ELECTRON-SPIN RESONANCE OF POLYACETYLENE AND ASF5-DOPED POLYACETYLENE

被引:336
作者
GOLDBERG, IB
CROWE, HR
NEWMAN, PR
HEEGER, AJ
MACDIARMID, AG
机构
[1] UNIV PENN,RES STRUCT MATTER LAB,PHILADELPHIA,PA 19104
[2] UNIV PENN,DEPT PHYS & SURG,PHILADELPHIA,PA 19104
[3] UNIV PENN,DEPT CHEM,PHILADELPHIA,PA 19104
关键词
D O I
10.1063/1.437613
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The results of an electron spin resonance (ESR) study of trans-polyacetylene, before and after doping with AsF5, are reported. The undoped polymer exhibits a Lorentzian line (g = 2.00263) indicative of motional narrowing from a mobile unpaired electron species. Measurement of the intensity indicates a Curie law susceptibility with approximately one unpaired electron per 3 × 103 carbon atoms in agreement with earlier studies. From these results and comparison with earlier data on the cis polymer, it is suggested that the ESR signal arises from a mobile defect in the π system. Utilizing an apparatus which allows in situ AsF5 doping of a polyacetylene sample in the microwave cavity, we have monitored the ESR signal during the doping process. The spin resonance line narrows and increases in intensity, with no detectable g shift, as the doping proceeds. At high doping levels the line becomes asymmetric with a characteristic Dysonian line shape consistent with metallic behavior. © 1979 American Institute of Physics.
引用
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页码:1132 / 1136
页数:5
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