Chengshuang Zhou, Jinwon Oh, Michael L. Stone, Sydney Richardson, Pin‐Hung Chung, Jorge Osio‐Norgaard, Bang T. Nhan, Abinash Kumar, Miaofang Chi, Matteo Cargnello
{"title":"在多孔氧化物中封装金属纳米粒子的一般方法","authors":"Chengshuang Zhou, Jinwon Oh, Michael L. Stone, Sydney Richardson, Pin‐Hung Chung, Jorge Osio‐Norgaard, Bang T. Nhan, Abinash Kumar, Miaofang Chi, Matteo Cargnello","doi":"10.1002/adma.202409710","DOIUrl":null,"url":null,"abstract":"Encapsulation of metal nanoparticles within oxide materials has been shown as an effective strategy to improve activity, selectivity, and stability in several catalytic applications. Several approaches have been proposed to encapsulate nanoparticles, such as forming core‐shell structures, growing ordered structures (zeolites or metal‐organic frameworks) on nanoparticles, or directly depositing support materials on nanoparticles. Here, a general nanocasting method is demonstrated that can produce diverse encapsulated metal@oxide structures with different compositions (Pt, Pd, Rh) and multiple types of oxides (Al<jats:sub>2</jats:sub>O<jats:sub>3</jats:sub>, Al<jats:sub>2</jats:sub>O<jats:sub>3</jats:sub>‐CeO<jats:sub>2</jats:sub>, ZrO<jats:sub>2</jats:sub>, ZnZrO<jats:sub>x</jats:sub>, In<jats:sub>2</jats:sub>O<jats:sub>3</jats:sub>, Mn<jats:sub>2</jats:sub>O<jats:sub>3</jats:sub>, TiO<jats:sub>2</jats:sub>) while controlling the size and dispersion of nanoparticles and the porous structure of the oxide. Metal@polymer structures are first prepared, and then the oxide precursor is infiltrated into such structures and the resulting material is calcined to form the metal@oxide structures. Most Pt@oxides catalysts show similar catalytic activity, demonstrating the availability of surface Pt sites in the encapsulated structures. However, the Pt@Mn<jats:sub>2</jats:sub>O<jats:sub>3</jats:sub> sample showed much higher CO oxidation activity, while also being stable under aging conditions. This work demonstrated a robust nanocasting method to synthesize metal@oxide structures, which can be utilized in catalysis to finely tune metal‐oxide interfaces.","PeriodicalId":114,"journal":{"name":"Advanced Materials","volume":null,"pages":null},"PeriodicalIF":27.4000,"publicationDate":"2024-11-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A General Approach for Metal Nanoparticle Encapsulation Within Porous Oxides\",\"authors\":\"Chengshuang Zhou, Jinwon Oh, Michael L. Stone, Sydney Richardson, Pin‐Hung Chung, Jorge Osio‐Norgaard, Bang T. Nhan, Abinash Kumar, Miaofang Chi, Matteo Cargnello\",\"doi\":\"10.1002/adma.202409710\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Encapsulation of metal nanoparticles within oxide materials has been shown as an effective strategy to improve activity, selectivity, and stability in several catalytic applications. Several approaches have been proposed to encapsulate nanoparticles, such as forming core‐shell structures, growing ordered structures (zeolites or metal‐organic frameworks) on nanoparticles, or directly depositing support materials on nanoparticles. Here, a general nanocasting method is demonstrated that can produce diverse encapsulated metal@oxide structures with different compositions (Pt, Pd, Rh) and multiple types of oxides (Al<jats:sub>2</jats:sub>O<jats:sub>3</jats:sub>, Al<jats:sub>2</jats:sub>O<jats:sub>3</jats:sub>‐CeO<jats:sub>2</jats:sub>, ZrO<jats:sub>2</jats:sub>, ZnZrO<jats:sub>x</jats:sub>, In<jats:sub>2</jats:sub>O<jats:sub>3</jats:sub>, Mn<jats:sub>2</jats:sub>O<jats:sub>3</jats:sub>, TiO<jats:sub>2</jats:sub>) while controlling the size and dispersion of nanoparticles and the porous structure of the oxide. Metal@polymer structures are first prepared, and then the oxide precursor is infiltrated into such structures and the resulting material is calcined to form the metal@oxide structures. Most Pt@oxides catalysts show similar catalytic activity, demonstrating the availability of surface Pt sites in the encapsulated structures. However, the Pt@Mn<jats:sub>2</jats:sub>O<jats:sub>3</jats:sub> sample showed much higher CO oxidation activity, while also being stable under aging conditions. This work demonstrated a robust nanocasting method to synthesize metal@oxide structures, which can be utilized in catalysis to finely tune metal‐oxide interfaces.\",\"PeriodicalId\":114,\"journal\":{\"name\":\"Advanced Materials\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":27.4000,\"publicationDate\":\"2024-11-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advanced Materials\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1002/adma.202409710\",\"RegionNum\":1,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Materials","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/adma.202409710","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
摘要
在一些催化应用中,将金属纳米颗粒封装在氧化物材料中已被证明是提高活性、选择性和稳定性的有效策略。封装纳米颗粒的方法有多种,如形成核壳结构、在纳米颗粒上生长有序结构(沸石或金属有机框架)或直接在纳米颗粒上沉积支撑材料。在这里,我们展示了一种通用的纳米铸造方法,它可以生产出不同成分(铂、钯、铑)和多种类型氧化物(Al2O3、Al2O3-CeO2、ZrO2、ZnZrOx、In2O3、Mn2O3、TiO2)的各种封装金属@氧化物结构,同时控制纳米粒子的尺寸和分散性以及氧化物的多孔结构。首先制备金属@聚合物结构,然后将氧化物前驱体渗入此类结构中,并对所得材料进行煅烧,形成金属@氧化物结构。大多数 Pt@ 氧化物催化剂都显示出类似的催化活性,这表明封装结构中存在表面铂位点。然而,Pt@Mn2O3 样品显示出更高的 CO 氧化活性,同时在老化条件下也很稳定。这项工作展示了一种合成金属@氧化物结构的稳健的纳米铸造方法,这种方法可用于催化领域,对金属-氧化物界面进行微调。
A General Approach for Metal Nanoparticle Encapsulation Within Porous Oxides
Encapsulation of metal nanoparticles within oxide materials has been shown as an effective strategy to improve activity, selectivity, and stability in several catalytic applications. Several approaches have been proposed to encapsulate nanoparticles, such as forming core‐shell structures, growing ordered structures (zeolites or metal‐organic frameworks) on nanoparticles, or directly depositing support materials on nanoparticles. Here, a general nanocasting method is demonstrated that can produce diverse encapsulated metal@oxide structures with different compositions (Pt, Pd, Rh) and multiple types of oxides (Al2O3, Al2O3‐CeO2, ZrO2, ZnZrOx, In2O3, Mn2O3, TiO2) while controlling the size and dispersion of nanoparticles and the porous structure of the oxide. Metal@polymer structures are first prepared, and then the oxide precursor is infiltrated into such structures and the resulting material is calcined to form the metal@oxide structures. Most Pt@oxides catalysts show similar catalytic activity, demonstrating the availability of surface Pt sites in the encapsulated structures. However, the Pt@Mn2O3 sample showed much higher CO oxidation activity, while also being stable under aging conditions. This work demonstrated a robust nanocasting method to synthesize metal@oxide structures, which can be utilized in catalysis to finely tune metal‐oxide interfaces.
期刊介绍:
Advanced Materials, one of the world's most prestigious journals and the foundation of the Advanced portfolio, is the home of choice for best-in-class materials science for more than 30 years. Following this fast-growing and interdisciplinary field, we are considering and publishing the most important discoveries on any and all materials from materials scientists, chemists, physicists, engineers as well as health and life scientists and bringing you the latest results and trends in modern materials-related research every week.