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Zinc metal, as the mainstream anode material of aqueous batteries, faces severe side reactions and notorious dendrite growth. Surface passivation of Zn anodes with a protective layer is one of the effective strategies to address these issues. The previous reports have focused on applying different components as surface layers while neglecting the impact of their crystallographic orientation on electrochemical performance. Here, a ZIF-8 layer is prepared as a model to elucidate this effect on the Zn anode. DFT calculations indicate that ZIF-8(200), compared to ZIF-8(110) and ZIF-8(211), exhibits a lower d-band center, a smaller difference in d-p band centers, and a weaker HO adsorption, thereby inhibiting hydrogen evolution as confirmed by experimental results. Meanwhile, ZIF-8(200) also increases the interfacial interaction between ZIF-8 and Zn, enhances the mechanical properties, and suppresses the dendrite growth. The small pores of ZIF-8 restrict the migration of SO -, I-, and VO , thus enabling the selective transport of Zn. Thus, the preferential orientation of ZIF-8(200) significantly improves the electrochemical performance of the Zn anodes. These results demonstrate a new way to improve the electrochemical performance of Zn anodes through crystal engineering of surface layers.
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http://dx.doi.org/10.1002/anie.202509952 | DOI Listing |
ACS Sens
September 2025
METU MEMS Center, Ankara 06530, Türkiye.
Cardiovascular diseases (CVDs) remain a leading cause of death, particularly in developing countries, where their incidence continues to rise. Traditional CVD diagnostic methods are often time-consuming and inconvenient, necessitating more efficient alternatives. Rapid and accurate measurement of cardiac biomarkers released into body fluids is critical for early detection, timely intervention, and improved patient outcomes.
View Article and Find Full Text PDFAnal Chem
September 2025
Jiangsu Key Laboratory for Molecular and Medical Biotechnology, College of Life Sciences, Nanjing Normal University, Nanjing 210023, P. R. China.
Electroactive bacteria (EAB) hold great promise for the development of electrochemical biosensors given their unique ability to transfer electrons extracellularly via specialized pathways, a process termed extracellular electron transfer (EET). Ongoing research aims to overcome current limitations and fully harness the potential of EABs for high-performance biosensing applications. Herein, we report the fabrication of an electrochemical microsensor based on biomineralized electroactive bacteria, specifically MR-1.
View Article and Find Full Text PDFDalton Trans
September 2025
Department of Chemistry, University of Zululand, Private Bag X1001, KwaDlangezwa 3880, South Africa.
To overcome the potential issue of active site blockage by surfactants in colloidal synthesis, alternative synthetic approaches must be explored. In this study, we investigated both solvent-free and colloidal thermolysis routes to synthesize nickel sulfides (NiS and NiS) using sulfur-based Ni complexes, [Ni(SCO(CH))] (Ni-Xan) and [Ni(SCN(CH))] (Ni-DTC) as precursors. The solvent-free decomposition of these complexes produced ligand-free NiS and NiS in the absence or presence of triphenylphosphine (TPP), respectively.
View Article and Find Full Text PDFSmall
September 2025
School of Chemistry and Chemical Engineering, Key Lab of Fuel Cell Technology of Guangdong Province, South China University of Technology, Guangzhou, 510641, China.
Aggregation-induced electrochemiluminescence (AIECL) is a promising strategy for enhancing electrochemiluminescence (ECL) efficiency by minimizing energy loss of excited-state ECL emitters. However, rational design of high-efficiency AIECL emitters is hindered by limited mechanistic understanding and an unclear structure-performance relationship. To address this, four supramolecular coordination frameworks (SCFs) with varying π-bridge structures are synthesized using pyridine-functionalized tetraphenylethene (TPE) as the ligand and Pt(II) as the coordination center.
View Article and Find Full Text PDFSmall
September 2025
School of Mechanical Engineering, Yonsei University, 50, Yonsei-ro, Seodaemun-gu, Seoul, 03722, Republic of Korea.
Core-shell electrodes provide a potential and innovative approach for significantly enhancing the performance and capacity of supercapacitors (SCs) by combining two distinct materials. The capabilities of these advanced electrodes surpass those of conventional single electrodes. Specifically, these exhibit better energy storage, higher power density, and improved overall performance.
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