Tandem Catalysis Driven by Nitrogen Spillover in a Core–Shell Heterostructure for Direct Ammonia Fuel Cells
Source abstract
Abstract
ABSTRACT Low‐temperature direct ammonia fuel cells (DAFCs) are promising yet challenged by slow ammonia oxidation reaction (AOR) kinetics and severe catalyst poisoning. To address such bottlenecks, we design a vertically aligned NiCo 2 O 4 @NiCo 2 S 4 core–shell heterostructure where the NiCo 2 S 4 shell stands for NH 3 activization and the NiCo 2 O 4 core serves for N 2 generation. The built‐in electric field at the heterointerface, together with the bimetallic synergy introduced by Ni doping, enables the optimization of electron configuration via work function engineering. Driven by the adsorption energy gradient across heterointerface, the efficient *N spillover promotes the regeneration of NH 3 adsorption sites and facilitates the efficient desorption of N 2 , leading to a refined tandem catalytic pathway of NH 3 ‐*N‐N 2 . Consequently, NiCo 2 O 4 @NiCo 2 S 4 achieves a high current density of 972 mA cm −2 at 80 °C in a three‐electrode system and delivers 20‐h stability, offering a novel strategy for high‐performance, poison‐tolerant AOR anodes.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Ammonia Synthesis and Nitrogen Reduction · Electrocatalysts for Energy Conversion · Advancements in Solid Oxide Fuel Cells
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Key Laboratory of Superlight Materials and Surface Technology of Ministry of Education College of Materials Science and Chemical Engineering Harbin Engineering University Harbin China
School of Mechanical and Aerospace Engineering Nanyang Technological University Singapore Singapore
Y2, 2nd Floor, Building 2 Xixi Legu Creative Pioneering Park Hangzhou Zhejiang China
Funding
Heilongjiang Postdoctoral Science Foundation · Fundamental Research Funds for the Central Universities
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