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Zhang, Lei
Publications (10 of 12) Show all publications
Pati, P. B., Damas, G., Tian, L., Fernandes, D. L. A., Zhang, L., Bayrak Pehlivan, I., . . . Tian, H. (2017). An experimental and theoretical study of an efficient polymer nano-photocatalyst for hydrogen evolution. Energy & Environmental Science, 10(6), 1372-1376
Open this publication in new window or tab >>An experimental and theoretical study of an efficient polymer nano-photocatalyst for hydrogen evolution
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2017 (English)In: Energy & Environmental Science, ISSN 1754-5692, E-ISSN 1754-5706, Vol. 10, no 6, p. 1372-1376Article in journal (Refereed) Published
Abstract [en]

In this work, we report a highly efficient organic polymer nano-photocatalyst for light driven proton reduction. The system renders an initial rate of hydrogen evolution up to 50 +/- 0.5 mmol g(-1) h(-1), which is the fastest rate among all other reported organic photocatalysts. We also experimentally and theoretically prove that the nitrogen centre of the benzothiadiazole unit plays a crucial role in the photocatalysis and that the Pdots structure holds a close to ideal geometry to enhance the photocatalysis.

Keywords
CATALYSTS; H-2; SYSTEM; ENVIRONMENTAL SCIENCES; CELLS; CONJUGATED POLYMERS; ENERGY & FUELS; ARTIFICIAL PHOTOSYNTHESIS; WATER; ENGINEERING, CHEMICAL; GENERATION; CHEMISTRY, MULTIDISCIPLINARY; VISIBLE-LIGHT
National Category
Polymer Chemistry Engineering and Technology
Identifiers
urn:nbn:se:uu:diva-332949 (URN)10.1039/c7ee00751e (DOI)000403320300009 ()
Funder
Knut and Alice Wallenberg FoundationSwedish Energy AgencyÅForsk (Ångpanneföreningen's Foundation for Research and Development)Stiftelsen Olle Engkvist ByggmästareStandUp
Available from: 2017-11-02 Created: 2017-11-02 Last updated: 2019-12-03Bibliographically approved
Pati, P. B., Zhang, L., Philippe, B., Fernández-Terán, R., Ahmadi, S., Tian, L., . . . Tian, H. (2017). Insights into the Mechanism of a Covalently Linked Organic Dye-Cobaloxime Catalyst System for Dye-Sensitized Solar Fuel Devices. ChemSusChem, 10(11), 2480-2495
Open this publication in new window or tab >>Insights into the Mechanism of a Covalently Linked Organic Dye-Cobaloxime Catalyst System for Dye-Sensitized Solar Fuel Devices
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2017 (English)In: ChemSusChem, ISSN 1864-5631, E-ISSN 1864-564X, Vol. 10, no 11, p. 2480-2495Article in journal (Refereed) [Artistic work] Published
Abstract [en]

A covalently-linked organic dye-cobaloxime catalyst system is developed by facile click reaction for mechanistic studies and application in a dye sensitized solar fuel device based on mesoporous NiO. This system has been systematically investigated by photophysical measurements, density functional theory, time resolved fluorescence, transient absorption spectroscopy as well as photoelectron spectroscopy. The results show that irradiation of the dye-catalyst on NiO leads to ultrafast hole injection into NiO from the excited dye, followed by a fast electron transfer to reduce the catalyst unit. Moreover, they suggest that the dye undergoes structural changes in the excited state and that excitation energy transfer occurs between neighboring molecules. The photoelectrochemical experiments also show the hydrogen production by this system-based NiO photocathode. The axial chloride ligands of the catalyst are released during photocatalysis to create the active sites for proton reduction. A working mechanism of the dye-catalyst on photocathode is eventually proposed on the basis of this study.

Keywords
DSSFDs, electron transfer, Cobaloxime catalyst
National Category
Physical Chemistry
Research subject
Chemistry with specialization in Chemical Physics
Identifiers
urn:nbn:se:uu:diva-301412 (URN)10.1002/cssc.201700285 (DOI)000403005900021 ()
Available from: 2016-08-23 Created: 2016-08-23 Last updated: 2017-12-28Bibliographically approved
Hao, Y., Yang, W., Zhang, L., Jiang, R., Mijangos, E., Saygili, Y., . . . Boschloo, G. (2016). A small electron donor in cobalt complex electrolyte significantly improves efficiency in dye-sensitized solar cells. Nature Communications, 7, Article ID 13934.
Open this publication in new window or tab >>A small electron donor in cobalt complex electrolyte significantly improves efficiency in dye-sensitized solar cells
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2016 (English)In: Nature Communications, ISSN 2041-1723, E-ISSN 2041-1723, Vol. 7, article id 13934Article in journal (Refereed) Published
Abstract [en]

Photoelectrochemical approach to solar energy conversion demands a kinetic optimization of various light-induced electron transfer processes. Of great importance are the redox mediator systems accomplishing the electron transfer processes at the semiconductor/electrolyte interface, therefore affecting profoundly the performance of various photoelectrochemical cells. Here, we develop a strategy-by addition of a small organic electron donor, tris(4-methoxyphenyl)amine, into state-of-art cobalt tris(bipyridine) redox electrolyte-to significantly improve the efficiency of dye-sensitized solar cells. The developed solar cells exhibit efficiency of 11.7 and 10.5%, at 0.46 and one-sun illumination, respectively, corresponding to a 26% efficiency improvement compared with the standard electrolyte. Preliminary stability tests showed the solar cell retained 90% of its initial efficiency after 250 h continuous one-sun light soaking. Detailed mechanistic studies reveal the crucial role of the electron transfer cascade processes within the new redox system.

National Category
Physical Chemistry
Identifiers
urn:nbn:se:uu:diva-310194 (URN)10.1038/ncomms13934 (DOI)000390223200001 ()
Funder
Swedish Research CouncilSwedish Energy AgencyKnut and Alice Wallenberg FoundationStiftelsen Olle Engkvist Byggmästare
Note

Yan Hao and Wenxing Yang contributed equally to this work.

Available from: 2016-12-12 Created: 2016-12-12 Last updated: 2018-08-16Bibliographically approved
Sheibani, E., Zhang, L., Liu, P., Xu, B., Mijangos, E., Boschloo, G., . . . Tian, H. (2016). A study of oligothiophene–acceptor dyes in p-type dye-sensitized solar cells. RSC Advances, 6(22), 18165-18177
Open this publication in new window or tab >>A study of oligothiophene–acceptor dyes in p-type dye-sensitized solar cells
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2016 (English)In: RSC Advances, ISSN 2046-2069, E-ISSN 2046-2069, Vol. 6, no 22, p. 18165-18177Article in journal (Refereed) Published
Abstract [en]

Two new dyes, E1 and E2, equipped with triphenylamine as the electron donor, oligothiophene as the linkerand different electron acceptor groups, have been designed and synthesized as photosensitizers for p-typedye-sensitized solar cells (p-DSCs). A systematic study of the effect of molecular structures on the observedphotophysical properties, the electron/hole recombination process, the overall performance and theinterfacial charge separation was carried out. Transient absorption spectroscopy (TAS) shows that the E1dye with a napthoilene-1,2-benzimidazole (NBI) unit as the acceptor has a longer lifetime in the reducedstate than the E2 dye with a malononitrile subunit on the NiO surface.

National Category
Physical Chemistry
Identifiers
urn:nbn:se:uu:diva-280839 (URN)10.1039/c5ra26310g (DOI)000370717900043 ()
Funder
Swedish Research CouncilSwedish Energy AgencyKnut and Alice Wallenberg FoundationÅForsk (Ångpanneföreningen's Foundation for Research and Development), 14-452Stiftelsen Olle Engkvist Byggmästare
Available from: 2016-03-15 Created: 2016-03-15 Last updated: 2017-11-30
Zhang, L. (2016). Exploring Electron Transfer Dynamics of Novel Dye Sensitized Photocathodes: Towards Solar Cells and Solar Fuels. (Doctoral dissertation). Uppsala: Acta Universitatis Upsaliensis
Open this publication in new window or tab >>Exploring Electron Transfer Dynamics of Novel Dye Sensitized Photocathodes: Towards Solar Cells and Solar Fuels
2016 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

The design of dyes for NiO-based dye-sensitized solar cells (DSSCs) has drawn attention owing to their potential applications in photocatalysis and because they are indispensable for the development of tandem dye-sensitized solar cells. The understanding of the electron transfer mechanisms and dynamics is beneficial to guide further dye design and further improve the performance of photocathode in solar cells and solar fuel devices.

Time-resolved spectroscopy techniques, especially femtosecond and nanosecond transient absorption spectroscopy, supply sufficient resolution to get insights into the charge transfer processes in p-type dye sensitized solar cell and solar fuel devices. In paper I-V, several kinds of novel organic “push-pull” and inorganic charge transfer dyes for sensitization of p-type NiO, were systematically investigated by time-resolved spectroscopy, and photo-induced charge transfer dynamics of the organic/inorganic dyes were summarized. The excited state and reduced state intermediates were investigated in solution phase as references to confirm the charge injection and recombination on the NiO surface. The charge recombination kinetics is remarkably heterogeneous in some cases occurring on time scales spanning at least six orders of magnitude even for the same dye.

In this thesis, we also proposed a novel concept of solid state p-type dye sensitized solar cells (p-ssDSSCs) for the first time (paper VI), using an organic dye P1 as sensitizer on mesoporous NiO and phenyl-C61-butyric acid methyl ester (PCBM) as electron conductor. Femtosecond and nanosecond transient absorption spectroscopy gave evidence for sub-ps hole injection from excited P1 to NiO, followed by electron transfer from P1●- to PCBM. The p-ssDSSCs device showed an impressive 620 mV open circuit photovoltage.

Chapter 6 (paper VII) covers the study of electron transfer mechanisms in a covalently linked dye-catalyst (PB-2) sensitized NiO photocathode, towards hydrogen producing solar fuel devices. Hole injection from excited dye (PB-2*) into NiO VB takes place on dual time scales, and the reduced PB-2 (PB-2●-) formed then donates an electron to the catalyst unit.  The subsequent regeneration efficiency of PB-2 by the catalyst unit (the efficiency of catalyst reduction) is determined to ca. 70%.

Place, publisher, year, edition, pages
Uppsala: Acta Universitatis Upsaliensis, 2016. p. 80
Series
Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology, ISSN 1651-6214 ; 1418
Keywords
Electron transfer, Laser spectroscopy, Femtosecond spectroscopy, Transient absorption, NiO, DSSCs, DSSFDs, Charge separation, Solar energy conversion, Nanosecond photolysis, Photophysics
National Category
Chemical Sciences
Research subject
Chemistry with specialization in Chemical Physics
Identifiers
urn:nbn:se:uu:diva-302263 (URN)978-91-554-9678-4 (ISBN)
Public defence
2016-10-21, Häggsalen, Ångströmlaboratoriet, Lägerhyddsvägen 1, Uppsala, 13:15 (English)
Opponent
Supervisors
Available from: 2016-09-27 Created: 2016-08-31 Last updated: 2016-10-11
Zhang, L., Favereau, L., Farre, Y., Maufroy, A., Pellegrin, Y., Blart, E., . . . Hammarström, L. (2016). Molecular-structure control of electron transferdynamics of push–pull porphyrins as sensitizers forNiO based dye sensitized solar cells. RSC Advances, 6(81), 77184-77194
Open this publication in new window or tab >>Molecular-structure control of electron transferdynamics of push–pull porphyrins as sensitizers forNiO based dye sensitized solar cells
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2016 (English)In: RSC Advances, ISSN 2046-2069, E-ISSN 2046-2069, Vol. 6, no 81, p. 77184-77194Article in journal (Refereed) Published
Abstract [en]

Porphyrin dyes were synthesized for use in p-type (NiO) dye sensitized solar cells based on different designprinciples. One porphyrin was designed with a significant charge transfer character in the excited statebecause of push–pull effects of the substituents. Another porphyrin had instead an appended NDIacceptor group (NDI ¼ naphthalene diimide). The dyes were characterized by spectroscopic,electrochemical and DFT methods. Solar cells based on sensitized, meso-porous NiO showed ratherpoor performance compared to other organic dyes, but with a clear improvement for the dye with theNDI acceptor. Ultrafast transient absorption spectroscopy and nanosecond laser photolysis showed thathole injection into NiO was followed by unusually rapid charge recombination, predominantly ona 50–100 ps time scale, which is likely the main reason for the poor photovoltaic performance. Againthe porphyrin with the NDI group showed a more long-lived charge separation that should lead to betterdye regeneration in a solar cell, which can explain its better photovoltaic performance.

Keywords
porphyrins, electron transfer dynamics, NiO
National Category
Physical Chemistry
Research subject
Chemistry with specialization in Chemical Physics
Identifiers
urn:nbn:se:uu:diva-301387 (URN)10.1039/c6ra15195g (DOI)000382482200011 ()
Funder
EU, European Research Council, Marches-278845Swedish Energy Agency
Available from: 2016-08-22 Created: 2016-08-22 Last updated: 2017-11-28Bibliographically approved
Farré, Y., Zhang, L., Pellegrin, Y., Planchat, A., Blart, E., Boujtita, M., . . . Odobel, F. (2016). Second Generation of DiketopyrrolopyrroleDyes for NiO based Dye-Sensitized Solar Cells. The Journal of Physical Chemistry C, 120(15), 7923-7940
Open this publication in new window or tab >>Second Generation of DiketopyrrolopyrroleDyes for NiO based Dye-Sensitized Solar Cells
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2016 (English)In: The Journal of Physical Chemistry C, ISSN 1932-7447, E-ISSN 1932-7455, Vol. 120, no 15, p. 7923-7940Article in journal (Refereed) Published
Abstract [en]

In this study, four new diketopyrrolopyrrole (DPP) sensitizers, with a dicarboxylated triphenylamine anchoring group for attachment to NiO, were prepared and their electronic absorption, emission and electrochemical properties were recorded. The nature of the electronic excited-states was also modeled with TD-DFT quantum chemistry calculations. The photovoltaic performances of these new dyes were characterized in NiO-based dye-sensitized solar cells (DSCs) with the classical iodide/triiodide and cobaltII/III-polypyridine electrolytes, in which they proved to be quite active. Laser spectroscopy on dye/NiO/electrolyte films gave evidence for ultrafast hole injection into NiO (0.2-10 ps time scales). For the dyes with an appended naphtalenediimide (NDI) acceptor unit, ultrafast electron transfer to the NDI dramatically prolonged the lifetime of the charge separated state NiO(+)/dye-, from the ps time scale to an average lifetime ≈ 0.25 ms, which is among the slowest charge recombinations ever reported for dye/NiO systems. This allowed for efficient regeneration by CoIIIpolypyridine electrolytes, which translated into much improved PV-performance compared to the DPP dyes without appended NDI. Overall, these results underscore the suitability of DPP as sensitizers for NiO-based photoelectrochemical devices for photovoltaic and photocatalysis.

National Category
Physical Chemistry
Identifiers
urn:nbn:se:uu:diva-280841 (URN)10.1021/acs.jpcc.5b12489 (DOI)000374811100004 ()
Funder
EU, European Research Council, Marches -278845Knut and Alice Wallenberg FoundationSwedish Energy AgencySwedish Research Council
Available from: 2016-03-15 Created: 2016-03-15 Last updated: 2017-11-30Bibliographically approved
Zhang, L., Boschloo, G., Hammarström, L. & Tian, H. (2016). Solid state p-type dye-sensitized solar cells: concept, experiment and mechanism. Physical Chemistry, Chemical Physics - PCCP, 18(7), 5080-5085
Open this publication in new window or tab >>Solid state p-type dye-sensitized solar cells: concept, experiment and mechanism
2016 (English)In: Physical Chemistry, Chemical Physics - PCCP, ISSN 1463-9076, E-ISSN 1463-9084, Vol. 18, no 7, p. 5080-5085Article in journal (Refereed) Published
Abstract [en]

Solid state p-type dye-sensitized solar cells (p-ssDSCs) have been proposed and fabricated for the first time, using the organic dye P1 as the sensitizer on mesoporous NiO and phenyl-C61-butyric acid methyl ester (PCBM) as the electron conductor. The p-ssDSC has shown an impressive open circuit photovoltage of 620 mV. Femtosecond and nanosecond transient absorption spectroscopy has given evidence for sub-ps hole injection from the excited P1 to NiO, followed by electron transfer from P1˙ to PCBM.

National Category
Physical Chemistry
Identifiers
urn:nbn:se:uu:diva-280843 (URN)10.1039/C5CP05247E (DOI)000370421500001 ()
Funder
Knut and Alice Wallenberg FoundationSwedish Energy Agency
Available from: 2016-03-15 Created: 2016-03-15 Last updated: 2017-11-30Bibliographically approved
Zhang, L., Favereau, L., Farre, Y., Mijangos, E., Pellegrin, Y., Blart, E., . . . Hammarström, L. (2016). Ultrafast and slow charge recombination dynamics of diketopyrrolopyrrole–NiO dye sensitized solar cells. Physical Chemistry, Chemical Physics - PCCP, 18, 18515-18527
Open this publication in new window or tab >>Ultrafast and slow charge recombination dynamics of diketopyrrolopyrrole–NiO dye sensitized solar cells
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2016 (English)In: Physical Chemistry, Chemical Physics - PCCP, ISSN 1463-9076, E-ISSN 1463-9084, Vol. 18, p. 18515-18527Article in journal (Refereed) Published
Abstract [en]

In a photophysical study, two diketopyrrolopyrrole (DPP)-based sensitizers functionalized with4-thiophenecarboxylic acid as an anchoring group and a bromo (DPPBr) or dicyanovinyl (DPPCN2)group, and a dyad consisting of a DPP unit linked to a naphthalenediimide group (DPP–NDI), wereinvestigated both in solution and grafted on mesoporous NiO films. Femtosecond transient absorptionmeasurements indicate that ultrafast hole injection occurred predominantly on a timescale of B200 fs,whereas the subsequent charge recombination occurred on a surprisingly wide range of timescales,from tens of ps to tens of ms; this kinetic heterogeneity is much greater than is typically observed fordye-sensitized TiO2 or ZnO. Also, in contrast to what is typically observed for dye-sensitized TiO2, therewas no significant dependence on the excitation power of the recombination kinetics, which can beexplained by the hole density being comparatively higher near the valence band of NiO beforeexcitation. The additional acceptor group in DPP–NDI provided a rapid electron shift and stabilizedcharge separation up to the ms timescale. This enabled efficient (B95%) regeneration of NDI bya CoIII(dtb)3 electrolyte (dtb = 4,40-di-tert-butyl-2,20-bipyridine), according to transient absorptionmeasurements. The regeneration of DPPBr and DPPCN2 by CoIII(dtb)3 was instead inefficient, as mostrecombination for these dyes occurred on the sub-ns timescale. The transient spectroscopy data thuscorroborated the trend of the published photovoltaic properties of dye-sensitized solar cells (DSSCs)based on these dyes on mesoporous NiO, and show the potential of a design strategy with a secondaryacceptor bound to the dye. The study identifies rapid initial recombination between the dye and NiO asthe main obstacle to obtaining high efficiencies in NiO-based DSSCs; these recombination componentsmay be overlooked when studies are conducted using only methods with ns resolution or slower.

Keywords
Ultrafast, pDSSCs, Charge recombination
National Category
Physical Chemistry
Research subject
Chemistry with specialization in Physical Chemistry
Identifiers
urn:nbn:se:uu:diva-300147 (URN)10.1039/c6cp01762b (DOI)000379486200081 ()27338174 (PubMedID)
Funder
Swedish Energy AgencyKnut and Alice Wallenberg Foundation
Available from: 2016-08-03 Created: 2016-08-03 Last updated: 2017-11-28Bibliographically approved
Warnan, J., Pellegrin, Y., Blart, E., Zhang, L., Brown, A., Hammarström, L., . . . Odobel, F. (2014). Acetylacetone anchoring group for NiO-based dye-sensitized solar cell. Dyes and pigments, 105, 174-179
Open this publication in new window or tab >>Acetylacetone anchoring group for NiO-based dye-sensitized solar cell
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2014 (English)In: Dyes and pigments, ISSN 0143-7208, E-ISSN 1873-3743, Vol. 105, p. 174-179Article in journal (Refereed) Published
Abstract [en]

In this article, the viability of the first push pull (nitrophenyl and hexyl-thiophene as acceptor and donor unit respectively) sensitizer functionalized with acetylacetone (acac) anchoring group was assessed for application in p-type dye sensitized solar cells (Ni0-based). An effective synthetic strategy to introduce the acac directly to an aryl moiety was developed. Then, the UV visible absorption, emission and electrochemical properties of this new sensitizer were determined. FT-IR spectroscopy revealed an effective binding of the acac group to NiO surface while time-dependent density functional theory (TDDFT) calculations predicted a strong charge-transfer transition with no component of the LUMO centred on the acac. Ultrafast hole injection (<200 fs) from the dye excited state into the valence band (VB) of NiO was experimentally demonstrated by transient absorption spectroscopy studies. It was also shown that excitation of the sensitizer leads to the formation of a twisted intramolecular charge transfer (TICT) state. Finally, the photovoltaic performances of this dye were investigated in NiO based solar cells using the iodide/triiodide electrolyte. We measured promising power conversion efficiencies higher than that of the coumarin 043 benchmark reference albeit with a weaker light harvesting efficiency.

Keywords
Photovoltaic, p-Type semiconductor, Photoinduced hole injection, Photoelectrochemistry, Surface coating, Time dependent density functional theory
National Category
Chemical Engineering
Identifiers
urn:nbn:se:uu:diva-225504 (URN)10.1016/j.dyepig.2014.01.026 (DOI)000335111600024 ()
Available from: 2014-06-24 Created: 2014-06-04 Last updated: 2017-12-05Bibliographically approved
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