Wenxiu Yang , Jinfeng Zhang , Quanlong Xu , Yun Yang , Lijie Zhang
{"title":"Bimetallic AuCu Alloy Decorated Covalent Organic Frameworks for Efficient Photocatalytic Hydrogen Production","authors":"Wenxiu Yang , Jinfeng Zhang , Quanlong Xu , Yun Yang , Lijie Zhang","doi":"10.3866/PKU.WHXB202312014","DOIUrl":null,"url":null,"abstract":"<div><div>Covalent organic frameworks (COFs) represent a kind of novel crystalline porous organic substances with extended <em>π</em>-conjugation framework and tunable structures, which display great promise in photocatalysis. However, unadorned COFs suffer from sluggish reaction kinetics, and a cocatalyst is essentially needed to reduce the activation barrier toward specific surface reaction and accelerate reaction kinetics. In this work, bimetallic alloys serving as co-catalysts were decorated on COFs to enhance the photocatalytic hydrogen evolution performance. By precisely-tuning the ratio of AuCu alloy, the resultant Au<sub>1</sub>Cu<sub>5</sub>/COF-TpPa displays the highest photocatalytic hydrogen generation rate (8.24 mmol∙g<sup>−1</sup>∙h<sup>−1</sup>), even surpassing the Pt modified COF-TpPa (6.51 mmol∙h<sup>−1</sup>∙g<sup>−1</sup>). According to the systematic characterizations and theoretical calculation, Au<sub>1</sub>Cu<sub>5</sub>/COF-TpPa exhibits the significantly enhanced charge carrier separation efficiency and reduced H* formation energy barrier, thus possessing high photocatalytic performance. This work affords a valuable approach to advancing COF-based photocatalysts by employing bimetallic alloy cocatalysts.</div><div><span><figure><span><img><ol><li><span><span>Download: <span>Download high-res image (117KB)</span></span></span></li><li><span><span>Download: <span>Download full-size image</span></span></span></li></ol></span></figure></span></div></div>","PeriodicalId":6964,"journal":{"name":"物理化学学报","volume":"40 10","pages":"Article 2312014"},"PeriodicalIF":10.8000,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"物理化学学报","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1000681824001589","RegionNum":2,"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
Abstract
Covalent organic frameworks (COFs) represent a kind of novel crystalline porous organic substances with extended π-conjugation framework and tunable structures, which display great promise in photocatalysis. However, unadorned COFs suffer from sluggish reaction kinetics, and a cocatalyst is essentially needed to reduce the activation barrier toward specific surface reaction and accelerate reaction kinetics. In this work, bimetallic alloys serving as co-catalysts were decorated on COFs to enhance the photocatalytic hydrogen evolution performance. By precisely-tuning the ratio of AuCu alloy, the resultant Au1Cu5/COF-TpPa displays the highest photocatalytic hydrogen generation rate (8.24 mmol∙g−1∙h−1), even surpassing the Pt modified COF-TpPa (6.51 mmol∙h−1∙g−1). According to the systematic characterizations and theoretical calculation, Au1Cu5/COF-TpPa exhibits the significantly enhanced charge carrier separation efficiency and reduced H* formation energy barrier, thus possessing high photocatalytic performance. This work affords a valuable approach to advancing COF-based photocatalysts by employing bimetallic alloy cocatalysts.