水稳定性过氧化物纳米管阵列在功能化聚氧化铝的诱导下增强了电荷载流子的传输,可用于高效光还原铀(VI)

IF 6.1 1区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR
Yanli Yang, Keke Guo, Xue Bai, Maochun Zhu, Siyue Wang and Shuxia Liu
{"title":"水稳定性过氧化物纳米管阵列在功能化聚氧化铝的诱导下增强了电荷载流子的传输,可用于高效光还原铀(VI)","authors":"Yanli Yang, Keke Guo, Xue Bai, Maochun Zhu, Siyue Wang and Shuxia Liu","doi":"10.1039/D4QI02393E","DOIUrl":null,"url":null,"abstract":"<p >Since metal halide perovskites (MHPs) possess excellent optoelectronic performances, constructing MHP-based photocatalysts is a promising strategy to promote photocatalytic uranium(<small>VI</small>) reduction. However, the instability of MHPs in water limits their practical application, which is still a major issue and challenge. In this work, we constructed a perovskite nanotube array-based catalyst encapsulated by a functionalized POM, (HMTA)<small><sub>3</sub></small>Pb<small><sub>2</sub></small>Br<small><sub>7</sub></small>@STA-PW<small><sub>12</sub></small>, which can maintain stability in water for 10 hours under stirring conditions. It is noteworthy that considering the “electron-sponge” property of POMs, STA-PW<small><sub>12</sub></small> acting as an electronic transfer medium not only increases the stability of the catalyst in water due to the hydrophobic long-chain STA but also contributes to the separation of photogenerated carriers and enhances charge transfer from (HMTA)<small><sub>3</sub></small>Pb<small><sub>2</sub></small>Br<small><sub>7</sub></small> to PW<small><sub>12</sub></small>, which significantly enhances the photocatalytic activity. The enhanced electron carrier mobility (<em>μ</em><small><sub>e</sub></small>) (1.1 cm<small><sup>2</sup></small> V<small><sup>−1</sup></small> s<small><sup>−1</sup></small>) and carrier diffusion length (245 nm) of (HMTA)<small><sub>3</sub></small>Pb<small><sub>2</sub></small>Br<small><sub>7</sub></small>@STA-PW<small><sub>12</sub></small> further illustrate its effective charge carrier transfer. DFT calculations further indicate the transition of electrons from (HMTA)<small><sub>3</sub></small>Pb<small><sub>2</sub></small>Br<small><sub>7</sub></small> to PW<small><sub>12</sub></small>, which greatly inhibits the recombination of photogenerated carriers, thereby advancing electron transfer. Finally, the synthesized catalyst exhibits an excellent performance in the photocatalytic removal of U(<small>VI</small>) with a removal rate of 99.3% at a U(<small>VI</small>) concentration of 40 ppm after 40 min under simulated sunlight.</p>","PeriodicalId":79,"journal":{"name":"Inorganic Chemistry Frontiers","volume":" 1","pages":" 261-272"},"PeriodicalIF":6.1000,"publicationDate":"2024-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Water-stable perovskite nanotube array with enhanced transport of charge carriers induced by functionalized polyoxometalate for the highly efficient photoreduction of uranium(vi)†\",\"authors\":\"Yanli Yang, Keke Guo, Xue Bai, Maochun Zhu, Siyue Wang and Shuxia Liu\",\"doi\":\"10.1039/D4QI02393E\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Since metal halide perovskites (MHPs) possess excellent optoelectronic performances, constructing MHP-based photocatalysts is a promising strategy to promote photocatalytic uranium(<small>VI</small>) reduction. However, the instability of MHPs in water limits their practical application, which is still a major issue and challenge. In this work, we constructed a perovskite nanotube array-based catalyst encapsulated by a functionalized POM, (HMTA)<small><sub>3</sub></small>Pb<small><sub>2</sub></small>Br<small><sub>7</sub></small>@STA-PW<small><sub>12</sub></small>, which can maintain stability in water for 10 hours under stirring conditions. It is noteworthy that considering the “electron-sponge” property of POMs, STA-PW<small><sub>12</sub></small> acting as an electronic transfer medium not only increases the stability of the catalyst in water due to the hydrophobic long-chain STA but also contributes to the separation of photogenerated carriers and enhances charge transfer from (HMTA)<small><sub>3</sub></small>Pb<small><sub>2</sub></small>Br<small><sub>7</sub></small> to PW<small><sub>12</sub></small>, which significantly enhances the photocatalytic activity. The enhanced electron carrier mobility (<em>μ</em><small><sub>e</sub></small>) (1.1 cm<small><sup>2</sup></small> V<small><sup>−1</sup></small> s<small><sup>−1</sup></small>) and carrier diffusion length (245 nm) of (HMTA)<small><sub>3</sub></small>Pb<small><sub>2</sub></small>Br<small><sub>7</sub></small>@STA-PW<small><sub>12</sub></small> further illustrate its effective charge carrier transfer. DFT calculations further indicate the transition of electrons from (HMTA)<small><sub>3</sub></small>Pb<small><sub>2</sub></small>Br<small><sub>7</sub></small> to PW<small><sub>12</sub></small>, which greatly inhibits the recombination of photogenerated carriers, thereby advancing electron transfer. Finally, the synthesized catalyst exhibits an excellent performance in the photocatalytic removal of U(<small>VI</small>) with a removal rate of 99.3% at a U(<small>VI</small>) concentration of 40 ppm after 40 min under simulated sunlight.</p>\",\"PeriodicalId\":79,\"journal\":{\"name\":\"Inorganic Chemistry Frontiers\",\"volume\":\" 1\",\"pages\":\" 261-272\"},\"PeriodicalIF\":6.1000,\"publicationDate\":\"2024-11-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Inorganic Chemistry Frontiers\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2025/qi/d4qi02393e\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, INORGANIC & NUCLEAR\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Inorganic Chemistry Frontiers","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/qi/d4qi02393e","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
引用次数: 0

摘要

由于金属卤化物过氧化物(MHPs)具有优异的光电性能,因此构建基于 MHPs 的光催化剂是促进光催化还原铀(VI)的一种前景广阔的策略。然而,MHPs 在水中的不稳定性限制了其实际应用,这仍然是一个重大问题和挑战。在本文中,我们构建了一种由功能化 POMs 封装的基于包晶纳米管阵列的催化剂 (HMTA)3Pb2Br7@STA-PW12,该催化剂在搅拌条件下可在水中保持稳定 10 小时。值得注意的是,考虑到 POMs 的 "电子海绵 "特性,STA-PW12 作为电子传递介质,不仅由于长链 STA 的疏水性提高了催化剂在水中的稳定性,还有助于分离光生载流子,增强电荷从 (HMTA)3Pb2Br7 向 PW12 的转移,从而显著提高光催化活性。(HMTA)3Pb2Br7@STA-PW12 增强的电子载流子迁移率(μe)(1.1 cm2 V-1 s-1)和载流子扩散长度(245 nm)进一步说明了其有效的电荷载流子转移。DFT 计算进一步表明,电子从 (HMTA)3Pb2Br7 向 PW12 过渡,极大地抑制了光生载流子的重组,从而促进了电子转移。最后,合成的催化剂在光催化去除 U(VI)方面表现优异,在模拟阳光下 40 分钟后,U(VI)浓度为 40 ppm 时的去除率为 99.3%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Water-stable perovskite nanotube array with enhanced transport of charge carriers induced by functionalized polyoxometalate for the highly efficient photoreduction of uranium(vi)†

Water-stable perovskite nanotube array with enhanced transport of charge carriers induced by functionalized polyoxometalate for the highly efficient photoreduction of uranium(vi)†

Since metal halide perovskites (MHPs) possess excellent optoelectronic performances, constructing MHP-based photocatalysts is a promising strategy to promote photocatalytic uranium(VI) reduction. However, the instability of MHPs in water limits their practical application, which is still a major issue and challenge. In this work, we constructed a perovskite nanotube array-based catalyst encapsulated by a functionalized POM, (HMTA)3Pb2Br7@STA-PW12, which can maintain stability in water for 10 hours under stirring conditions. It is noteworthy that considering the “electron-sponge” property of POMs, STA-PW12 acting as an electronic transfer medium not only increases the stability of the catalyst in water due to the hydrophobic long-chain STA but also contributes to the separation of photogenerated carriers and enhances charge transfer from (HMTA)3Pb2Br7 to PW12, which significantly enhances the photocatalytic activity. The enhanced electron carrier mobility (μe) (1.1 cm2 V−1 s−1) and carrier diffusion length (245 nm) of (HMTA)3Pb2Br7@STA-PW12 further illustrate its effective charge carrier transfer. DFT calculations further indicate the transition of electrons from (HMTA)3Pb2Br7 to PW12, which greatly inhibits the recombination of photogenerated carriers, thereby advancing electron transfer. Finally, the synthesized catalyst exhibits an excellent performance in the photocatalytic removal of U(VI) with a removal rate of 99.3% at a U(VI) concentration of 40 ppm after 40 min under simulated sunlight.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Inorganic Chemistry Frontiers
Inorganic Chemistry Frontiers CHEMISTRY, INORGANIC & NUCLEAR-
CiteScore
10.40
自引率
7.10%
发文量
587
审稿时长
1.2 months
期刊介绍: The international, high quality journal for interdisciplinary research between inorganic chemistry and related subjects
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信