{"title":"具有高合金化度的超细钯金纳米线用于将甲烷直接氧化为 C1 氧化合物","authors":"Linhui Tan, Yi Shi, Yueshan Xu, Xue Zhang, Daoxiong Wu, Zhitong Wang, Juanxiu Xiao, Huan Wen, Jing Li, Xinlong Tian, Peilin Deng","doi":"10.1002/cjoc.202400591","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>The direct oxidation of methane (CH<sub>4</sub>) into high-valued C1 oxygenates production has garnered increased attention in effectively using vast CH<sub>4</sub> and alleviating the global energy crisis. However, due to the high cleavage energy of C—H bond and low polarity of CH<sub>4</sub> molecule, it is difficult to activate the first C—H bond. Furthermore, C1 oxygenates are readily inclined to be oxidized to CO<sub>2</sub>, because their weaker C—H bond comparing with CH<sub>4</sub> molecule, resulting in poor selectivity. Herein, we designed ultrathin Pd<sub><i>x</i></sub>Au<sub><i>y</i></sub> alloy NWs supported on ZSM-5 (Z-5) to investigate the direct oxidation of CH<sub>4</sub> to high value-added oxygenate under mild conditions. By precisely adjusting the molar ratio of Pd/Au and alloying degree, Pd<sub>9</sub>Au<sub>1</sub>NWs/Z-5 showed an excellent yield of 11.57 mmol·g<sup>–l</sup>·h<sup>–1</sup> and the outstanding selectivity of 95.1% for C1 oxygenates (CH<sub>3</sub>OH, CH<sub>3</sub>OOH and HCOOH). The <i>in-situ</i> spectroscopic and mechanism analysis proved that the enhanced catalytic performance of Pd<sub>9</sub>Au<sub>1</sub>NWs/Z-5 was ascribed to the stable one-dimensional nanostructure and the strong synergy effect with high alloying PdAu, which could increase the adsorption capacity of CH<sub>4</sub> molecules on Pd atoms to promote the CH<sub>4</sub> conversion. This work offers valuable insights into the design concept of high-efficient catalysts and the structure-activity relationship for the direct oxidation of CH<sub>4</sub>.</p>\n <p>\n </p>\n </div>","PeriodicalId":151,"journal":{"name":"Chinese Journal of Chemistry","volume":"42 23","pages":"2999-3005"},"PeriodicalIF":5.5000,"publicationDate":"2024-08-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Ultrathin PdAu Nanowires with High Alloying Degree for the Direct Oxidation of Methane to C1 Oxygenates\",\"authors\":\"Linhui Tan, Yi Shi, Yueshan Xu, Xue Zhang, Daoxiong Wu, Zhitong Wang, Juanxiu Xiao, Huan Wen, Jing Li, Xinlong Tian, Peilin Deng\",\"doi\":\"10.1002/cjoc.202400591\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n <p>The direct oxidation of methane (CH<sub>4</sub>) into high-valued C1 oxygenates production has garnered increased attention in effectively using vast CH<sub>4</sub> and alleviating the global energy crisis. However, due to the high cleavage energy of C—H bond and low polarity of CH<sub>4</sub> molecule, it is difficult to activate the first C—H bond. Furthermore, C1 oxygenates are readily inclined to be oxidized to CO<sub>2</sub>, because their weaker C—H bond comparing with CH<sub>4</sub> molecule, resulting in poor selectivity. Herein, we designed ultrathin Pd<sub><i>x</i></sub>Au<sub><i>y</i></sub> alloy NWs supported on ZSM-5 (Z-5) to investigate the direct oxidation of CH<sub>4</sub> to high value-added oxygenate under mild conditions. By precisely adjusting the molar ratio of Pd/Au and alloying degree, Pd<sub>9</sub>Au<sub>1</sub>NWs/Z-5 showed an excellent yield of 11.57 mmol·g<sup>–l</sup>·h<sup>–1</sup> and the outstanding selectivity of 95.1% for C1 oxygenates (CH<sub>3</sub>OH, CH<sub>3</sub>OOH and HCOOH). The <i>in-situ</i> spectroscopic and mechanism analysis proved that the enhanced catalytic performance of Pd<sub>9</sub>Au<sub>1</sub>NWs/Z-5 was ascribed to the stable one-dimensional nanostructure and the strong synergy effect with high alloying PdAu, which could increase the adsorption capacity of CH<sub>4</sub> molecules on Pd atoms to promote the CH<sub>4</sub> conversion. This work offers valuable insights into the design concept of high-efficient catalysts and the structure-activity relationship for the direct oxidation of CH<sub>4</sub>.</p>\\n <p>\\n </p>\\n </div>\",\"PeriodicalId\":151,\"journal\":{\"name\":\"Chinese Journal of Chemistry\",\"volume\":\"42 23\",\"pages\":\"2999-3005\"},\"PeriodicalIF\":5.5000,\"publicationDate\":\"2024-08-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chinese Journal of Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/cjoc.202400591\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chinese Journal of Chemistry","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cjoc.202400591","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Ultrathin PdAu Nanowires with High Alloying Degree for the Direct Oxidation of Methane to C1 Oxygenates
The direct oxidation of methane (CH4) into high-valued C1 oxygenates production has garnered increased attention in effectively using vast CH4 and alleviating the global energy crisis. However, due to the high cleavage energy of C—H bond and low polarity of CH4 molecule, it is difficult to activate the first C—H bond. Furthermore, C1 oxygenates are readily inclined to be oxidized to CO2, because their weaker C—H bond comparing with CH4 molecule, resulting in poor selectivity. Herein, we designed ultrathin PdxAuy alloy NWs supported on ZSM-5 (Z-5) to investigate the direct oxidation of CH4 to high value-added oxygenate under mild conditions. By precisely adjusting the molar ratio of Pd/Au and alloying degree, Pd9Au1NWs/Z-5 showed an excellent yield of 11.57 mmol·g–l·h–1 and the outstanding selectivity of 95.1% for C1 oxygenates (CH3OH, CH3OOH and HCOOH). The in-situ spectroscopic and mechanism analysis proved that the enhanced catalytic performance of Pd9Au1NWs/Z-5 was ascribed to the stable one-dimensional nanostructure and the strong synergy effect with high alloying PdAu, which could increase the adsorption capacity of CH4 molecules on Pd atoms to promote the CH4 conversion. This work offers valuable insights into the design concept of high-efficient catalysts and the structure-activity relationship for the direct oxidation of CH4.
期刊介绍:
The Chinese Journal of Chemistry is an international forum for peer-reviewed original research results in all fields of chemistry. Founded in 1983 under the name Acta Chimica Sinica English Edition and renamed in 1990 as Chinese Journal of Chemistry, the journal publishes a stimulating mixture of Accounts, Full Papers, Notes and Communications in English.