Yanbin Zhu, Xiaoju Yang, Yan Wei, Peize Li, Shujie Liu, Muqin Wang, Xuan Yang, Yongqing Fu, Yan Shen, Mingkui Wang
{"title":"硅质沸石中纳米晶簇In2Cu3O6的高效CO2甲烷化","authors":"Yanbin Zhu, Xiaoju Yang, Yan Wei, Peize Li, Shujie Liu, Muqin Wang, Xuan Yang, Yongqing Fu, Yan Shen, Mingkui Wang","doi":"10.1021/acscatal.4c07480","DOIUrl":null,"url":null,"abstract":"This work reports CO<sub>2</sub> methanation with high Faraday efficiency and production selectivity on In<sub>2</sub>Cu<sub>3</sub>O<sub>6</sub> nanoclusters encapsulated in siliceous MFI zeolite (In<sub>2</sub>Cu<sub>3</sub>O<sub>6</sub>@zeolite) by modulating the pH and buffering capacity of electrolytes. Using an aqueous electrolyte of KHCO<sub>3</sub> and K<sub>2</sub>CO<sub>3</sub> saturated with CO<sub>2</sub>, the In<sub>2</sub>Cu<sub>3</sub>O<sub>6</sub>@zeolite electrode achieves a superior electrocatalytic Faraday efficiency of 74.1% for CO<sub>2</sub> methanation and a retention rate of ∼90% after a 40 h long stability test. This represents one of the highest Faraday efficiency values for CO<sub>2</sub> methanation. In situ spectroscopic characterization of intermediates shows that the high selectivity for methanation in aqueous electrolytes is due to the enriched protonation and associated pH buffering effect enabled by the encapsulation of In<sub>2</sub>Cu<sub>3</sub>O<sub>6</sub> nanoclusters in MFI zeolite channels. When such an In<sub>2</sub>Cu<sub>3</sub>O<sub>6</sub>@zeolite catalyst is used as the cathode of an aprotic Li-CO<sub>2</sub> battery, a high full-discharge capacity of 28,992 mAh g<sup>–1</sup> at 100 mA g<sup>–1</sup> and excellent cycling performance over 200 cycles at 400 mA g<sup>–1</sup> can be achieved.","PeriodicalId":9,"journal":{"name":"ACS Catalysis ","volume":"79 1","pages":""},"PeriodicalIF":13.1000,"publicationDate":"2025-02-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"In2Cu3O6 Nanocluster in Siliceous Zeolite for Efficient CO2 Methanation\",\"authors\":\"Yanbin Zhu, Xiaoju Yang, Yan Wei, Peize Li, Shujie Liu, Muqin Wang, Xuan Yang, Yongqing Fu, Yan Shen, Mingkui Wang\",\"doi\":\"10.1021/acscatal.4c07480\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"This work reports CO<sub>2</sub> methanation with high Faraday efficiency and production selectivity on In<sub>2</sub>Cu<sub>3</sub>O<sub>6</sub> nanoclusters encapsulated in siliceous MFI zeolite (In<sub>2</sub>Cu<sub>3</sub>O<sub>6</sub>@zeolite) by modulating the pH and buffering capacity of electrolytes. Using an aqueous electrolyte of KHCO<sub>3</sub> and K<sub>2</sub>CO<sub>3</sub> saturated with CO<sub>2</sub>, the In<sub>2</sub>Cu<sub>3</sub>O<sub>6</sub>@zeolite electrode achieves a superior electrocatalytic Faraday efficiency of 74.1% for CO<sub>2</sub> methanation and a retention rate of ∼90% after a 40 h long stability test. This represents one of the highest Faraday efficiency values for CO<sub>2</sub> methanation. In situ spectroscopic characterization of intermediates shows that the high selectivity for methanation in aqueous electrolytes is due to the enriched protonation and associated pH buffering effect enabled by the encapsulation of In<sub>2</sub>Cu<sub>3</sub>O<sub>6</sub> nanoclusters in MFI zeolite channels. When such an In<sub>2</sub>Cu<sub>3</sub>O<sub>6</sub>@zeolite catalyst is used as the cathode of an aprotic Li-CO<sub>2</sub> battery, a high full-discharge capacity of 28,992 mAh g<sup>–1</sup> at 100 mA g<sup>–1</sup> and excellent cycling performance over 200 cycles at 400 mA g<sup>–1</sup> can be achieved.\",\"PeriodicalId\":9,\"journal\":{\"name\":\"ACS Catalysis \",\"volume\":\"79 1\",\"pages\":\"\"},\"PeriodicalIF\":13.1000,\"publicationDate\":\"2025-02-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Catalysis \",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1021/acscatal.4c07480\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Catalysis ","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acscatal.4c07480","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
摘要
这项工作报道了通过调节pH值和电解质的缓冲能力,在硅质MFI沸石(In2Cu3O6@zeolite)中封装的In2Cu3O6纳米团簇上具有高法拉第效率和生产选择性的CO2甲烷化。使用饱和CO2的KHCO3和K2CO3水溶液电解质,In2Cu3O6@zeolite电极在40 h的稳定性测试后,实现了CO2甲烷化的良好电催化法拉第效率(74.1%)和保持率(~ 90%)。这代表了二氧化碳甲烷化的最高法拉第效率值之一。中间体的原位光谱表征表明,水溶液中甲烷化的高选择性是由于在MFI沸石通道中包封In2Cu3O6纳米团簇可以增强质子化和相关的pH缓冲作用。当这种In2Cu3O6@zeolite催化剂用作非质子锂-二氧化碳电池的阴极时,在100 mA g-1下可达到28,992 mAh g-1的高全放电容量,在400 mA g-1下可达到200次以上的优异循环性能。
In2Cu3O6 Nanocluster in Siliceous Zeolite for Efficient CO2 Methanation
This work reports CO2 methanation with high Faraday efficiency and production selectivity on In2Cu3O6 nanoclusters encapsulated in siliceous MFI zeolite (In2Cu3O6@zeolite) by modulating the pH and buffering capacity of electrolytes. Using an aqueous electrolyte of KHCO3 and K2CO3 saturated with CO2, the In2Cu3O6@zeolite electrode achieves a superior electrocatalytic Faraday efficiency of 74.1% for CO2 methanation and a retention rate of ∼90% after a 40 h long stability test. This represents one of the highest Faraday efficiency values for CO2 methanation. In situ spectroscopic characterization of intermediates shows that the high selectivity for methanation in aqueous electrolytes is due to the enriched protonation and associated pH buffering effect enabled by the encapsulation of In2Cu3O6 nanoclusters in MFI zeolite channels. When such an In2Cu3O6@zeolite catalyst is used as the cathode of an aprotic Li-CO2 battery, a high full-discharge capacity of 28,992 mAh g–1 at 100 mA g–1 and excellent cycling performance over 200 cycles at 400 mA g–1 can be achieved.
期刊介绍:
ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels.
The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.