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Li, Y., Wu, X., Zuo, G., Wang, Y., Liu, X., Ma, Y., . . . Cai, W. (2023). An n-n Heterojunction Configuration for Efficient Electron Transport in Organic Photovoltaic Devices. Advanced Functional Materials, 33(9), Article ID 2209728.
Open this publication in new window or tab >>An n-n Heterojunction Configuration for Efficient Electron Transport in Organic Photovoltaic Devices
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2023 (English)In: Advanced Functional Materials, ISSN 1616-301X, E-ISSN 1616-3028, Vol. 33, no 9, article id 2209728Article in journal (Refereed) Published
Abstract [en]

Selective electron transport and extraction are essential to the operation of photovoltaic devices. Electron transport layer (ETL) is therefore critical to organic photovoltaics (OPV). Herein, an ETL configuration is presented comprising a solution-processed n-n organic heterojunction to enhance electron transport and hole blocking, and boost power conversion efficiency (PCE) in OPV. Specifically, the n-n heterojunction is constructed by stacking a narrow-band n-type conjugated polymer layer (PNDIT-F3N) and a wide-band n-type conjugated molecule layer (Phen-NaDPO). Based on the ultraviolet photoelectron spectroscopy measurement and numerical simulation of current density-voltage characteristics, the formation of the built-in potential is investigated. In three OPVs with different active layers, substantial improvements are observed in performance following the introduction of this ETL configuration. The performance enhancement arises from the combination of selective carrier transport properties and reduced recombination. Another contributing factor is the good film-forming quality of the new ETL configuration, where the surface energies of the related materials are well-matched. The n-n organic heterojunction represents a viable and promising ETL construction strategy for efficient OPV devices.

Place, publisher, year, edition, pages
WILEY-V C H VERLAG GMBH, 2023
Keywords
electron transport layers; n-n heterojunctions; organic photovoltaic devices; selective carrier transports
National Category
Condensed Matter Physics
Identifiers
urn:nbn:se:liu:diva-190782 (URN)10.1002/adfm.202209728 (DOI)000899349000001 ()
Note

Funding Agencies|National Natural Science Foundation of China; National Key Research & Development Program of China; Guangdong Basic and Applied Basic Research Foundation; Fundamental Research Funds for the Central Universities; Key Projects of Joint Fund of Basic and Applied Basic Research Fund of Guangdong Province; Science and Technology Planning Project of Guangzhou; [61804065]; [62104083]; [2017YFA0206600]; [2021A1515012561]; [21621008]; [2019B1515120073]; [201605030008]; [202201010447]

Available from: 2023-01-02 Created: 2023-01-02 Last updated: 2024-02-13Bibliographically approved
Jiang, S., Xiong, S., Wu, H., Zhao, D., You, X., Xu, Y., . . . Bao, Q. (2023). In Situ Reconstruction of Hole-Selective Perovskite Heterojunction with Graded Energetics Toward Highly Efficient and Stable Solar Cells. Advanced Energy Materials, 13(27), Article ID 2300983.
Open this publication in new window or tab >>In Situ Reconstruction of Hole-Selective Perovskite Heterojunction with Graded Energetics Toward Highly Efficient and Stable Solar Cells
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2023 (English)In: Advanced Energy Materials, ISSN 1614-6832, E-ISSN 1614-6840, Vol. 13, no 27, article id 2300983Article in journal (Refereed) Published
Abstract [en]

Perovskite solar cells (PSCs) have demonstrated a high power conversion efficiency, however, the large energy loss due to non-radiative recombination is the main challenge for further performance enhancement. Here, a surface treatment strategy is developed by heat-induced decomposition of a thin interlayer 2,7-Naphthaleneditriflate (NAP) to in situ reconstruct perovskite energetics. It is verified that the reconstructed perovskite surface energetics match better with the upper hole transport layer compared to the intrinsic condition. Spontaneous generation of n/n(-) homojunctions between the perovskite film bulk and the surface region promotes hole extraction, enhancing built-in electric field, and thus significantly suppresses charge recombination at such perovskite hole-selective heterojunctions. Moreover, the surface decomposed fluorine-rich complexes passivate the defects and improve the crystallinity of the perovskite film. These advantages are confirmed by a remarkably improved efficiency from 20.52% for the control device to 23.37% for the treated one with excellent stability. The work provides a promising approach of in situ reconstructing perovskite surface and interface for the design of highly efficient and stable PSCs.

Place, publisher, year, edition, pages
WILEY-V C H VERLAG GMBH, 2023
Keywords
charge transport; charge-selective heterojunction; efficiency; nonradiative recombination; perovskite solar cells
National Category
Other Chemistry Topics
Identifiers
urn:nbn:se:liu:diva-196831 (URN)10.1002/aenm.202300983 (DOI)001004552400001 ()
Note

Funding Agencies|National Natural Science Foundation of China [22279034, 52261145698]; National Key Research and Development Program of China [2022YFB3803300]; Shanghai Science and Technology Innovation Action Plan [22ZR1418900]; Fundamental Research Funds for the Central Universities; East China Normal University (ECNU) Multifunctional Platform for Innovation; China Postdoctoral Science Foundation [BX20220089]

Available from: 2023-08-24 Created: 2023-08-24 Last updated: 2024-03-28Bibliographically approved
Chen, Z., Liu, X., Wang, H., Liu, X., Hou, L. & Gao, F. (2023). Photoluminescence Enhancement for Efficient Mixed-Halide Blue Perovskite Light-Emitting Diodes. Advanced Optical Materials, 11(6), Article ID 2202528.
Open this publication in new window or tab >>Photoluminescence Enhancement for Efficient Mixed-Halide Blue Perovskite Light-Emitting Diodes
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2023 (English)In: Advanced Optical Materials, ISSN 2162-7568, E-ISSN 2195-1071, Vol. 11, no 6, article id 2202528Article in journal (Refereed) Published
Abstract [en]

The development of highly efficient blue perovskite light-emitting diodes (PeLEDs) remains a big challenge, requiring more fundamental investigations. In this work, significant photoluminescence enhancement in mixed halide blue perovskite films is demonstrated by using a molecule, benzylphosphonic acid, which eventually doubles the external quantum efficiency to 6.3% in sky-blue PeLEDs. The photoluminescence enhancement is achieved by forming an oxide-bonded perovskite surface at grain boundaries and suppressing electron-phonon interaction, which enhances the radiative recombination rate and reduces the nonradiative recombination rate, respectively. Moreover, severe thermal quenching is observed in the blue perovskite films, which can be explained by a two-step mechanism involving exciton dissociation and electron-phonon interaction. The results suggest that enhancing the radiative recombination rate and reducing the electron-phonon interaction-induced nonradiative recombination rate are crucial for achieving blue perovskite films with strong emission at or above room temperature.

Place, publisher, year, edition, pages
WILEY-V C H VERLAG GMBH, 2023
Keywords
blue perovskites; light-emitting diodes; mixed halides; PeLEDs; photoluminescence
National Category
Materials Chemistry
Identifiers
urn:nbn:se:liu:diva-191627 (URN)10.1002/adom.202202528 (DOI)000914788900001 ()
Note

Funding Agencies|Swedish Energy Agency Energimyndigheten [48758-1]; China Postdoctoral Science Foundation [2020M673055]; NSFC [61774077]; Research and Development Program in Key Areas of Guangdong Province [2019B1515120073, 2019B090921002, 2019B010132004]; [895679]

Available from: 2023-02-06 Created: 2023-02-06 Last updated: 2024-02-27Bibliographically approved
Ghorbani Shiraz, H., Ullah Khan, Z., Pere, D., Liu, X., Coppel, Y., Fahlman, M., . . . Crispin, X. (2022). 3R-TaS2 as an Intercalation-Dependent Electrified Interface for Hydrogen Reduction and Oxidation Reactions. The Journal of Physical Chemistry C, 126(40), 17056-17065
Open this publication in new window or tab >>3R-TaS2 as an Intercalation-Dependent Electrified Interface for Hydrogen Reduction and Oxidation Reactions
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2022 (English)In: The Journal of Physical Chemistry C, ISSN 1932-7447, E-ISSN 1932-7455, Vol. 126, no 40, p. 17056-17065Article in journal (Refereed) Published
Abstract [en]

Hydrogen technology, as a future breakthrough for the energy industry, has been defined as an environmentally friendly, renewable, and high-power energy carrier. The green production of hydrogen, which mainly relies on electrocatalysts, is limited by the high cost and/ or the performance of the catalytic system. Recently, studies have been conducted in search of bifunctional electrocatalysts accelerating both the hydrogen evolution reaction (HER) and the hydrogen oxidation reaction (HOR). Herein, we report the investigation of the high efficiency bifunctional electrocatalyst TaS2 for both the HER and the HOR along with the asymmetric effect of inhibition by organic intercalation. The linear organic agent, to boost the electron donor property and to ease the process of intercalation, provides a higher interlayer gap in the tandem structure of utilized nanosheets. XRD and XPS data reveal an increase in the interlayer distance of 22%. The HER and the HOR were characterized in a Pt group metal-free electrochemical system. The pristine sample shows a low overpotential of -0.016 Vat the onset. The intercalated sample demonstrates a large shift in its performance for the HER. It is revealed that the intercalation is a potential key strategy for tuning the performance of this family of catalysts. The inhibition of the HER by intercalation is considered as the increase in the operational window of a water-based electrolyte on a negative electrode, which is relevant to technologies of electrochemical energy storage.

Place, publisher, year, edition, pages
American Chemical Society (ACS), 2022
National Category
Other Chemical Engineering
Identifiers
urn:nbn:se:liu:diva-189795 (URN)10.1021/acs.jpcc.2c04290 (DOI)000869704900001 ()
Note

Funding Agencies|Swedish Research Council [VR 2016-05990]; Knut and Alice Wallenberg Foundation [KAW 2019.0604, 2021.0195]; Karl Erik Onnesjos Foundation; Swedish Government Strategic Research Area in Materials Science on Advanced Functional Materials at Linkoping University (Faculty Grant SFO-MatLiU) [2009-00971]

Available from: 2022-11-08 Created: 2022-11-08 Last updated: 2023-12-06Bibliographically approved
Jiang, S., Xiong, S., Dong, W., Li, D., Yan, Y., Jia, M., . . . Bao, Q. (2022). Constructing Chromium Multioxide Hole-Selective Heterojunction for High-Performance Perovskite Solar Cells. Advanced Science, 9(30), Article ID 2203681.
Open this publication in new window or tab >>Constructing Chromium Multioxide Hole-Selective Heterojunction for High-Performance Perovskite Solar Cells
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2022 (English)In: Advanced Science, E-ISSN 2198-3844, Vol. 9, no 30, article id 2203681Article in journal (Refereed) Published
Abstract [en]

Perovskite solar cells (PSCs) suffer from significant nonradiative recombination at perovskite/charge transport layer heterojunction, seriously limiting their power conversion efficiencies. Herein, solution-processed chromium multioxide (CrOx) is judiciously selected to construct a MAPbI(3)/CrOx/Spiro-OMeTAD hole-selective heterojunction. It is demonstrated that the inserted CrOx not only effectively reduces defect sites via redox shuttle at perovskite contact, but also decreases valence band maximum (VBM)-HOMO offset between perovskite and Spiro-OMeTAD. This will diminish thermionic losses for collecting holes and thus promote charge transport across the heterojunction, suppressing both defect-assisted recombination and interface carrier recombination. As a result, a remarkable improvement of 21.21% efficiency with excellent device stability is achieved compared to 18.46% of the control device, which is among the highest efficiencies for polycrystalline MAPbI(3) based n-i-p planar PSCs reported to date. These findings of this work provide new insights into novel charge-selective heterojunctions for further enhancing efficiency and stability of PSCs.

Place, publisher, year, edition, pages
Wiley, 2022
Keywords
charge transport; efficiency; hole-selective heterojunction; nonradiative recombination; perovskite solar cells
National Category
Other Chemical Engineering
Identifiers
urn:nbn:se:liu:diva-188443 (URN)10.1002/advs.202203681 (DOI)000846622500001 ()36031391 (PubMedID)
Note

Funding Agencies|National Science Foundation of China [21875067]; Shanghai Science and Technology Innovation Action Plan [22ZR1418900]; Fundamental Research Funds for the Central Universities; Shanghai Rising-Star [19QA1403100]; East China Normal University (ECNU) Multifunctional Platform for Innovation; open research fund of Songshan Lake Materials Laboratory [2021SLABFK02]; National Key Research and Development Program of China [2017YFA0206600]; National Natural Science Foundation of China [51922032, 21961160720]

Available from: 2022-09-14 Created: 2022-09-14 Last updated: 2023-06-22Bibliographically approved
Chen, J.-D., Li, L., Qin, C.-C., Ren, H., Li, Y.-Q., Ou, Q.-D., . . . Tang, J.-X. (2022). Hot-electron emission-driven energy recycling in transparent plasmonic electrode for organic solar cells. InfoMat, 4(3), Article ID e12285.
Open this publication in new window or tab >>Hot-electron emission-driven energy recycling in transparent plasmonic electrode for organic solar cells
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2022 (English)In: InfoMat, ISSN 2567-3165, Vol. 4, no 3, article id e12285Article in journal (Refereed) Published
Abstract [en]

Plasmonic metal electrodes with subwavelength nanostructures are promising for enhancing light harvesting in photovoltaics. However, the nonradiative damping of surface plasmon polaritons (SPPs) during coupling with sunlight results in the conversion of the excited hot-electrons to heat, which limits the absorption of light and generation of photocurrent. Herein, an energy recycling strategy driven by hot-electron emission for recycling the SPP energy trapped in the plasmonic electrodes is proposed. A transparent silver-based plasmonic metal electrode (A-PME) with a periodic hexagonal nanopore array is constructed, which is combined with a luminescent organic emitter for radiative recombination of the injected hot-electrons. Owing to the suppressed SPP energy loss via broadband hot-electron emission, the A-PME achieves an optimized optical transmission with an average transmittance of over 80% from 380 to 1200 nm. Moreover, the indium-tin-oxide-free organic solar cells yield an enhanced light harvesting with a power conversion efficiency of 16.1%.

Place, publisher, year, edition, pages
Wiley, 2022
Keywords
energy recycling; hot-electron emission; organic solar cells; plasmonic electrode; surface plasmon polariton
National Category
Atom and Molecular Physics and Optics
Identifiers
urn:nbn:se:liu:diva-182792 (URN)10.1002/inf2.12285 (DOI)000746931900001 ()
Note

Funding Agencies|ARC Centre of Excellence for Future LowEnergy Electronics Technologies (FLEET); Collaborative Innovation Center of Suzhou Nano Science Technology; Jiangsu Provincial Research Scheme of Natural Science for Higher Education Institutions [19KJB510056]; Natural Science Foundation of Jiangsu Province of ChinaNatural Science Foundation of Jiangsu Province [BK20190815]; National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [11804084, 12074104, 62075061, 61905171, 51873138]; 333 program [BRA2019061]

Available from: 2022-02-14 Created: 2022-02-14 Last updated: 2023-08-22Bibliographically approved
Zhang, Q., Zhang, H., Wu, Z., Wang, C., Zhang, R., Yang, C., . . . Fahlman, M. (2022). Natural Product Betulin-Based Insulating Polymer Filler in Organic Solar Cells. Solar RRL, 6(9), Article ID 2200381.
Open this publication in new window or tab >>Natural Product Betulin-Based Insulating Polymer Filler in Organic Solar Cells
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2022 (English)In: Solar RRL, E-ISSN 2367-198X, Vol. 6, no 9, article id 2200381Article in journal (Refereed) Published
Abstract [en]

Introduction of filler materials into organic solar cells (OSCs) are a promising strategy to improve device performance and thermal/mechanical stability. However, the complex interactions between the state-of-the-art OSC materials and filler require careful selection of filler materials and OSC fabrication to achieve lower cost and improved performance. In this work, the introduction of a natural product betulin-based insulating polymer as filler in various OSCs is investigated. Donor-acceptor-insulator ternary OSCs are developed with improved open-circuit voltage due to decreased trap-assisted recombination. Furthermore, filler-induced vertical phase separation due to mismatched surface energy can strongly affect charge collection at the bottom interface and limit the filler ratio. A quasi-bilayer strategy is used in all-polymer systems to circumvent this problem. Herein, the variety of filler materials in OSCs to biomass is broadened, and the filler strategy is made a feasible and promising strategy toward highly efficient, eco, and low-cost OSCs.

Place, publisher, year, edition, pages
Wiley-V C H Verlag GMBH, 2022
Keywords
betulin; filler strategy; organic solar cells
National Category
Textile, Rubber and Polymeric Materials
Identifiers
urn:nbn:se:liu:diva-186508 (URN)10.1002/solr.202200381 (DOI)000809737000001 ()
Note

Funding Agencies|Knut and Alice Wallenberg Foundation (KAW) through the Wallenberg Wood Science Center; Swedish Energy Agency [45411-1]; Swedish Research Council [2016-05498, 2016-05990, 2020-04538, 2018-06048]; STINT grant [CH2017-7163]; Swedish Government Strategic Research Area in Materials Science on Functional Materials at Linkoping University [2009 00971]

Available from: 2022-06-29 Created: 2022-06-29 Last updated: 2024-01-10Bibliographically approved
Wang, Y., Zhong, K., Li, H., Dai, Y., Zhang, H., Zuo, J., . . . Tang, J. (2021). Bimetallic hybrids modified with carbon nanotubes as cathode catalysts for microbial fuel cell: Effective oxygen reduction catalysis and inhibition of biofilm formation. Journal of Power Sources, 485, Article ID 229273.
Open this publication in new window or tab >>Bimetallic hybrids modified with carbon nanotubes as cathode catalysts for microbial fuel cell: Effective oxygen reduction catalysis and inhibition of biofilm formation
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2021 (English)In: Journal of Power Sources, ISSN 0378-7753, E-ISSN 1873-2755, Vol. 485, article id 229273Article in journal (Refereed) Published
Abstract [en]

As a promising energy conversion equipment, the performance of microbial fuel cell (MFC) is affected by slow kinetics of oxygen reduction reaction (ORR). It is of great significance to explore electrocatalysts with high activity for sustainable energy applications. Herein, we synthesize the in-situ grown carbon nanotubes decorated electrocatalyst derived from copper-based metal organic frameworks (MOFs) co-doped with cobalt and nitrogen (CuCo@NCNTs) through straightforward immersion and pyrolysis process. The carbon nanotubes produced by metallic cobalt and high-activity bimetallic active sites formed by nitrogen doping enable CuCo@NCNTs to have the best oxygen reduction reaction (ORR) performance in alkaline electrolyte, with limit current density of 5.88 mA cm-2 and onset potential of 0.91 V (vs. RHE). Moreover, CuCo@NCNTs nanocomposite exhibits obvious antibacterial activity, and inhibiting the biofilm on cathode surface in antibacterial test and biomass quantification. The maximum power density (2757 mW m-3) of MFC modified with CuCo@NCNTs is even higher than Pt/C catalyst (2313 mW m-3). In short, CuCo@NCNTs nanocomposite can be an alternative cathode catalyst for MFC.

Place, publisher, year, edition, pages
Amsterdam, Netherlands: Elsevier, 2021
Keywords
Metal organic frameworks; Oxygen reduction reaction; Microbial fuel cell; Antibacterial; Biofilm
National Category
Other Chemical Engineering
Identifiers
urn:nbn:se:liu:diva-185081 (URN)10.1016/j.jpowsour.2020.229273 (DOI)000607098200001 ()2-s2.0-85097459188 (Scopus ID)
Note

Funding Agencies: National Natural Science Foundation of China (NSFC) [51208122, 51778156, 51708142, 51708143]; Pearl River S&T Nova Program of Guangzhou [201806010191]; Science and Technology Program of Guangzhou [201707010256]; Guangzhou Universitys Training Program for Excellent New-recruited Doctors [YB201710]; Guangzhou Universitys Training Program of Innovation Ability for Postgraduates [2019GDJC-M07]

Available from: 2022-05-16 Created: 2022-05-16 Last updated: 2022-06-03Bibliographically approved
Chen, Y., Liu, X., Braun, S. & Fahlman, M. (2021). Understanding Interface Dipoles at an Electron Transport Material/Electrode Modifier for Organic Electronics. ACS Applied Materials and Interfaces, 13(39), 47218-47225
Open this publication in new window or tab >>Understanding Interface Dipoles at an Electron Transport Material/Electrode Modifier for Organic Electronics
2021 (English)In: ACS Applied Materials and Interfaces, ISSN 1944-8244, E-ISSN 1944-8252, Vol. 13, no 39, p. 47218-47225Article in journal (Refereed) Published
Abstract [en]

Interface dipoles formed at an electrolyte/electrode interface have been widely studied and interpreted using the "double dipole step" model, where the dipole vector is determined by the size and/or range of motion of the charged ions. Some electron transport materials (ETMs) with lone pairs of electrons on heteroatoms exhibit a similar interfacial behavior. However, the origin of the dipoles in such materials has not yet been explored in great depth. Herein, we systematically investigate the influence of the lone pair of electrons on the interface dipole through three pyridine derivatives B2-B4PyMPM. Experiments show that different positions of nitrogen atoms in the three materials give rise to different hydrogen bonds and molecular orientations, thereby affecting the areal density and direction of the lone pair of electrons. The interface dipoles of the three materials predicted by the "double dipole step" model are in good agreement with the ultraviolet photoelectron spectroscopy results both in spin-coated and vacuum-deposited films. These findings help to better understand the ETMs/electrode interfacial behaviors and provide new guidelines for the molecular design of the interlayer.

Place, publisher, year, edition, pages
American Chemical Society (ACS), 2021
Keywords
Interface dipole, Electron transport material, Hydrogen bond, Molecular orientation, Organic electronics
National Category
Materials Chemistry
Identifiers
urn:nbn:se:liu:diva-180703 (URN)10.1021/acsami.1c13172 (DOI)000706187100099 ()34551513 (PubMedID)
Note

Funding agencies: The Swedish Research Council (project grants no. 2016-05498, 2016-05990, and 2020-04538), The Swedish Government Strategic Research Area in Materials Science on Functional Materials at Linköping University (Faculty Grant SFO Mat LiU no. 2009 00971), The Open Fund of the State Key Laboratory of Luminescent Materials and Devices (South China University of Technology)

Available from: 2021-11-01 Created: 2021-11-01 Last updated: 2021-11-17Bibliographically approved
Qin, L., Tao, Q., Liu, L., Jiang, J., Liu, X., Fahlman, M., . . . Zhang, F. (2020). Flexible Solid-State Asymmetric Supercapacitors with Enhanced Performance Enabled by Free-Standing MXene-Biopolymer Nanocomposites and Hierarchical Graphene-RuOx Paper Electrodes. Batteries & Supercaps, 3(7), 604-610
Open this publication in new window or tab >>Flexible Solid-State Asymmetric Supercapacitors with Enhanced Performance Enabled by Free-Standing MXene-Biopolymer Nanocomposites and Hierarchical Graphene-RuOx Paper Electrodes
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2020 (English)In: Batteries & Supercaps, E-ISSN 2566-6223, Vol. 3, no 7, p. 604-610Article in journal (Refereed) Published
Abstract [en]

Two-dimensional (2D) transition metal carbides and carbonitrides, called MXenes, with metallic conductivity and hydrophilic surfaces, show great promise as electrode materials for supercapacitors. A major drawback of 2D nanomaterials is the re-stacking of the nanosheets, which prevents full utilization of surface area and blocks the access of the electrolyte. In this study, a free-standing nanocomposite paper electrode is realized by combining Mo1.33C MXene and positively charged biopolymer lignin (the second most abundant biopolymer in nature, L-DEA). The self-assembled layered architecture with alternating polymer and MXene flakes increases the interlayer space to promote ion transport, and with combining charge storage capability of the lignin derivative and MXene in an interpenetrating MXene/L-DEA nanocomposite, which offers an impressive capacitance of 503.7 F g(-1). Moreover, we demonstrate flexible solid-state asymmetric supercapacitors (ASCs) using Mo1.33C@L-DEA as the negative electrode and electrochemically exfoliated graphene with ruthenium oxide (EG@RuOx) as the positive electrode. This asymmetric device operates at a voltage window of 1.35 V, which is about two times wider than that of a symmetric Mo1.33C@L-DEA based supercapacitor. Finally, the ASCs can deliver an energy density of 51.9 Wh kg(-1) at a power density of 338.5 W kg(-1), with 86 % capacitance retention after 10000 charge-discharge cycles.

Place, publisher, year, edition, pages
WILEY-V C H VERLAG GMBH, 2020
Keywords
MXene; nanocomposite paper electrode; graphene; biopolymer; asymmetric supercapacitors
National Category
Materials Chemistry
Identifiers
urn:nbn:se:liu:diva-166200 (URN)10.1002/batt.202000044 (DOI)000530007200001 ()
Note

Funding Agencies|Swedish Energy AgencySwedish Energy Agency [EM 42033-1]; Swedish Government Strategic Research Area in Material Science on Functional Materials at Linkoping University (Faculty Grant SFO-Mat-LiU) [200900971]; Swedish Research CouncilSwedish Research Council [2017-04123]; SSF Synergy program [EM160004]; Knut and Alice Wallenberg (KAW) FoundationKnut & Alice Wallenberg Foundation [KAW 2015.0043]; National Natural Science Foundation of ChinaNational Natural Science Foundation of China [61774077]; Open Fund of the State Key Laboratory of Luminescent Materials and Devices [2018-skllmd-12]; Fundamental Research Funds for the Central UniversitiesFundamental Research Funds for the Central Universities

Available from: 2020-06-09 Created: 2020-06-09 Last updated: 2022-09-02Bibliographically approved
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ORCID iD: ORCID iD iconorcid.org/0000-0002-3190-2774

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