Porosity and thickness effect of Pd–Cu–Si metallic glasses on electrocatalytic hydrogen production and storage
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in: Materials and Design, Jahrgang 210.2021, Nr. 15 November, 110099, 07.09.2021.
Publikationen: Beitrag in Fachzeitschrift › Artikel › Forschung › (peer-reviewed)
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TY - JOUR
T1 - Porosity and thickness effect of Pd–Cu–Si metallic glasses on electrocatalytic hydrogen production and storage
AU - Sarac, Baran
AU - Karazehir, Tolga
AU - Yüce, E.
AU - Mühlbacher, Marlene
AU - Sarac, A. Sezai
AU - Eckert, Jürgen
N1 - Publisher Copyright: © 2021 The Authors
PY - 2021/9/7
Y1 - 2021/9/7
N2 - This contribution places emphasis on tuning pore architecture and film thickness of mesoporous Pd–Cu–Si thin films sputtered on Si/SiO2 substrates for enhanced electrocatalytic and hydrogen sorption/desorption activity and their comparison with the state-of-the-art thin film electrocatalysts. Small Tafel slope of 43 mV dec–1 for 1250 nm thick coating on 2 µm diameter pores with 4.2 µm interspacing electrocatalyst with comparable hydrogen overpotentials to the literature suggests its use for standard fuel cells. The largest hydrogen sorption has been attained for the 250 nm thick electrocatalyst on 5 µm pore diameter with 12 µm interspacing (2189 µC cm−2 per CV cycle), making it possible for rapid storage systems. Moreover, the charge transfer resistance described by an equivalent circuit model has an excellent correlation with Tafel slopes. Along with its very low Tafel slope of 42 mV dec–1 10 nm thick electrocatalyst on 2 µm diameter pores with 4.2 µm interspacing has the highest capacitive response of ∼ 0.001 S sn cm−2 and is promising to be used as a nano-charger and hydrogen sensor. The findings of Si/SiO2 supported mesoporous Pd-based metallic glass (MG) assemblies suggest a similar design applicability for crystalline systems and other MG types.
AB - This contribution places emphasis on tuning pore architecture and film thickness of mesoporous Pd–Cu–Si thin films sputtered on Si/SiO2 substrates for enhanced electrocatalytic and hydrogen sorption/desorption activity and their comparison with the state-of-the-art thin film electrocatalysts. Small Tafel slope of 43 mV dec–1 for 1250 nm thick coating on 2 µm diameter pores with 4.2 µm interspacing electrocatalyst with comparable hydrogen overpotentials to the literature suggests its use for standard fuel cells. The largest hydrogen sorption has been attained for the 250 nm thick electrocatalyst on 5 µm pore diameter with 12 µm interspacing (2189 µC cm−2 per CV cycle), making it possible for rapid storage systems. Moreover, the charge transfer resistance described by an equivalent circuit model has an excellent correlation with Tafel slopes. Along with its very low Tafel slope of 42 mV dec–1 10 nm thick electrocatalyst on 2 µm diameter pores with 4.2 µm interspacing has the highest capacitive response of ∼ 0.001 S sn cm−2 and is promising to be used as a nano-charger and hydrogen sensor. The findings of Si/SiO2 supported mesoporous Pd-based metallic glass (MG) assemblies suggest a similar design applicability for crystalline systems and other MG types.
KW - Electrochemical circuit modeling
KW - Hydrogen evolution reaction
KW - Hydrogen storage
KW - Metallic glass
KW - Polarization
KW - Thin film
UR - http://www.scopus.com/inward/record.url?scp=85114794626&partnerID=8YFLogxK
U2 - 10.1016/j.matdes.2021.110099
DO - 10.1016/j.matdes.2021.110099
M3 - Article
AN - SCOPUS:85114794626
VL - 210.2021
JO - Materials and Design
JF - Materials and Design
SN - 0264-1275
IS - 15 November
M1 - 110099
ER -