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Kumar, P., You, S. & Vomiero, A. (2023). Recent Progress in Materials and Device Design for Semitransparent Photovoltaic Technologies. Advanced Energy Materials, 13(39), Article ID 2301555.
Open this publication in new window or tab >>Recent Progress in Materials and Device Design for Semitransparent Photovoltaic Technologies
2023 (English)In: Advanced Energy Materials, ISSN 1614-6832, E-ISSN 1614-6840, Vol. 13, no 39, article id 2301555Article, review/survey (Refereed) Published
Abstract [en]

Semitransparent photovoltaic (STPV) solar cells offer an immense opportunity to expand the scope of photovoltaics to special applications such as windows, facades, skylights, and so on. These new opportunities have encouraged researchers to develop STPVs using traditional thin-film solar cell technologies (amorphous-Si, CdTe, and CIGS or emerging solar cells (organic, perovskites, and dye-sensitized). There are considerable improvements in both power conversion efficiency (PCE) and semitransparency of these STPV devices. This review studies the device structure of state-of-the-art STPV devices and thereby analyzes the different approaches toward maximizing the product of PCE and average visible transmittance. The origins of PCE losses during the opaque-to-semitransparent transition in the different STPV technologies are discussed. In addition, critical practical aspects relevant to all STPV devices, such as compatibility of the top transparent electrode with the device structure, buffer layer optimization, light management engineering, scale-up, and stability, are also reported. This overview is expected to facilitate researchers across different technologies to identify and overcome the challenges toward achieving higher light utilization efficiencies in STPVs.

Place, publisher, year, edition, pages
John Wiley & Sons, 2023
Keywords
building integrated photovoltaics, semitransparent solar cells, transparent conductive electrodes, visible light transmittance
National Category
Materials Chemistry
Research subject
Experimental Physics
Identifiers
urn:nbn:se:ltu:diva-101570 (URN)10.1002/aenm.202301555 (DOI)2-s2.0-85169672434 (Scopus ID)
Funder
Knut and Alice Wallenberg FoundationThe Kempe Foundations
Note

Validerad;2023;Nivå 2;2023-11-09 (hanlid);

Full text license: CC BY

Available from: 2023-10-16 Created: 2023-10-16 Last updated: 2023-11-09Bibliographically approved
Taranova, A., Akbar, K., Yusupov, K., You, S., Polewczyk, V., Mauri, S., . . . Vomiero, A. (2023). Unraveling the optoelectronic properties of CoSbx intrinsic selective solar absorber towards high-temperature surfaces. Nature Communications, 14(1), Article ID 7280.
Open this publication in new window or tab >>Unraveling the optoelectronic properties of CoSbx intrinsic selective solar absorber towards high-temperature surfaces
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2023 (English)In: Nature Communications, E-ISSN 2041-1723, Vol. 14, no 1, article id 7280Article in journal (Refereed) Published
Abstract [en]

The combination of the ability to absorb most of the solar radiation and simultaneously suppress infrared re-radiation allows selective solar absorbers (SSAs) to maximize solar energy to heat conversion, which is critical to several advanced applications. The intrinsic spectral selective materials are rare in nature and only a few demonstrated complete solar absorption. Typically, intrinsic materials exhibit high performances when integrated into complex multilayered solar absorber systems due to their limited spectral selectivity and solar absorption. In this study, we propose CoSbx (2 < x < 3) as a new exceptionally efficient SSA. Here we demonstrate that the low bandgap nature of CoSbx endows broadband solar absorption (0.96) over the solar spectral range and simultaneous low emissivity (0.18) in the mid-infrared region, resulting in a remarkable intrinsic spectral solar selectivity of 5.3. Under 1 sun illumination, the heat concentrates on the surface of the CoSbx thin film, and an impressive temperature of 101.7 °C is reached, demonstrating the highest value among reported intrinsic SSAs. Furthermore, the CoSbx was tested for solar water evaporation achieving an evaporation rate of 1.4 kg m−2 h−1. This study could expand the use of narrow bandgap semiconductors as efficient intrinsic SSAs with high surface temperatures in solar applications.

Place, publisher, year, edition, pages
Springer Nature, 2023
National Category
Energy Engineering Atom and Molecular Physics and Optics
Research subject
Experimental Physics
Identifiers
urn:nbn:se:ltu:diva-102498 (URN)10.1038/s41467-023-42839-6 (DOI)
Funder
The Kempe FoundationsKnut and Alice Wallenberg FoundationLuleå University of TechnologyEuropean Commission, No 881603, No 861857
Note

Validerad;2023;Nivå 2;2023-11-17 (joosat);

Funder: European Union - NextGenerationEU; Göran Gustafsson foundation;

CC BY 4.0 License

Available from: 2023-11-17 Created: 2023-11-17 Last updated: 2023-11-17Bibliographically approved
Kumar, P., You, S. & Vomiero, A. (2022). CuSCN as a hole transport layer in an inorganic solution-processed planar Sb2S3 solar cell, enabling carbon-based and semitransparent photovoltaics. Journal of Materials Chemistry C, 10(43), 16273-16282
Open this publication in new window or tab >>CuSCN as a hole transport layer in an inorganic solution-processed planar Sb2S3 solar cell, enabling carbon-based and semitransparent photovoltaics
2022 (English)In: Journal of Materials Chemistry C, ISSN 2050-7526, E-ISSN 2050-7534, Vol. 10, no 43, p. 16273-16282Article in journal (Refereed) Published
Abstract [en]

Sb2S3 is an emerging inorganic photovoltaic absorber material with attractive properties such as high absorption coefficient, stability, earth-abundance, non-toxicity, and low-temperature solution processability. Furthermore, with a bandgap of ca. 1.7 eV, it can also be used in semitransparent or tandem solar cell applications. Here, an inorganic wide-bandgap hole transport layer (HTL), copper thiocyanate (CuSCN), is used in an Sb2S3 solar cell employing a simple planar geometry. The compact and highly transparent CuSCN HTL was compatible with the low-cost, blade-coated carbon/Ag electrode and a semitransparent solar cell device. With Au and carbon/Ag electrodes, chemical bath deposited Sb2S3 solar cells achieved power conversion efficiencies (PCEs) of 1.75% and 1.95%, respectively. At the same time, a preliminary semitransparent Sb2S3 device with an ultrathin Au (similar to 15 nm) electrode showed a good average visible transmittance (AVT) of 26.7% at a PCE of 1.65%.

Place, publisher, year, edition, pages
Royal Society of Chemistry, 2022
National Category
Atom and Molecular Physics and Optics
Research subject
Experimental Physics
Identifiers
urn:nbn:se:ltu:diva-93960 (URN)10.1039/d2tc03420d (DOI)000870358700001 ()2-s2.0-85141036857 (Scopus ID)
Funder
Knut and Alice Wallenberg FoundationThe Kempe Foundations
Note

Validerad;2022;Nivå 2;2022-11-29 (marisr)

Available from: 2022-11-10 Created: 2022-11-10 Last updated: 2023-05-08Bibliographically approved
Cailotto, S., Massari, D., Gigli, M., Campalani, C., Bonini, M., You, S., . . . Crestini, C. (2022). N-Doped Carbon Dot Hydrogels from Brewing Waste for Photocatalytic Wastewater Treatment. ACS Omega, 7(5), 4052-4061
Open this publication in new window or tab >>N-Doped Carbon Dot Hydrogels from Brewing Waste for Photocatalytic Wastewater Treatment
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2022 (English)In: ACS Omega, E-ISSN 2470-1343, Vol. 7, no 5, p. 4052-4061Article in journal (Refereed) Published
Abstract [en]

The brewery industry annually produces huge amounts of byproducts that represent an underutilized, yet valuable, source of biobased compounds. In this contribution, the two major beer wastes, that is, spent grains and spent yeasts, have been transformed into carbon dots (CDs) by a simple, scalable, and ecofriendly hydrothermal approach. The prepared CDs have been characterized from the chemical, morphological, and optical points of view, highlighting a high level of N-doping, because of the chemical composition of the starting material rich in proteins, photoluminescence emission centered at 420 nm, and lifetime in the range of 5.5–7.5 ns. With the aim of producing a reusable catalytic system for wastewater treatment, CDs have been entrapped into a polyvinyl alcohol matrix and tested for their dye removal ability. The results demonstrate that methylene blue can be efficiently adsorbed from water solutions into the composite hydrogel and subsequently fully degraded by UV irradiation.

Place, publisher, year, edition, pages
American Chemical Society (ACS), 2022
National Category
Physical Chemistry Food Engineering
Research subject
Experimental Physics
Identifiers
urn:nbn:se:ltu:diva-89385 (URN)10.1021/acsomega.1c05403 (DOI)000757780800001 ()35155899 (PubMedID)2-s2.0-85124252978 (Scopus ID)
Funder
The Kempe FoundationsKnut and Alice Wallenberg Foundation
Note

Validerad;2022;Nivå 2;2022-02-23 (joosat);

Funder: Ca′ Foscari University (FPI2019)

Available from: 2022-02-23 Created: 2022-02-23 Last updated: 2022-04-07Bibliographically approved
Campalani, C., Cattaruzza, E., Zorzi, S., Vomiero, A., You, S., Matthews, L., . . . Perosa, A. (2021). Biobased Carbon Dots: From Fish Scales to Photocatalysis. Nanomaterials, 11(2), Article ID 524.
Open this publication in new window or tab >>Biobased Carbon Dots: From Fish Scales to Photocatalysis
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2021 (English)In: Nanomaterials, E-ISSN 2079-4991, Vol. 11, no 2, article id 524Article in journal (Refereed) Published
Abstract [en]

The synthesis, characterization and photoreduction ability of a new class of carbon dots made from fish scales is here described. Fish scales are a waste material that contains mainly chitin, one of the most abundant natural biopolymers, and collagen. These components make the scales rich, not only in carbon, hydrogen and oxygen, but also in nitrogen. These self-nitrogen-doped carbonaceous nanostructured photocatalyst were synthesized from fish scales by a hydrothermal method in the absence of any other reagents. The morphology, structure and optical properties of these materials were investigated. Their photocatalytic activity was compared with the one of conventional nitrogen-doped carbon dots made from citric acid and diethylenetriamine in the photoreduction reaction of methyl viologen.

Place, publisher, year, edition, pages
MDPI, 2021
Keywords
carbon dots, sustainability, bio-sourced functional materials, metal-free photoredox catalysis, circular economy, circular chemistry
National Category
Other Physics Topics
Research subject
Experimental Physics
Identifiers
urn:nbn:se:ltu:diva-83211 (URN)10.3390/nano11020524 (DOI)000622890300001 ()33670807 (PubMedID)2-s2.0-85101463642 (Scopus ID)
Note

Validerad;2021;Nivå 2;2021-03-09 (alebob)

Available from: 2021-03-09 Created: 2021-03-09 Last updated: 2023-10-28Bibliographically approved
Alberoni, C., Barroso-Martín, I., Infantes-Molina, A., Rodríguez-Castellón, E., Talon, A., Zhao, H., . . . Moretti, E. (2021). Ceria doping boosts methylene blue photodegradation in titania nanostructures. Materials Chemistry Frontiers, 5(11), 4138-4152
Open this publication in new window or tab >>Ceria doping boosts methylene blue photodegradation in titania nanostructures
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2021 (English)In: Materials Chemistry Frontiers, E-ISSN 2052-1537, Vol. 5, no 11, p. 4138-4152Article in journal (Refereed) Published
Abstract [en]

Ceria-doped titania photocatalysts (ceria loading 0.25–5.0 wt%) were synthesized by hydrothermal methods for water remediation. Nanotubes (CeTNTx) and nanoparticles (CeTNPx) were obtained. Ceria doping was applied to tune the electronic properties of nanostructured titania, boosting its photocatalytic activity. CeTNT nanostructures contained anatase as the only titania phase, whereas the CeTNP series consisted of both anatase and rutile polymorphs. The Ce addition induced a decrease in the energy gap, allowing enhancement of visible light harvesting. The photodegradation of methylene blue, MB, in aqueous solution was chosen to study the influence of the morphology and the ceria loading on the photocatalytic response, under UV and solar light. Both CeO2–TiO2 nanoparticles and nanotubes were found to be very active under UV light. The highest MB degradation rates were obtained for the 0.25 wt% CeO2 doping, for both nanotubes and nanoparticles (0.123 and 0.146 min−1, respectively), able to photodegrade completely the dye after 120 min. The two samples are stable after a 3-cycle reusability test. The photo-response under simulated solar light confirmed that doping titania with ceria allows harvesting visible light absorption, enhancing its photoactivity. A maximum efficiency of 85% under simulated sunlight at a degradation rate of 0.054 min−1 was obtained. Transient photoluminescence confirmed that MB acts as a charge scavenger for the composite system. These results pointed out ceria-doped titania nanostructures as a promising class of photocatalysts for the degradation of dyes and other hazardous organic compounds in wastewater.

Place, publisher, year, edition, pages
Royal Society of Chemistry, 2021
National Category
Materials Chemistry
Research subject
Experimental Physics
Identifiers
urn:nbn:se:ltu:diva-84247 (URN)10.1039/D1QM00068C (DOI)000642224500001 ()2-s2.0-85107440607 (Scopus ID)
Funder
The Kempe FoundationsKnut and Alice Wallenberg FoundationÅForsk (Ångpanneföreningen's Foundation for Research and Development)
Note

Validerad;2021;Nivå 2;2021-06-14 (beamah);

Finansiär: Ministry of Science, Innovation and Universities (RTI2018-099668-BC22); FEDER funds; Ministry of Economy and Competitiveness (RyC-2015-17870);

Available from: 2021-05-10 Created: 2021-05-10 Last updated: 2022-04-29Bibliographically approved
Solomon, G., Gilzad Kohan, M., Vagin, M., Rigoni, F., Mazzaro, R., Natile, M. M., . . . Vomiero, A. (2021). Decorating vertically aligned MoS2 nanoflakes with silver nanoparticles for inducing a bifunctional electrocatalyst towards oxygen evolution and oxygen reduction reaction. Nano Energy, 81, Article ID 105664.
Open this publication in new window or tab >>Decorating vertically aligned MoS2 nanoflakes with silver nanoparticles for inducing a bifunctional electrocatalyst towards oxygen evolution and oxygen reduction reaction
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2021 (English)In: Nano Energy, ISSN 2211-2855, E-ISSN 2211-3282, Vol. 81, article id 105664Article in journal (Refereed) Published
Abstract [en]

Catalysts capable of improving the performance of oxygen evolution reaction (OER) and oxygen reduction reactions (ORR) are essential for the advancement of renewable energy technologies. Herein, Ag-decorated vertically aligned MoS2 nanoflakes are developed via magnetron co-sputtering and investigated as electrocatalyst towards OER and ORR. Due to the presence of silver, the catalyst shows more than 1.5 times an increase in the roughness-normalized rate of OER, featuring a very low Tafel slope (58.6 mv dec−1), thus suggesting that the catalyst surface favors the thermodynamics of hydroxyl radical (OH•) adsorption with the deprotonation steps being the rate-determining steps. The improved performance is attributed to the strong interactions between OOH intermediates and the Ag surface which reduces the activation energy. Rotating ring disk electrode (RRDE) analysis shows that the net disk currents on the Ag-MoS2 sample are two times higher at 0.65 V compared to MoS2, demonstrating the co-catalysis effect of silver doping. Based on the rate constant values, Ag-MoS2 proceeds through a mixed 4 electron and a 2 + 2 serial route reduction mechanism, in which the ionized hydrogen peroxide is formed as a mobile intermediate. The presence of silver decreases the electron transfer number and increases the peroxide yield due to the interplay of a 2 + 2 electron reduction pathway. A 2.5–6 times faster conversion rate of peroxide to OH- observed due to the presence of silver, indicating its effective cocatalyst nature. This strategy can help in designing a highly active bifunctional catalyst that has great potential as a viable alternative to precious-metal-based catalysts.Graphica

Place, publisher, year, edition, pages
Elsevier, 2021
Keywords
Oxygen evolution reaction (OER), Oxygen reduction reaction (ORR), Electrocatalys, tBifunctional catalyst, Magnetron co-sputtering
National Category
Other Physics Topics
Research subject
Experimental Physics
Identifiers
urn:nbn:se:ltu:diva-82322 (URN)10.1016/j.nanoen.2020.105664 (DOI)000620327900002 ()2-s2.0-85098781620 (Scopus ID)
Funder
Vinnova, 2015-01513Knut and Alice Wallenberg FoundationEU, Horizon 2020, 654002, 785219The Kempe FoundationsLuleå University of TechnologySwedish Research Council, 2019-05577
Note

Validerad;2021;Nivå 2;2021-01-12 (alebob);

Finansiär: MIUR-PON TARANTO (ARS01_00637)

Available from: 2021-01-12 Created: 2021-01-12 Last updated: 2022-01-14Bibliographically approved
Zhao, H., Liu, G., You, S., Camargo, F. V. A., Zavelani-Rossi, M., Wang, X., . . . Gong, X. (2021). Gram-scale synthesis of carbon quantum dots with a large Stokes shift for the fabrication of eco-friendly and high-efficiency luminescent solar concentrators. Energy & Environmental Science, 14(1), 396-406
Open this publication in new window or tab >>Gram-scale synthesis of carbon quantum dots with a large Stokes shift for the fabrication of eco-friendly and high-efficiency luminescent solar concentrators
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2021 (English)In: Energy & Environmental Science, ISSN 1754-5692, E-ISSN 1754-5706, Vol. 14, no 1, p. 396-406Article in journal (Refereed) Published
Abstract [en]

Luminescent solar concentrators (LSCs) are large-area sunlight collectors coupled to small area solar cells, for efficient solar-to-electricity conversion. The three key points for the successful market penetration of LSCs are: (i) removal of light losses due to reabsorption during light collection; (ii) high light-to-electrical power conversion efficiency of the final device; (iii) long-term stability of the LSC structure related to the stability of both the matrix and the luminophores. Among various types of fluorophores, carbon quantum dots (C-dots) offer a wide absorption spectrum, high quantum yield, non-toxicity, environmental friendliness, low-cost, and eco-friendly synthetic methods. However, they are characterized by a relatively small Stokes shift, compared to inorganic quantum dots, which limits the highest external optical efficiency that can be obtained for a large-area single-layer LSC (>100 cm2) based on C-dots below 2%. Herein, we report highly efficient large-area LSCs (100–225 cm2) based on colloidal C-dots synthesized via a space-confined vacuum-heating approach. This one batch reaction could produce Gram-scale C-dots with a high quantum yield (QY) (∼65%) using eco-friendly citric acid and urea as precursors. Thanks to their very narrow size distribution, the C-dots produced via the space-confined vacuum-heating approach had a large Stokes shift of 0.53 eV, 50% larger than C-dots synthesized via a standard solvothermal reaction using the same precursors with a similar absorption range. The large-area LSC (15 × 15 × 0.5 cm3) prepared by using polyvinyl pyrrolidone (PVP) polymer as a matrix exhibited an external optical efficiency of 2.2% (under natural sun irradiation, 60 mW cm−2, uncharacterized spectrum). After coupling to silicon solar cells, the LSC exhibited a power conversion efficiency (PCE) of 1.13% under natural sunlight illumination (20 mW cm−2, uncharacterized spectrum). These unprecedented results were obtained by completely suppressing the reabsorption losses during light collection, as proved by optical spectroscopy. These findings demonstrate the possibility of obtaining eco-friendly, high-efficiency, large-area LSCs through scalable production techniques, paving the way to the lab-to-fab transition of this kind of devices.

Place, publisher, year, edition, pages
Royal Society of Chemistry, 2021
National Category
Other Physics Topics
Research subject
Experimental Physics
Identifiers
urn:nbn:se:ltu:diva-81657 (URN)10.1039/D0EE02235G (DOI)000611850000018 ()2-s2.0-85100495565 (Scopus ID)
Note

Validerad;2021;Nivå 2;2021-02-22 (johcin)

Available from: 2020-11-27 Created: 2020-11-27 Last updated: 2023-10-28Bibliographically approved
Gilzad Kohan, M., You, S., Camellini, A., Concina, I., Rossi, M. Z. & Vomiero, A. (2021). Optical field coupling in ZnO nanorods decorated with silver plasmonic nanoparticles. Journal of Materials Chemistry C, 9(43), 15452-15462
Open this publication in new window or tab >>Optical field coupling in ZnO nanorods decorated with silver plasmonic nanoparticles
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2021 (English)In: Journal of Materials Chemistry C, ISSN 2050-7526, E-ISSN 2050-7534, Vol. 9, no 43, p. 15452-15462Article in journal (Refereed) Published
Abstract [en]

Characterizing carrier redistribution due to optical field modulation in a plasmonic hot-electron/semiconductor junction can be used to raise the framework for harnessing the carrier decay of plasmonic metals in more efficient conversion systems. In this work we comprehensively studied the carrier redistribution mechanisms of a 1-dimensional (1D) metal-semiconductor Schottky architecture, holding the dual feature of a hot-electron plasmonic system and a simple metal/semiconductor junction. We obtained a strongly enhanced external quantum efficiency (EQE) of the plasmonic Ag decorated ZnO semiconductor in both the band-edge region of ZnO and the corresponding plasmonic absorption profile of the Ag NPs (visible region). Simultaneously, the insertion of an insulating Al2O3 intermediate layer between Ag NPs and ZnO resulted in a parallel distinction of the two main non-radiative carrier transfer mechanisms of plasmonic NPs, i.e. direct electron transfer (DET) and plasmonic induced resonance energy transfer (PIRET). The multi-wavelength transient pump-probe spectroscopy indicated the very fast plasmonic radiative transfer dynamics of the system in <500 fs below 389 nm. We demonstrate a 13% increase of photogenerated current in ZnO upon visible irradiation as a result of non-radiative plasmonic hot-electron injection from Ag NPs. Overall, our device encompasses several effective solutions for designing a plasmonic system featuring non-radiative electron-electron plasmonic dephasing and high photoconversion efficiencies.

Place, publisher, year, edition, pages
Royal Society of Chemistry, 2021
National Category
Condensed Matter Physics
Research subject
Experimental Physics
Identifiers
urn:nbn:se:ltu:diva-87361 (URN)10.1039/d1tc03032a (DOI)000700916000001 ()2-s2.0-85119323967 (Scopus ID)
Funder
The Kempe FoundationsEU, Horizon 2020, 654002Knut and Alice Wallenberg FoundationVinnova
Note

Validerad;2021;Nivå 2;2021-11-29 (johcin);

Artikeln har tidigare förekommit som manuskript i avhandling

Available from: 2021-10-04 Created: 2021-10-04 Last updated: 2021-11-29Bibliographically approved
Lontio Fomekong, R., You, S., Frohnhoven, R., Ludwig, T., Mathur, S. & Saruhan, B. (2021). Self-decoration of Barium Titanate with Rhodium-NP via a facile co-precipitation route for NO sensing in hot gas environment. Sensors and actuators. B, Chemical, 338, Article ID 129848.
Open this publication in new window or tab >>Self-decoration of Barium Titanate with Rhodium-NP via a facile co-precipitation route for NO sensing in hot gas environment
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2021 (English)In: Sensors and actuators. B, Chemical, ISSN 0925-4005, E-ISSN 1873-3077, Vol. 338, article id 129848Article in journal (Refereed) Published
Abstract [en]

There is an urgent need to develop real-time gas sensors capable of detection under hot-gas (> 400 °C) flow, for applications such as exhaust emission control. In this context, Rh-doped BaTiO3 has been prepared by a co-precipitation route and heat-treated at 900 °C under 2% hydrogen to obtain in-situ Rh-nanoparticle decoration of submicron BaTiO3 particles. X-ray diffraction, Raman, and X-Ray photoelectron spectrometry analysis confirm the presence of Barium Titanate phases and the substitution of Ti4+ by Rh3+. According to the analytic evidence, thermal hydrogen treatment leads probably to Rhodium diffusion out of titanate lattice, yielding a self-decoration of the nano-sized Barium Titanate particles. Further NO-sensing tests revealed that the sensors produced by deposition of this in-situ Rh-loaded BaTiO3 on the interdigitated electrodes (IDE) yield a significant increase of selectivity and response (∼18 % for 200 ppm NO) towards NO, for the first time, under a hot-gas environment reaching up to 900 °C as synthetic humid air being the carrier gas. The calculated response and recovery times are reasonable, and observed reproducibility confirms suitability to practical applications. Relying on the carried investigations, this good sensing performance can be explained by the creation of excessive oxygen vacancies resulting from Rhodium's surface diffusion. Moreover, it is to claim that excellent catalytic activity of Rhodium plays a key role in enhancing NO-sensing performance.

Place, publisher, year, edition, pages
Elsevier, 2021
Keywords
Rh-loaded BaTiO3, co-precipitation, high-temperature sensor, nitrogen oxide
National Category
Physical Chemistry
Research subject
Experimental Physics
Identifiers
urn:nbn:se:ltu:diva-83401 (URN)10.1016/j.snb.2021.129848 (DOI)000641349500006 ()2-s2.0-85103251162 (Scopus ID)
Note

Validerad;2021;Nivå 2;2021-04-13 (johcin);

Finansiär: DLR-DAAD Fellowship (284)

Available from: 2021-03-25 Created: 2021-03-25 Last updated: 2021-05-18Bibliographically approved
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Identifiers
ORCID iD: ORCID iD iconorcid.org/0000-0001-7475-6394

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