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Fan, Lizhou
Publications (5 of 5) Show all publications
Guo, Y., Yao, Z., Timmer, B. J. J., Sheng, X., Fan, L., Li, Y., . . . Sun, L. (2019). Boosting nitrogen reduction reaction by bio-inspired FeMoS containing hybrid electrocatalyst over a wide pH range. Nano Energy, 62, 282-288
Open this publication in new window or tab >>Boosting nitrogen reduction reaction by bio-inspired FeMoS containing hybrid electrocatalyst over a wide pH range
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2019 (English)In: Nano Energy, ISSN 2211-2855, E-ISSN 2211-3282, Vol. 62, p. 282-288Article in journal (Refereed) Published
Abstract [en]

A facile preparation of bio-inspired and morphology controllable catalytic electrode FeS@MoS2/CFC, featuring a carbon fiber cloth (CFC) covered with FeS dotted MoS2 nanosheets, has been established. Synergy between the CFC as a self-standing conductive substrate and the FeS nanoparticle dotted MoS2 nanosheets with abundant active sites makes the noble-metal-free catalytic electrode FeS@MoS2/CFC highly efficient in nitrogen reduction reaction (NRR), with an ammonia production rate of 8.45 mu g h(-1) cm(-2) and excellent long-term stability at -0.5 V in pH neutral electrolyte. Further electrolysis in acidic and alkaline electrolytes revealed the overall NRR catalytic activity of this electrode over a wide pH range.

Place, publisher, year, edition, pages
Elsevier, 2019
Keywords
FeS nanoparticles, MoS2 nanosheets, Nitrogen reduction reaction, Bioinspired catalysts
National Category
Chemical Sciences
Identifiers
urn:nbn:se:kth:diva-255360 (URN)10.1016/j.nanoen.2019.05.051 (DOI)000474636100033 ()2-s2.0-85065865579 (Scopus ID)
Note

QC 20190731

Available from: 2019-07-31 Created: 2019-07-31 Last updated: 2019-07-31Bibliographically approved
Zhang, P., Sheng, X., Chen, X., Fang, Z., Jiang, J., Wang, M., . . . Sun, L. (2019). Paired Electrocatalytic Oxygenation and Hydrogenation of Organic Substrates with Water as the Oxygen and Hydrogen Source. Angewandte Chemie International Edition, 58(27), 9155-9159
Open this publication in new window or tab >>Paired Electrocatalytic Oxygenation and Hydrogenation of Organic Substrates with Water as the Oxygen and Hydrogen Source
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2019 (English)In: Angewandte Chemie International Edition, ISSN 1433-7851, E-ISSN 1521-3773, Vol. 58, no 27, p. 9155-9159Article in journal (Refereed) Published
Abstract [en]

The use of water as an oxygen and hydrogen source for the paired oxygenation and hydrogenation of organic substrates to produce valuable chemicals is of utmost importance as a means of establishing green chemical syntheses. Inspired by the active Ni3+ intermediates involved in electro-catalytic water oxidation by nickel-based materials, we prepared NiBx as a catalyst and used water as the oxygen source for the oxygenation of various organic compounds. NiBx was further employed as both an anode and a cathode in a paired electrosynthesis cell for the respective oxygenation and hydrogenation of organic compounds, with water as both the oxygen and hydrogen source. Conversion efficiency and selectivity of >= 99% were observed during the oxygenation of 5-hydroxy-methylfurfural to 2,5-furandicarboxylic acid and the simultaneous hydrogenation of p-nitrophenol to p-aminophenol. This paired electrosynthesis cell has also been coupled to a solar cell as a stand-alone reactor in response to sunlight.

Place, publisher, year, edition, pages
Wiley-VCH Verlagsgesellschaft, 2019
Keywords
electrochemistry, green chemical synthesis, hydrogenation, oxygenation, water
National Category
Chemical Sciences
Identifiers
urn:nbn:se:kth:diva-255764 (URN)10.1002/anie.201903936 (DOI)000476691200033 ()31025774 (PubMedID)2-s2.0-85066906976 (Scopus ID)
Note

QC 20190816

Available from: 2019-08-16 Created: 2019-08-16 Last updated: 2019-08-16Bibliographically approved
Fan, L., Zhang, P., Zhang, B., Daniel, Q., Timmer, B., Zhang, F. & Sun, L. (2018). 3D Core-Shell NiFeCr Catalyst on a Cu Nanoarray for Water Oxidation: Synergy between Structural and Electronic Modulation. ACS ENERGY LETTERS, 3(12), 2865-2874
Open this publication in new window or tab >>3D Core-Shell NiFeCr Catalyst on a Cu Nanoarray for Water Oxidation: Synergy between Structural and Electronic Modulation
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2018 (English)In: ACS ENERGY LETTERS, ISSN 2380-8195, Vol. 3, no 12, p. 2865-2874Article in journal (Refereed) Published
Abstract [en]

Low cost transition metal-based electrocatalysts for water oxidation and understanding their structure-activity relationship are greatly desired for clean and sustainable chemical fuel production. Herein, a core-shell (CS) NiFeCr metal/metal hydroxide catalyst was fabricated on a 3D Cu nanoarray by a simple electrodeposition-activation method. A synergistic promotion effect between electronic structure modulation and nanostructure regulation was presented on a CS-NiFeCr oxygen evolution reaction (OER) catalyst: the 3D nanoarchitecture facilitates the mass transport process, the in situ formed interface metal/metal hydroxide heterojunction accelerates the electron transfer, and the electronic structure modulation by Cr incorporation improves the reaction kinetics. Benefiting from the synergy between structural and electronic modulation, the catalyst shows excellent activity toward water oxidation under alkaline conditions: overpotential of 200 mV at 10 mA/cm(2) current density and Tafel slope of 28 mV/dec. This work opens up a new window for understanding the structure-activity relationship of OER catalysts and encourages new strategies for development of more advanced OER catalysts.

Place, publisher, year, edition, pages
AMER CHEMICAL SOC, 2018
National Category
Chemical Sciences
Identifiers
urn:nbn:se:kth:diva-241005 (URN)10.1021/acsenergylett.8b01897 (DOI)000453805100003 ()2-s2.0-85056263175 (Scopus ID)
Note

QC 20190109

Available from: 2019-01-09 Created: 2019-01-09 Last updated: 2019-08-20Bibliographically approved
Zhang, P., Li, L., Nordlund, D., Chen, H., Fan, L., Zhang, B., . . . Sun, L. (2018). Dendritic core-shell nickel-iron-copper metal/metal oxide electrode for efficient electrocatalytic water oxidation. Nature Communications, 9(1), Article ID 381.
Open this publication in new window or tab >>Dendritic core-shell nickel-iron-copper metal/metal oxide electrode for efficient electrocatalytic water oxidation
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2018 (English)In: Nature Communications, ISSN 2041-1723, E-ISSN 2041-1723, Vol. 9, no 1, article id 381Article in journal (Refereed) Published
Abstract [en]

Electrochemical water splitting requires efficient water oxidation catalysts to accelerate the sluggish kinetics of water oxidation reaction. Here, we report a promisingly dendritic core-shell nickel-iron-copper metal/metal oxide electrode, prepared via dealloying with an electrodeposited nickel-iron-copper alloy as a precursor, as the catalyst for water oxidation. The as-prepared core-shell nickel-iron-copper electrode is characterized with porous oxide shells and metallic cores. This tri-metal-based core-shell nickel-iron-copper electrode exhibits a remarkable activity toward water oxidation in alkaline medium with an overpotential of only 180 mV at a current density of 10 mA cm-2. The core-shell NiFeCu electrode exhibits pH-dependent oxygen evolution reaction activity on the reversible hydrogen electrode scale, suggesting that non-concerted proton-electron transfers participate in catalyzing the oxygen evolution reaction. To the best of our knowledge, the as-fabricated core-shell nickel-iron-copper is one of the most promising oxygen evolution catalysts.

Place, publisher, year, edition, pages
Nature Publishing Group, 2018
National Category
Other Chemistry Topics
Identifiers
urn:nbn:se:kth:diva-222290 (URN)10.1038/s41467-017-02429-9 (DOI)2-s2.0-85041107994 (Scopus ID)
Note

QC 20180206

Available from: 2018-02-06 Created: 2018-02-06 Last updated: 2018-02-06Bibliographically approved
Zhang, B., Li, Y., Valvo, M., Fan, L., Daniel, Q., Zhang, P., . . . Sun, L. (2017). Electrocatalytic Water Oxidation Promoted by 3 D Nanoarchitectured Turbostratic Δ-MnOx on Carbon Nanotubes. ChemSusChem, 10(22), 4472-4478
Open this publication in new window or tab >>Electrocatalytic Water Oxidation Promoted by 3 D Nanoarchitectured Turbostratic Δ-MnOx on Carbon Nanotubes
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2017 (English)In: ChemSusChem, ISSN 1864-5631, E-ISSN 1864-564X, Vol. 10, no 22, p. 4472-4478Article in journal (Refereed) Published
Abstract [en]

The development of manganese-based water oxidation electrocatalysts is desirable for the production of solar fuels, as manganese is earth-abundant, inexpensive, non-toxic, and has been employed by the Photosystem II in nature for a billion years. Herein, we directly constructed a 3 D nanoarchitectured turbostratic δ-MnOx on carbon nanotube-modified nickel foam (MnOx/CNT/NF) by electrodeposition and a subsequent annealing process. The MnOx/CNT/NF electrode gives a benchmark catalytic current density (10 mA cm−2) at an overpotential (η) of 270 mV under alkaline conditions. A steady current density of 19 mA cm−2 is obtained during electrolysis at 1.53 V for 1.0 h. To the best of our knowledge, this work represents the most efficient manganese-oxide-based water oxidation electrode and demonstrates that manganese oxides, as a structural and functional model of oxygen-evolving complex (OEC) in Photosystem II, can also become comparable to those of most Ni- and Co-based catalysts.

Place, publisher, year, edition, pages
Wiley-VCH Verlag, 2017
Keywords
artificial photosynthesis, electrochemistry, manganese, turbostratic manganese oxide, water oxidation, Carbon, Carbon nanotubes, Electrocatalysts, Electrodes, Foams, Nanotubes, Nickel, Oxidation, Oxides, Yarn, Alkaline conditions, Annealing process, Catalytic current, Co-based catalysts, Oxygen-evolving complexes, Turbostratic, Manganese oxide, carbon nanotube, manganese derivative, oxide, water, catalysis, chemistry, electrochemical analysis, electrode, molecular mimicry, oxidation reduction reaction, photosystem II, procedures, solar energy, Electrochemical Techniques, Manganese Compounds, Nanotubes, Carbon, Oxidation-Reduction, Photosystem II Protein Complex
National Category
Other Chemistry Topics
Identifiers
urn:nbn:se:kth:diva-227139 (URN)10.1002/cssc.201700824 (DOI)000416158500023 ()28675680 (PubMedID)2-s2.0-85035013364 (Scopus ID)
Note

QC 20180503

Available from: 2018-05-03 Created: 2018-05-03 Last updated: 2019-02-07Bibliographically approved
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