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21.
A non-conjugated polymer acceptor PF1-TS4 was firstly synthesized by embedding a thioalkyl segment in the mainchain, which shows excellent photophysical properties on par with a fully conjugated polymer, with a low optical band gap of 1.58 eV and a high absorption coefficient >105 cm−1, a high LUMO level of −3.89 eV, and suitable crystallinity. Matched with the polymer donor PM6, the PF1-TS4-based all-PSC achieved a power conversion efficiency (PCE) of 8.63 %, which is ≈45 % higher than that of a device based on the small molecule acceptor counterpart IDIC16. Moreover, the PF1-TS4-based all-PSC has good thermal stability with ≈70 % of its initial PCE retained after being stored at 85 °C for 180 h, while the IDIC16-based device only retained ≈50 % of its initial PCE when stored at 85 °C for only 18 h. Our work provides a new strategy to develop efficient polymer acceptor materials by linkage of conjugated units with non-conjugated thioalkyl segments.  相似文献   
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Hideyuki Tatsuno  Kasper S. Kjr  Kristjan Kunnus  Tobias C. B. Harlang  Cornelia Timm  Meiyuan Guo  Pavel Chbera  Lisa A. Fredin  Robert W. Hartsock  Marco E. Reinhard  Sergey Koroidov  Lin Li  Amy A. Cordones  Olga Gordivska  Om Prakash  Yizhu Liu  Mads G. Laursen  Elisa Biasin  Frederik B. Hansen  Peter Vester  Morten Christensen  Kristoffer Haldrup  Zoltn Nmeth  Dorottya Srosin Szemes   va Bajnczi  Gyrgy Vank  Tim B. Van Driel  Roberto Alonso‐Mori  James M. Glownia  Silke Nelson  Marcin Sikorski  Henrik T. Lemke  Dimosthenis Sokaras  Sophie E. Canton  Asmus O. Dohn  Klaus B. Mller  Martin M. Nielsen  Kelly J. Gaffney  Kenneth Wrnmark  Villy Sundstrm  Petter Persson  Jens Uhlig 《Angewandte Chemie (International ed. in English)》2020,59(1):364-372
Iron N‐heterocyclic carbene (NHC) complexes have received a great deal of attention recently because of their growing potential as light sensitizers or photocatalysts. We present a sub‐ps X‐ray spectroscopy study of an FeIINHC complex that identifies and quantifies the states involved in the deactivation cascade after light absorption. Excited molecules relax back to the ground state along two pathways: After population of a hot 3MLCT state, from the initially excited 1MLCT state, 30 % of the molecules undergo ultrafast (150 fs) relaxation to the 3MC state, in competition with vibrational relaxation and cooling to the relaxed 3MLCT state. The relaxed 3MLCT state then decays much more slowly (7.6 ps) to the 3MC state. The 3MC state is rapidly (2.2 ps) deactivated to the ground state. The 5MC state is not involved in the deactivation pathway. The ultrafast partial deactivation of the 3MLCT state constitutes a loss channel from the point of view of photochemical efficiency and highlights the necessity to screen transition‐metal complexes for similar ultrafast decays to optimize photochemical performance.  相似文献   
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A high statistics measurement of the Lambda(+)(c) lifetime from the Fermilab fixed-target FOCUS photoproduction experiment is presented. We describe the analysis technique with particular attention to the determination of the systematic uncertainty. The measured value of 204.6 +/- 3.4 (stat) +/- 2.5 (syst) fs from 8034 +/- 122 Lambda(+)(c)-->pK(-)pi(+) decays represents a significant improvement over the present world average.  相似文献   
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Both Shubnikov-de Haas and de Haas-van Alphen oscillations are reported for C8nAsF5 (n=1,2, is the stage number). The observed oscillations are interpreted in terms of a tight-binding model for the band structure, and good agreement with both band parameters and effective carrier masses is found. In addition, the effective charge transfer per AsF5 molecule (f=.37 for stage 1, =.41 for stage 2) is in basic agreement with previous determinations.  相似文献   
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From a sample of 1172 +/- 61 D(+)-->pi(-)pi(+)pi(+) decays, we find gamma(D(+)-->pi(-)pi(+)pi(+))/gamma(D(+)-->K-pi(+)pi(+)) = 0.0311 +/- 0.0018(+0.0016)(-0.0026). Using a coherent amplitude analysis to fit the Dalitz plot of these decays, we find strong evidence that a scalar resonance of mass 478(+24)(-23) +/- 17 MeV/c(2) and width 324(+42)(-40) +/- 21 MeV/c(2) accounts for approximately half of all decays.  相似文献   
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This article reports our discovery that poly(ethylene glycol) (PEG) can quantitatively be functionalized by transesterification using Candida antarctica lipase B (Novozyme 435) as the catalyst. α‐ω telechelic PEG‐methacrylates and PEG‐acetates were successfully prepared using commercially available PEGs with both narrow and broad molecular weight distribution. 1H and 13C NMR together with MALDI‐TOF mass spectroscopy verified the expected structures. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 3024–3028, 2008  相似文献   
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