{"id":70,"date":"2015-02-27T14:28:51","date_gmt":"2015-02-27T19:28:51","guid":{"rendered":"http:\/\/caslabs.case.edu\/sauve\/?page_id=70"},"modified":"2025-10-27T11:38:10","modified_gmt":"2025-10-27T15:38:10","slug":"publications","status":"publish","type":"page","link":"https:\/\/caslabs.case.edu\/sauve\/publications\/","title":{"rendered":"Publications"},"content":{"rendered":"

At Case Western Reserve University:<\/span><\/h3>\n
    \n
  1. Knight, L. R.; Tran, Q. D.; Raufman, D.; Paparella, A. A.; Brancel, C. D.; Jadhav, N.; Rodrigues, V.; Zou, Q.; Jimenez, J. C.; Wu, S.; Zhu, L.; Sauve, G. \u201cSide chain engineering of near-IR aza-BODIPY dyes enable processable films with high hole mobility in diodes\u201d Phys. Chem. C<\/em>. 2025<\/strong>, ASAP https:\/\/doi.org\/10.1021\/acs.jpcc.5c04202<\/a>\"\"<\/a><\/li>\n
  2. Knight, L. R.; Tritt, M. M.; Tran, Q. D.; Zhang, H.; Zhu, L.; Sauve, G. \u201cGreen solvent-processable poly(3-hexylthiophene) derivative maintains high hole mobility in diodes\u201d Synthetic Metals<\/em>. 2025<\/strong>, 314, 117940. https:\/\/doi.org\/10.1016\/j.synthmet.2025.117940<\/a>
    \n    \"\"<\/a><\/li>\n
  3. Knight, L.; Tran, Q.; Bushnell, A.; Wongwirat, T.; Honghu, Z.; Zhu, L.; Sauve, G. \u201cComparing the effects of side chain dipole-dipole interactions and hydrogen bonding on the mechanical and electrical properties of poly(3-hexylthiophene)\u201d ACS Appl. Polym. Mater.<\/em> 2025<\/strong>, 7, 4, 2337-2346. https:\/\/doi.org\/10.1021\/acsapm.4c03426<\/a>
    \n    \"\"<\/a><\/li>\n
  4. Knight, L.; Jimenez, J. C.; Tran, Q.; Zhao, M.; Pugh, M<\/u>. H.; Brancel, C<\/u>. D.; Zhang, H.; Li, R.; Yuan, Y.; Zhu, L.; Sauv\u00e9, G. \u201cTuning the charge transport properties of non-planar zinc(II) complexes of azadipyrromethene using solubilizing groups\u201d Advance Article,\n
  5. Tran, Q. D.; Knight, L. R.; Rui, G.; Mason, G. T.; Kulatunga, P.; Bushnell, A<\/u>. J.; Hou, B<\/u>.; Zhu, L.; Rondeau-Gagn\u00e9, S.; Sauv\u00e9, G. \u201cEster side chain functionalization enhances mechanical properties of poly(3-hexylthiophene) while maintaining high hole mobility: Macromolecules <\/em>2024, <\/strong>57, 4544-4555.\u00a0https:\/\/doi.org\/10.1021\/acs.macromol.3c01886<\/a>
    \n    \"\"<\/a><\/li>\n
  6. Jimenez, J. C.; Tran, Q.; Pugh, Madison H<\/u>.; Brancel, C. D.<\/u>; Rheingold, A. L.; Sauv\u00e9, G. \u201cZinc(II) complexes of azadipyrromethene: Effect of nature and placement of solubilizing groups on structural, thermal, electrochemical and optical properties\u201d Dyes Pigm.<\/em> 2023<\/strong>, 208, 110858. https:\/\/doi.org\/10.1016\/j.dyepig.2022.110858<\/a>\"\"<\/a><\/li>\n
  7. Zhao, M.; Jimenez, J. C.; Wang, C.; Rui, G.; Ma, T.; Lu, C.; Rheingold, A. L.; Li, R.; Zhu, L.; Sauv\u00e9, G. \u201cMonofluorination of the naphthyls promotes pi-pi. Stacking and increase electron mobiity of non-planar zinc(II) complexes of. Di(naphthylethynyl) azadipyrromethene\u201d Phys. Chem. C<\/em>, 2022<\/strong>, 126, 15, 6543-6555. https:\/\/doi.org\/10.1021\/acs.jpcc.1c09734<\/a>\"\"<\/a><\/li>\n
  8. Jimenez, J. C.; Zhou, Z.; Rheingold, A. L.; Parker, S. M.; Sauv\u00e9, G. \u201cTuning the properties of azadipyrromethene-based near-infrared dyes using intramolecular BO chelation and peripheral substitutions\u201d Inorg. Chem.<\/i> 2021<\/b>, 60, 13320-13331.<\/a> \"\"<\/a><\/li>\n
  9. Lu, C.<\/u>; Wang, C.; Jimenez, J. C.; Rheingold, A. L.; Sauv\u00e9, G.\u00a0 \u201cLarge non-planar conjugated molecule with strong intermolecular interactions achieved with homoleptic Zn(II) complex of di(5-quinolylethynyl)-tetraphenylazadipyrromethene\u201d ACS Omega<\/i>, 2020<\/b>, 5, 31467-31472.<\/a>
    \n    \"\"<\/a><\/li>\n
  10. Wang, C.; Zhao, M.; Rheingold, A.; Sauv\u00e9, G. \u201cStructure-property study of homoleptic zinc(II) complexes of di(arylethynyl) azadipyrromethene as non-fullerene acceptors for organic photovoltaics: Effect of aryl group\u201d Phys. Chem. C<\/em>, 2020<\/strong>, 124, 8541-8549.<\/a>\"\"<\/a><\/li>\n
  11. Wang, C.; Daddario, C.; Peji\u0107, S.; Sauv\u00e9, G. \u201cSynthesis and properties of azadipyrromethene-based complexes with nitrile substitution\u201d J. Org. Chem.\u00a0<\/em>2020<\/strong>, 6, <\/em>714-722.<\/a> DOI: 10.1002\/ejoc.201901736.\"\"<\/a><\/li>\n
  12. Wang, C.; Wei, P.; Ngai, J. H. L.; Rheingold, A. L.; Gray, T. G.; Li, Y.; Pentzer, E.; Li, R.; Zhu, L.; Sauv\u00e9, G. \u201cOrganic photovoltaics with high industrial accessibility using a zinc(II) complex of di(naphthylethynyl)azadipyrromethene as non-fullerene acceptor\u201d Mater. Chem. A.<\/em> 2019<\/strong>, 7, 24614-24625.<\/a>\"\"<\/a><\/li>\n
  13. Fernando, R.; Peji\u0107, S.; Thomsen, A M..<\/u>; Wang, C.; Sauv\u00e9, G. \u201cAzadipyrromethene-based near-IR dyes with styryl substituents at the pyrrolic positions for organic photovoltaic applications\u201d Dyes Pigm.<\/em>, 2019<\/strong>, 168, 257-263<\/a>.\"\"<\/a><\/li>\n
  14. Sauv\u00e9, G. \u201cDesigning alternative non-fullerene molecular electron acceptors for solution-processable organic photovoltaics\u201d Chem. Rec<\/em>. (Special Edition: New Directions in Organic Solar Cells), 2019<\/strong>, 19, 1-16<\/a>. A personal Account<\/em>.\"\"<\/a><\/li>\n
  15. Wang, C.; Zhang, Z.; Peji\u0107, S.; Li, R.; Fukuto, M.; Zhu, L.; Sauv\u00e9, G. \u201cHigh dielectric constant semiconducting poly(3-alkylthiophene)s from side chain modification with polar sulfinyl and sulfonyl groups\u201d Macromolecule<\/em>, 2018<\/strong>, 51, 9368-9381.<\/a>\"\"<\/a><\/li>\n
  16. Dai, Y; Wang, C.; Chiu, L.-Y.; Abbasi, K.; Tolbert, B.; Sauv\u00e9, G.; Yen, Y.; Liu, C.C. \u201cApplication of bioconjugation chemistry on biosensor fabrication for detection of TAR-DNA binding protein 43\u201d Biosens. Bioelectron.\u00a0<\/i>2018<\/b>, 117, 60-67.<\/a>\"\"<\/a><\/li>\n
  17. DiScipio, R.; Sauv\u00e9, G.; Crespo-Hernandez, C. E. \u201cPhotodynamics in metal-chelating tetraphenylazadipyrromethene complexes: Implications for their potential use as photovoltaic materials\u201d Phys. Chem. C\u00a0<\/em>2018<\/strong>, 122, 13579-13589.<\/a>\"\"<\/a><\/li>\n
  18. Peji\u0107, S.; Thomsen, A. M.<\/u>; Etheridge, F. S.; Fernando, R.; Wang, C.; Sauv\u00e9, G. \u201cFluorination increases the electron mobility of zinc azadipyrromethene-based elecron acceptors and enhances the performance of fullerene-free organic solar cells\u201d Mater. Chem. C \u00a0<\/em>2018<\/strong>, 6, 3990-3998.<\/a>\"\"<\/a><\/li>\n
  19. Saini, A.; Etheridge, F. S.; Peters, K. C.; Peji\u0107, S.; Gao, L.; Hellring, S. D.; Schuele, D. E.; Sauv\u00e9, G.; Singer, K. D. \u201cAqueous deposition of a semiconducting polymer by electrocoating\u201d Electron.\u00a0<\/em>2018<\/strong>, 53, 332-338<\/a>.\"\"<\/a><\/li>\n
  20. Zhao, Z.; Zhang, Z.; Pejic, S.; Zhang, G.; Zhu, Y.; Liu, H.*; Litt, M.; Sauve, G.<\/strong>*; Zhu, L.* \u201cSynergistic dielectric and semiconducting properties in fluorescein monopotassium salt random copolymers\u201d Polymer<\/em> 2017<\/strong>, 114, 189-198<\/a>.\"\"<\/a><\/li>\n
  21. Vogelbaum, H. S.; Sauv\u00e9, G.* <\/strong>\u201cRecently developed high-efficiency organic photoactive materials for printable photovoltaic cells: a mini review\u201d Synth.\u00a0Met.<\/em> 2017<\/strong>, 223, 107-121.<\/a><\/li>\n
  22. Smith, Z. C.; Wright, Z. M.; Arnold, A. M.; Sauv\u00e9, G.<\/strong>; McCullough, R. D.; Sydlik, S. A.* \u201cIncreased Toughness and Excellent Electronic Properties in Regioregular Random Copolymers of 3-Alkylthiophenes and Thiophene\u201d Adv.\u00a0<\/em>Electron. Mater.<\/em> 2017, 3, 1600316<\/strong>.<\/a>\"\"<\/a><\/li>\n
  23. Etheridge, F. S.; Fernando, R. J.; Peji\u0107, S.; Zeller, M.; Sauv\u00e9, G.*<\/strong> \u201cSynthesis and Characterization of Fluorinated Azadipyrromethene Complexes as Acceptors for Organic Photovoltaics\u201d Beilstein J. Org. Chem.<\/em> 2016<\/strong>, 12, 1925-1938<\/a>.\"\"<\/a><\/li>\n
  24. Sauve, G.*<\/strong>, Fernando, R. \u201cBeyond Fullerenes: Designing alternative molecular electron acceptors for solution-processable bulk heterojunction organic photovoltaics\u201d, Phys, Chem. Lett.<\/em> 2015<\/strong>, 6, 3770-3780.<\/a>\"\"<\/a><\/span><\/li>\n
  25. Daddario, C. M.; Han, Q.; Zeller, M.; Sauve, G.*<\/strong> \u201cAzadipyrromethene-based near-infrared dyes: Effect of thienylethynyl substitution at the distal and proximal phenyls\u201d, Eur. J. Inorg. Chem. <\/em>2015<\/strong>\u00a06,3770-3780<\/a>. \"\"<\/a><\/em><\/span><\/li>\n
  26. Etheridge, F. S.; Fernando, R.; Golen, J. A.; Rheingold, A. L.; Sauve, G.*<\/strong> \u201cTuning optoelectronic properties of core-substituted naphthalene diimides by the selective conversion of imides to monothioimides\u201d, RSC Adv<\/em>. 2015<\/strong>,5, 46534-46539<\/a>.\"\"<\/a><\/span><\/li>\n
  27. Fernando, R.; Etheridge, F.; Muller, E.; Sauve, G.*<\/strong> \u201cEffect of vinylphenyl N-substituent on the opto-electronic properties of core-substituted naphthalenediimides\u201d, New<\/em> J. Chem.<\/em> 2015<\/strong>, 39, 2506-2514<\/a>.\"\"<\/a><\/span><\/li>\n
  28. Senevirathna, W.; Liao, J.-Y.; Gu, J.; Porter, M.; Wang, C.; Fernando, R.; Sauve, G.*<\/strong> \u201cSynthesis, characterization and photovoltaic properties of electron accepting azadipyrromethene-based dyes: effect of pyrrolic substituents\u201d, J. Mater. Chem. A<\/em>, 2015<\/strong>, 3, 4203-4214<\/a>.\"\"<\/a><\/span><\/li>\n
  29. Mao, Z.; Le, T.; Vakhshouri, K.; Fernando, R.; Ruan, F.; Muller, E.; Gomez, E. D.; Sauve, G.*<\/strong> \u201cCore-substituted naphthalene diimide acceptor-based organic solar cell: effect of processing additive\u201d, Org. Electron<\/em>, 2014<\/strong>, 15, 3384-3391<\/a>.\"\"<\/a><\/span><\/li>\n
  30. Mao Z.; Senevirathna, W.; Liao, J.-Y.; Gu, J.; Vajjala Kesava, S.; Guo, C.; Gomez, E. D.; Sauve, G<\/strong>. \u201cAzadipyrromethene-based Zn(II) complexes as non-planar conjugated electron acceptors for organic photovoltaics\u201d, Adv. Mater.<\/em>, 2014<\/strong>, 26, 6290-6294<\/a>.\"\"<\/a><\/span><\/li>\n
  31. Senevirathna, W.; Daddario, C. M.; Sauve, G.<\/strong> \u201cDensity functional theory study predicts low reorganization energies for azadipyrromethene-based metal complexes\u201d, J. Phys. Chem. Lett.<\/em>, 2014<\/strong>, 5, 935-941<\/a>.\"\"<\/a><\/span><\/li>\n
  32. Fernando, R.; Mao, Z.; Muller, E.; Ruan, F.; Sauv\u00e9, G.<\/strong> \u201cTuning the organic solar cell performance of acceptor 2,6-dialkylaminonaphthalene diimides by varying a linker between the imide nitrogen and a thiophene group\u201d, J. Phys. Chem. C.<\/em>,\u00a02014<\/strong>, 118, 3433-3442<\/a>.\"\"<\/a><\/span><\/li>\n
  33. Senevirathna, W.; Sauv\u00e9, G.* <\/strong>“Introducing 3D conjugated acceptors with intense red absorption: homoleptic metal (II) complexes of di(phenylacetylene) azadipyrromethene”, J. Mater. Chem. C<\/em>, 2013<\/strong>, 1, 6684-6694<\/a>.\"\"<\/a><\/span><\/li>\n
  34. Fernando, R.; Mao, Z.; Sauv\u00e9, G.* <\/strong>“Synthesis and Characterization of Rod-like Oligomers Incorporating 2,6-dialkylamino Core-substituted Naphthalene Diimide” Org. Electron.<\/em>2013<\/strong>, 14, 1683-1692<\/a>.\"\"<\/a><\/span><\/li>\n
  35. Mao, Z.; Vakhshouri, K.; Jaye, C.; Fischer, D. A.; Fernando, \u00a0R.; DeLongchamp, D. M.; Gomez, \u00a0E. D.; Sauv\u00e9, G.*<\/strong> \u201cSynthesis of Perfluoroalkyl End-Functionalized Poly(3-hexylthiophene) and the Effect of Fluorinated End-Groups on Solar Cell Performance\u201d Macromolecules<\/em>, 2013<\/strong>, 46, 103-112<\/a>.\"\"<\/a><\/span><\/li>\n
  36. Gao, L.; Tang, S.; Zhu, L.; Sauv\u00e9, G.*<\/strong> \u201cSynthesis and Characterization of Azadipyrromethene- alt<\/em>– p<\/em>-Phenylene Ethynylene Conjugated Polymers and Their Chelates\u201d Macromolecules<\/em> 2012<\/strong>, 45, 7404-7412<\/a>.\"\"<\/a><\/span><\/li>\n
  37. Gao, L.; Senevirathna, R.; Sauv\u00e9, G.<\/strong>. “Azadipyrromethene-Based Conjugated Oligomers with Near-IR Absorption and High Electron Affinity” Org. Lett.<\/em>, 2011<\/strong>, 13, 5354-5357<\/a>.\"\"<\/a><\/span><\/li>\n<\/ol>\n

    Prior to Case Western Reserve University:<\/span><\/h3>\n
      \n
    1. Sauv\u00e9, G.<\/strong>; Javier, A. E.; Zhang, R.; Liu, J.; Sydlik, S. A.; Kowalewski,T.; McCullough, R. D. “Well-defined, high molecular weight poly(3-alkylthiophene)s in thin-film transistors: side chain invariance in field-effect mobility” J. Mater. Chem.<\/em>, 2010<\/strong>, 20, 3195-3201<\/a>.<\/span><\/li>\n
    2. Osaka, I.; Zhang, R.; Sauv\u00e9, G.<\/strong>; Smilgies, D.-M.; Kowalewski, T.; McCullough, R. D. “High-Lamellar Ordering and Amorphous-Like p-Network in Short-Chain thiazolothiazole-Thiophene Copolymers Lead to High Mobilities’, J. Am. Chem. Soc.<\/em>, 2009<\/strong>, 131(7), 2521-2529.<\/span><\/li>\n
    3. Liu, J.; Zhang, R.; Sauv\u00e9, G.<\/strong>; Kowalewski, T.; McCullough, R. D. “Highly Disordered Polymer Field Effect Transistors: N-alkyl dithieno[3,2-b:2′,3′-d]pyrroles-based Copolymers with Surprisingly High Charge Carrier Mobilities”, J. Am. Chem. Soc.<\/em>, 2008<\/strong>, 130(39), 13167-13176.<\/span><\/li>\n
    4. Singh, K. A.; Sauv\u00e9, G.<\/strong>; Zhang, R.; Kowalewski, T.; McCullough, R. D.; Porter, L. M. “Dependence of Field-Effect Mobility and Contact Resistance on Nanostructure in Regioregular Poly(3-hexylthiophene) Thin Film Transistors”, Appl. Phys. Lett.<\/em>, 2008<\/strong>, 92, 263303.<\/span><\/li>\n
    5. Osaka, I.; Sauv\u00e9, G.<\/strong>; Zhang, R.; Kowalewski, T.; McCullough, R. D. “Novel Thiophene-Thiazolothiazole Copolymers for Organic Field-Effect Transistors”, Adv. Mater.<\/em>, 2007<\/strong>,19(23) 4160-4165.<\/span><\/li>\n
    6. Sauv\u00e9, G.<\/strong>; McCullough, R. D. “High Field-Effect Mobilities for Diblock Copolymers of Poly(3-hexylthiophene) and Poly(methyl acrylate)”, Adv. Mater.<\/em>, 2007<\/strong>, 19(14) 1822-1825<\/a>.<\/span><\/li>\n
    7. Li, B.; Santhanmam, S.; Schultz, L.; Jeffries-EL, M.; Iovu, M. C.; Sauv\u00e9, G.<\/strong>; Cooper, J.; Zhang, R.; Revelli, J. C.; Kusne, A. G.; Snyder, J. L.; Kowalewski, T.; Weiss, L. E.; McCullough, R. D.; Fedder, G. K.; Lambeth, D. N.; “Inkjet Printed Chemical Sensor Array Based on Polythiophene Conductive Polymers”, Sensors and Actuators, B: Chemical<\/em>, 2007<\/strong>, B123, 651-660.<\/span><\/li>\n
    8. Li, B.; Sauv\u00e9, G.<\/strong>; Iovu, M. C.; Zhang, R.; Cooper, J.; Santhanam, S.; Schultz, L.; Revelli, J. C.; Kusne, A. G.; Kowalewski, T.; Snyder, J. L.; Weiss, L. E.; Fedder, G. K.; McCullough, R. D.; Lambeth, D. N.; “Volatile Organic Compound Detection Using Nanostructured Copolymers”, Nano Lett.<\/em>, 2006<\/strong>, 6 (8) 1598-1602.<\/span><\/li>\n
    9. Zhang, R.; Li, B.; Iovu, M.; Jeffries-EL, M.; Sauv\u00e9, G.<\/strong>; Cooper, J.; Jia, S.; Tristram-Nagle, S.; Smilgies, D. M.; Lambeth, D. N.; McCullough, R. D.; Kowalewski, T. “Nanostructure Dependence of Field-Effect Mobility in Regioregular Poly(3-hexylthiophene) Thin Film Field Effect Transistors”, J. Am. Chem. Soc.<\/em>, 2006<\/strong>, 128(11), 3480-3481.<\/span><\/li>\n
    10. Jeffries-EL, M.; Sauv\u00e9, G.<\/strong>; McCullough, R. D. “Facile Synthesis of End-Functionalized Regioregular Poly(3-alkylthiophene)s via Modified Grignard Metathesis Reaction”, Macromolecules<\/em>, 2005<\/strong>, 38(25), 10346-10352<\/a>.<\/span><\/li>\n
    11. Ewbank, P. C.; Loewe, R. S.; Zhai, L.; Reddinger, J.; Sauv\u00e9, G.<\/strong>; McCullough, R. D. “Regioregular Poly(thiophene-3-alkanoic acid)s: Water Soluble Conducting Polymers Suitable for Chromatic Chemosensing in Solution and Solid State”, Tetrahedron<\/em>, 2004<\/strong>, 60(49), 11269-11275.<\/span><\/li>\n
    12. Jeffries-EL, M.; Sauv\u00e9, G.<\/strong>; McCullough, R. D. “In-situ End-group Functionalization of Regioregular Poly(3-alkylthiophene) Using the Grignard Metathesis Polymerization Method”, Adv. Mater.<\/em>, 2004<\/strong>, 16(12), 1017-1019.<\/span><\/li>\n
    13. Sauv\u00e9, G.<\/strong>; Cass, M. E.; Coia, G.; Doig, S. J.; Lauermann, I.; Pomykal, K. E.; Lewis, N. S. “Dye Sensitization of Nanocrystalline Titanium Dioxide with Osmium and Ruthenium Polypyridyl Complexes”, J. Phys. Chem. B<\/em>, 2000<\/strong>, 104, 6821-6836<\/a>.<\/span><\/li>\n
    14. Sauv\u00e9, G.<\/strong>; Cass, M. E.; Doig, S. J.; Lauermann, I.; Pomykal, K. E.; Lewis, N. S. “High Quantum Yield Sensitization of Nanocrystalline Titanium Dioxide Photoelectrodes with cis-Dicyanobis(4,4′-dicarboxy-2,2′-bipyridine)osmium(II) or Tris(4,4′-dicarboxy-2,2′-bipyridine)osmium(II) Complexes”, J. Phys. Chem. B<\/em>, 2000<\/strong>, 104, 3488-3491.<\/span><\/li>\n
    15. Kamat, P. V.; Sauv\u00e9, G.<\/strong>; Guldi, D. M.; Asmus, K.-D. “Radical Reactions of C84”, Res. Chem. Intermed.<\/em>, 1997<\/strong>, 23, 575-585.<\/span><\/li>\n
    16. Sauv\u00e9 G.<\/strong>; Kamat, P. V.; Thomas, K. G.; Thomas, K. J.; Das, S.; George, M. V. “Photochemistry of Squaraine Dyes: Excited Triplet State and Redox Properties of Crown Ether Squaraines”, J. Phys. Chem.<\/em>, 1996<\/strong>, 100(6), 2117-2123.<\/span><\/li>\n
    17. Serpone, N.; Sauv\u00e9, G.<\/strong>; Koch, R.; Tahiri, H.; Pichat, P.; Piccinini, P.; Pelizzetti, E.; Hidaka, H. “Standardization Protocole of Process Efficiencies and Activation Parameters in Heterogeneous Photocatalysis: Relative Photonic Efficiencies xr”, J. Photochem. Photobiol. A: Chem.<\/em>, 1996<\/strong>, 94(2,3), 191-203.<\/span><\/li>\n
    18. Sauv\u00e9, G.<\/strong>; Kamat, P. V.; Ruoff, R. S. “Excited Triplet and Reduced Forms of C84”, J. Phys. Chem<\/em>, 1995<\/strong>, 99, 2162-2165.<\/span><\/li>\n
    19. Sauv\u00e9, G.<\/strong>; Dimitrijevic, N. M.; Kamat, P. V. “Singlet and Triplet Excited State Behaviors of C60 in Nonreactive and Reactive Polymer Films”, J. Phys. Chem.<\/em>, 1995<\/strong>, 99, 1199-1203.<\/span><\/li>\n
    20. Serpone, N.; Terzian, R.; Lawless, D.; Kennepohl, P.; Sauv\u00e9, G.<\/strong> “On the Usage of Turnover Numbers and Quantum Yields in Heterogeneous Photocatalysis”, J. Photochem. Photobiol., A: Chem.<\/em>, 1993<\/strong>, 73(1), 11-16.<\/span><\/li>\n<\/ol>\n

       <\/p>\n

      Book chapters<\/span><\/h3>\n

      Sauve, G. <\/strong>\u201cNon-Fullerene Acceptors\u201d in \u201cWorld Scientific Handbook of Organic Optoelectronic Devices\u201d, Editor-in-chief: Franky So, Volume 2: \u201cOrganic Photovoltaics (OPVs)\u201d Editor: Barry C Thompson. World Scientific, Aug 2018<\/strong>, p. 31-87.<\/p>\n

      Ewbank, P. C.; Stefan, Mihaela C.; Sauve, G.<\/strong>; McCullough R. D., “Synthesis, characterization and properties of regioregular polythiophene-based materials, in Handbook of Thiophene-based Materials:Applications in Organic Electronics and Photonics”, Wiley, 2009<\/strong>.<\/span><\/p>\n

      <\/div>\n","protected":false},"excerpt":{"rendered":"

      At Case Western Reserve University:<\/p>\n

      \tKnight, L. R.; Tran, Q. D.; Raufman, D.; Paparella, A. A.; Brancel, C. D.; Jadhav, N.; Rodrigues, V.; Zou, Q.; Jimenez, J. C.; Wu, S.; Zhu, L.; Sauve, G. \u201cSide chain engineering of near-IR aza-BODIPY dyes enable processable films with high hole mobility in diodes\u201d Phys. Chem. C<\/em>. 2025<\/strong>, ASAP https:\/\/doi.org\/10.1021\/acs.jpcc.5c04202<\/a><\/a>
      \n \tKnight, L. R.; Tritt, M. M.; Tran, Q. D.; Zhang, H.; Zhu, L.; Sauve, G. \u201cGreen solvent-processable poly(3-hexylthiophene) derivative maintains high hole mobility in diodes\u201d Synthetic Metals<\/em>. 2025<\/strong>,<\/p>\n

      Continue reading… Publications<\/span><\/a><\/p>\n","protected":false},"author":181,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"spay_email":""},"_links":{"self":[{"href":"https:\/\/caslabs.case.edu\/sauve\/wp-json\/wp\/v2\/pages\/70"}],"collection":[{"href":"https:\/\/caslabs.case.edu\/sauve\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/caslabs.case.edu\/sauve\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/caslabs.case.edu\/sauve\/wp-json\/wp\/v2\/users\/181"}],"replies":[{"embeddable":true,"href":"https:\/\/caslabs.case.edu\/sauve\/wp-json\/wp\/v2\/comments?post=70"}],"version-history":[{"count":10,"href":"https:\/\/caslabs.case.edu\/sauve\/wp-json\/wp\/v2\/pages\/70\/revisions"}],"predecessor-version":[{"id":656,"href":"https:\/\/caslabs.case.edu\/sauve\/wp-json\/wp\/v2\/pages\/70\/revisions\/656"}],"wp:attachment":[{"href":"https:\/\/caslabs.case.edu\/sauve\/wp-json\/wp\/v2\/media?parent=70"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}