Activity and durability of Pt-Ni nanocage electocatalysts in proton exchange membrane fuel cells

[Display omitted] •Pt-Ni nanocages were investigated as catalysts for PEM fuel cells.•Pt-Ni nanocages showed higher ex-situ and in-situ ORR activity than commercial Pt/C.•Pt-Ni nanocages were highly stable in the ORR environment, not prone to dissolution.•Pt-Ni nanocage stability and activity were b...

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Veröffentlicht in:Applied catalysis. B, Environmental Environmental, 2017-04, Vol.203 (C), p.927-935
Hauptverfasser: Peng, Xiong, Zhao, Shuai, Omasta, Travis J., Roller, Justin M., Mustain, William E.
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container_end_page 935
container_issue C
container_start_page 927
container_title Applied catalysis. B, Environmental
container_volume 203
creator Peng, Xiong
Zhao, Shuai
Omasta, Travis J.
Roller, Justin M.
Mustain, William E.
description [Display omitted] •Pt-Ni nanocages were investigated as catalysts for PEM fuel cells.•Pt-Ni nanocages showed higher ex-situ and in-situ ORR activity than commercial Pt/C.•Pt-Ni nanocages were highly stable in the ORR environment, not prone to dissolution.•Pt-Ni nanocage stability and activity were both significantly superior to Pt/C. A Ni-rich Pt-Ni alloy was synthesized via a solvothermal method and transformed into platinum-nickel nanocage catalysts (PNCs) by applying a two-phase corrosion process. The catalysts were physically and electrochemically characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM) and both cyclic and linear sweep voltammetry using a rotating disk electrode (RDE). During the RDE testing, the half-wave potential of the PNC was 30mV higher compared to that of a commercial Pt/C catalyst for the oxygen reduction reaction (ORR). The RDE experiments showed that the specific and mass activity of the PNC was 2 and 4 times greater than Pt/C, respectively, at 0.9V. Catalyst-coated membranes (CCMs) were fabricated with the Pt-Ni nanocages using an automated air-assisted cylindrical liquid jet sprayer system. The PNC CCMs were loaded into proton exchange membrane fuel cells (PEMFC) for activity and stability testing. The CCMs showed no obvious Pt and Ni dissolution and redeposition in the membrane even after 30K cycles. The performance and electrochemically active surface area (ECSA) retention of the PNC was far superior to commercial Pt/C, just short of the US Department of Energy (DOE) 2020 targets, suggesting that Pt-alloy nanocages are very promising candidates for high-performing commercial PEMFCs.
doi_str_mv 10.1016/j.apcatb.2016.10.081
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A Ni-rich Pt-Ni alloy was synthesized via a solvothermal method and transformed into platinum-nickel nanocage catalysts (PNCs) by applying a two-phase corrosion process. The catalysts were physically and electrochemically characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM) and both cyclic and linear sweep voltammetry using a rotating disk electrode (RDE). During the RDE testing, the half-wave potential of the PNC was 30mV higher compared to that of a commercial Pt/C catalyst for the oxygen reduction reaction (ORR). The RDE experiments showed that the specific and mass activity of the PNC was 2 and 4 times greater than Pt/C, respectively, at 0.9V. Catalyst-coated membranes (CCMs) were fabricated with the Pt-Ni nanocages using an automated air-assisted cylindrical liquid jet sprayer system. The PNC CCMs were loaded into proton exchange membrane fuel cells (PEMFC) for activity and stability testing. The CCMs showed no obvious Pt and Ni dissolution and redeposition in the membrane even after 30K cycles. The performance and electrochemically active surface area (ECSA) retention of the PNC was far superior to commercial Pt/C, just short of the US Department of Energy (DOE) 2020 targets, suggesting that Pt-alloy nanocages are very promising candidates for high-performing commercial PEMFCs.</description><identifier>ISSN: 0926-3373</identifier><identifier>EISSN: 1873-3883</identifier><identifier>DOI: 10.1016/j.apcatb.2016.10.081</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Catalysts ; Chemical synthesis ; Corrosion ; Diffraction ; Dissolution ; Durability ; Electron microscopy ; Energy policy ; Federal agencies ; Fuel cells ; Fuel technology ; High performance ; Membranes ; Nanocage ; Nanostructure ; Nickel ; Nickel base alloys ; Oxygen reduction ; PEM fuel cell ; Phase (cyclic) ; Photoelectron spectroscopy ; Platinum ; Platinum base alloys ; Proton exchange membrane fuel cells ; Rotating disks ; Spectroscopy ; Spectrum analysis ; Sprays ; Stability ; Studies ; Transmission electron microscopy ; X ray photoelectron spectroscopy ; X-ray diffraction</subject><ispartof>Applied catalysis. 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B, Environmental</title><description>[Display omitted] •Pt-Ni nanocages were investigated as catalysts for PEM fuel cells.•Pt-Ni nanocages showed higher ex-situ and in-situ ORR activity than commercial Pt/C.•Pt-Ni nanocages were highly stable in the ORR environment, not prone to dissolution.•Pt-Ni nanocage stability and activity were both significantly superior to Pt/C. A Ni-rich Pt-Ni alloy was synthesized via a solvothermal method and transformed into platinum-nickel nanocage catalysts (PNCs) by applying a two-phase corrosion process. The catalysts were physically and electrochemically characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM) and both cyclic and linear sweep voltammetry using a rotating disk electrode (RDE). During the RDE testing, the half-wave potential of the PNC was 30mV higher compared to that of a commercial Pt/C catalyst for the oxygen reduction reaction (ORR). The RDE experiments showed that the specific and mass activity of the PNC was 2 and 4 times greater than Pt/C, respectively, at 0.9V. Catalyst-coated membranes (CCMs) were fabricated with the Pt-Ni nanocages using an automated air-assisted cylindrical liquid jet sprayer system. The PNC CCMs were loaded into proton exchange membrane fuel cells (PEMFC) for activity and stability testing. The CCMs showed no obvious Pt and Ni dissolution and redeposition in the membrane even after 30K cycles. The performance and electrochemically active surface area (ECSA) retention of the PNC was far superior to commercial Pt/C, just short of the US Department of Energy (DOE) 2020 targets, suggesting that Pt-alloy nanocages are very promising candidates for high-performing commercial PEMFCs.</description><subject>Catalysts</subject><subject>Chemical synthesis</subject><subject>Corrosion</subject><subject>Diffraction</subject><subject>Dissolution</subject><subject>Durability</subject><subject>Electron microscopy</subject><subject>Energy policy</subject><subject>Federal agencies</subject><subject>Fuel cells</subject><subject>Fuel technology</subject><subject>High performance</subject><subject>Membranes</subject><subject>Nanocage</subject><subject>Nanostructure</subject><subject>Nickel</subject><subject>Nickel base alloys</subject><subject>Oxygen reduction</subject><subject>PEM fuel cell</subject><subject>Phase (cyclic)</subject><subject>Photoelectron spectroscopy</subject><subject>Platinum</subject><subject>Platinum base alloys</subject><subject>Proton exchange membrane fuel cells</subject><subject>Rotating disks</subject><subject>Spectroscopy</subject><subject>Spectrum analysis</subject><subject>Sprays</subject><subject>Stability</subject><subject>Studies</subject><subject>Transmission electron microscopy</subject><subject>X ray photoelectron spectroscopy</subject><subject>X-ray diffraction</subject><issn>0926-3373</issn><issn>1873-3883</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp9kE1P3DAQhi0EEgv0H_RglXO2_iCJfam0QtBWQm0PcDbOZNz1KmtvbS9i_30dpeee7Bk9M3rmJeQjZ2vOePd5t7YHsGVYi1rV1popfkZWXPWykUrJc7JiWnSNlL28JFc57xhjQgq1Iq8bKP7NlxO1YaTjMdnBT3MZHf1Vmh-eBhsi2N9IcUIo9VvsdMolUx_oIcUSA8V32NpQkT3uh2QDUnfEiQJOU74hF85OGT_8e6_Jy-PD8_235unn1-_3m6cGWs5KM6BmTtuxZ7LXTGsU0PW6BQvQ2XYcBz52TjplhWgHrllnBy0dsK7tW6eUltfk07I35uJNBl8QthBDqNKG33EumazQ7QJV8T9HzMXs4jGF6mW4loJrIZSo1N1CQYo5J3TmkPzeppPhzMyBm51ZAjdz4HO3Bl7HvixjWM9885hmCwyAo0-zxBj9_xf8Ba3ei2s</recordid><startdate>20170401</startdate><enddate>20170401</enddate><creator>Peng, Xiong</creator><creator>Zhao, Shuai</creator><creator>Omasta, Travis J.</creator><creator>Roller, Justin M.</creator><creator>Mustain, William E.</creator><general>Elsevier B.V</general><general>Elsevier BV</general><general>Elsevier</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7ST</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>JG9</scope><scope>KR7</scope><scope>L7M</scope><scope>SOI</scope><scope>OTOTI</scope></search><sort><creationdate>20170401</creationdate><title>Activity and durability of Pt-Ni nanocage electocatalysts in proton exchange membrane fuel cells</title><author>Peng, Xiong ; 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B, Environmental</jtitle><date>2017-04-01</date><risdate>2017</risdate><volume>203</volume><issue>C</issue><spage>927</spage><epage>935</epage><pages>927-935</pages><issn>0926-3373</issn><eissn>1873-3883</eissn><abstract>[Display omitted] •Pt-Ni nanocages were investigated as catalysts for PEM fuel cells.•Pt-Ni nanocages showed higher ex-situ and in-situ ORR activity than commercial Pt/C.•Pt-Ni nanocages were highly stable in the ORR environment, not prone to dissolution.•Pt-Ni nanocage stability and activity were both significantly superior to Pt/C. A Ni-rich Pt-Ni alloy was synthesized via a solvothermal method and transformed into platinum-nickel nanocage catalysts (PNCs) by applying a two-phase corrosion process. The catalysts were physically and electrochemically characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM) and both cyclic and linear sweep voltammetry using a rotating disk electrode (RDE). During the RDE testing, the half-wave potential of the PNC was 30mV higher compared to that of a commercial Pt/C catalyst for the oxygen reduction reaction (ORR). The RDE experiments showed that the specific and mass activity of the PNC was 2 and 4 times greater than Pt/C, respectively, at 0.9V. Catalyst-coated membranes (CCMs) were fabricated with the Pt-Ni nanocages using an automated air-assisted cylindrical liquid jet sprayer system. The PNC CCMs were loaded into proton exchange membrane fuel cells (PEMFC) for activity and stability testing. The CCMs showed no obvious Pt and Ni dissolution and redeposition in the membrane even after 30K cycles. The performance and electrochemically active surface area (ECSA) retention of the PNC was far superior to commercial Pt/C, just short of the US Department of Energy (DOE) 2020 targets, suggesting that Pt-alloy nanocages are very promising candidates for high-performing commercial PEMFCs.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><doi>10.1016/j.apcatb.2016.10.081</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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subjects Catalysts
Chemical synthesis
Corrosion
Diffraction
Dissolution
Durability
Electron microscopy
Energy policy
Federal agencies
Fuel cells
Fuel technology
High performance
Membranes
Nanocage
Nanostructure
Nickel
Nickel base alloys
Oxygen reduction
PEM fuel cell
Phase (cyclic)
Photoelectron spectroscopy
Platinum
Platinum base alloys
Proton exchange membrane fuel cells
Rotating disks
Spectroscopy
Spectrum analysis
Sprays
Stability
Studies
Transmission electron microscopy
X ray photoelectron spectroscopy
X-ray diffraction
title Activity and durability of Pt-Ni nanocage electocatalysts in proton exchange membrane fuel cells
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