Publications by authors named "Bingyan Mo"

Developing economical and efficient catalyst for hydrogen generation from ammonia borane (AB) hydrolysis is still a huge challenge. As an alternative strategy, the functional group regulation of metal nanoparticles (NPs)-based catalysts is believed to be capable of improving the catalytic activity. Herein, a series of Ni/TiCT-Y (T = F, -OH; Y denotes etching time (d)) catalysts are synthesized and show remarkably enhanced catalytic activity on the hydrolysis of AB in contrast to the corresponding without regulating.

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Photocatalytic oxidation of sulfide into sulfoxide has attracted extensive attention as an environmentally friendly strategy for chemical transformations or toxic chemicals degradation. Herein, we construct a series of In S /NU-1000 heterojunction photocatalysts, which can efficiently catalyze the oxidation of sulfides to form sulfoxides as the sole product under LED lamp (full-spectrum) illumination in air at room temperature. Especially, the sulfur mustard simulant, 2-chloroethyl ethyl sulfide (CEES), can also be photocatalytically oxidized with In S /NU-1000 to afford nontoxic 2-chloroethyl ethyl sulfoxide (CEESO) selectively and effectively.

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Porous two-dimensional metal-organic framework (2D-MOF) nanosheets Zr-BTB-H4TBAPy and PCN-134-2D were synthesized and characterized by X-ray diffraction (XRD), N2 adsorption-desorption, scanning electron microscopy (SEM), transmission electron microscopy (TEM), atomic force microscopy (AFM) and zeta potential and subjected to dye adsorption and separation investigation. These 2D-MOF nanosheets are ultrathin, have large surface area and high water stability and can selectively adsorb cationic dyes, rhodamine B (RhB) and methylene blue (MLB), from aqueous solutions, with removal rates of nearly 100% within 10 min. The adsorption kinetic results showed that Zr-BTB-H4TBAPy and PCN-134-2D could effectively and selectively remove cationic dyes from water, followed a pseudo-second-order kinetic model and fitted well with the Freundlich isotherm.

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Herein, a surface site engineering strategy is used to construct a porous Z-scheme heterojunction photocatalyst for photocatalytic hydrogen evolution (PHE) by integration of BiOI in a mesoporous Zr-based metal-organic framework (MOF) NU-1000. Three high-quality and highly dispersed BiOI@NU-1000 heterojunction materials are synthesized, and a set of methods is used to characterize these materials, indicating that the BiOI@NU-1000 heterojunction can retain high porosity and crystallinity of the parent NU-1000. Furthermore, the built-in electric field of the BiOI@NU-1000 composite can effectively tune the band gap, promote the separation of photoinduced charge carriers, improve photocurrent intensity, and reduce photoelectric impedance.

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