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ONE-POT SYNTHESIS OF INTERESTING 3D γ-MnOOH NETWORKS
HAIQIU LIU,MINDONG CHEN,FEI TENG,YUJIAN JIN,Na Li,Lili Wang,SUNQI LOU,XIA HUA,KAI WANG,Peng Sun 성균관대학교(자연과학캠퍼스) 성균나노과학기술원 2014 NANO Vol.9 No.7
Three-dimensional (3D) γ-MnOOH networks are successfully prepared by one-pot solvothermalmethod without using any catalyst. The samples are characterized by X-ray diffraction (XRD),scanning electron microscopy (SEM) and high-resolution transmission electron microscopy(HRTEM). It is found that the amounts of urea and H2O2 added, reaction temperature and timehave important infuences on the samples. It is interesting that the 3D networks are formed fromthe oriented attachment (OA) of Mn3O4 octahedrons; and that the phase transformation from Mn3O4 to γ-MnOOH occurs via the protonation of Mn3O4. This study is expected to offer a facileapproach to the syntheses of new, intricate nanostructures.
NOVEL HIERARCHICAL NANORODS OF SILICON-DOPED Bi2O2CO3 AND ITS PHOTOCATALYTIC ACTIVITY
Peng Sun,MINDONG CHEN,YUNXUAN ZHAO,JUAN XU,WENQING YAO,YONGFA ZHU,FEI TENG,YUJIAN JIN 성균관대학교(자연과학캠퍼스) 성균나노과학기술원 2014 NANO Vol.9 No.8
The silicon-doped Bi2O2CO3 nanorods with the interesting hierarchical structure are synthesized by a simple hydrothermal method. The samples are characterized by XRD, X-ray photoelectron spectroscopy (XPS), scanning electron microscope (SEM), high-resolution transmission electron microscopy (HRTEM), Ultraviolet-visible diffuse refectance spectra (UV-DRS) and nitrogen sorption isotherms. It is found that with the increase of silicon content, the XRD peak of the sample significantly shifts toward a low diffraction angle and the particle morphologies change from nanosheets, nanoflowers to hierarchical nanorods. Moreover, the silicon-doped Bi2O2CO3 hierarchical nanorods exhibit improved photocatalytic degradation activities for different types of dyes under simulated solar light irradiation. The improved activity has been mainly attributed to the unique hierarchical nanorods structure and the formation of Si–O–Bi bonds.
Zhuang Wang,Se Wang,MINDONG CHEN,Defu Xu,Lili Tang,Degao Wang 대한화학회 2015 Bulletin of the Korean Chemical Society Vol.36 No.6
Simulations at multiple levels were performed to investigate the aqueous adsorption of phthalate esters (PAEs) on carbon nanoparticles and to find the competitive effect of a low molecular weight natural organic acid (benzoic acid) on the adsorption process. Six PAEs of varying alkyl side chain lengths and three carbon-based nanomaterials including a single-walled carbon nanotube (SWNT), double-walled carbon nanotube (DWNT), and graphene (G) were studied. Results showed that the adsorption energies calculated using density functional theory increase with increasing length of the PAE alkyl chain. G exhibits higher adsorption capacity for the PAEs than SWNT and DWNT. The absolute adsorption energies of these systems also display a positive linear correlation with the hydrophobicity of the PAE molecules. Molecular dynamics simulations indicate that the presence of neutral/anionic benzoic acid in water alleviates the PAE adsorption. Furthermore, anionic benzoic acid exerts more impact on the PAE adsorption than the neutral form.
SYNTHESIS AND CHARGE–DISCHARGE PROPERTIES OF POROUS CO3O4 NANOROD BUNDLE ELECTRODE
FEI TENG,JUN WANG,MINDONG CHEN,DENNIS DESHENG MNEG 성균관대학교(자연과학캠퍼스) 성균나노과학기술원 2012 NANO Vol.7 No.5
The Co3O4 nanorod bundles are synthesized by a hydrothermal method. The samples are characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), electron diffraction (ED), X-ray powder diffractometer (XRD), and nitrogen adsorption. It is important that the as-obtained Co3O4 nanorod bundles are assembled by nanoparticles. The porous nanorod bundle electrode exhibits a higher rate capacity and a higher reverse capability for lithium ion battery than the solid nanorods, which is attributed to the high surface area and the porous structure.
Leilei Xu,Xueying Wen,Mindong Chen,Chufei Lv,Yan Cui,Xianyun Wu,Cai-e Wu,Zhichao Miao,Xun Hu 한국공업화학회 2021 Journal of Industrial and Engineering Chemistry Vol.100 No.-
The mesoporous nanosponge MFI silicate zeolite was facilely fabricated by employing the long chainammonium as the structure-directing agent. The zeolite with both mesoporous and microporouschannels were selected as the support of Ni-La catalysts for methanation of CO2. Various techniques wereused to characterize the catalysts systematically. The effects of the La2O3 promotor and pore morphologyof the support on the catalytic performance were carefully investigated. Our study demonstrated that Lapromoter could be beneficial to the increase of the surface basicity and the enhancement of the metallicNi dispersion. This would intensify the processes of the CO2 chemisorption and H2 dissociation in CO2methanation. Besides, we also found that the catalyst supported on mesoporous nanosponge MFI zeoliteperformed higher activity and better long-term stability than the reference catalysts supported on bulkMFI and MCM-48, suggesting that the synergistic effect between the mesoporous and microporouschannels displayed unique advantages. Kinetic study revealed that both the nanosponge structure andLa2O3 promoter contributed to decreasing the reaction activation energy. Therefore, the present highlydispersed Ni-La catalyst over mesoporous nanosponge MFI zeolite promised a potential catalystcandidate for low-temperature CO2 methanation reaction.
Yiyu Shi,Leilei Xu,Mindong Chen,Bo Yang,Ge Cheng,Cai-e Wu,Zhichao Miao,Ning Wang,Xun Hu 한국공업화학회 2022 Journal of Industrial and Engineering Chemistry Vol.105 No.-
In this work, the uniform Cu2O submicron-cubes were facilely synthesized by liquid phase reductionmethod. Then, the Cu2O submicron-cubes were further oxidized into Cu2O-CuO heterojunction with tunableCu2+/Cu+ ratios and CuO submicron-cubes by controlling the calcination temperature. The phasetransition period during calcination was real-time monitored by the in-situ XRD and in-situ DRIFTS. The obtained materials were investigated as the catalysts of CO oxidation. The results revealed thatthe Cu2O-CuO heterojunction catalysts performed much higher catalytic activities than the Cu2O andCuO counterparts. Because the synergistic effect of the heterojunction (Cu2+/Cu+) could increase the surfaceoxygen vacancy concentration. Furthermore, it was also found that only the Cu2O-CuO heterojunctionstructure with the appropriate Cu2+/Cu+ ratio behaved the optimum catalytic activity. The kineticstudies indicated that the apparent activation energy of CO oxidation was greatly affected by the Cu2+/Cu+ ratio. Therefore, these Cu2O-CuO submicron-cubes with heterostructure were considered as thepromising CO oxidation catalysts.
Hui Yang,Xueying Wen,Siyuan Yin,Yixin Zhang,Cai-e Wu,Liang Xu,Jian Qiu,Xun Hu,Leilei Xu,Mindong Chen 한국공업화학회 2023 Journal of Industrial and Engineering Chemistry Vol.128 No.-
In this work, the La(OH)3 nanorods were successfully synthesized by precisely regulating the parametersof the hydrothermal method. Then, a series of Ni-based CO2 methanation catalysts were fabricated via theincipient-wetness impregnation and deposition–precipitation methods by employing the La(OH)3 nanorodsas the supports. The influences of the support morphology and the preparation method on the metalsupportinteraction, Ni dispersion, and the surface basicity were carefully investigated based on varioustechniques, such as XRD, SEM, H2-TPR, CO2-TPD, XPS, ect. It was found that the rod-shaped La(OH)3 supportedcatalyst prepared by the deposition–precipitation method performed the optimum activity andstability. The reason for this could be derived from the confinement effect of the crystal plane of therod-shaped support, which would promote the formation of the strong metal-support interaction andthe construction of the Ni-La interface with high activity. Furthermore, the online-tandem TG-MS andin-situ DRIFTS technologies were used to investigate the thermal decomposition performance of the catalystprecursors in the calcination process and the reaction intermediates of the CO2 methanation. Therefore, the fundamental roles of support morphology and catalyst preparation method were expectedto direct the advancement of the Ni-based nanostructured catalysts with outstanding low-temperatureperformances.