中文版 | English
题名

Pressure induced polymerization of acetylide anions in CaC2 and 10(7) fold enhancement of electrical conductivity

作者
通讯作者Li, Kuo
发表日期
2017-01
DOI
发表期刊
ISSN
2041-6520
EISSN
2041-6539
卷号8期号:1页码:298-304
摘要

Transformation between different types of carbon-carbon bonding in carbides often results in a dramatic change of physical and chemical properties. Under external pressure, unsaturated carbon atoms form new covalent bonds regardless of the electrostatic repulsion. It was predicted that calcium acetylide (also known as calcium carbide, CaC2) polymerizes to form calcium polyacetylide, calcium polyacenide and calcium graphenide under high pressure. In this work, the phase transitions of CaC2 under external pressure were systematically investigated, and the amorphous phase was studied in detail for the first time. Polycarbide anions like C-6(6-) are identified with gas chromatography-mass spectrometry and several other techniques, which evidences the pressure induced polymerization of the acetylide anions and suggests the existence of the polyacenide fragment. Additionally, the process of polymerization is accompanied with a 10(7) fold enhancement of the electrical conductivity. The polymerization of acetylide anions demonstrates that high pressure compression is a viable route to synthesize novel metal polycarbides and materials with extended carbon networks, while shedding light on the synthesis of more complicated metal organics.

相关链接[来源记录]
收录类别
语种
英语
重要成果
NI论文
学校署名
其他
资助项目
DOE-BES[DE-FG02-99ER45775] ; DOE-BES[DE-AC02-06CH11357]
WOS研究方向
Chemistry
WOS类目
Chemistry, Multidisciplinary
WOS记录号
WOS:000391454500033
出版者
EI入藏号
20165203190684
EI主题词
Covalent Bonds ; Electric Conductivity ; Gas Chromatography ; High Pressure Engineering ; Ions ; Mass Spectrometry ; Organometallics ; Polymerization
EI分类号
Electricity: Basic Concepts And Phenomena:701.1 ; Chemistry:801 ; Physical Chemistry:801.4 ; Chemical Operations:802.3 ; Organic Compounds:804.1 ; Inorganic Compounds:804.2 ; Polymerization:815.2
来源库
Web of Science
引用统计
被引频次[WOS]:18
成果类型期刊论文
条目标识符http://sustech.caswiz.com/handle/2SGJ60CL/29289
专题理学院_物理系
作者单位
1.Ctr High Pressure Sci & Technol Adv Res HPSTAR, POB 8009, Beijing 100088, Peoples R China
2.Carnegie Inst Sci, Geophys Lab, Washington, DC 20015 USA
3.COFCO Nutr & Hlth Res Inst, Beijing Key Lab Nutr Hlth & Food Safety, Beijing 100209, Peoples R China
4.Agilent Technol China Co Ltd, Wangjingbei Rd, Beijing 100102, Peoples R China
5.Univ Durham, Dept Chem, South Rd, Durham DH1 3LE, England
6.Oak Ridge Natl Lab, Spallat Neutron Source, Oak Ridge, TN 37830 USA
7.Oak Ridge Natl Lab, Ctr Nanophase Mat Sci, Oak Ridge, TN 37831 USA
8.Carnegie Inst Sci, Geophys Lab, HPSynC, Argonne, IL 60439 USA
9.Southern Univ Sci & Technol, Dept Phys, Shenzhen, Peoples R China
10.Chinese Acad Sci, Inst Phys, Beijing 100190, Peoples R China
11.Collaborat Innovat Ctr Quantum Matter, Beijing, Peoples R China
12.European Spallat Source ERIC, Lund, Sweden
推荐引用方式
GB/T 7714
Zheng, Haiyan,Wang, Lijuan,Li, Kuo,et al. Pressure induced polymerization of acetylide anions in CaC2 and 10(7) fold enhancement of electrical conductivity[J]. Chemical Science,2017,8(1):298-304.
APA
Zheng, Haiyan.,Wang, Lijuan.,Li, Kuo.,Yang, Youyou.,Wang, Yajie.,...&Jin, Changqing.(2017).Pressure induced polymerization of acetylide anions in CaC2 and 10(7) fold enhancement of electrical conductivity.Chemical Science,8(1),298-304.
MLA
Zheng, Haiyan,et al."Pressure induced polymerization of acetylide anions in CaC2 and 10(7) fold enhancement of electrical conductivity".Chemical Science 8.1(2017):298-304.
条目包含的文件
文件名称/大小 文献类型 版本类型 开放类型 使用许可 操作
c6sc02830f.pdf(1577KB)----开放获取--浏览
个性服务
原文链接
推荐该条目
保存到收藏夹
查看访问统计
导出为Endnote文件
导出为Excel格式
导出为Csv格式
Altmetrics Score
谷歌学术
谷歌学术中相似的文章
[Zheng, Haiyan]的文章
[Wang, Lijuan]的文章
[Li, Kuo]的文章
百度学术
百度学术中相似的文章
[Zheng, Haiyan]的文章
[Wang, Lijuan]的文章
[Li, Kuo]的文章
必应学术
必应学术中相似的文章
[Zheng, Haiyan]的文章
[Wang, Lijuan]的文章
[Li, Kuo]的文章
相关权益政策
暂无数据
收藏/分享
文件名: c6sc02830f.pdf
格式: Adobe PDF
文件名: c6sc02830f.pdf
格式: Adobe PDF
所有评论 (0)
[发表评论/异议/意见]
暂无评论

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。