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首页> 外文期刊>Journal of Porphyrins and Phthalocyanines >Formation and photoinduced properties of zinc porphyrin-SWCNT and zinc phthalocyanine-SWCNT nanohybrids using diameter sorted nanotubes assembled via metal-ligand coordination and π–π stacking
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Formation and photoinduced properties of zinc porphyrin-SWCNT and zinc phthalocyanine-SWCNT nanohybrids using diameter sorted nanotubes assembled via metal-ligand coordination and π–π stacking

机译:锌卟啉-SWCNT和酞菁锌-SWCNT纳米杂化体的形成及其光诱导性能,通过金属配体配位和π-π堆叠组装而成的直径排序纳米管

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摘要

Photoinduced electron transfer processes in self-assembled zinc porphyrin (ZnP) or zinc phthalocyanine (ZnPc) with semiconducting (7,6)- and (6,5)-enriched SWCNTs were investigated. To bind photosensitizers to SWCNTs, first, pyrene covalently functionalized with a phenylimidazole (Im-Pyr) entity was treated with SWCNTs. Exfoliation of SWCNTs occurred due to π–π stacking of pyrene with nanotubes walls leaving the imidazole entity that was subsequently used to coordinate ZnP or ZnPc in o-dichlorobenzene (DCB). The donor-acceptor nanohybrids thus formed were characterized by TEM imaging, steady-state UV-visible-near IR absorption and fluorescence spectra. Free-energy calculations suggested possibility of electron transfer from the photoexcited ZnP or ZnPc to Im-Pyr/SWCNT(n,m) in the nanohybrids. Consequently, steady-state and time-resolved fluorescence studies revealed efficient quenching of the singlet excited state of ZnP or ZnPc with therate constants of charge separation (kCS) in the range of (3–6) × 109 s-1. Nanosecond transient absorption technique confirmed the electron transfer products, ZnP·+←Im-Pyr/SWCNT·- and ZnPc·+←Im-Pyr/SWCNT·- (and opposite charged pairs) having characteristic absorptions with the decay rate constants due to charge recombination (kCR) in the range of (1.4–2.4) × 107 s-1, corresponding to lifetimes of radical ion-pairs in the 70–100 ns range. The SWCNT·- was further utilized to mediate electrons to hexyl-viologen dication (HV2+) resulting in an electron-accumulation process in the presence of sacrificial electron donor, offering additional proof for the occurrence of photoinduced charge-separation and potential utilization of these materials in light energy harvesting applications. Further, photoelectrochemical cells have been constructed on FTO/SnO2 electrodes to verify their ability to directly convert light into electricity. An IPCE efficiency of up to 7% has been achieved in case of ZnP←Im-Pyr/SWCNT modified electrode.
机译:研究了自组装锌卟啉(ZnP)或酞菁锌(ZnPc)中富含半导体(7,6)和(6,5)的SWCNT的光诱导电子转移过程。为了将光敏剂与SWCNT结合,首先,将用苯基咪唑(Im-Pyr)实体共价官能化的pyr用SWCNT处理。 SWCNT的剥离是由于of与纳米管壁的π-π堆积而留下的咪唑实体,随后该咪唑实体用于配位邻二氯苯(DCB)中的ZnP或ZnPc。通过TEM成像,稳态UV-可见-近红外吸收和荧光光谱表征由此形成的供体-受体纳米杂化物。自由能计算表明,纳米杂化物中电子可能从光激发的ZnP或ZnPc转移到Im-Pyr / SWCNT(n,m)。因此,稳态和时间分辨荧光研究表明,ZnP或ZnPc的单重激发态有效猝灭,电荷分离速率常数(kCS)在(3-6)×109 s-1范围内。纳秒瞬态吸收技术证实了电子转移产物ZnP·+←Im-Pyr / SWCNT·-和ZnPc·+←Im-Pyr / SWCNT·-(和相反的电荷对)具有特征吸收,并且由于电荷而具有衰减率常数重组(kCR)在(1.4–2.4)×107 s-1的范围内,对应于70–100 ns范围内的自由基离子对的寿命。 SWCNT·-进一步用于介导电子至己基紫胶指示剂(HV2 +),在牺牲电子供体存在的情况下导致电子蓄积过程,为这些材料发生光致电荷分离和潜在利用提供了额外的证据在光能收集应用中。此外,已经在FTO / SnO2电极上构建了光电化学电池,以验证其将光直接转换为电的能力。 ZnP←Im-Pyr / SWCNT修饰电极的IPCE效率高达7%。

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  • 来源
    《Journal of Porphyrins and Phthalocyanines》 |2011年第10期|p.1033-1043|共11页
  • 作者单位

    Sushanta K. Das Department of Chemistry, University of North Texas, 1155 Union Circle, #305070, Denton, TX 76203-5017, USA Navaneetha K. Subbaiyan Department of Chemistry, University of North Texas, 1155 Union Circle, #305070, Denton, TX 76203-5017, USA Francis D'Souza Corresponding author, tel: +940-369-8832, fax: +940-565-4318.SPP full member in good standing.Department of Chemistry, University of North Texas, 1155 Union Circle, #305070, Denton, TX 76203-5017, USAFrancis.DSouza@UNT.edu Atula S. D. Sandanayaka School of Materials Science, Japan Advanced Institute of Science and Technology (JAIST), Nomi, Ishikawa 923-1292, Japan Takatsugu Wakahara Fullerene Engineering Group, Advanced Nano Materials Laboratory, National Institute for Materials Science, 1-1 Namiki, Tsukuba, Ibaraki 305-0044, Japan Osamu Ito Corresponding author.Fullerene Engineering Group, Advanced Nano Materials Laboratory, National Institute for Materials Science, 1-1 Namiki, Tsukuba, Ibaraki 305-0044, JapanCarbonPhotoScience, Kita-Nakayama, 2-1-6, Izumi-ku, Sendai 98-3215, Japanito@tagen.tohoku.ac.jp;

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  • 正文语种 eng
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  • 关键词

    charge stabilization, diameter sorted single walled carbon nanotubes, donor-acceptor nanohybrids, photocatalysis, photoelectrochemistry, photoinduced electron transfer.;

    机译:电荷稳定;直径排序的单壁碳纳米管;施主-受体纳米杂化物;光催化;光电化学;光致电子转移。;

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