TY - JOUR
T1 - Insights into the Proton-Coupled Electron Transfer Mechanism in Fuel Cells
AU - Anwar, Muhammad Faisal
AU - Yu, Yong
AU - Rasool, Shahzad
AU - Akbar, Nabeela
AU - Huang, Jianbing
AU - Singh, Manish
AU - Gupta, Priyanka
AU - Wan, Shuo
AU - Huang, Qiu An
AU - Yang, Fan
AU - Khalid, Muhammad
AU - Raza, Rizwan
AU - Wang, Jun
AU - Lu, Yuzheng
AU - Yun, Sining
AU - Zhu, Bin
N1 - Publisher Copyright:
© 2025 American Chemical Society.
PY - 2025/3/26
Y1 - 2025/3/26
N2 - Proton-coupled electron transfer (PCET) is not only an important fundamental process in energy systems but also a pivotal factor in enhancing electrocatalytic functions in fuel cells (FCs). This article investigates the PCET mechanism in low-temperature (300-500 °C) protonic ceramic fuel cells, focusing on its role in catalyzing the hydrogen oxidation reaction and the oxygen reduction reaction. Our findings reveal that PCET significantly enhances the electrocatalytic activity by mitigating polarization losses, reducing charge-transfer resistance by 1 to 2 orders of magnitude, and thereby accelerating the reaction kinetics compared to scenarios without PCET. Importantly, changes in relaxation time upon proton injection evidence the robustness of PCET. The marked reduction in activation energy to 0.31 eV further illustrates how PCET overcomes energy barriers, facilitating more efficient reaction pathways. These insights highlight the critical role of PCET in optimizing the electrocatalytic performance of FCs, underscoring its significant importance in advancing FC technology.
AB - Proton-coupled electron transfer (PCET) is not only an important fundamental process in energy systems but also a pivotal factor in enhancing electrocatalytic functions in fuel cells (FCs). This article investigates the PCET mechanism in low-temperature (300-500 °C) protonic ceramic fuel cells, focusing on its role in catalyzing the hydrogen oxidation reaction and the oxygen reduction reaction. Our findings reveal that PCET significantly enhances the electrocatalytic activity by mitigating polarization losses, reducing charge-transfer resistance by 1 to 2 orders of magnitude, and thereby accelerating the reaction kinetics compared to scenarios without PCET. Importantly, changes in relaxation time upon proton injection evidence the robustness of PCET. The marked reduction in activation energy to 0.31 eV further illustrates how PCET overcomes energy barriers, facilitating more efficient reaction pathways. These insights highlight the critical role of PCET in optimizing the electrocatalytic performance of FCs, underscoring its significant importance in advancing FC technology.
KW - electrocatalyst
KW - electrochemical proton injection
KW - hydrogen oxidation reaction
KW - oxygen reduction reaction
KW - proton ceramic fuel cell
KW - proton-coupled electron transfer
UR - https://www.scopus.com/pages/publications/105001487889
U2 - 10.1021/acsami.5c00203
DO - 10.1021/acsami.5c00203
M3 - 文章
C2 - 40096473
AN - SCOPUS:105001487889
SN - 1944-8244
VL - 17
SP - 18371
EP - 18382
JO - ACS Applied Materials and Interfaces
JF - ACS Applied Materials and Interfaces
IS - 12
ER -