浏览全部资源
扫码关注微信
吉林大学, 超分子结构与材料教育部重点实验室,吉林 长春,130012
收稿日期:2004-08-19,
修回日期:2005-01-10,
纸质出版日期:2006-01-20
移动端阅览
李茂, 路萍, 张海全, 陆丹, 马於光. 含芴聚合物电子亲合能和电离能的确定[J]. 发光学报, 2006,27(1): 80-84
LI Mao, LU Ping, ZHANG Hai-quan, LU Dan, MA Yu-guang. Electrochemical Determination of the Ionization Potential and Electron Affinity of PF Derivatives[J]. Chinese Journal of Luminescence, 2006,27(1): 80-84
通过循环伏安法测量了若干含芴交替共聚物的氧化还原电位
并通过氧化还原的起始电位点来确定聚合物的能级结构。从结果分析
在聚芴中引入系列的基团改变了聚合物的电离能、电子亲合能及带隙能。其中引入联吡啶后
带隙能变化不大
但电子亲合能明显升高
增加了电子的注入能力;引入带有七元环的联苯
特别是引入间位连接带有七元环的联苯后
带隙能明显增加。与聚芴比较
七元环聚合物电离能(
I
p
)从5.60eV增加到5.81eV
而电子亲合能(
E
a
)从2.05eV增加到2.42eV
带隙能从3.55eV增加到3.82eV。这与光谱得到的带隙能得到了较好的对应。
Cyclic voltammetry measurements for the blue-emitting conjugated PF and its derivatives were reported.Both oxidation and reduction potentials onsets were determined and thus the ionization potentials
I
p
and electron affinities
E
a
of the polymers under the same experimental condition were estimated. The oxidative potential onset of PF was at 0.97 V and the reductive potential onset at-2.58 V. In order to increase the electron-accepting ability
the bipyridine units were introduced to the polymer backbone (PP). PP3(with 50% bipyridine content) displayed greater potential change in the reductive potential (-0.37 V) compared with PF because the bipyridine in PP3 is an electron-deficient. PP3 showed a good electro-accepted ability. The
E
a
was increased from the 2.05 eV to 1.92 eV compared with that of PF. In the anodic scan
the onsets of oxidation of PS
PO
PC and PD was at 1.10
1.11
1.10 and 1.06 V which correspond to the ionization potential (
I
p
) values of 5.73
5.74
5.73 and 5.69 eV.The electron affi-nity (
E
a
) values of the polymers were determined to be 2.16
2.08
1.92 and 1.96 eV. The incorporation of the seven-membered ring moiety into the polymer backbone led to wider bandgaps. It indicates that the seven-membered ring compound was an efficient segment for tailoring the band gap of the conjugated polymer. The shift of redox potential
change of the ionization potential and electron affinity were due to the different seven-membered ring structures. The band gap of the PF derivatives was increased by introducing the seven-membered ring
especially for the meta-linkage polymers. The electrochemical energy gap agrees well with the optical energy for these copolymers.
Lu Ping,Zhang Haiquan,Shen Fangzhong,et al.A wide-bandgap semiconducting polymer for ultraviolet and blue light emitting diodes[J].Macromol.Chem.Phys.,2003,204:2274-2280.
Zhang H Q,Yang B,Zheng Y,et al.New biphenyl derivative with planer phenyl-phenyl conformation in crystal at room temperature exhibits highly efficient UV light-emitting[J].J.Phys.Chem.B,108:9571-9573.
Inbasekaran M,Woo E,Wu W,et al.Fluorene homopolymers and copolymers[J].Synth.Met.,2002,111-112:397-401.
Chen Zhizhong,Li Fushan,Gong Qihuang.Novel blue organic light-emitting diodes and materials[J].Chin.J.Lumin.(发光学报),2005,26(6):743-747 (in Chinese).
Osaheni J A,Jenekhe S A,Perlstein J.Photogeneration of charge carriers in bilayer assemblies of conjugated rigid-rod polymers[J].J.Phys.Chem.,1994,98:12727-12736.
Shirota Y,Kuwabara Y,Inada H.Multilayered organic electroluminescent device using a novel starburst molecule,4,4',4-tris(3-methylphenylphenylamino)triphenylamine,as a hole transport material[J].Appl.Phys.Lett.,1994,65:807-809.
Alvarado S F,Libioulle L,Seidler P F.STM-excited luminescence on organic materials[J].Synth.Met.,1997,91:69-72.
Kim Joo-Hyun,Lee Hoo-Sung.Improvement of efficiency of the single-layer polymerlight-emitting diodes:the exciton confinement in the emitting layer by conjugated 1,3,4-oxadiazole[J].Synth.Met.,2004,114:169-176.
Bredas J L,Silbey R,Boudreaux D S,et al.Chain-length dependence of electronic and electrochemical properties of conjugated systems:polyacetylene,polyphenylene,polythiophene,and polypyrrole[J].J.Am.Chem.Soc.,1983,105:6555-6559.
Leeuw D M de,Simenon M M J,Brown A R,et al.Stability of n-type doped conducting polymers and consequences for polymeric microelectronic devices[J].Synth.Met.,1997,87:53-59.
Cervini R,Li X C,Spencer G W C,et al.Electrochemical and optical studies of PPV derivatives and poly(aromatic oxadiazoles)[J].Synth.Met.,1997,84:359-360.
Ding Bangdong,Zhang Jimei,Zhu Wenqing,et al.Convenient electrochemical method to determine the energy level of organic electroluminescent materials[J].Chin.J.Lumin.(发光学报),2003,24(6):606-611 (in Chinese).
Lu Hong-Fang,Chan Hardy S O,Ng Siu-Choon.Synthesis,characterization,and electronic and optical properties of donor-acceptor conjugated polymers based on alternating bis(3-alkylthiophene) and pyridine moieties[J].Macromolecules,2003,36:1543-1552.
Ding Jianfu,Tao Ye,Day M,et al.Electrochemical and fluorescent properties of alternating copolymers of 9,9-dioctyl-fluorene and oxadiazole as blue electroluminescent and electron transport materials[J].J.Opt.A:Pure Appl.Opt.4,2002,4:S267-S272.
Kreyenschmidt M,Uckert F,Mullen K A.New soluble poly(p-phenylene) with tetrahydropyrene repeating units[J].Macromolecules,1995,28:4577-4582.
Anderson J D,McDonald E M,Lee P A,et al.Electrochemistry and electrogenerated chemiluminescence processes of the components of aluminum quinolate/triarylamine,and related organic light-emitting diodes[J].J.Am.Chem.Soc.,1998,120:9646-9655.
Janietz S,Bradley D D C,Grell M,et al.Electrochemical determination of the ionization potential and electron affinity of poly(9,9-dioctylfluorene)[J].Appl.Phys.Lett.,1998,73:2453-2455.
Chen Z K,Huang W,Wang L H,et al.A family of electroluminescent silyl-Substituted poly(p-phenylenevinylene)s:synthesis,characterization,and structure-property relationships[J].Macromolecules,2000,33:9015-9025.
0
浏览量
186
下载量
7
CSCD
关联资源
相关文章
相关作者
相关机构