Low-loading IrO2 supported on Pt for catalysis of PEM water electrolysis and regenerative fuel cells

[Display omitted] •IrO2 supported on Pt having a hemispheric core-shell structure was constructed to be used as OER and HOR electrode for URFC.•Significant performance, 7.1 A cm−2 at 2.0 Vcell, was achieved in PEMWE with only 0.16 mgIr cm−2 including a stability demonstrated for 220 h.•49% of round...

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Veröffentlicht in:Applied catalysis. B, Environmental Environmental, 2020-09, Vol.272, p.118955, Article 118955
Hauptverfasser: Lim, Ahyoun, Kim, Junyoung, Lee, Hye Jin, Kim, Hyoung-Juhn, Yoo, Sung Jong, Jang, Jong Hyun, Young Park, Hee, Sung, Yung-Eun, Park, Hyun S.
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container_start_page 118955
container_title Applied catalysis. B, Environmental
container_volume 272
creator Lim, Ahyoun
Kim, Junyoung
Lee, Hye Jin
Kim, Hyoung-Juhn
Yoo, Sung Jong
Jang, Jong Hyun
Young Park, Hee
Sung, Yung-Eun
Park, Hyun S.
description [Display omitted] •IrO2 supported on Pt having a hemispheric core-shell structure was constructed to be used as OER and HOR electrode for URFC.•Significant performance, 7.1 A cm−2 at 2.0 Vcell, was achieved in PEMWE with only 0.16 mgIr cm−2 including a stability demonstrated for 220 h.•49% of round trip efficiency at 0.4 A cm−2 was achieved in PEM-URFC with 0.83 mg(Pt+Ir) cm−2 of total noble catalysts. A unitized regenerative fuel cell (URFC), an electrochemical device operated in both water electrolysis (WE) and fuel cell (FC) modes, is a promising technology in interconverting renewable electricity and chemical fuels within a compact system. However, Proton-exchange membrane-based URFCs usually employ a significant amount of precious metal catalysts, e.g., up to 4 mg(Pt+IrO2) cm−2, to achieve high efficiency in round-trip operations. Here, we present a PEM-URFC electrode that uses only 0.8 mg(Pt+Ir) cm−2 without compromising the performance of URFC. IrO2-shells (70 nm) layered upon hemispherical Pt particles (Pt@IrO2) are formed using sequential electrodeposition over Ti-felt electrodes. A 100 % improvement in WE compared to performance without Pt supports and superior mass activity (44 A mgIr−1 at 2 Vcell) with an insignificant degradation rate of 155 μV h−1 at 0.4 A cm−2 are demonstrated. In addition, high round-trip efficiency of 49 % at 0.4 A cm−2 in URFC is achieved.
doi_str_mv 10.1016/j.apcatb.2020.118955
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A unitized regenerative fuel cell (URFC), an electrochemical device operated in both water electrolysis (WE) and fuel cell (FC) modes, is a promising technology in interconverting renewable electricity and chemical fuels within a compact system. However, Proton-exchange membrane-based URFCs usually employ a significant amount of precious metal catalysts, e.g., up to 4 mg(Pt+IrO2) cm−2, to achieve high efficiency in round-trip operations. Here, we present a PEM-URFC electrode that uses only 0.8 mg(Pt+Ir) cm−2 without compromising the performance of URFC. IrO2-shells (70 nm) layered upon hemispherical Pt particles (Pt@IrO2) are formed using sequential electrodeposition over Ti-felt electrodes. A 100 % improvement in WE compared to performance without Pt supports and superior mass activity (44 A mgIr−1 at 2 Vcell) with an insignificant degradation rate of 155 μV h−1 at 0.4 A cm−2 are demonstrated. In addition, high round-trip efficiency of 49 % at 0.4 A cm−2 in URFC is achieved.</description><identifier>ISSN: 0926-3373</identifier><identifier>EISSN: 1873-3883</identifier><identifier>DOI: 10.1016/j.apcatb.2020.118955</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Catalysis ; Catalysts ; Chemical fuels ; Electrochemistry ; Electrodeposition ; Electrodes ; Electrolysis ; Electrolytic cells ; Fuel cells ; Fuel technology ; Iridium ; Oxygen evolution catalysts ; Proton exchange membrane water electrolysis ; Regenerative fuel cells ; Titanium ; Unitized regenerative fuel cell</subject><ispartof>Applied catalysis. 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B, Environmental</title><description>[Display omitted] •IrO2 supported on Pt having a hemispheric core-shell structure was constructed to be used as OER and HOR electrode for URFC.•Significant performance, 7.1 A cm−2 at 2.0 Vcell, was achieved in PEMWE with only 0.16 mgIr cm−2 including a stability demonstrated for 220 h.•49% of round trip efficiency at 0.4 A cm−2 was achieved in PEM-URFC with 0.83 mg(Pt+Ir) cm−2 of total noble catalysts. A unitized regenerative fuel cell (URFC), an electrochemical device operated in both water electrolysis (WE) and fuel cell (FC) modes, is a promising technology in interconverting renewable electricity and chemical fuels within a compact system. However, Proton-exchange membrane-based URFCs usually employ a significant amount of precious metal catalysts, e.g., up to 4 mg(Pt+IrO2) cm−2, to achieve high efficiency in round-trip operations. Here, we present a PEM-URFC electrode that uses only 0.8 mg(Pt+Ir) cm−2 without compromising the performance of URFC. IrO2-shells (70 nm) layered upon hemispherical Pt particles (Pt@IrO2) are formed using sequential electrodeposition over Ti-felt electrodes. A 100 % improvement in WE compared to performance without Pt supports and superior mass activity (44 A mgIr−1 at 2 Vcell) with an insignificant degradation rate of 155 μV h−1 at 0.4 A cm−2 are demonstrated. 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B, Environmental</jtitle><date>2020-09-05</date><risdate>2020</risdate><volume>272</volume><spage>118955</spage><pages>118955-</pages><artnum>118955</artnum><issn>0926-3373</issn><eissn>1873-3883</eissn><abstract>[Display omitted] •IrO2 supported on Pt having a hemispheric core-shell structure was constructed to be used as OER and HOR electrode for URFC.•Significant performance, 7.1 A cm−2 at 2.0 Vcell, was achieved in PEMWE with only 0.16 mgIr cm−2 including a stability demonstrated for 220 h.•49% of round trip efficiency at 0.4 A cm−2 was achieved in PEM-URFC with 0.83 mg(Pt+Ir) cm−2 of total noble catalysts. A unitized regenerative fuel cell (URFC), an electrochemical device operated in both water electrolysis (WE) and fuel cell (FC) modes, is a promising technology in interconverting renewable electricity and chemical fuels within a compact system. However, Proton-exchange membrane-based URFCs usually employ a significant amount of precious metal catalysts, e.g., up to 4 mg(Pt+IrO2) cm−2, to achieve high efficiency in round-trip operations. Here, we present a PEM-URFC electrode that uses only 0.8 mg(Pt+Ir) cm−2 without compromising the performance of URFC. IrO2-shells (70 nm) layered upon hemispherical Pt particles (Pt@IrO2) are formed using sequential electrodeposition over Ti-felt electrodes. A 100 % improvement in WE compared to performance without Pt supports and superior mass activity (44 A mgIr−1 at 2 Vcell) with an insignificant degradation rate of 155 μV h−1 at 0.4 A cm−2 are demonstrated. In addition, high round-trip efficiency of 49 % at 0.4 A cm−2 in URFC is achieved.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><doi>10.1016/j.apcatb.2020.118955</doi><orcidid>https://orcid.org/0000-0003-0238-5971</orcidid><orcidid>https://orcid.org/0000-0002-7960-9729</orcidid><orcidid>https://orcid.org/0000-0001-8558-9368</orcidid><orcidid>https://orcid.org/0000-0002-1563-8328</orcidid></addata></record>
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source ScienceDirect Journals (5 years ago - present)
subjects Catalysis
Catalysts
Chemical fuels
Electrochemistry
Electrodeposition
Electrodes
Electrolysis
Electrolytic cells
Fuel cells
Fuel technology
Iridium
Oxygen evolution catalysts
Proton exchange membrane water electrolysis
Regenerative fuel cells
Titanium
Unitized regenerative fuel cell
title Low-loading IrO2 supported on Pt for catalysis of PEM water electrolysis and regenerative fuel cells
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