Search for: All records

This review revisits critical descriptors to assess the performance of Zn–air batteries. The recent progress of inorganic nanoporous metal films as self-standing air electrodesfor Zn–air batteries is systematically summarized and analyzed. 

Abstract Direct ethanol fuel cells have been widely investigated as nontoxic and low-corrosive energy conversion devices with high energy and power densities. It is still challenging to develop high-activity and durable catalysts for a complete ethanol oxidation reaction on the anode and accelerated oxygen reduction reaction on the cathode. The materials’ physics and chemistry at the catalytic interface play a vital role in determining the overall performance of the catalysts. Herein, we propose a Pd/Co@N-C catalyst that can be used as a model system to study the synergism and engineering at the solid-solid interface. Particularly, the transformation of amorphous carbon to highly graphitic carbon promoted by cobalt nanoparticles helps achieve the spatial confinement effect, which prevents structural degradation of the catalysts. The strong catalyst-support and electronic effects at the interface between palladium and Co@N-C endow the electron-deficient state of palladium, which enhances the electron transfer and improved activity/durability. The Pd/Co@N-C delivers a maximum power density of 438 mW cm −2 in direct ethanol fuel cells and can be operated stably for more than 1000 hours. This work presents a strategy for the ingenious catalyst structural design that will promote the development of fuel cells and other sustainable energy-related technologies. 

Employing the strong metal-support interaction (SMSI) effect for promoting the catalyst's activity toward the oxygen reduction reaction (ORR) is promising due to the electronic structure optimization and high utilization efficiency of platinum group metal (PGM) catalysts. Metal oxides as alternative supports for PGMs facilitate intrinsic activity and improve durability as compared to conventional carbon supports. However, the restricted mass and electron transfer at the metal/support interface need to be addressed. Herein, to strengthen the interaction at the metal/support interfaces and improve the utilization efficiency of PGM, an ultralow loading of Pd was embedded in a surface-oxygenated PdNiMnO porous film. The Mn-doping was designed to promote surface oxygenation using a facile anodization process that created sufficiently exposed interfaces between Pd and the support, strengthening the SMSI effects at the Pd/oxygenated support interface for enhancing ORR performance. Furthermore, the Ni-containing oxygenated catalyst served as both the active component for the oxygen evolution reaction (OER) and the functional support for stabilizing Pd, making PdNiMnO a bifunctional catalyst for zinc–air flow batteries (ZAFB). As a proof-of-concept, the ZAFB (PdNiMnO) shows a maximal power density of 211.6 mW cm −2 and outstanding cycling stability for over 2000 h with a minimal voltage gap of 0.69 V at a current density of 10 mA cm −2 , superior to the state-of-the-art catalysts. 

Abstract Oxygen reduction reaction (ORR) is an electrochemical reaction in which dissolved oxygen in an electrolyte is reduced to OH⁻/H₂O when receiving electrons. This reaction plays a crucial role in shaping the efficiency of both metal–air batteries and fuel cells, and precious metals are the dominant catalysts carrying out the ORR in their cathodes. However, how to manipulate the electronic structure of precious metals as active sites to further promote ORR performance and maximize the utilization rate is still under development. Metal oxide serves as suitable and promising support that can strongly interact with precious metals for both activity and durability enhancement. Herein, we present recent research updates on strong precious metal–metal oxide interaction (SPMMOI) utilized in ORR. We start by introducing the background of ORR, the issues to be solved, and its practical applications followed by a thorough discussion of the reaction mechanism and comprehensive evaluation protocols of performance. We then provide a complete understanding of the working principle of SPMMOI and highlight the related advances. Finally, we summarize the merits of the precious metal–metal oxide system and propose the research direction as well as some urgent problems to be addressed in the future. 

Rechargeable zinc–air batteries (ZABs) show enticing prospects as next‐generation energy conversion and storage technology due to their unique merits of environmental friendliness, low cost, impressive energy density, and high security. However, the dendrite growth, surface passivation, and metal anode corrosion, as well as the sluggish reaction kinetics, deficient bifunctionality, high platinum group metals (PGMs) dependence, and corrosion of carbon‐based materials for air cathodes, are the main problems hindering the large‐scale application of ZABs. Herein, the fundamental principles of ZABs are first introduced. The detailed discussions will be focused on the electrochemical aspects of the metal anode and air cathode by making a comprehensive comparison of the recent progress in the field. Lastly, brief perspectives on the further development of rechargeable ZABs are introduced. This review aims to provide a better understanding of electrode design for ZABs, which will provide guidelines for the design and fabrication of high‐performance and cost‐effective ZABs.