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| 1 | The fabrication of biomimetic biphasic CAN-PAC hydrogel with a seamless interfacial layer applied in osteochondral defect repair显示文摘Cartilage tissue engineering based on biomimetic scaffolds has become a rapidly developing strategy for repairing cartilage defects. In this study, a biphasic CAN-PAC hydrogel for osteochondral defect(OCD)regeneration was fabricated based on the density difference between the two layers via a thermally reactive,rapid cross-linking method. The upper hydrogel was cross-linked by CSMA and NIPAm, and the lower hydrogel was composed of PECDA, AAm and PEGDA. The interface between the two layers was first grafted by the physical cross-linking of calcium gluconate and alginate, followed by the chemical cross-linking of the carbon-carbon double bonds in the other components. The pore sizes of the upper and lower hydrogels were ~ 187.4 and ~ 112.6 μm, respectively. The moduli of the upper and lower hydrogels were ~ 0.065 and~ 0.261 MPa. This prepared bilayer hydrogel exhibited the characteristics of mimetic composition, mimetic structure and mimetic stiffness, which provided a microenvironment for sustaining cell attachment and viability. Meanwhile, the biodegradability and biocompatibility of the CAN-PAC hydrogel were examined in vivo. Furthermore, an osteochondral defect model was developed in rabbits, and the bilayer hydrogels were implanted into the defect. The regenerated tissues in the bilayer hydrogel group exhibited new translucent cartilage and repaired subchondral bone, indicating that the hydrogel can enhance the repair of osteochondral defects. | Jinfeng Liao Taoran Tian Sirong Shi Xueping Xie Quanquan Ma Guo Li Yunfeng Lin | 2017 | Bone Research2017，5，2： | 10 |
| 2 | Experimental and mechanistic understanding of photo-oxidation of methanol catalyzed by CuO/TiO2-spindle nanocomposite:Oxygen vacancy engineering显示文摘We report experimental and mechanistic understanding of methanol oxidation to produce methyl formate using CuO/Ti02-spindle composite as a promising photocatalyst under mild conditions with over 97%conversion and 83%selectivity.The catalysts are obtained via precise depositing of CuO nanoclusters(size:~3.5 nm)at the{101}facet of the TiO2 to optimally tune exciton recombination through oxygen vacancies generation,evidenced by photoluminescence and Raman spectroscopy measurements.The turnover frequency(TOF)and the apparent quantum efficiency(AQE)of the 7%CuO/TiO2-spindle composites reach up to 23.8 molmethanol·gcat^-1·h^-1 and 55.2%at 25℃,respectively,which are substantially higher than these previously reported photocatalysts.Further,the in-situ attenuated total reflection infrared spectroscopy analysis reveals that the methanol oxidation most likely takes place through the conversion of adsorbed methoxy(CH30^*)to formaldehyde(CHO^*)intermediate,a subject of major debate for a long time.The adsorbed formaldehyde(CHO^*)thus produced reacts with another CH30^*species in its close proximity to form the final product of methyl formate.Results of this study provide insights into the reaction mechanism,and offer guidelines to systematically develop and apply photocatalysts for methanol conversion and related reactions via surface engineering. | Quanquan Shi Zhaoxian Qin Changlin Yu Ammara Waheed Hui Xu Yong Gao Hadi Abroshan Gao Li | 2020 | Nano Research2020，13，4： | 3 |
| 3 | Synergistic effects of PtFe/CeO_(2)catalysts afford high catalytic performance in selective hydrogenation of cinnamaldehyde显示文摘Selective hydrogenation of unsaturated aldehydes remains a grand challenge in controlling chemoselectivity up to now.We synthesized a series of PtFex/CeO_(2)catalysts,which were characterized by X-ray diffraction(XRD),transmission electron microscopy(TEM),X-ray photoelectron spectroscopy(XPS)as well as temperature-programmed-reduction by hydrogen(H2-TPR).The catalytic performance of PtFex/CeO_(2),including cinnamaldehyde(CAL)conversion and selectivity toward cinnamyl alcohol(COL),is improved remarkably by introduction of Fe species in the Pt particles in the selective CAL hydrogenation under mild conditions.XPS results indicate that the electron transfer from Fe to Pt promotes CAL adsorption,resulting in the enhanced CAL conversion.And the COL selectivity is improved by CAL adsorption via an interaction of C=O group with surface oxygen defect sites because of interaction between PtFe and CeO_(2)support.In all,this study may provide some hints to design efficient nano Pt particles for the selective hydrogenation. | Xia Gong Quanquan Shi Xinyu Zhang Jinmei Li Guichen Ping Hui Xu Hongjing Ding Gao Li | 2023 | Journal of Rare Earths2023，41，2： | 0 |
| 4 | Morphology effects in MnCeO_(x)solid solution-catalyzed NO reduction with CO:Active sites,water tolerance,reaction pathway显示文摘Morphological effects of nanoparticles are crucial in many solid-catalyzed chemical transformations.We herein prepared two manganese-ceria solid solutions,well-defined MnCeO_(x)nanorods and MnCeO_(x)-nanocubes,exposing preferentially(111)and(100)facets of ceria,respectively.The incorporation of Mn dopant into ceria lattice strongly enhanced the catalytic performance in the NO reduction with CO.MnCeO_(x)(111)catalyst outperformed MnCeO_(x)(100)counterpart due to its higher population density of oxygen vacancy defects.In-situ infrared spectroscopy investigations indicated that the reaction pathway over MnCeO_(x)and pristine CeO_(2)is similar and that besides the direct pathway,an indirect pathway via adsorbed hyponitrite as an intermediate cannot be ruled out.X-ray photoelectron and Raman spectroscopies as well as first-principles density functional theory(DFT)calculations indicate that the enhanced catalytic performance of MnCeO_(x)can be traced back to its“Mn–OL(VÖ)–Mn–OL(VÖ)–Ce”connectivities.The Mn dopant strongly facilitates the formation of surface oxygen vacancies(VÖ)by liberating surface lattice oxygen(OL)via CO*+OL→CO_(2)*+VÖand promotes the reduction of NO,according to NO*+VÖ→N*+OL and 2N*→N_(2).The Mn dopant impact on both the adsorption of CO and activation of OL reveals that a balance between these two effects is critical for facilitating all reaction steps. | Quanquan Shi Yifei Zhang Zhiwen Li Zhongkang Han Liangliang Xu Alfons Baiker Gao Li | 2023 | Nano Research2023，16，5： | 0 |
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