Baozong Li

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Name: 李宝宗; BaoZong Li
Organization: Soochow University , China
Department: Department of Polymer Science and Engineering
Title: Professor(PhD)

TOPICS

Co-reporter:Jiangang Li, Changzhen Shao, Baozong Li, Yi Li, Chundong Wang, Yonggang Yang
Materials Letters 2017 Volume 188() pp:308-311
Publication Date(Web):1 February 2017
DOI:10.1016/j.matlet.2016.09.103
•Helical m-phenylenediamine-formaldehyde resin nanotubes were prepared.•High N-doped helical carbonaceous nanofibers were produced after pyrolysis process.•The N-doped carbonaceous nanofibers showed good electrochemical performance.•The doped N is beneficial to enhance the Li+ storage capacity.The great demand for high-power lithium-ion batteries (LIBs) has spurred extensive research on carbonaceous electrode materials. In this work, a novel high nitrogen-doped helical carbonaceous nanofiber derived from pyrolytic resins was fabricated. Helical m-phenylenediamine-formaldehyde resin nanotubes were prepared via a sol-gel duplication method using a chiral amphiphile as the template. Then, the obtained resin nanotubes were subject to carbonize at 600 °C under Ar atmosphere, forming helical carbonaceous nanofibers with N content of 12.4 wt%. The inner tunnels were disappeared owing to the thermal contraction. Wide angle X-ray diffraction and Raman spectrum analysis verify that the obtained nanofibers were amorphous carbon predominantly. The electrochemical characterization reveals that the in-situ nitrogen-doped carbonaceous nanofibers exhibit high specific capacity, together with long cycle time and excellent rate capability.
Co-reporter:Huayan Sun;Jiaming Qin;Yi Li
Chemical Research in Chinese Universities 2017 Volume 33( Issue 1) pp:119-121
Publication Date(Web):2017 February
DOI:10.1007/s40242-016-6168-5
Circular dichroism(CD) is usually used to study supramolecular chirality. With the development of CD methods, diffuse transmission CD(DTCD) and diffuse reflectance CD(DRCD) have been developed. However, the relationship among CD, DTCD and DRCD has not been well-studied. A chiral low molecular weight gelator was synthesized, which can result in a transparent physical gel in deionized water. The field-emission electron microscopy images show that the gel is able to self-assemble into left-handed helical fibers. The CD and DTCD spectra are almost identical, but they partially differ from the DRCD spectrum. Based on the TD-DFT calculated CD spectrum, the DRCD spectrum is shown to be more accurate.
Co-reporter:Zeli Xiao, Yanwei Zhao, Zhibin Huang, Yi Li, Baozong Li
Materials Letters 2014 Volume 135() pp:233-236
Publication Date(Web):15 November 2014
DOI:10.1016/j.matlet.2014.06.131
•Silica nanoflakes with spherical mesopores were prepared.•The pore architectures were controlled by the F127 block copolymer.•The morphologies were controlled by the organic self-assemblies.A pair of chiral low-molecular-weight amphiphiles (LMWAs) was synthesized from phenylglycine, which forms a viscous solution in water. Mesoporous silica nanoflakes were prepared via a dual-templating approach using F127 block copolymer and the LMWAs. The morphologies and pore architectures of the silica nanoflakes were studied using transmission electron microscopy, field-emission scanning electron microscopy, powder X-ray diffraction, and N2 sorptions. The spherical mesopores opened onto the surfaces of the nanoflakes and were organized in a two-dimensional, hexagonal-like structure. We believe that the pore architectures and morphologies were controlled by the F127 block copolymer and the self-assembly of the LMWAs, respectively. This kind of material has potential for applications in separation and catalysis.
Co-reporter:Qing Wang, Bao-Zong Li, Yi Li
Chinese Chemical Letters 2014 Volume 25(Issue 2) pp:253-256
Publication Date(Web):February 2014
DOI:10.1016/j.cclet.2013.10.028
Helical 1,2-ethylene–silica nanofibers with lamellar mesopores on the surfaces and twisted rod-like mesopores inside were prepared according to literature procedures. After carbonization, helical carbon/silica nanofibers with lamellar mesopores on the surfaces and twisted rod-like micropores inside were obtained. The morphologies and pore architectures of the carbon/silica nanofibers were characterized using transmission electron microscopy, field-emission scanning electron microscopy, powder X-ray diffraction and N2 sorptions. Although the mesopores inside shrank into micropores, the helical nanostructure remained. Moreover, several carbon/silica nanofibers with lamellar mesopores on the surfaces and concentric circular micropores inside were also obtained. After being calcined in air, helical silica nanofibers with lamellar mesopores on the surfaces and twisted rod-like micropores inside were produced as well.Helical 1,2-ethylene-silica nanofibers were prepared according to the literature procedures. After carbonization, helical carbon/silica nanofibers with lamellar mesopores on the surfaces and twisted rod-like micropores inside were obtained.
Co-reporter:Dan Liu, Yong-Min Guo, Yi Li, Bao-Zong Li
Chinese Chemical Letters 2014 Volume 25(Issue 6) pp:879-882
Publication Date(Web):June 2014
DOI:10.1016/j.cclet.2014.01.039
Left-handed, coiled, 4,4′-biphenylene bridged polybissilsesquioxane, tubular nanoribbons were prepared according to the published literature. After carbonization and removal of silica using HF aqueous solution, left-handed, coiled, carbonaceous, tubular nanoribbons were obtained. The left-handed, coiled, carbonaceous, tubular nanoribbons were characterized using field-emission scanning electron microscopy, transmission electron microscopy, powder X-ray diffraction, Raman spectrophotometer, diffuse reflectance circular dichroism (DRCD), and N2 adsorptions. Micropores were formed due to the removal of silica. The nitrogen BET surface area is 1727 m2/g. A broad, positive DRCD signal, identified at 400–800 nm, indicates the carbonaceous, tubular nanoribbons exhibit optical activity. The helical pitch is proposed to play an important role in the position of the DRCD signal.Left-handed coiled, 4,4′-biphenylene bridged polybissilsesquioxane, tubular nanoribbons were prepared according to the literature. After carbonization and removal of silica using HF aqueous solution, left-handed coiled, carbonaceous, tubular nanoribbons were obtained. The resulting samples were constructed as double layers of nanoribbons with micropores formed in this process. Moreover, the obtained samples exhibited optical activity.
Co-reporter:Li-Qing Ma, Hao Chen, Yong-Min Guo, Bao-Zong Li, Yi Li
Chinese Chemical Letters 2014 Volume 25(Issue 10) pp:1363-1366
Publication Date(Web):October 2014
DOI:10.1016/j.cclet.2014.05.035
Single-handed helical phenolic resin nanofibers were synthesized through a supramolecular templating approach using the supramolecular self-assemblies of a pair of chiral low-molecular-weight amphiphiles as the templates and 2,4-dihydroxybenzoic acid and formaldehyde as the precursors. The phenolic resin nanofibers were characterized using field-emission scanning electron microscopy, transmission electron microscopy and diffused reflection circular dichroism. The results indicated that the chirality of the supramolecular self-assemblies was successfully transferred to the phenolic resin nanofibers. The left- and right-handed helical phenolic resin nanofibers exhibited opposite optical activity.Single-handed helical phenolic resin nanofibers were synthesized through a supramolecular templating approach using the self-assemblies of a pair of chiral low-molecular-weight amphiphiles as the templates and 2,4-dihydroxybenzoic acid and formaldehyde as the precursors. The left- and right-handed helical phenolic resin nanofibers exhibited opposite optical activity.
Co-reporter:Chuanyong Zhang, Hongjing Huo, Yi Li, Baozong Li, Yonggang Yang
Materials Letters 2013 Volumes 102–103() pp:50-52
Publication Date(Web):July 2013
DOI:10.1016/j.matlet.2013.03.105
•Helical CdS nanotubes were prepared through a sol–gel transcription approach.•The CdS nanotubes were constructed by nanocrystals.•The handedness of the nanotubes follows that of the organic self-assemblies.CdS nanoparticles attracted much attention for their potential applications for biomedical imaging, sensing and light-emitting diodes. Up to now, varieties of nanostructures have been prepared. Here, single-handed helical CdS nanotubes were prepared through a sol–gel transcription approach using the self-assembly of a pair of chiral low-molecular-weight gelators as the templates. The results indicated that the handedness of the CdS nanotubes was controlled by that of the organic self-assembled structures. Wide-angle X-ray diffraction patterns indicated that the nanotubes were constructed by crystals with a mixture of cubic and hexagonal structures. Electrostatic interaction between Cd2+ and perchloride was proposed to drive the adsorption of Cd2+ on the surfaces of the chiral organic self-assemblies.Graphical abstract
Co-reporter:Feng-Wen Hou, Li-Min Wu, Yong-Min Guo, Yi Li, Bao-Zong Li
Chinese Chemical Letters 2013 Volume 24(Issue 8) pp:770-772
Publication Date(Web):August 2013
DOI:10.1016/j.cclet.2013.04.040
Single-handed helical silica nanotubes were prepared according to the literature procedures, using the self-assemblies of a pair of chiral cationic low-molecular-weight gelators as the templates. A chirality indicator, 4,4′-bis(triethoxysilyl)-1,1′-biphenyl, was developed to determine the chirality of the silica nanotubes. The chirality of the surfaces and the bulky walls of the silica nanotubes were understood from the twist of the biphenylene rings.Single-handed helical silica nanotubes were prepared according to the literature procedures, using the self-assemblies of a pair of chiral cationic low-molecular-weight gelators as the templates. A chirality indicator, 4,4′-bis(triethoxysilyl)-1,1′-biphenyl, was developed to determine the chirality of the silica nanotubes. The chirality of the surfaces and the bulky walls of the silica nanotubes were understood from the twist of the biphenylene rings.
Co-reporter:Yun Yue Pu, Yi Li, Wei Zhuang, Ming Zhang, Bao Zong Li, Yong Gang Yang
Chinese Chemical Letters 2012 Volume 23(Issue 10) pp:1201-1204
Publication Date(Web):October 2012
DOI:10.1016/j.cclet.2012.07.010
Helical mesoporous silica nanorods were prepared using cetyltrimethylammonium bromide and achiral alcohols as the co-structure-directing agents. They were characterized using field-emission scanning electron microscopy, transmission electron microscopy, nitrogen sorptions, and small angle X-ray diffraction. The length of the silica nanorods increases with increasing the length of the alcohols. When n-heptanol and n-octanol were used, helical mesoporous silica nanorods with lamellar mesopores on the surfaces were obtained.
Co-reporter:Yuanli Chen;Min Xiao;Wei Zhuang;Yi Li;Yonggang Yang
Chinese Journal of Chemistry 2012 Volume 30( Issue 7) pp:1582-1588
Publication Date(Web):
DOI:10.1002/cjoc.201280026

Abstract

Silicas with hierarchical porous architectures attracted much attention, due to their potential applications in catalysis and separation. Generally, they were prepared through dual- or triple-templating approaches. Herein, mesoporous silica nanoparticles with rod-like pore channels inside and lamellar mesopores on the surfaces were prepared using the self-assemblies of a chiral low-molecular-weight amphiphile as templates through a single-templating approach. The formation of the lamellar mesopores was studied by taking field-emission scanning electron microscopy and transmission electron microscopy images after different reaction times. The lamellar pores were proposed to be formed by merging rod-like micelles during the sol-gel process. Moreover, helical nanofibers with rod-like pore channels inside and lamellar mesopores on the surfaces were prepared with the addition of n-octanol as a co-structure-directing agent.

Co-reporter:Xiaojuan Liu, Wei Zhuang, Baozong Li, Limin Wu, Sibing Wang, Yi Li and Yonggang Yang  
Chemical Communications 2011 vol. 47(Issue 25) pp:7215-7217
Publication Date(Web):31 May 2011
DOI:10.1039/C1CC11769F
Helical periodic mesoporous 1,4-phenylene-silica nanorods with chiral crystalline walls were prepared using the self-assembly of a pair of enantiomers as templates.
Co-reporter:Ming Zhang;Yi Li;Lifeng Bi;Wei Zhuang;Sibing Wang;Yuanli Chen;Yonggang Yang
Chinese Journal of Chemistry 2011 Volume 29( Issue 5) pp:933-941
Publication Date(Web):
DOI:10.1002/cjoc.201190191

Abstract

The morphologies and pore architectures of mesoporous ethenylene-silica were controlled using cetyltrimethylammonium bromide (CTAB) as template and (S)-β-citronellol as a co-structure-directing agent under basic conditions. When the (S)-β-citronellol/CTAB molar ratios are in the range of 0.75–2.0, helical nanofibers were obtained. With increasing the (S)-β-citronellol/CTAB molar ratio, the lengths of the nanofibers increases. Lamellar mesopores were identified on the surfaces of the nanofibers prepared in the (S)-β-citronellol/CTAB molar ratio range of 1.5–2.0. At the (S)-β-citronellol/CTAB molar ratio of 2.5:1, nanoparticles with nanoflakes on the surfaces were obtained. The field emission scanning electron microscopy images taken after different reaction times indicated that the helical pitches of the nanofibers decreased with increasing the reaction time. Helical 1,4-phenylene-silica and methylene-silica nanofibers were also prepared. The results indicated that the morphologies and pore architectures of the obtained organic-inorganic hybrid silicas are also sensitive to the hybrid silica precursors. Helical ethenylene-silica nanofibers with lamellar mesopores on their surfaces can be also prepared using the mixtures of CTAB and racemic citronellol within a narrower citronellol/CTAB molar ratio range.

Co-reporter:Yuxia Chen;Sibing Wang;Xiaojuan Liu;Yi Li;Dr. Baozong Li;Yonggang Yang
Chinese Journal of Chemistry 2010 Volume 28( Issue 10) pp:1941-1945
Publication Date(Web):
DOI:10.1002/cjoc.201090323

Abstract

Left-handed double twisted silica nanoribbons were prepared through a sol-gel transcription approach in the mixtures of ethanol and water. The self-assemblies of a chiral low-molecular-weight amphiphile served as the templates. The samples were characterized using X-ray diffraction, transmission electron microscope and scanning electron microscope. These double twisted silica nanoribbons were several micrometers in length, 50 to 70 nm in wideness, about 15 nm in thickness. The silica nanoribbons can be prepared in a large scale.

Co-reporter:Xiaojuan Liu, Wei Zhuang, Baozong Li, Limin Wu, Sibing Wang, Yi Li and Yonggang Yang
Chemical Communications 2011 - vol. 47(Issue 25) pp:NaN7217-7217
Publication Date(Web):2011/05/31
DOI:10.1039/C1CC11769F
Helical periodic mesoporous 1,4-phenylene-silica nanorods with chiral crystalline walls were prepared using the self-assembly of a pair of enantiomers as templates.
Poly[decyl(2-methylpropyl)silylene]
4-((4-Methoxyphenyl)ethynyl)benzoic acid
Poly[decyl[(2S)-2-methylbutyl]silylene]
Hydroxyl
L-Alanine, N-(1-oxooctadecyl)-L-alanyl-