Yuanming Hou , Xiaocheng Song , Yanqing Zhang , Tingting Ren , Jiaxin Wang , Jingyi Qin , Jianjun Yang , Zhengzheng Xie , Zhihong Tian , Zhongjie Guan , Xianwei Fu , Shilong Jiao , Qiuye Li , Erling Li
{"title":"氮化镧系元素纳米片上的 0D/2D 肖特基异质结 CsPbBr3 纳米晶体用于增强电荷转移和二氧化碳光电还原","authors":"Yuanming Hou , Xiaocheng Song , Yanqing Zhang , Tingting Ren , Jiaxin Wang , Jingyi Qin , Jianjun Yang , Zhengzheng Xie , Zhihong Tian , Zhongjie Guan , Xianwei Fu , Shilong Jiao , Qiuye Li , Erling Li","doi":"10.1016/j.flatc.2024.100720","DOIUrl":null,"url":null,"abstract":"<div><p>Solar-driven conversion of CO<sub>2</sub> to value-added chemical fuels has been regarded as a promising strategy for solving the climate problem and energy crisis. To realize this goal, it is vital to design photocatalysts with abundant catalytic active sites and excellent charge separation efficiency. Here, perovskite nanocrystals (CsPbBr<sub>3</sub>) were anchored on two-dimensional molybdenum nitride (MoN) using an in-situ growth method, forming a new and effective 0D/2D CsPbBr<sub>3</sub>@MoN (CPB@MoN) nanoheterosturcture with close contact interface for CO<sub>2</sub> photoreduction. The introduction of MoN, acting as a charge transfer channel, could quickly trap the photoinduced charge from CsPbBr<sub>3</sub> and provide abundant catalytic sites for CO<sub>2</sub> photocatalytic reactions. For optimized CsPbBr<sub>3</sub>@MoN composites, the CO yield was 13.86μmol/gh<sup>−1</sup> without any sacrificial reagent, which was a 4.5-fold enhancement of the pure CsPbBr<sub>3</sub>. Further, in-situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) revealed the catalytic mechanism for the CO<sub>2</sub> photoreduction process. This work provides a new platform for constructing superior perovskite/MoN-based photocatalysts for photocatalytic CO<sub>2</sub> reduction.</p></div>","PeriodicalId":316,"journal":{"name":"FlatChem","volume":"47 ","pages":"Article 100720"},"PeriodicalIF":5.9000,"publicationDate":"2024-07-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"0D/2D Schottky heterojunction of CsPbBr3 nanocrystals on MoN nanosheets for enhancing charge transfer and CO2 photoreduction\",\"authors\":\"Yuanming Hou , Xiaocheng Song , Yanqing Zhang , Tingting Ren , Jiaxin Wang , Jingyi Qin , Jianjun Yang , Zhengzheng Xie , Zhihong Tian , Zhongjie Guan , Xianwei Fu , Shilong Jiao , Qiuye Li , Erling Li\",\"doi\":\"10.1016/j.flatc.2024.100720\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Solar-driven conversion of CO<sub>2</sub> to value-added chemical fuels has been regarded as a promising strategy for solving the climate problem and energy crisis. To realize this goal, it is vital to design photocatalysts with abundant catalytic active sites and excellent charge separation efficiency. Here, perovskite nanocrystals (CsPbBr<sub>3</sub>) were anchored on two-dimensional molybdenum nitride (MoN) using an in-situ growth method, forming a new and effective 0D/2D CsPbBr<sub>3</sub>@MoN (CPB@MoN) nanoheterosturcture with close contact interface for CO<sub>2</sub> photoreduction. The introduction of MoN, acting as a charge transfer channel, could quickly trap the photoinduced charge from CsPbBr<sub>3</sub> and provide abundant catalytic sites for CO<sub>2</sub> photocatalytic reactions. For optimized CsPbBr<sub>3</sub>@MoN composites, the CO yield was 13.86μmol/gh<sup>−1</sup> without any sacrificial reagent, which was a 4.5-fold enhancement of the pure CsPbBr<sub>3</sub>. Further, in-situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) revealed the catalytic mechanism for the CO<sub>2</sub> photoreduction process. This work provides a new platform for constructing superior perovskite/MoN-based photocatalysts for photocatalytic CO<sub>2</sub> reduction.</p></div>\",\"PeriodicalId\":316,\"journal\":{\"name\":\"FlatChem\",\"volume\":\"47 \",\"pages\":\"Article 100720\"},\"PeriodicalIF\":5.9000,\"publicationDate\":\"2024-07-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"FlatChem\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2452262724001144\",\"RegionNum\":3,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"FlatChem","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2452262724001144","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
摘要
太阳能驱动的一氧化碳到高附加值化学燃料的转化一直被认为是解决气候问题和能源危机的一个有前途的战略。要实现这一目标,设计具有丰富催化活性位点和优异电荷分离效率的光催化剂至关重要。在这里,利用原位生长方法将过氧化物纳米晶体(CsPbBr)锚定在二维氮化钼(MoN)上,形成了一种新型、有效的 0D/2D CsPbBr@MoN (CPB@MoN)纳米异构体,其界面接触紧密,可用于 CO 的光氧化还原。作为电荷转移通道,MoN 的引入可快速捕获来自 CsPbBr 的光诱导电荷,并为 CO 光催化反应提供丰富的催化位点。对于优化的 CsPbBr@MoN 复合材料,在不使用任何牺牲试剂的情况下,CO 产率为 13.86μmol/gh,是纯 CsPbBr 的 4.5 倍。此外,原位漫反射红外傅立叶变换光谱(DRIFTS)揭示了 CO 光还原过程的催化机理。这项工作为构建用于光催化还原 CO 的优质包晶石/MoN 基光催化剂提供了一个新平台。
0D/2D Schottky heterojunction of CsPbBr3 nanocrystals on MoN nanosheets for enhancing charge transfer and CO2 photoreduction
Solar-driven conversion of CO2 to value-added chemical fuels has been regarded as a promising strategy for solving the climate problem and energy crisis. To realize this goal, it is vital to design photocatalysts with abundant catalytic active sites and excellent charge separation efficiency. Here, perovskite nanocrystals (CsPbBr3) were anchored on two-dimensional molybdenum nitride (MoN) using an in-situ growth method, forming a new and effective 0D/2D CsPbBr3@MoN (CPB@MoN) nanoheterosturcture with close contact interface for CO2 photoreduction. The introduction of MoN, acting as a charge transfer channel, could quickly trap the photoinduced charge from CsPbBr3 and provide abundant catalytic sites for CO2 photocatalytic reactions. For optimized CsPbBr3@MoN composites, the CO yield was 13.86μmol/gh−1 without any sacrificial reagent, which was a 4.5-fold enhancement of the pure CsPbBr3. Further, in-situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) revealed the catalytic mechanism for the CO2 photoreduction process. This work provides a new platform for constructing superior perovskite/MoN-based photocatalysts for photocatalytic CO2 reduction.
期刊介绍:
FlatChem - Chemistry of Flat Materials, a new voice in the community, publishes original and significant, cutting-edge research related to the chemistry of graphene and related 2D & layered materials. The overall aim of the journal is to combine the chemistry and applications of these materials, where the submission of communications, full papers, and concepts should contain chemistry in a materials context, which can be both experimental and/or theoretical. In addition to original research articles, FlatChem also offers reviews, minireviews, highlights and perspectives on the future of this research area with the scientific leaders in fields related to Flat Materials. Topics of interest include, but are not limited to, the following: -Design, synthesis, applications and investigation of graphene, graphene related materials and other 2D & layered materials (for example Silicene, Germanene, Phosphorene, MXenes, Boron nitride, Transition metal dichalcogenides) -Characterization of these materials using all forms of spectroscopy and microscopy techniques -Chemical modification or functionalization and dispersion of these materials, as well as interactions with other materials -Exploring the surface chemistry of these materials for applications in: Sensors or detectors in electrochemical/Lab on a Chip devices, Composite materials, Membranes, Environment technology, Catalysis for energy storage and conversion (for example fuel cells, supercapacitors, batteries, hydrogen storage), Biomedical technology (drug delivery, biosensing, bioimaging)