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Atomic–Level Interfacial Regulation Enables Efficient Chlorine Redox Chemistry in Rechargeable H 2 ─Cl 2 Batteries
Yingnan Cao and Zhenzhen Wang contributed equally to this work. Conflicts of Interest The authors declare no conflicts of interest. Data Availability Statement The data that support the findings of this study are available from the corresponding author upon reasonable request. Supporting Information Filename Description anie73737-sup-0001-SuppMat.docx19.3 MB Supporting File: anie73737-sup-0001-SuppMat.docx.
Immobilization of Single Ni Sites and Separated Pd Clusters in Covalent Organic Framework for Enhanced Electrochemical Reduction of Nitrite to Ammonia Click to copy article link Article link copied!
Abstract Click to copy section linkSection link copied! The electrochemical reduction of nitrite (NO2–) to ammonia (NH3) offers a promising strategy for simultaneously purifying wastewater and producing value-added chemicals. The metal active site struggles to simultaneously optimize the adsorption strengths of NO2– and H*, resulting in a mismatch between the kinetics of intermediate activation and hydrogenation.
Conjugated C≡C Linked Organic Polymers With Thiadiazole-Induced Electron-Ion Decoupling Toward Long-Life Lithium Metal Anode
1 Introduction Lithium-metal batteries (LMBs) dominate the consumer market including electric vehicles and portable devices, primarily due to their substantially higher theoretical capacity when compared to conventional lithium-ion batteries [1]. This characteristic offers enormous potential for applications in large-scale energy storage scenarios, significantly enhancing their range and efficiency [2-4].
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