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The key aspect of the photoelectrochemical CO reduction reaction (PEC CO RR) lies in designing cathode materials that can generate high-energy photoelectrons, enabling the activation and conversion of CO into high-value products. In this study, a coaxially wrapped ZnO@ZnSe array heterostructure was synthesized using a simple anion exchange strategy and metallic Bi nanoparticles (NPs) were subsequently deposited on the surface to construct a Bi/ZnO@ZnSe photocathode with high CO conversion capability. This array photocathode possesses a large aspect ratio, which simultaneously satisfies a low charge carrier migration path and a large specific surface area that facilitates mass transfer. Additionally, the barrier formed at the n-n heterojunction interface hinders the transfer of high-energy photoelectrons from ZnSe to lower energy levels, resulting in their rapid capture by Bi while maintaining a relatively long lifetime. These captured electrons act as active sites, efficiently converting CO into CO with a Faradaic efficiency above 88.9 % at -0.9 V vs. RHE and demonstrating superior stability. This work provides a novel approach for synthesizing high-energy photoelectrode materials with long lifetimes.
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http://dx.doi.org/10.1002/cssc.202401436 | DOI Listing |
Chem Soc Rev
September 2025
Beijing Key Laboratory of Photoelectronic/Electrophotonic Conversion Materials, Key Laboratory of Cluster Science, Ministry of Education, Advanced Technology Research Institute (Jinan), Frontiers Science Center for High Energy Material, School of Chemistry and Chemical Engineering, Beijing Institute
Proton exchange membrane fuel cells (PEMFCs) represent a promising clean and efficient energy conversion technology. Enhancing the efficiency of the oxygen reduction reaction (ORR) at the cathode is crucial for improving overall cell performance. Beyond the intrinsic activity of the catalyst, mass transport at the oxygen-water-catalyst three-phase boundary (TPB) in the catalyst layers (CLs) significantly influences ORR kinetics.
View Article and Find Full Text PDFNanomicro Lett
September 2025
Guangdong Provincial Key Laboratory of New Energy Materials Service Safety, College of Materials Science and Engineering, Shenzhen University, Shenzhen, 518060, People's Republic of China.
Chloride-based solid electrolytes are considered promising candidates for next-generation high-energy-density all-solid-state batteries (ASSBs). However, their relatively low oxidative decomposition threshold (~ 4.2 V vs.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
Frontiers Science Center for High Energy Material, Key Laboratory of Cluster Science, Ministry of Education, Beijing Key Laboratory of Photoelectronic/Electrophotonic Conversion Materials, School of Interdisciplinary Science, School of Chemistry and Chemical Engineering, Beijing Institute of Technol
Hydrogen peroxide (HO) is a green oxidant widely used in a variety of industries. Photocatalytic generation of HO from water and oxygen by sunlight is an appealing strategy compared to the high energy consumption of the industrial anthraquinone process. However, the low activity and selectivity of the two-step single-electron oxygen reduction reaction (ORR) during the photocatalytic process greatly restricts the HO production efficiency.
View Article and Find Full Text PDFSmall
September 2025
University of Münster, Institute of Organic Chemistry, Corrensstr. 36, 48149, Münster, Germany.
The development of next-generation Lithium-ion batteries (LIBs) to meet the demands of advancing technology and energy storage requires focus on the formation of effective interphases on both the positive and negative electrodes. Different promising approaches to facilitate effective interphase formation are already known Out of these, the incorporation of film-forming electrolyte additives is a straight-forward strategy to achieve this goal. In the presented study, a bifunctional electrolyte additive, (5-methyl-2-oxo-1,3-dioxol-4-yl)methyl thiophene-3-carboxylate composed of two functional motifs, vinylene carbonate (VC) and thiophene, is reported.
View Article and Find Full Text PDFJ Colloid Interface Sci
August 2025
State Key Laboratory of Advanced Fiber Materials, College of Materials Science and Engineering, Donghua University, Shanghai 201620, China. Electronic address:
Lithium-ion batteries incorporating Si-based anodes and nickel-rich LiNiCoMnO (NCM) cathodes offer exceptional energy density compared to conventional systems. However, they still suffer from two critical challenges: irreversible lithium loss at the anode and interfacial degradation at the cathode. To simultaneously resolve both issues, we propose a bifunctional prelithiation strategy using a novel LiAlO (LAO) material, which has remained unexplored due to sluggish delithiation kinetics and poorly understood lithium extraction mechanisms.
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