TY - JOUR
T1 - Designing High Interfacial Conduction beyond Bulk via Engineering the Semiconductor-Ionic Heterostructure CeO2-δ/BaZr0.8Y0.2O3for Superior Proton Conductive Fuel Cell and Water Electrolysis Applications
AU - Xing, Yueming
AU - Zhu, Bin
AU - Hong, Liang
AU - Xia, Chen
AU - Wang, Baoyuan
AU - Wu, Yan
AU - Cai, Hongdong
AU - Rauf, Sajid
AU - Huang, Jianbing
AU - Asghar, Muhammad Imran
AU - Yang, Yang
AU - Lin, Wen Feng
N1 - Publisher Copyright:
© 2022 American Chemical Society. All rights reserved.
PY - 2022/12/26
Y1 - 2022/12/26
N2 - Proton ceramic fuel cells (PCFCs) are an emerging clean energy technology; however, a key challenge persists in improving the electrolyte proton conductivity, e.g., around 10-3-10-2S cm-1at 600 °C for the well-known BaZr0.8Y0.2O3(BZY), that is far below the required 0.1 S cm-1. Herein, we report an approach for tuning BZY from low bulk to high interfacial conduction by introducing a semiconductor CeO2-δforming a semiconductor-ionic heterostructure CeO2-δ/BZY. The interfacial conduction was identified by a significantly higher conductivity obtained from the BZY grain boundary than that of the bulk and a further improvement from the CeO2-δ/BZY which achieved a remarkably high proton conductivity of 0.23 S cm-1. This enabled a high peak power of 845 mW cm-2at 520 °C from a PCFC using the CeO2-δ/BZY as the electrolyte, in strong contrast to the BZY bulk conduction electrolyte with only 229 mW cm-2. Furthermore, the CeO2-δ/BZY fuel cell was operated under water electrolysis mode, exhibiting a very high current density output of 3.2 A cm-2corresponding to a high H2production rate, under 2.0 V at 520 °C. The band structure and a built-in-field-assisted proton transport mechanism have been proposed and explained. This work demonstrates an efficient way of tuning the electrolyte from low bulk to high interfacial proton conduction to attain sufficient conductivity required for PCFCs, electrolyzers, and other advanced electrochemical energy technologies.
AB - Proton ceramic fuel cells (PCFCs) are an emerging clean energy technology; however, a key challenge persists in improving the electrolyte proton conductivity, e.g., around 10-3-10-2S cm-1at 600 °C for the well-known BaZr0.8Y0.2O3(BZY), that is far below the required 0.1 S cm-1. Herein, we report an approach for tuning BZY from low bulk to high interfacial conduction by introducing a semiconductor CeO2-δforming a semiconductor-ionic heterostructure CeO2-δ/BZY. The interfacial conduction was identified by a significantly higher conductivity obtained from the BZY grain boundary than that of the bulk and a further improvement from the CeO2-δ/BZY which achieved a remarkably high proton conductivity of 0.23 S cm-1. This enabled a high peak power of 845 mW cm-2at 520 °C from a PCFC using the CeO2-δ/BZY as the electrolyte, in strong contrast to the BZY bulk conduction electrolyte with only 229 mW cm-2. Furthermore, the CeO2-δ/BZY fuel cell was operated under water electrolysis mode, exhibiting a very high current density output of 3.2 A cm-2corresponding to a high H2production rate, under 2.0 V at 520 °C. The band structure and a built-in-field-assisted proton transport mechanism have been proposed and explained. This work demonstrates an efficient way of tuning the electrolyte from low bulk to high interfacial proton conduction to attain sufficient conductivity required for PCFCs, electrolyzers, and other advanced electrochemical energy technologies.
KW - ceramic proton-conducting electrolyte
KW - interface engineering
KW - proton ceramic fuel cells
KW - semiconductor-ionic heterostructure
KW - solid oxide water electrolysis cell
UR - https://www.scopus.com/pages/publications/85144483012
U2 - 10.1021/acsaem.2c02995
DO - 10.1021/acsaem.2c02995
M3 - 文章
AN - SCOPUS:85144483012
SN - 2574-0962
VL - 5
SP - 15373
EP - 15384
JO - ACS Applied Energy Materials
JF - ACS Applied Energy Materials
IS - 12
ER -