Aug. 2014

Article Contents

Chinese Optics> 2014> 7(4): 588-599.

QIAO Zi-wen, GAO Bing-rong, CHEN Qi-dai, WANG Hai-yu, WANG Lei. Ultrafast spectroscopy techniques and their complementary usages[J]. Chinese Optics, 2014, 7(4): 588-599. doi: 10.3788/CO.20140704.0588

Citation:

QIAO Zi-wen, GAO Bing-rong, CHEN Qi-dai, WANG Hai-yu, WANG Lei. Ultrafast spectroscopy techniques and their complementary usages[J].Chinese Optics, 2014, 7(4): 588-599.doi:10.3788/CO.20140704.0588

QIAO Zi-wen, GAO Bing-rong, CHEN Qi-dai, WANG Hai-yu, WANG Lei. Ultrafast spectroscopy techniques and their complementary usages[J]. Chinese Optics, 2014, 7(4): 588-599. doi: 10.3788/CO.20140704.0588

Citation:

QIAO Zi-wen, GAO Bing-rong, CHEN Qi-dai, WANG Hai-yu, WANG Lei. Ultrafast spectroscopy techniques and their complementary usages[J].Chinese Optics, 2014, 7(4): 588-599.doi:10.3788/CO.20140704.0588

PDF( 1260 KB)

Ultrafast spectroscopy techniques and their complementary usages

doi:10.3788/CO.20140704.0588

1.
Electronic Information Products Supervision Inspection Institute of Jilin Province, Changchun 130021, China;
2.
State Key Laboratory on Integrated Optoelectronics, College of Electronic Science and Engineering, Jilin University, Changchun 130012, China

Received Date:18 Mar 2014
Rev Recd Date:15 May 2014
Publish Date:25 Jul 2014

Abstract

Abstract

Ultrafast spectroscopy techniques are powerful tools for exploring the excited-state processes of materials. In this paper, we introduced femtosecond time-resolved fluorescence technique and femtosecond pump-probe technique in detail, including the fundamental principles of systems, optical paths and data processing metheds, as well as the advantage and disadvantage in different implemental schemes. At last, in order to reveal the complementary role, we provided an example in which the scientific problems were solved comprehensively and reliably by combinative usage of the two systems.
- ultrafast spectroscopy,
- fluorescence upconversion,
- pump-probe

FullText(HTML)

References (1)

References

[1] KAHLOW M A,JARZEBA W,DUBRUIL T P,et al.. Ultrafast emission spectroscopy in the ultraviolet by time-gated upconversion[J].Rev. Sci. Instrum.,1988,59:1098-1109.
[2] HIRSCH M D,MARCUS M A,LEWIS A,et al.. A method for measuring picosecond phemomena in photolabile species: the emission lifetime of bacteriorhodopsin[J].Biophys. J.,1976,16:1399-1409.
[3] BARBARA P F,KANG T J,JARZEBA W,et al.. Subpicosecond fluorescence measurements-application in chemistry[J].SPIE,1988,910:123-129.
[4] NAKAMURA R,KANEMATSU Y. Femtosecond spectral snapshots based on electronic optical Kerr effect[J].Rev. Sci. Instrum.,2004,75:636-644.
[5] NAKAMURA R,KANEMATSU Y. A simple and effective method for femtosecond spectral snapshots[J].J. Lumin.,2001,94-95:559-563.
[6] YU B L,BYKOV A B,QIU T,et al. Femtosecond optical Kerr shutter using lead-bismuth-gallium oxide glass[J].Opt. Commun.,2003,215:407-411.
[7] FOGGI P,BUSSOTTI L,NEWUWAHL F. Photophysical and photochemical applications of femtosecond time-resolved transient absorption spectroscopy[J].International J Photoenergy,2001,3:103-109.
[8] DHAR L,ROGERS J A,NELSON K A. Time-resolved vibrational spectroscopy in the impulsive limit[J].Chem. Rev.,1994,94:157.
[9] ALFANO R R,SHAPIRO S L. Emission in the region 4000 to 7000 Åvia four-photon coupling in glass[J].Phys. Rev. Lett.,1970,24:584.
[10] PENZKOFER A,KAISER W. Generation of picosecond light continua by parametric four-photon interactions in liquids and solids[J].Opt. Quantum Electron.,1977,9:315.
[11] SMITH W L,LIU P,BLOAMBERGEN N. Superbroadening in H₂O and D₂O by self-focused picosecond pulses from a YAlG:Nd laser[J].Phys. Rev. A,1977,15:2396.
[12] BEIKE S,GASE R,VOGLER K. On the generation of picosecond light continua depending on various nonlinear processes[J].Opt. Quantum Electron.,1980,12:9.
[13] YAMAGUCHI S,HAMAGUCHI H. Femtosecond ultraviolet-visible absorption study of all-trans-13 cis-9 cis photoisomerization of retinal[J].J. Chem. Phys.,1998,109:476692-476703.
[14] STOKKUM V,ALARSEN D,GRONDELLE R. Global and target analysis of time-resolved spectra[J].Biochimica et Biophysica Acta-Bioenergetics,2004,1657:82-104.
[15] GAO B R,WANG H Y,HAO Y W,et al.. Time-resolved fluorescence study of aggregation-induced emission enhancement by restriction of intramolecular charge transfer state[J].J. Phys. Chem. B,2010,114:128-134.
[16] GAO B R,WANG H Y,YANG Z Y,et al.. Comparative time resolved study of two aggregation induced emissive molecules[J].J. Phys. Chem. C,2011,115:16150-16154.
[17] 杨智勇,王亚峰,张汉壮,等. 异质二聚体反应中心的电荷转移过程[J]. 发光学报,2012,11:1177-1180. YANG ZH Y,WANG Y F,ZHANG H ZH,et al.. Study of electron transfer process of heterodimer reaction center[J].Chinese J. Luminescence,2012,11:1177-1180.(in Chinese)
[18] 王亚峰,王岩,孙琳,等. 具有开闭环性质的荧光素与螺吡喃双官能团融合分子的超快光谱研究[J]. 发光学报,2013,34(9):1118-1121. WANG Y F,WANG Y,SUN L,et al.. Study on the properties of bifunctional fused molecule consisted of spriopyran and fluorescein units using ultrafast spectroscopy[J].Chinese J. Luminescence,2013,34(9):1118-1121.(in Chinese)
[19] WANG H,WANG H Y,GAO B R,et al.. Exciton diffusion and charge transfer dynamics in nano phase-separated P3HT:PCBM blend films[J].Nanoscale,2011,3:2280-2285.
[20] 张伟,余汉城,王惠,等. 侧链基团对聚合物薄膜瞬态发光性能的影响[J]. 发光学报,2007,28(4):521-525. ZHANG W,YU H CH,WANG H,et al.. The influence of the side-chain groups on luminescence of porphyrin side-chain polymers[J].Chinese J. Luminescence,2007,28(4):521-525.(in Chinese)
[21] PAN L Y,ZHANG Y L,WANG H Y,et al. Hierarchical self-assembly of CdTe quantum dots into hyperbranched nanobundles:suppression of biexciton Auger recombination[J].Nanoscale,2011,3:2882-2888.
[22] HAO Y W,WANG H Y,JIANG Y,et al.. Hybrid states dynamics of gold nanorods/dye J-aggregate under strong coupling[J].Angew. Chem. Int. Ed.,2011,50:7824-7828.
[23] JIANG Y,WANG H Y,XIE L P,et al. Study of electron-phonon coupling dynamics in Au nanorods by transient depolarization measurements[J].J. Phys. Chem. C,2010,114:2913-2917.
[24] WANG H,GAO B R,JIANG Y,et al.. Surface plasmon enhanced absorption dynamics of regioregular poly(3-hexylthiophene)[J].Appl. Phys. Lett.,2011,98:251501.
[25] LUO J D,XIE Z L,LAM J W Y,et al.. Aggregation-induced emission of 1-methyl-1,2,3,4,5-pentaphenylsilole[J].Chem. Commun.,2001:1740-1741.
[26] XIE Z Q,YANG B,LI F,et al. Cross dipole stacking in the crystal of distyrylbenzene derivative: the approach toward high solid-state luminescence efficiency[J].J. Am. Chem. Soc.,2005,127:14152-14153.
[27] CHEN J W,LAW C C W,LAM J W Y,et al.. Synthesis,light emission, nanoaggregation, and restricted intramolecular rotation of 1,1-substituted 2,3,4,5-tetraphenylsiloles[J].Chem. Mater.,2003,15:1535-1546.
[28] LI Y P,LI F,ZHANG H Y,et al.. Tight intermolecular packing through supramolecular interactions in crystals of cyano substituted oligo(para-phenylene vinylene):a key factor for aggregation-induced emission[J].Chem. Commun.,2007:231-233.
[29] REN Y,LAM J W Y,DONG Y Q,et al.. Enhanced emission efficiency and excited state lifetime due to restricted intramolecular motion in silole aggregates[J].J. Phys. Chem. B,2005,109:1135-1140.
[30] WANG H,ZHANG H,ABOU-ZIED O K,et al.. Femtosecond fluorescence upconversion studies of excited-state proton-transfer dynamics in 2-(2'-hydroxyphenyl)benzoxazole(HBO) in liquid solution and DNA[J].Chem. Phys. Lett.,2003,367:599-608.
[31] LI Y P,SHEN F Z,WANG H,et al.. Supramolecular network conducting the formation of uniaxially oriented molecular crystal of cyano substituted oligo(p-phenylene vinylene) and its amplified spontaneous emission(ASE) behavior[J].Chem. Mater.,2008,20:7312-7318.