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Maximum Theoretical Efficiency Limit of Photovoltaic Devices: Effect of Band Structure on Excited State Entropy.

The journal of physical chemistry letters

Osterloh FE.
PMID: 26278444
J Phys Chem Lett. 2014 Oct 02;5(19):3354-9. doi: 10.1021/jz501740n. Epub 2014 Sep 17.

The Shockley-Queisser analysis provides a theoretical limit for the maximum energy conversion efficiency of single junction photovoltaic cells. But besides the semiconductor bandgap no other semiconductor properties are considered in the analysis. Here, we show that the maximum conversion...

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Osterloh FE. Maximum Theoretical Efficiency Limit of Photovoltaic Devices: Effect of Band Structure on Excited State Entropy. J Phys Chem Lett. 2014;5(19):3354-9doi: 10.1021/jz501740n.
Osterloh, F. E. (2014). Maximum Theoretical Efficiency Limit of Photovoltaic Devices: Effect of Band Structure on Excited State Entropy. The journal of physical chemistry letters, 5(19), 3354-9. https://doi.org/10.1021/jz501740n
Osterloh, Frank E. "Maximum Theoretical Efficiency Limit of Photovoltaic Devices: Effect of Band Structure on Excited State Entropy." The journal of physical chemistry letters vol. 5,19 (2014): 3354-9. doi: https://doi.org/10.1021/jz501740n
Osterloh FE. Maximum Theoretical Efficiency Limit of Photovoltaic Devices: Effect of Band Structure on Excited State Entropy. J Phys Chem Lett. 2014 Oct 02;5(19):3354-9. doi: 10.1021/jz501740n. Epub 2014 Sep 17. PMID: 26278444.
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Boosting the Efficiency of Suspended Photocatalysts for Overall Water Splitting.

The journal of physical chemistry letters

Osterloh FE.
PMID: 26277937
J Phys Chem Lett. 2014 Aug 07;5(15):2510-1. doi: 10.1021/jz501342j.

No abstract available.

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Osterloh FE. Boosting the Efficiency of Suspended Photocatalysts for Overall Water Splitting. J Phys Chem Lett. 2014;5(15):2510-1doi: 10.1021/jz501342j.
Osterloh, F. E. (2014). Boosting the Efficiency of Suspended Photocatalysts for Overall Water Splitting. The journal of physical chemistry letters, 5(15), 2510-1. https://doi.org/10.1021/jz501342j
Osterloh, Frank E. "Boosting the Efficiency of Suspended Photocatalysts for Overall Water Splitting." The journal of physical chemistry letters vol. 5,15 (2014): 2510-1. doi: https://doi.org/10.1021/jz501342j
Osterloh FE. Boosting the Efficiency of Suspended Photocatalysts for Overall Water Splitting. J Phys Chem Lett. 2014 Aug 07;5(15):2510-1. doi: 10.1021/jz501342j. PMID: 26277937.
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Planar gold nanoparticle clusters as microscale mirrors.

Journal of the American Chemical Society

Kim JY, Osterloh FE.
PMID: 16551068
J Am Chem Soc. 2006 Mar 29;128(12):3868-9. doi: 10.1021/ja057958k.

Dispersible microscale mirror particles were synthesized by linkage of citrate-coated gold nanoparticles and 3-aminopropylsilyl-modified Ca2Nb3O10 perovskite nanoplates. The mirror particles reflect 14-19% of light in the 500-800 nm wavelength interval with retention of polarization. Due to their directional reflection...

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Kim JY, Osterloh FE. Planar gold nanoparticle clusters as microscale mirrors. J Am Chem Soc. 2006;128(12):3868-9doi: 10.1021/ja057958k.
Kim, J. Y., & Osterloh, F. E. (2006). Planar gold nanoparticle clusters as microscale mirrors. Journal of the American Chemical Society, 128(12), 3868-9. https://doi.org/10.1021/ja057958k
Kim, Jin Young, and Osterloh, Frank E. "Planar gold nanoparticle clusters as microscale mirrors." Journal of the American Chemical Society vol. 128,12 (2006): 3868-9. doi: https://doi.org/10.1021/ja057958k
Kim JY, Osterloh FE. Planar gold nanoparticle clusters as microscale mirrors. J Am Chem Soc. 2006 Mar 29;128(12):3868-9. doi: 10.1021/ja057958k. PMID: 16551068.
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Alkanethiol-induced structural rearrangements in silica-gold core-shell-type nanoparticle clusters: an opportunity for chemical sensor engineering.

Langmuir : the ACS journal of surfaces and colloids

Osterloh F, Hiramatsu H, Porter R, Guo T.
PMID: 15986699
Langmuir. 2004 Jun 22;20(13):5553-8. doi: 10.1021/la0348719.

Electrostatically bonded SiO2.Au nanoparticle clusters form by reaction of 3-aminopropylsilane-modified SiO2 spheres (470 nm) with citrate-coated gold nanoparticles (9.7 nm) in water. Reaction of the clusters with 0.01 M KBr or HCl solution induces desorption of the gold nanoparticles...

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Osterloh F, Hiramatsu H, Porter R, et al. Alkanethiol-induced structural rearrangements in silica-gold core-shell-type nanoparticle clusters: an opportunity for chemical sensor engineering. Langmuir. 2004;20(13):5553-8doi: 10.1021/la0348719.
Osterloh, F., Hiramatsu, H., Porter, R., & Guo, T. (2004). Alkanethiol-induced structural rearrangements in silica-gold core-shell-type nanoparticle clusters: an opportunity for chemical sensor engineering. Langmuir : the ACS journal of surfaces and colloids, 20(13), 5553-8. https://doi.org/10.1021/la0348719
Osterloh, Frank, et al. "Alkanethiol-induced structural rearrangements in silica-gold core-shell-type nanoparticle clusters: an opportunity for chemical sensor engineering." Langmuir : the ACS journal of surfaces and colloids vol. 20,13 (2004): 5553-8. doi: https://doi.org/10.1021/la0348719
Osterloh F, Hiramatsu H, Porter R, Guo T. Alkanethiol-induced structural rearrangements in silica-gold core-shell-type nanoparticle clusters: an opportunity for chemical sensor engineering. Langmuir. 2004 Jun 22;20(13):5553-8. doi: 10.1021/la0348719. PMID: 15986699.
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Fe3O4-LiMo3Se3 nanoparticle clusters as superparamagnetic nanocompasses.

Langmuir : the ACS journal of surfaces and colloids

Osterloh FE, Hiramatsu H, Dumas RK, Liu K.
PMID: 16207056
Langmuir. 2005 Oct 11;21(21):9709-13. doi: 10.1021/la051498r.

A scaleable chemical approach to functional nanoscale analogues of the magnetic compasses in magnetotactic bacteria is described. LiMo(3)Se(3)-Fe(3)O(4) nanowire-nanoparticle composites were synthesized by a reaction of 3-iodopropionic acid treated LiMo(3)Se(3) nanowire bundles with oleic acid-stabilized Fe(3)O(4) nanoparticles of 2.8,...

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Osterloh FE, Hiramatsu H, Dumas RK, et al. Fe3O4-LiMo3Se3 nanoparticle clusters as superparamagnetic nanocompasses. Langmuir. 2005;21(21):9709-13doi: 10.1021/la051498r.
Osterloh, F. E., Hiramatsu, H., Dumas, R. K., & Liu, K. (2005). Fe3O4-LiMo3Se3 nanoparticle clusters as superparamagnetic nanocompasses. Langmuir : the ACS journal of surfaces and colloids, 21(21), 9709-13. https://doi.org/10.1021/la051498r
Osterloh, Frank E, et al. "Fe3O4-LiMo3Se3 nanoparticle clusters as superparamagnetic nanocompasses." Langmuir : the ACS journal of surfaces and colloids vol. 21,21 (2005): 9709-13. doi: https://doi.org/10.1021/la051498r
Osterloh FE, Hiramatsu H, Dumas RK, Liu K. Fe3O4-LiMo3Se3 nanoparticle clusters as superparamagnetic nanocompasses. Langmuir. 2005 Oct 11;21(21):9709-13. doi: 10.1021/la051498r. PMID: 16207056.
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Photocatalytic water oxidation with nonsensitized IrO2 nanocrystals under visible and UV light.

Journal of the American Chemical Society

Frame FA, Townsend TK, Chamousis RL, Sabio EM, Dittrich T, Browning ND, Osterloh FE.
PMID: 21524069
J Am Chem Soc. 2011 May 18;133(19):7264-7. doi: 10.1021/ja200144w. Epub 2011 Apr 27.

Rutile IrO(2) is known as being among the best electrocatalysts for water oxidation. Here we report on the unexpected photocatalytic water oxidation activity of 1.98 nm ± 0.11 nm succinic acid-stabilized IrO(2) nanocrystals. From aqueous persulfate and silver nitrate...

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Frame FA, Townsend TK, Chamousis RL, et al. Photocatalytic water oxidation with nonsensitized IrO2 nanocrystals under visible and UV light. J Am Chem Soc. 2011;133(19):7264-7doi: 10.1021/ja200144w.
Frame, F. A., Townsend, T. K., Chamousis, R. L., Sabio, E. M., Dittrich, T., Browning, N. D., & Osterloh, F. E. (2011). Photocatalytic water oxidation with nonsensitized IrO2 nanocrystals under visible and UV light. Journal of the American Chemical Society, 133(19), 7264-7. https://doi.org/10.1021/ja200144w
Frame, F Andrew, et al. "Photocatalytic water oxidation with nonsensitized IrO2 nanocrystals under visible and UV light." Journal of the American Chemical Society vol. 133,19 (2011): 7264-7. doi: https://doi.org/10.1021/ja200144w
Frame FA, Townsend TK, Chamousis RL, Sabio EM, Dittrich T, Browning ND, Osterloh FE. Photocatalytic water oxidation with nonsensitized IrO2 nanocrystals under visible and UV light. J Am Chem Soc. 2011 May 18;133(19):7264-7. doi: 10.1021/ja200144w. Epub 2011 Apr 27. PMID: 21524069.
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Differences in DOM of rewetted and natural peatlands - Results from high-field FT-ICR-MS and bulk optical parameters.

The Science of the total environment

Herzsprung P, Osterloh K, von Tümpling W, Harir M, Hertkorn N, Schmitt-Kopplin P, Meissner R, Bernsdorf S, Friese K.
PMID: 28215801
Sci Total Environ. 2017 May 15;586:770-781. doi: 10.1016/j.scitotenv.2017.02.054. Epub 2017 Feb 16.

Peatlands can be a potential source of dissolved organic matter (DOM) in fresh water catchment areas. The quantity and quality of DOM can differ between pristine, degraded and rewetted peatlands. Due to the large scale and continuing losses of...

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Herzsprung P, Osterloh K, von Tümpling W, et al. Differences in DOM of rewetted and natural peatlands - Results from high-field FT-ICR-MS and bulk optical parameters. Sci Total Environ. 2017;586:770-781doi: 10.1016/j.scitotenv.2017.02.054.
Herzsprung, P., Osterloh, K., von Tümpling, W., Harir, M., Hertkorn, N., Schmitt-Kopplin, P., Meissner, R., Bernsdorf, S., & Friese, K. (2017). Differences in DOM of rewetted and natural peatlands - Results from high-field FT-ICR-MS and bulk optical parameters. The Science of the total environment, 586770-781. https://doi.org/10.1016/j.scitotenv.2017.02.054
Herzsprung, Peter, et al. "Differences in DOM of rewetted and natural peatlands - Results from high-field FT-ICR-MS and bulk optical parameters." The Science of the total environment vol. 586 (2017): 770-781. doi: https://doi.org/10.1016/j.scitotenv.2017.02.054
Herzsprung P, Osterloh K, von Tümpling W, Harir M, Hertkorn N, Schmitt-Kopplin P, Meissner R, Bernsdorf S, Friese K. Differences in DOM of rewetted and natural peatlands - Results from high-field FT-ICR-MS and bulk optical parameters. Sci Total Environ. 2017 May 15;586:770-781. doi: 10.1016/j.scitotenv.2017.02.054. Epub 2017 Feb 16. PMID: 28215801.
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Synthesis, Electrochemistry, and Reversible Interconversion among Perhalogenated Hydroxyphenyl Ni(II) Porphyrins, Porphodimethenes, and Porpho-5,15-bis-paraquinone Methide.

Inorganic chemistry

Cong L, Chahal MK, Osterloh R, Sankar M, Kadish KM.
PMID: 31633340
Inorg Chem. 2019 Nov 04;58(21):14361-14376. doi: 10.1021/acs.inorgchem.9b01642. Epub 2019 Oct 21.

Two octahalogenated nickel(II) hydroxyphenylporphyrins were synthesized and characterized as to their electrochemical and spectroscopic properties as well as their reactivity in neutral, acidic, and basic nonaqueous media. The newly synthesized complexes are represented as NiPorCl

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Cong L, Chahal MK, Osterloh R, et al. Synthesis, Electrochemistry, and Reversible Interconversion among Perhalogenated Hydroxyphenyl Ni(II) Porphyrins, Porphodimethenes, and Porpho-5,15-bis-paraquinone Methide. Inorg Chem. 2019;58(21):14361-14376doi: 10.1021/acs.inorgchem.9b01642.
Cong, L., Chahal, M. K., Osterloh, R., Sankar, M., & Kadish, K. M. (2019). Synthesis, Electrochemistry, and Reversible Interconversion among Perhalogenated Hydroxyphenyl Ni(II) Porphyrins, Porphodimethenes, and Porpho-5,15-bis-paraquinone Methide. Inorganic chemistry, 58(21), 14361-14376. https://doi.org/10.1021/acs.inorgchem.9b01642
Cong, Lei, et al. "Synthesis, Electrochemistry, and Reversible Interconversion among Perhalogenated Hydroxyphenyl Ni(II) Porphyrins, Porphodimethenes, and Porpho-5,15-bis-paraquinone Methide." Inorganic chemistry vol. 58,21 (2019): 14361-14376. doi: https://doi.org/10.1021/acs.inorgchem.9b01642
Cong L, Chahal MK, Osterloh R, Sankar M, Kadish KM. Synthesis, Electrochemistry, and Reversible Interconversion among Perhalogenated Hydroxyphenyl Ni(II) Porphyrins, Porphodimethenes, and Porpho-5,15-bis-paraquinone Methide. Inorg Chem. 2019 Nov 04;58(21):14361-14376. doi: 10.1021/acs.inorgchem.9b01642. Epub 2019 Oct 21. PMID: 31633340.
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Wavelength dependent photochemical charge transfer at the Cu.

Chemical communications (Cambridge, England)

Wu Z, Cheung G, Wang J, Zhao Z, Osterloh FE.
PMID: 30047953
Chem Commun (Camb). 2018 Aug 09;54(65):9023-9026. doi: 10.1039/c8cc04123g.

The understanding of the photochemical charge transfer properties of powdered semiconductors is of relevance to artificial photosynthesis and the production of solar fuels. Here we use surface photovoltage spectroscopy to probe photoelectrochemical charge transfer between bismuth vanadate (BiVO4) and...

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Wu Z, Cheung G, Wang J, et al. Wavelength dependent photochemical charge transfer at the Cu. Chem Commun (Camb). 2018;54(65):9023-9026doi: 10.1039/c8cc04123g.
Wu, Z., Cheung, G., Wang, J., Zhao, Z., & Osterloh, F. E. (2018). Wavelength dependent photochemical charge transfer at the Cu. Chemical communications (Cambridge, England), 54(65), 9023-9026. https://doi.org/10.1039/c8cc04123g
Wu, Zongkai, et al. "Wavelength dependent photochemical charge transfer at the Cu." Chemical communications (Cambridge, England) vol. 54,65 (2018): 9023-9026. doi: https://doi.org/10.1039/c8cc04123g
Wu Z, Cheung G, Wang J, Zhao Z, Osterloh FE. Wavelength dependent photochemical charge transfer at the Cu. Chem Commun (Camb). 2018 Aug 09;54(65):9023-9026. doi: 10.1039/c8cc04123g. PMID: 30047953.
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Focal random selection closes the gender gap in competitiveness.

Science advances

Berger J, Osterloh M, Rost K.
PMID: 33219019
Sci Adv. 2020 Nov 20;6(47). doi: 10.1126/sciadv.abb2142. Print 2020 Nov.

Gender differences in choosing to enter competitions are an important cause of the leaky pipeline for women in leadership roles and represent a considerable waste of human resources. We used an incentivized laboratory experiment to evaluate whether the introduction...

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Berger J, Osterloh M, Rost K. Focal random selection closes the gender gap in competitiveness. Sci Adv. 2020;6(47)doi: 10.1126/sciadv.abb2142.
Berger, J., Osterloh, M., & Rost, K. (2020). Focal random selection closes the gender gap in competitiveness. Science advances, 6(47), . https://doi.org/10.1126/sciadv.abb2142
Berger, Joël, et al. "Focal random selection closes the gender gap in competitiveness." Science advances vol. 6,47 (2020). doi: https://doi.org/10.1126/sciadv.abb2142
Berger J, Osterloh M, Rost K. Focal random selection closes the gender gap in competitiveness. Sci Adv. 2020 Nov 20;6(47). doi: 10.1126/sciadv.abb2142. Print 2020 Nov. PMID: 33219019; PMCID: PMC7679159.
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Old Dog, New Tricks: Innocent, Five-coordinate Cyanocobalt Corroles.

Inorganic chemistry

Osterloh WR, Desbois N, Quesneau V, Brandès S, Fleurat-Lessard P, Fang Y, Blondeau-Patissier V, Paolesse R, Gros CP, Kadish KM.
PMID: 32452674
Inorg Chem. 2020 Jun 15;59(12):8562-8579. doi: 10.1021/acs.inorgchem.0c01037. Epub 2020 May 26.

Three mono-CN ligated anionic cobalt A

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Osterloh WR, Desbois N, Quesneau V, et al. Old Dog, New Tricks: Innocent, Five-coordinate Cyanocobalt Corroles. Inorg Chem. 2020;59(12):8562-8579doi: 10.1021/acs.inorgchem.0c01037.
Osterloh, W. R., Desbois, N., Quesneau, V., Brandès, S., Fleurat-Lessard, P., Fang, Y., Blondeau-Patissier, V., Paolesse, R., Gros, C. P., & Kadish, K. M. (2020). Old Dog, New Tricks: Innocent, Five-coordinate Cyanocobalt Corroles. Inorganic chemistry, 59(12), 8562-8579. https://doi.org/10.1021/acs.inorgchem.0c01037
Osterloh, W Ryan, et al. "Old Dog, New Tricks: Innocent, Five-coordinate Cyanocobalt Corroles." Inorganic chemistry vol. 59,12 (2020): 8562-8579. doi: https://doi.org/10.1021/acs.inorgchem.0c01037
Osterloh WR, Desbois N, Quesneau V, Brandès S, Fleurat-Lessard P, Fang Y, Blondeau-Patissier V, Paolesse R, Gros CP, Kadish KM. Old Dog, New Tricks: Innocent, Five-coordinate Cyanocobalt Corroles. Inorg Chem. 2020 Jun 15;59(12):8562-8579. doi: 10.1021/acs.inorgchem.0c01037. Epub 2020 May 26. PMID: 32452674.
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Nickel(II) monobenzoporphyrins and chlorins: synthesis, electrochemistry and anion sensing properties.

Dalton transactions (Cambridge, England : 2003)

Kumar S, Chaudhri N, Osterloh WR, Kadish KM, Sankar M.
PMID: 34779452
Dalton Trans. 2021 Nov 30;50(46):17086-17100. doi: 10.1039/d1dt03122h.

A series of nickel(II) monobenzochlorins (MBCs) and monobenzoporphyrins (MBPs) containing

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Kumar S, Chaudhri N, Osterloh WR, et al. Nickel(II) monobenzoporphyrins and chlorins: synthesis, electrochemistry and anion sensing properties. Dalton Trans. 2021;50(46):17086-17100doi: 10.1039/d1dt03122h.
Kumar, S., Chaudhri, N., Osterloh, W. R., Kadish, K. M., & Sankar, M. (2021). Nickel(II) monobenzoporphyrins and chlorins: synthesis, electrochemistry and anion sensing properties. Dalton transactions (Cambridge, England : 2003), 50(46), 17086-17100. https://doi.org/10.1039/d1dt03122h
Kumar, Sandeep, et al. "Nickel(II) monobenzoporphyrins and chlorins: synthesis, electrochemistry and anion sensing properties." Dalton transactions (Cambridge, England : 2003) vol. 50,46 (2021): 17086-17100. doi: https://doi.org/10.1039/d1dt03122h
Kumar S, Chaudhri N, Osterloh WR, Kadish KM, Sankar M. Nickel(II) monobenzoporphyrins and chlorins: synthesis, electrochemistry and anion sensing properties. Dalton Trans. 2021 Nov 30;50(46):17086-17100. doi: 10.1039/d1dt03122h. PMID: 34779452.
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Showing 1 to 12 of 74 entries