Hong Liu

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.

Biopolymer/Calcium phosphate scaffolds for bone tissue engineering.

Abstract: With nearly 30 years of progress, tissue engineering has shown promise in developing solutions for tissue repair and regeneration. Scaffolds, together with cells and growth factors, are key components of this development. Recently, an increasing number of studies have reported on the design and fabrication of scaffolding materials. In particular, inspired by the nature of bone, polymer/ceramic composite scaffolds have been studied extensively. The purpose of this paper is to review the recent progress of the naturally derived biopolymers and the methods applied to generate biomimetic biopolymer/calcium phosphate composites as well as their biomedical applications in bone tissue engineering.

Hierarchical microsphere of MoNi porous nanosheets as electrocatalyst and cocatalyst for hydrogen evolution reaction

Abstract: In industrial water electrolysis cell, the electrocatalyst has a sluggish water dissociation kinetics leading to low electrocatalytic activity for the generation of H2 from water splitting. This work reports a hierarchical microsphere constructed by MoNi porous nanosheets derived from NiMoO4 microsphere, as a rapid Tafel-step-decided electrocatalyst towards hydrogen evolution reaction (HER). Consequently, the synthesized MoNi hierarchical microsphere (MoNi HM) electrocatalyst exhibits an onset potential of as small as −7 mV vs. RHE, an operating potential of 72 mV for 10 mA cm−2, and a low Tafel slope of 36.6 mV per decade in 1.0 M KOH. Furthermore, MoNi HM as cocatalyst and CdS nanowires as photocatalyst are physically mixed (MoNi HM/CdS NWs) and presentes a champion photocatalytic performance for H2 production with a prominent H2 generation rate of as high as 151.7 μmol mg-1 h−1 at λ > 420 nm light illumination. The large contact area between MoNi nanosheets and CdS nanowires endows the fast separation of photogenerated charge carriers to significantly facilitate the photocatalytic H2 production.

Novel visible-light driven Mn0.8Cd0.2S/g-C3N4 composites: Preparation and efficient photocatalytic hydrogen production from water without noble metals

Abstract: A series of novel visible light-responsive Mn 0.8 Cd 0.2 S/g-C 3 N 4 hybrid materials with different g-C 3 N 4 contents were synthesized via a facile hydrothermal method. The obtained Mn 0.8 Cd 0.2 S/g-C 3 N 4 composites displayed highly efficient photocatalytic activities for H 2 evolution from aqueous solutions containing sacrificial reagents (Na 2 S and Na 2 SO 3 ) under visible light ( λ > 420 nm) even without noble metal co-catalysts. The highest H 2 evolution rate of 4.0 mmol h −1 g −1 (with an apparent quantum efficiency of 4.1% at 420 nm) was achieved on the Mn 0.8 Cd 0.2 S/g-C 3 N 4 (10 wt%) sample, which was about 3.40 times higher than that of pure Mn 0.8 Cd 0.2 S. The enhanced photocatalytic activity of Mn 0.8 Cd 0.2 S/g-C 3 N 4 composites should be attributed to the well-matched band structure and intimate contact interfaces between Mn 0.8 Cd 0.2 S and g-C 3 N 4 , which led to the effective transfer and separation of the photogenerated charge carriers. In addition, the Mn 0.8 Cd 0.2 S/g-C 3 N 4 photocatalysts showed good stability during the photocatalytic water splitting to hydrogen under visible light. A possible mechanism of the enhanced photocatalytic activity of Mn 0.8 Cd 0.2 S/g-C 3 N 4 was also proposed.

Fe2N nanoparticles boosting FeNx moieties for highly efficient oxygen reduction reaction in Fe-N-C porous catalyst

Abstract: Replacing Pt-based electrocatalysts for the oxygen reduction reaction (ORR) with high performance and low-cost non-precious metal catalysts is crucial for the commercialization of fuel cells. Herein, we present a highly efficient Fe-N-C porous ORR electrocatalyst with FeNxmoieties promoted by Fe2N nanoparticles derived from Fe-doped zeolitic imidazolate framework. The best-performing Fe-N-C/HPC-NH3catalyst exhibits a superior ORR activity with an onset (E0) and half-wave (E1/2) potential of 0.945 and 0.803 V (RHE), respectively, which is comparable to those of the commercial Pt/C in acidic media. Probing and acid-leaching experiments prove that FeNx moieties play an important role in the ORR and the Fe2N can further improve the ORR activity. Density functional theory calculation reveals a synergistic effect that the existence of Fe2N weakens the adsorption of ORR intermediates on active sites and lowers the reaction free energy of the potential limiting step, thus facilitating the ORR. Both experimental evidence and theoretical analysis for the enhancement of ORR activity by Fe2N decoration in Fe-N-C catalyst might inspire a new strategy for rational design of high performance non-precious metal catalysts.

I and i

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 …

疟原虫var基因转换速率变化导致抗原变异[英]／Paul H, Robert P, Christodoulou Z, et al//Proc Natl Acad Sci U S A

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。

The chemistry of two-dimensional layered transition metal dichalcogenide nanosheets

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.