Tianyi Huang, Jianyu Han, Zhongqiu Li, Yixin Hong, Xiaofei Gu, Yafeng Wu, Prof. Yuanjian Zhang, Prof. Songqin Liu
{"title":"Unraveling the Essential Role of Consecutive Protonation Steps in Photocatalytic CO2 Reduction when Using Au Nanorods in a MOF","authors":"Tianyi Huang, Jianyu Han, Zhongqiu Li, Yixin Hong, Xiaofei Gu, Yafeng Wu, Prof. Yuanjian Zhang, Prof. Songqin Liu","doi":"10.1002/anie.202500269","DOIUrl":null,"url":null,"abstract":"<p>The proton-coupled electron transfer process (PCET) plays a crucial role in both natural and artificial photosynthesis, including CO<sub>2</sub> fixation chemistry. However, difficulties in capturing the transient intermediates generated during the protonation process impede the clarification of the fundamental mechanism behind photocatalytic CO<sub>2</sub> reduction. Herein, we report a general killing two birds with one stone strategy by spatially confining Au nanorods within a typical porphyrin metal–organic framework (MOF). Interestingly, 2.4-fold increase in CH<sub>4</sub>/CO selectivity and 12-fold increase in CH<sub>4</sub> production were observed after loading of Au nanorods, indicative of a strengthened protonation process in the photocatalytic CO<sub>2</sub> reduction. More importantly, the plasmonic effect from Au nanorods simultaneously boosted the in situ Raman signals of *CO and *CHO intermediates on the Au−O−Zr active site. The evident protonation process was further clarified in a control H/D kinetic isotope experiment. This work highlights the significance of successive protonation steps for boosting CH<sub>4</sub> production in photocatalytic CO<sub>2</sub> reduction.</p>","PeriodicalId":125,"journal":{"name":"Angewandte Chemie International Edition","volume":"64 16","pages":""},"PeriodicalIF":16.1000,"publicationDate":"2025-02-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Angewandte Chemie International Edition","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/anie.202500269","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
The proton-coupled electron transfer process (PCET) plays a crucial role in both natural and artificial photosynthesis, including CO2 fixation chemistry. However, difficulties in capturing the transient intermediates generated during the protonation process impede the clarification of the fundamental mechanism behind photocatalytic CO2 reduction. Herein, we report a general killing two birds with one stone strategy by spatially confining Au nanorods within a typical porphyrin metal–organic framework (MOF). Interestingly, 2.4-fold increase in CH4/CO selectivity and 12-fold increase in CH4 production were observed after loading of Au nanorods, indicative of a strengthened protonation process in the photocatalytic CO2 reduction. More importantly, the plasmonic effect from Au nanorods simultaneously boosted the in situ Raman signals of *CO and *CHO intermediates on the Au−O−Zr active site. The evident protonation process was further clarified in a control H/D kinetic isotope experiment. This work highlights the significance of successive protonation steps for boosting CH4 production in photocatalytic CO2 reduction.
质子耦合电子转移过程(PCET)在自然和人工光合作用中都起着至关重要的作用,其中包括CO2固定化学。然而,捕获质子化过程中产生的瞬态中间体的困难阻碍了光催化CO2还原背后的基本机制的阐明。在此,我们报告了一种通过将金纳米棒空间限制在典型卟啉MOF内的一石两鸟策略(Au@PCN-222)。有趣的是,负载Au纳米棒后,CH4/CO选择性增加了2.4倍,CH4产量增加了12倍,这表明光催化CO2还原过程中的质子化过程得到加强。更重要的是,Au纳米棒的等离子体效应同时增强了Au- o - zr活性位点上*CO和*CHO中间体的原位拉曼信号。在对照H/D动力学同位素实验中进一步阐明了明显的质子化过程。这项工作强调了在光催化CO2还原过程中连续质子化步骤对提高CH4产量的重要性。
期刊介绍:
Angewandte Chemie, a journal of the German Chemical Society (GDCh), maintains a leading position among scholarly journals in general chemistry with an impressive Impact Factor of 16.6 (2022 Journal Citation Reports, Clarivate, 2023). Published weekly in a reader-friendly format, it features new articles almost every day. Established in 1887, Angewandte Chemie is a prominent chemistry journal, offering a dynamic blend of Review-type articles, Highlights, Communications, and Research Articles on a weekly basis, making it unique in the field.