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Changing the pore structure and surface chemistry of hard carbon by coating it with a soft carbon to boost high-rate sodium storage
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作者 ZHONG Qin MO Ying +9 位作者 ZHOU Wang ZHENG Biao WU Jian-fang LIU Guo-ku Mohd Zieauddin Kufian Zurina Osman XU Xiong-wen GAO Peng YANG Le-zhi LIU Ji-lei 《新型炭材料(中英文)》 北大核心 2025年第3期651-665,共15页
Changes to the microstructure of a hard carbon(HC)and its solid electrolyte interface(SEI)can be effective in improving the electrode kinetics.However,achieving fast charging using a simple and inexpensive strategy wi... Changes to the microstructure of a hard carbon(HC)and its solid electrolyte interface(SEI)can be effective in improving the electrode kinetics.However,achieving fast charging using a simple and inexpensive strategy without sacrificing its initial Coulombic efficiency remains a challenge in sodium ion batteries.A simple liquid-phase coating approach has been used to generate a pitch-derived soft carbon layer on the HC surface,and its effect on the porosity of HC and SEI chemistry has been studied.A variety of structural characterizations show a soft carbon coating can increase the defect and ultra-micropore contents.The increase in ultra-micropore comes from both the soft carbon coatings and the larger pores within the HC that are partially filled by pitch,which provides more Na+storage sites.In-situ FTIR/EIS and ex-situ XPS showed that the soft carbon coating induced the formation of thinner SEI that is richer in NaF from the electrolyte,which stabilized the interface and promoted the charge transfer process.As a result,the anode produced fastcharging(329.8 mAh g^(−1)at 30 mA g^(−1)and 198.6 mAh g^(−1)at 300 mA g^(−1))and had a better cycling performance(a high capacity retention of 81.4%after 100 cycles at 150 mA g^(−1)).This work reveals the critical role of coating layer in changing the pore structure,SEI chemistry and diffusion kinetics of hard carbon,which enables rational design of sodium-ion battery anode with enhanced fast charging capability. 展开更多
关键词 Hard carbon Pitch-derived carbon coating Sodium-ion batteries Pore structure Surface chemistry
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Semi-quantitative analysis of the structural evolution of mesophase pitch-based carbon foams by Raman and FTIR spectroscopy
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作者 LIU Yue CHANG Sheng-kai +3 位作者 SU Zhan-peng HUANG Zu-jian QIN Ji YANG Jian-xiao 《新型炭材料(中英文)》 SCIE EI CAS CSCD 北大核心 2024年第4期668-680,共13页
Graphitized carbon foams(GFms)were prepared using mesophase pitch(MP)as a raw material by foaming(450℃),pre-oxidation(320℃),carbonization(1000℃)and graphitization(2800℃).The differences in structure and properties... Graphitized carbon foams(GFms)were prepared using mesophase pitch(MP)as a raw material by foaming(450℃),pre-oxidation(320℃),carbonization(1000℃)and graphitization(2800℃).The differences in structure and properties of GFms prepared from different MP precursors pretreated by ball milling or liquid phase extraction were investigated and compared,and semi-quantitative calculations were conducted on the Raman and FTIR spectra of samples at each preparation stage.Semi-quantitat-ive spectroscopic analysis provided detailed information on the structure and chemical composition changes of the MP and GFm de-rived from it.Combined with microscopic observations,the change from precursor to GFm was analyzed.The results showed that ball milling concentrated the distribution of aromatic molecules in the pitch,which contributed to uniform foaming to give a GFm with a uniform pore distribution and good properties.Liquid phase extraction helped remove light components while retaining large aromatics to form graphitic planes with the largest average size during post-treatment to produce a GFm with the highest degree of graphitization and the fewest open pores,giving the best compression resistance(2.47 MPa),the highest thermal conductivity(64.47 W/(m·K))and the lowest electrical resistance(13.02μΩ·m).Characterization combining semi-quantitative spectroscopic ana-lysis with microscopic observations allowed us to control the preparation of the MP-derived GFms. 展开更多
关键词 Mesophase pitch Carbon foams RAMAN FTIR GRAPHITIZATION
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铝掺杂对ZnO:Al薄膜结晶性能与微观组织的影响 被引量:1
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作者 陈建林 陈鼎 +1 位作者 张世英 陈振华 《中国有色金属学报》 EI CAS CSCD 北大核心 2009年第7期1284-1288,共5页
以二水合醋酸锌为原材料,采用溶胶-凝胶浸涂法在钠钙玻璃基片上制备了具有c轴择优取向的ZnO:Al薄膜,考察了铝掺杂浓度对薄膜结晶性与微观组织结构的影响。结果表明:铝掺杂使ZnO薄膜(002)晶面的2θ向高角度方向偏移,c轴择优取向性增强,... 以二水合醋酸锌为原材料,采用溶胶-凝胶浸涂法在钠钙玻璃基片上制备了具有c轴择优取向的ZnO:Al薄膜,考察了铝掺杂浓度对薄膜结晶性与微观组织结构的影响。结果表明:铝掺杂使ZnO薄膜(002)晶面的2θ向高角度方向偏移,c轴择优取向性增强,晶粒变小(15~20nm)。当铝掺杂浓度(摩尔分数)为1%~2%时,微观组织结构变得致密均匀;当铝掺杂浓度大于2%时,发生颗粒团聚现象;在高掺杂浓度下(5%和8%),出现大尺寸片状ZnO:Al晶粒异常长大,生长出特殊形貌的薄膜。 展开更多
关键词 ZNO:AL薄膜 铝掺杂 溶胶-凝胶法 择优取向生长
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