise construction of highly reactive nanostructures toward high-efficiency and highly stable flexible devices for energy conversion and storage.

25 citations


Cited by
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[...]

08 Dec 2001-BMJ
TL;DR: There is, I think, something ethereal about i —the square root of minus one, which seems an odd beast at that time—an intruder hovering on the edge of reality.
Abstract: There is, I think, something ethereal about i —the square root of minus one. I remember first hearing about it at school. It seemed an odd beast at that time—an intruder hovering on the edge of reality. Usually familiarity dulls this sense of the bizarre, but in the case of i it was the reverse: over the years the sense of its surreal nature intensified. It seemed that it was impossible to write mathematics that described the real world in …

33,785 citations

28 Jul 2005
TL;DR: PfPMP1)与感染红细胞、树突状组胞以及胎盘的单个或多个受体作用,在黏附及免疫逃避中起关键的作�ly.
Abstract: 抗原变异可使得多种致病微生物易于逃避宿主免疫应答。表达在感染红细胞表面的恶性疟原虫红细胞表面蛋白1(PfPMP1)与感染红细胞、内皮细胞、树突状细胞以及胎盘的单个或多个受体作用,在黏附及免疫逃避中起关键的作用。每个单倍体基因组var基因家族编码约60种成员,通过启动转录不同的var基因变异体为抗原变异提供了分子基础。

18,940 citations

Journal ArticleDOI
TL;DR: This Review describes how the tunable electronic structure of TMDs makes them attractive for a variety of applications, as well as electrically active materials in opto-electronics.
Abstract: Ultrathin two-dimensional nanosheets of layered transition metal dichalcogenides (TMDs) are fundamentally and technologically intriguing. In contrast to the graphene sheet, they are chemically versatile. Mono- or few-layered TMDs - obtained either through exfoliation of bulk materials or bottom-up syntheses - are direct-gap semiconductors whose bandgap energy, as well as carrier type (n- or p-type), varies between compounds depending on their composition, structure and dimensionality. In this Review, we describe how the tunable electronic structure of TMDs makes them attractive for a variety of applications. They have been investigated as chemically active electrocatalysts for hydrogen evolution and hydrosulfurization, as well as electrically active materials in opto-electronics. Their morphologies and properties are also useful for energy storage applications such as electrodes for Li-ion batteries and supercapacitors.

7,903 citations