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Designing new catalysts for synthetic fuels: general discussion.

Faraday discussions

Holt K, Jewell L, Niemantsverdriet H, Macheli L, Shozi M, Hutchings G, Wezendonk T, Bowker M, Catlow R, Adam S, Kooyman PJ, Hensen E, Hayward J, Coville N, Weststrate KJ, Fischer N, Roldan A, Redekop E, van Steen E, Friedrich H, Kuo DH, Bandaru H, Deeplal L, Zivkovic A, Naiker K, Tucker C, Mkhwanazi TPO, Bahnemann D, Neurock M, Petersen A, Forbes RP, Phaahlamohlaka T, Schulz H, Lennon D, Olsbye U, Wolf M, Kondrat S, Collier P, Sun X, Zheng Y, Corma A, Iglesia E, Nyathi T, Ma D, Bremmer M, Claeys M, Kapteijn F.
PMID: 28422221
Faraday Discuss. 2017 Apr 28;197:353-388. doi: 10.1039/c7fd90011b.

No abstract available.

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Holt K, Jewell L, Niemantsverdriet H, et al. Designing new catalysts for synthetic fuels: general discussion. Faraday Discuss. 2017;197:353-388doi: 10.1039/c7fd90011b.
Holt, K., Jewell, L., Niemantsverdriet, H., Macheli, L., Shozi, M., Hutchings, G., Wezendonk, T., Bowker, M., Catlow, R., Adam, S., Kooyman, P. J., Hensen, E., Hayward, J., Coville, N., Weststrate, K. J., Fischer, N., Roldan, A., Redekop, E., van Steen, E., Friedrich, H., Kuo, D. H., Bandaru, H., Deeplal, L., Zivkovic, A., Naiker, K., Tucker, C., Mkhwanazi, T. P. O., Bahnemann, D., Neurock, M., Petersen, A., Forbes, R. P., Phaahlamohlaka, T., Schulz, H., Lennon, D., Olsbye, U., Wolf, M., Kondrat, S., Collier, P., Sun, X., Zheng, Y., Corma, A., Iglesia, E., Nyathi, T., Ma, D., Bremmer, M., Claeys, M., & Kapteijn, F. (2017). Designing new catalysts for synthetic fuels: general discussion. Faraday discussions, 197353-388. https://doi.org/10.1039/c7fd90011b
Holt, Katherine, et al. "Designing new catalysts for synthetic fuels: general discussion." Faraday discussions vol. 197 (2017): 353-388. doi: https://doi.org/10.1039/c7fd90011b
Holt K, Jewell L, Niemantsverdriet H, Macheli L, Shozi M, Hutchings G, Wezendonk T, Bowker M, Catlow R, Adam S, Kooyman PJ, Hensen E, Hayward J, Coville N, Weststrate KJ, Fischer N, Roldan A, Redekop E, van Steen E, Friedrich H, Kuo DH, Bandaru H, Deeplal L, Zivkovic A, Naiker K, Tucker C, Mkhwanazi TPO, Bahnemann D, Neurock M, Petersen A, Forbes RP, Phaahlamohlaka T, Schulz H, Lennon D, Olsbye U, Wolf M, Kondrat S, Collier P, Sun X, Zheng Y, Corma A, Iglesia E, Nyathi T, Ma D, Bremmer M, Claeys M, Kapteijn F. Designing new catalysts for synthetic fuels: general discussion. Faraday Discuss. 2017 Apr 28;197:353-388. doi: 10.1039/c7fd90011b. PMID: 28422221.
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A comparison of cardiovascular risk factors for ten antipsychotic drugs in clinical practice.

Neuropsychiatric disease and treatment

Bodén R, Edman G, Reutfors J, Ostenson CG, Osby U.
PMID: 23682213
Neuropsychiatr Dis Treat. 2013;9:371-7. doi: 10.2147/NDT.S40554. Epub 2013 Mar 19.

It is well known that abdominal obesity, dyslipidemia, and insulin resistance are highly prevalent in patients receiving maintenance treatment with antipsychotics, but there is limited knowledge about the association between cardiovascular risk factors and treatment with antipsychotic drugs. In...

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Bodén R, Edman G, Reutfors J, et al. A comparison of cardiovascular risk factors for ten antipsychotic drugs in clinical practice. Neuropsychiatr Dis Treat. 2013;9:371-7doi: 10.2147/NDT.S40554.
Bodén, R., Edman, G., Reutfors, J., Ostenson, C. G., & Osby, U. (2013). A comparison of cardiovascular risk factors for ten antipsychotic drugs in clinical practice. Neuropsychiatric disease and treatment, 9371-7. https://doi.org/10.2147/NDT.S40554
Bodén, Robert, et al. "A comparison of cardiovascular risk factors for ten antipsychotic drugs in clinical practice." Neuropsychiatric disease and treatment vol. 9 (2013): 371-7. doi: https://doi.org/10.2147/NDT.S40554
Bodén R, Edman G, Reutfors J, Ostenson CG, Osby U. A comparison of cardiovascular risk factors for ten antipsychotic drugs in clinical practice. Neuropsychiatr Dis Treat. 2013;9:371-7. doi: 10.2147/NDT.S40554. Epub 2013 Mar 19. PMID: 23682213; PMCID: PMC3653763.
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CO2 sorption on MgO and CaO surfaces: a comparative quantum chemical cluster study.

The journal of physical chemistry. B

Jensen MB, Pettersson LG, Swang O, Olsbye U.
PMID: 16853136
J Phys Chem B. 2005 Sep 08;109(35):16774-81. doi: 10.1021/jp052037h.

A comparative quantum chemical study of CO2 adsorption on MgO and CaO has been carried out. Theoretical infrared (IR) frequencies are calculated and compared with IR experiments from the literature. The results show that CO2 adsorbs as monodentate on...

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Jensen MB, Pettersson LG, Swang O, et al. CO2 sorption on MgO and CaO surfaces: a comparative quantum chemical cluster study. J Phys Chem B. 2005;109(35):16774-81doi: 10.1021/jp052037h.
Jensen, M. B., Pettersson, L. G., Swang, O., & Olsbye, U. (2005). CO2 sorption on MgO and CaO surfaces: a comparative quantum chemical cluster study. The journal of physical chemistry. B, 109(35), 16774-81. https://doi.org/10.1021/jp052037h
Jensen, Morten B, et al. "CO2 sorption on MgO and CaO surfaces: a comparative quantum chemical cluster study." The journal of physical chemistry. B vol. 109,35 (2005): 16774-81. doi: https://doi.org/10.1021/jp052037h
Jensen MB, Pettersson LG, Swang O, Olsbye U. CO2 sorption on MgO and CaO surfaces: a comparative quantum chemical cluster study. J Phys Chem B. 2005 Sep 08;109(35):16774-81. doi: 10.1021/jp052037h. PMID: 16853136.
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Coke formation during the methanol-to-olefin conversion: in situ microspectroscopy on individual H-ZSM-5 crystals with different Brønsted acidity.

Chemistry (Weinheim an der Bergstrasse, Germany)

Mores D, Kornatowski J, Olsbye U, Weckhuysen BM.
PMID: 21305622
Chemistry. 2011 Mar 01;17(10):2874-84. doi: 10.1002/chem.201002624. Epub 2011 Feb 08.

Coke formation during the methanol-to-olefin (MTO) conversion has been studied at the single-particle level with in situ UV/Vis and confocal fluorescence microscopy. For this purpose, large H-ZSM-5 crystals differing in their Si/Al molar ratio have been investigated. During MTO,...

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Mores D, Kornatowski J, Olsbye U, et al. Coke formation during the methanol-to-olefin conversion: in situ microspectroscopy on individual H-ZSM-5 crystals with different Brønsted acidity. Chemistry. 2011;17(10):2874-84doi: 10.1002/chem.201002624.
Mores, D., Kornatowski, J., Olsbye, U., & Weckhuysen, B. M. (2011). Coke formation during the methanol-to-olefin conversion: in situ microspectroscopy on individual H-ZSM-5 crystals with different Brønsted acidity. Chemistry (Weinheim an der Bergstrasse, Germany), 17(10), 2874-84. https://doi.org/10.1002/chem.201002624
Mores, Davide, et al. "Coke formation during the methanol-to-olefin conversion: in situ microspectroscopy on individual H-ZSM-5 crystals with different Brønsted acidity." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 17,10 (2011): 2874-84. doi: https://doi.org/10.1002/chem.201002624
Mores D, Kornatowski J, Olsbye U, Weckhuysen BM. Coke formation during the methanol-to-olefin conversion: in situ microspectroscopy on individual H-ZSM-5 crystals with different Brønsted acidity. Chemistry. 2011 Mar 01;17(10):2874-84. doi: 10.1002/chem.201002624. Epub 2011 Feb 08. PMID: 21305622.
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Ti-STT: a new zeotype shape selective oxidation catalyst.

Chemical communications (Cambridge, England)

Eilertsen EA, Giordanino F, Lamberti C, Bordiga S, Damin A, Bonino F, Olsbye U, Lillerud KP.
PMID: 21975652
Chem Commun (Camb). 2011 Nov 21;47(43):11867-9. doi: 10.1039/c1cc15175d. Epub 2011 Oct 05.

A new zeotype titanium silicate oxidation catalyst with the STT topology has been synthesized from direct synthesis. Ti-STT has a microporous structure with small pore openings, allowing shape selective oxidation catalysis. The isomorphous substitution of Si by Ti in...

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Eilertsen EA, Giordanino F, Lamberti C, et al. Ti-STT: a new zeotype shape selective oxidation catalyst. Chem Commun (Camb). 2011;47(43):11867-9doi: 10.1039/c1cc15175d.
Eilertsen, E. A., Giordanino, F., Lamberti, C., Bordiga, S., Damin, A., Bonino, F., Olsbye, U., & Lillerud, K. P. (2011). Ti-STT: a new zeotype shape selective oxidation catalyst. Chemical communications (Cambridge, England), 47(43), 11867-9. https://doi.org/10.1039/c1cc15175d
Eilertsen, Einar André, et al. "Ti-STT: a new zeotype shape selective oxidation catalyst." Chemical communications (Cambridge, England) vol. 47,43 (2011): 11867-9. doi: https://doi.org/10.1039/c1cc15175d
Eilertsen EA, Giordanino F, Lamberti C, Bordiga S, Damin A, Bonino F, Olsbye U, Lillerud KP. Ti-STT: a new zeotype shape selective oxidation catalyst. Chem Commun (Camb). 2011 Nov 21;47(43):11867-9. doi: 10.1039/c1cc15175d. Epub 2011 Oct 05. PMID: 21975652.
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A new zirconium inorganic building brick forming metal organic frameworks with exceptional stability.

Journal of the American Chemical Society

Cavka JH, Jakobsen S, Olsbye U, Guillou N, Lamberti C, Bordiga S, Lillerud KP.
PMID: 18817383
J Am Chem Soc. 2008 Oct 22;130(42):13850-1. doi: 10.1021/ja8057953. Epub 2008 Sep 26.

Porous crystals are strategic materials with industrial applications within petrochemistry, catalysis, gas storage, and selective separation. Their unique properties are based on the molecular-scale porous character. However, a principal limitation of zeolites and similar oxide-based materials is the relatively...

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Cavka JH, Jakobsen S, Olsbye U, et al. A new zirconium inorganic building brick forming metal organic frameworks with exceptional stability. J Am Chem Soc. 2008;130(42):13850-1doi: 10.1021/ja8057953.
Cavka, J. H., Jakobsen, S., Olsbye, U., Guillou, N., Lamberti, C., Bordiga, S., & Lillerud, K. P. (2008). A new zirconium inorganic building brick forming metal organic frameworks with exceptional stability. Journal of the American Chemical Society, 130(42), 13850-1. https://doi.org/10.1021/ja8057953
Cavka, Jasmina Hafizovic, et al. "A new zirconium inorganic building brick forming metal organic frameworks with exceptional stability." Journal of the American Chemical Society vol. 130,42 (2008): 13850-1. doi: https://doi.org/10.1021/ja8057953
Cavka JH, Jakobsen S, Olsbye U, Guillou N, Lamberti C, Bordiga S, Lillerud KP. A new zirconium inorganic building brick forming metal organic frameworks with exceptional stability. J Am Chem Soc. 2008 Oct 22;130(42):13850-1. doi: 10.1021/ja8057953. Epub 2008 Sep 26. PMID: 18817383.
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Large zeolite H-ZSM-5 crystals as models for the methanol-to-hydrocarbons process: bridging the gap between single-particle examination and bulk catalyst analysis.

Chemistry (Weinheim an der Bergstrasse, Germany)

Hofmann JP, Mores D, Aramburo LR, Teketel S, Rohnke M, Janek J, Olsbye U, Weckhuysen BM.
PMID: 23649944
Chemistry. 2013 Jun 24;19(26):8533-42. doi: 10.1002/chem.201203351. Epub 2013 May 06.

The catalytic, deactivation, and regeneration characteristics of large coffin-shaped H-ZSM-5 crystals were investigated during the methanol-to-hydrocarbons (MTH) reaction at 350 and 500 °C. Online gas-phase effluent analysis and examination of retained material thereof were used to explore the bulk...

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Hofmann JP, Mores D, Aramburo LR, et al. Large zeolite H-ZSM-5 crystals as models for the methanol-to-hydrocarbons process: bridging the gap between single-particle examination and bulk catalyst analysis. Chemistry. 2013;19(26):8533-42doi: 10.1002/chem.201203351.
Hofmann, J. P., Mores, D., Aramburo, L. R., Teketel, S., Rohnke, M., Janek, J., Olsbye, U., & Weckhuysen, B. M. (2013). Large zeolite H-ZSM-5 crystals as models for the methanol-to-hydrocarbons process: bridging the gap between single-particle examination and bulk catalyst analysis. Chemistry (Weinheim an der Bergstrasse, Germany), 19(26), 8533-42. https://doi.org/10.1002/chem.201203351
Hofmann, Jan P, et al. "Large zeolite H-ZSM-5 crystals as models for the methanol-to-hydrocarbons process: bridging the gap between single-particle examination and bulk catalyst analysis." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 19,26 (2013): 8533-42. doi: https://doi.org/10.1002/chem.201203351
Hofmann JP, Mores D, Aramburo LR, Teketel S, Rohnke M, Janek J, Olsbye U, Weckhuysen BM. Large zeolite H-ZSM-5 crystals as models for the methanol-to-hydrocarbons process: bridging the gap between single-particle examination and bulk catalyst analysis. Chemistry. 2013 Jun 24;19(26):8533-42. doi: 10.1002/chem.201203351. Epub 2013 May 06. PMID: 23649944.
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The Nuclearity of the Active Site for Methane to Methanol Conversion in Cu-Mordenite: A Quantitative Assessment.

Journal of the American Chemical Society

Pappas DK, Martini A, Dyballa M, Kvande K, Teketel S, Lomachenko KA, Baran R, Glatzel P, Arstad B, Berlier G, Lamberti C, Bordiga S, Olsbye U, Svelle S, Beato P, Borfecchia E.
PMID: 30346154
J Am Chem Soc. 2018 Nov 14;140(45):15270-15278. doi: 10.1021/jacs.8b08071. Epub 2018 Nov 02.

The direct conversion of methane to methanol (MTM) is a reaction that has the potential to disrupt a great part of the synthesis gas-derived chemical industry. However, despite many decades of research, active enough catalysts and suitable processes for...

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Pappas DK, Martini A, Dyballa M, et al. The Nuclearity of the Active Site for Methane to Methanol Conversion in Cu-Mordenite: A Quantitative Assessment. J Am Chem Soc. 2018;140(45):15270-15278doi: 10.1021/jacs.8b08071.
Pappas, D. K., Martini, A., Dyballa, M., Kvande, K., Teketel, S., Lomachenko, K. A., Baran, R., Glatzel, P., Arstad, B., Berlier, G., Lamberti, C., Bordiga, S., Olsbye, U., Svelle, S., Beato, P., & Borfecchia, E. (2018). The Nuclearity of the Active Site for Methane to Methanol Conversion in Cu-Mordenite: A Quantitative Assessment. Journal of the American Chemical Society, 140(45), 15270-15278. https://doi.org/10.1021/jacs.8b08071
Pappas, Dimitrios K, et al. "The Nuclearity of the Active Site for Methane to Methanol Conversion in Cu-Mordenite: A Quantitative Assessment." Journal of the American Chemical Society vol. 140,45 (2018): 15270-15278. doi: https://doi.org/10.1021/jacs.8b08071
Pappas DK, Martini A, Dyballa M, Kvande K, Teketel S, Lomachenko KA, Baran R, Glatzel P, Arstad B, Berlier G, Lamberti C, Bordiga S, Olsbye U, Svelle S, Beato P, Borfecchia E. The Nuclearity of the Active Site for Methane to Methanol Conversion in Cu-Mordenite: A Quantitative Assessment. J Am Chem Soc. 2018 Nov 14;140(45):15270-15278. doi: 10.1021/jacs.8b08071. Epub 2018 Nov 02. PMID: 30346154.
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Deactivation of Zeolite Catalyst H-ZSM-5 during Conversion of Methanol to Gasoline: Operando Time- and Space-Resolved X-ray Diffraction.

The journal of physical chemistry letters

Rojo-Gama D, Mentel L, Kalantzopoulos GN, Pappas DK, Dovgaliuk I, Olsbye U, Lillerud KP, Beato P, Lundegaard LF, Wragg DS, Svelle S.
PMID: 29494162
J Phys Chem Lett. 2018 Mar 15;9(6):1324-1328. doi: 10.1021/acs.jpclett.8b00094. Epub 2018 Mar 05.

The deactivation of zeolite catalyst H-ZSM-5 by coking during the conversion of methanol to hydrocarbons was monitored by high-energy space- and time-resolved operando X-ray diffraction (XRD) . Space resolution was achieved by continuous scanning along the axial length of...

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Rojo-Gama D, Mentel L, Kalantzopoulos GN, et al. Deactivation of Zeolite Catalyst H-ZSM-5 during Conversion of Methanol to Gasoline: Operando Time- and Space-Resolved X-ray Diffraction. J Phys Chem Lett. 2018;9(6):1324-1328doi: 10.1021/acs.jpclett.8b00094.
Rojo-Gama, D., Mentel, L., Kalantzopoulos, G. N., Pappas, D. K., Dovgaliuk, I., Olsbye, U., Lillerud, K. P., Beato, P., Lundegaard, L. F., Wragg, D. S., & Svelle, S. (2018). Deactivation of Zeolite Catalyst H-ZSM-5 during Conversion of Methanol to Gasoline: Operando Time- and Space-Resolved X-ray Diffraction. The journal of physical chemistry letters, 9(6), 1324-1328. https://doi.org/10.1021/acs.jpclett.8b00094
Rojo-Gama, Daniel, et al. "Deactivation of Zeolite Catalyst H-ZSM-5 during Conversion of Methanol to Gasoline: Operando Time- and Space-Resolved X-ray Diffraction." The journal of physical chemistry letters vol. 9,6 (2018): 1324-1328. doi: https://doi.org/10.1021/acs.jpclett.8b00094
Rojo-Gama D, Mentel L, Kalantzopoulos GN, Pappas DK, Dovgaliuk I, Olsbye U, Lillerud KP, Beato P, Lundegaard LF, Wragg DS, Svelle S. Deactivation of Zeolite Catalyst H-ZSM-5 during Conversion of Methanol to Gasoline: Operando Time- and Space-Resolved X-ray Diffraction. J Phys Chem Lett. 2018 Mar 15;9(6):1324-1328. doi: 10.1021/acs.jpclett.8b00094. Epub 2018 Mar 05. PMID: 29494162.
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Conversion of methanol to hydrocarbons over zeolite ZSM-23 (MTT): exceptional effects of particle size on catalyst lifetime.

Chemical communications (Cambridge, England)

Molino A, Łukaszuk KA, Rojo-Gama D, Lillerud KP, Olsbye U, Bordiga S, Svelle S, Beato P.
PMID: 28555237
Chem Commun (Camb). 2017 Jun 22;53(51):6816-6819. doi: 10.1039/c6cc10118f.

A variety of synthetic procedures have been used to obtain zeolite ZSM-23 (MTT) catalysts with crystallite sizes ranging from the micrometer to nanometer scale. When the acidic zeolite is used as a catalyst for the methanol to hydrocarbon (MTH)...

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Molino A, Łukaszuk KA, Rojo-Gama D, et al. Conversion of methanol to hydrocarbons over zeolite ZSM-23 (MTT): exceptional effects of particle size on catalyst lifetime. Chem Commun (Camb). 2017;53(51):6816-6819doi: 10.1039/c6cc10118f.
Molino, A., Łukaszuk, K. A., Rojo-Gama, D., Lillerud, K. P., Olsbye, U., Bordiga, S., Svelle, S., & Beato, P. (2017). Conversion of methanol to hydrocarbons over zeolite ZSM-23 (MTT): exceptional effects of particle size on catalyst lifetime. Chemical communications (Cambridge, England), 53(51), 6816-6819. https://doi.org/10.1039/c6cc10118f
Molino, A, et al. "Conversion of methanol to hydrocarbons over zeolite ZSM-23 (MTT): exceptional effects of particle size on catalyst lifetime." Chemical communications (Cambridge, England) vol. 53,51 (2017): 6816-6819. doi: https://doi.org/10.1039/c6cc10118f
Molino A, Łukaszuk KA, Rojo-Gama D, Lillerud KP, Olsbye U, Bordiga S, Svelle S, Beato P. Conversion of methanol to hydrocarbons over zeolite ZSM-23 (MTT): exceptional effects of particle size on catalyst lifetime. Chem Commun (Camb). 2017 Jun 22;53(51):6816-6819. doi: 10.1039/c6cc10118f. PMID: 28555237.
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Formation and Functioning of Bimetallic Nanocatalysts: The Power of X-ray Probes.

Angewandte Chemie (International ed. in English)

Filez M, Redekop EA, Dendooven J, Ramachandran RK, Solano E, Olsbye U, Weckhuysen BM, Galvita VV, Poelman H, Detavernier C, Marin GB.
PMID: 30934165
Angew Chem Int Ed Engl. 2019 Sep 16;58(38):13220-13230. doi: 10.1002/anie.201902859. Epub 2019 Jul 24.

Bimetallic nanocatalysts are key enablers of current chemical technologies, including car exhaust converters and fuel cells, and play a crucial role in industry to promote a wide range of chemical reactions. However, owing to significant characterization challenges, insights in...

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Filez M, Redekop EA, Dendooven J, et al. Formation and Functioning of Bimetallic Nanocatalysts: The Power of X-ray Probes. Angew Chem Int Ed Engl. 2019;58(38):13220-13230doi: 10.1002/anie.201902859.
Filez, M., Redekop, E. A., Dendooven, J., Ramachandran, R. K., Solano, E., Olsbye, U., Weckhuysen, B. M., Galvita, V. V., Poelman, H., Detavernier, C., & Marin, G. B. (2019). Formation and Functioning of Bimetallic Nanocatalysts: The Power of X-ray Probes. Angewandte Chemie (International ed. in English), 58(38), 13220-13230. https://doi.org/10.1002/anie.201902859
Filez, Matthias, et al. "Formation and Functioning of Bimetallic Nanocatalysts: The Power of X-ray Probes." Angewandte Chemie (International ed. in English) vol. 58,38 (2019): 13220-13230. doi: https://doi.org/10.1002/anie.201902859
Filez M, Redekop EA, Dendooven J, Ramachandran RK, Solano E, Olsbye U, Weckhuysen BM, Galvita VV, Poelman H, Detavernier C, Marin GB. Formation and Functioning of Bimetallic Nanocatalysts: The Power of X-ray Probes. Angew Chem Int Ed Engl. 2019 Sep 16;58(38):13220-13230. doi: 10.1002/anie.201902859. Epub 2019 Jul 24. PMID: 30934165; PMCID: PMC6771619.
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Synchronizing gas injections and time-resolved data acquisition for perturbation-enhanced APXPS experiments.

The Review of scientific instruments

Redekop EA, Johansson N, Kokkonen E, Urpelainen S, Lopes da Silva F, Kaipio M, Nieminen HE, Rehman F, Miikkulainen V, Ritala M, Olsbye U.
PMID: 34243480
Rev Sci Instrum. 2021 Apr 01;92(4):044101. doi: 10.1063/5.0039957.

An experimental approach is described in which well-defined perturbations of the gas feed into an Ambient Pressure X-ray Photoelectron Spectroscopy (APXPS) cell are fully synchronized with the time-resolved x-ray photoelectron spectroscopy data acquisition. These experiments unlock new possibilities for...

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Redekop EA, Johansson N, Kokkonen E, et al. Synchronizing gas injections and time-resolved data acquisition for perturbation-enhanced APXPS experiments. Rev Sci Instrum. 2021;92(4):044101doi: 10.1063/5.0039957.
Redekop, E. A., Johansson, N., Kokkonen, E., Urpelainen, S., Lopes da Silva, F., Kaipio, M., Nieminen, H. E., Rehman, F., Miikkulainen, V., Ritala, M., & Olsbye, U. (2021). Synchronizing gas injections and time-resolved data acquisition for perturbation-enhanced APXPS experiments. The Review of scientific instruments, 92(4), 044101. https://doi.org/10.1063/5.0039957
Redekop, Evgeniy A, et al. "Synchronizing gas injections and time-resolved data acquisition for perturbation-enhanced APXPS experiments." The Review of scientific instruments vol. 92,4 (2021): 044101. doi: https://doi.org/10.1063/5.0039957
Redekop EA, Johansson N, Kokkonen E, Urpelainen S, Lopes da Silva F, Kaipio M, Nieminen HE, Rehman F, Miikkulainen V, Ritala M, Olsbye U. Synchronizing gas injections and time-resolved data acquisition for perturbation-enhanced APXPS experiments. Rev Sci Instrum. 2021 Apr 01;92(4):044101. doi: 10.1063/5.0039957. PMID: 34243480.
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Showing 1 to 12 of 46 entries