TY - JOUR
T1 - A strategy to promote the ORR electrocatalytic activity by the novel engineering bunched three-dimensional Pd-Cu alloy aerogel
AU - Wu, Xiaodong
AU - Ni, Chunsheng
AU - Man, Jianwei
AU - Shen, Xiaodong
AU - Cui, Sheng
AU - Chen, Xiangbao
N1 - Publisher Copyright:
© 2022 Elsevier B.V.
PY - 2023/2/15
Y1 - 2023/2/15
N2 - Pd has been considered as a potential substitution of the Pt-based electrocatalyst for oxygen reduction reaction (ORR) in the fields of fuel cells, however, the binding strength between the bare surface and the intermediates is much stronger than that on Pt, leading to its inferior ORR activity. Alloying noble metals with nonprecious metals provides a cost-effective strategy for electrocatalyst design. In this work, we have demonstrated a novel Pd3Cu aerogel electrocatalyst derived from a mild reduction agent via the self-assembly and freeze-drying technique. The resulting catalyst shows a typical three-dimensional and “pearl-like” aerogel structure. Combining the structural features and optimized chemical compositions, the Pd3Cu aerogel exhibits remarkable pH-independent performance over the commercial Pt/C electrocatalyst. Notably, the optimized Pd3Cu aerogel displays excellent ORR activity with a half-wave potential of 0.90 V vs RHE, with a limiting current density of 5.8 mA/cm2 under the alkaline conditions, which is among the best of the reported noble metal-based ORR electrocatalysts. In addition, the resulting Pd3Cu aerogel delivers excellent hydrogen evolution reaction (HER) and ethanol oxidation reaction (EOR) performance. Furthermore, the density functional theory (DFT) calculations reveal that the unique partially oxidized Pd3Cu aerogel has led to a shift-down of the d-band center of the active sites, which energetically optimizes the binding strength of the adsorbed O intermediate during the ORR process, therefore accelerating the ORR activity. These findings provide a new pathway for the integrated engineering of geometric and electronic structures of metal alloys to improve their electrocatalytic property.
AB - Pd has been considered as a potential substitution of the Pt-based electrocatalyst for oxygen reduction reaction (ORR) in the fields of fuel cells, however, the binding strength between the bare surface and the intermediates is much stronger than that on Pt, leading to its inferior ORR activity. Alloying noble metals with nonprecious metals provides a cost-effective strategy for electrocatalyst design. In this work, we have demonstrated a novel Pd3Cu aerogel electrocatalyst derived from a mild reduction agent via the self-assembly and freeze-drying technique. The resulting catalyst shows a typical three-dimensional and “pearl-like” aerogel structure. Combining the structural features and optimized chemical compositions, the Pd3Cu aerogel exhibits remarkable pH-independent performance over the commercial Pt/C electrocatalyst. Notably, the optimized Pd3Cu aerogel displays excellent ORR activity with a half-wave potential of 0.90 V vs RHE, with a limiting current density of 5.8 mA/cm2 under the alkaline conditions, which is among the best of the reported noble metal-based ORR electrocatalysts. In addition, the resulting Pd3Cu aerogel delivers excellent hydrogen evolution reaction (HER) and ethanol oxidation reaction (EOR) performance. Furthermore, the density functional theory (DFT) calculations reveal that the unique partially oxidized Pd3Cu aerogel has led to a shift-down of the d-band center of the active sites, which energetically optimizes the binding strength of the adsorbed O intermediate during the ORR process, therefore accelerating the ORR activity. These findings provide a new pathway for the integrated engineering of geometric and electronic structures of metal alloys to improve their electrocatalytic property.
KW - Aerogel
KW - Alloy
KW - D-band center
KW - Electrocatalyst
KW - Oxygen reduction reaction
UR - http://www.scopus.com/inward/record.url?scp=85143820879&partnerID=8YFLogxK
U2 - 10.1016/j.cej.2022.140293
DO - 10.1016/j.cej.2022.140293
M3 - 文章
AN - SCOPUS:85143820879
SN - 1385-8947
VL - 454
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
M1 - 140293
ER -