Muhammad Usman , Munzir H. Suliman , Maryam Abdinejad , Jesse Kok , Hussain Al Naji , Aasif Helal , Zain H. Yamani , Gabriele Centi
{"title":"在ZIF-8支架内使用铋纳米点进行高效CO2电还原生成甲酸","authors":"Muhammad Usman , Munzir H. Suliman , Maryam Abdinejad , Jesse Kok , Hussain Al Naji , Aasif Helal , Zain H. Yamani , Gabriele Centi","doi":"10.1016/j.ccst.2025.100450","DOIUrl":null,"url":null,"abstract":"<div><div>Zeolitic imidazolate frameworks (ZIFs) based electrocatalysts for CO<sub>2</sub> reduction offer unique possibilities for developing advanced materials for this reaction due to their ordered nanoporosity and pore environments, tunable characteristics and high affinity for CO<sub>2</sub>. Still, they were not investigated sufficiently. In this study, we developed a Bismuth nanodots embedded Zeolitic Imidazolate Framework-8 (BND-ZIF-8) electrocatalyst via a one-pot synthesis method for the electrochemical CO₂ reduction reaction (eCO₂RR). Comprehensive spectroscopic and electrochemical characterization confirmed the successful integration of Bismuth into the ZIF-8 matrix. The electrocatalytic performance of the BND-ZIF-8 was assessed in multiple reactor typologies such as H-cell, flow cell, and membrane electrode assembly (MEA) setups. Remarkable differences in the performances in the three cell configurations are evidenced. Notably, the MEA configuration exhibited a marked enhancement in formate selectivity, achieving a Faradic efficiency (FE) of up to 91 % at a current density of −150 mA cm<sup>‒</sup>². This work underscores the potential of Bi-ZIF-8 in advancing eCO₂RR while remarking on the crucial importance of the appropriate type of electrocatalytic experiments in assessing the material performance.</div></div>","PeriodicalId":9387,"journal":{"name":"Carbon Capture Science & Technology","volume":"16 ","pages":"Article 100450"},"PeriodicalIF":0.0000,"publicationDate":"2025-05-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Highly efficient CO2 electroreduction to formate using Bismuth nanodots within ZIF-8 scaffold\",\"authors\":\"Muhammad Usman , Munzir H. Suliman , Maryam Abdinejad , Jesse Kok , Hussain Al Naji , Aasif Helal , Zain H. Yamani , Gabriele Centi\",\"doi\":\"10.1016/j.ccst.2025.100450\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Zeolitic imidazolate frameworks (ZIFs) based electrocatalysts for CO<sub>2</sub> reduction offer unique possibilities for developing advanced materials for this reaction due to their ordered nanoporosity and pore environments, tunable characteristics and high affinity for CO<sub>2</sub>. Still, they were not investigated sufficiently. In this study, we developed a Bismuth nanodots embedded Zeolitic Imidazolate Framework-8 (BND-ZIF-8) electrocatalyst via a one-pot synthesis method for the electrochemical CO₂ reduction reaction (eCO₂RR). Comprehensive spectroscopic and electrochemical characterization confirmed the successful integration of Bismuth into the ZIF-8 matrix. The electrocatalytic performance of the BND-ZIF-8 was assessed in multiple reactor typologies such as H-cell, flow cell, and membrane electrode assembly (MEA) setups. Remarkable differences in the performances in the three cell configurations are evidenced. Notably, the MEA configuration exhibited a marked enhancement in formate selectivity, achieving a Faradic efficiency (FE) of up to 91 % at a current density of −150 mA cm<sup>‒</sup>². This work underscores the potential of Bi-ZIF-8 in advancing eCO₂RR while remarking on the crucial importance of the appropriate type of electrocatalytic experiments in assessing the material performance.</div></div>\",\"PeriodicalId\":9387,\"journal\":{\"name\":\"Carbon Capture Science & Technology\",\"volume\":\"16 \",\"pages\":\"Article 100450\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-05-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Carbon Capture Science & Technology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2772656825000892\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Carbon Capture Science & Technology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2772656825000892","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
基于沸石咪唑盐框架(ZIFs)的二氧化碳还原电催化剂由于其有序的纳米孔隙和孔环境、可调的特性和对二氧化碳的高亲和力,为开发用于该反应的先进材料提供了独特的可能性。然而,他们没有得到充分的调查。本研究采用一锅法制备了铋纳米点包埋咪唑酸分子筛骨架-8 (BND-ZIF-8)电催化剂,用于电化学CO₂还原反应(eCO₂RR)。综合光谱和电化学表征证实铋成功集成到ZIF-8基体中。BND-ZIF-8的电催化性能在多种反应器类型(如H-cell、flow cell和膜电极组件(MEA)设置)中进行了评估。三种电池配置的性能差异显著。值得注意的是,MEA结构显示出甲酸选择性的显著增强,在电流密度为- 150 mA cm -²时,达到高达91%的法拉迪效率(FE)。这项工作强调了Bi-ZIF-8在推进eCO₂RR方面的潜力,同时指出了适当类型的电催化实验在评估材料性能方面的重要性。
Highly efficient CO2 electroreduction to formate using Bismuth nanodots within ZIF-8 scaffold
Zeolitic imidazolate frameworks (ZIFs) based electrocatalysts for CO2 reduction offer unique possibilities for developing advanced materials for this reaction due to their ordered nanoporosity and pore environments, tunable characteristics and high affinity for CO2. Still, they were not investigated sufficiently. In this study, we developed a Bismuth nanodots embedded Zeolitic Imidazolate Framework-8 (BND-ZIF-8) electrocatalyst via a one-pot synthesis method for the electrochemical CO₂ reduction reaction (eCO₂RR). Comprehensive spectroscopic and electrochemical characterization confirmed the successful integration of Bismuth into the ZIF-8 matrix. The electrocatalytic performance of the BND-ZIF-8 was assessed in multiple reactor typologies such as H-cell, flow cell, and membrane electrode assembly (MEA) setups. Remarkable differences in the performances in the three cell configurations are evidenced. Notably, the MEA configuration exhibited a marked enhancement in formate selectivity, achieving a Faradic efficiency (FE) of up to 91 % at a current density of −150 mA cm‒². This work underscores the potential of Bi-ZIF-8 in advancing eCO₂RR while remarking on the crucial importance of the appropriate type of electrocatalytic experiments in assessing the material performance.