Enhanced Pyro-Photo Catalysis of the BaTiO3/NiB Catalyst for Dye Degradation Driven by Visible Light and Cold–Hot Cycles

IF 2.3 4区 化学 Q3 CHEMISTRY, PHYSICAL Catalysis Letters Pub Date : 2024-09-11 DOI:10.1007/s10562-024-04798-5
Mei Ma, Zhihua Liu, Jianguo Zhou
{"title":"Enhanced Pyro-Photo Catalysis of the BaTiO3/NiB Catalyst for Dye Degradation Driven by Visible Light and Cold–Hot Cycles","authors":"Mei Ma,&nbsp;Zhihua Liu,&nbsp;Jianguo Zhou","doi":"10.1007/s10562-024-04798-5","DOIUrl":null,"url":null,"abstract":"<div><p>The decomposition mechanism of dyes under the synergistic effect of pyroelectric catalysis and photocatalysis was systematically investigated using a BaTiO<sub>3</sub>/NiB catalyst in this paper, and the degradation efficiency of BaTiO<sub>3</sub>/NiB was 97.5% under light and 24 cycles of hot and cold at 25 ~ 65 °C, showing high pyroelectroic catalytic RhB decomposition activity and excellent recoverability. The degradation rate constants of RhB chromophore degradation by Pyro-photocatalytic coupled were 3.2 times as high as those of photocatalysis and 11.8 times as high as those of pyroelectric catalysis. In this study, we used light-assisted electrodeposition to deposit a thin layer of amorphous NiB acid salts onto the surface of a BaTiO<sub>3</sub> photoelectrode aiming to explore its influence on photocharge separation and the catalytic mechanism of NiB in the context of pollutant degradation. The synergies between the pyroelectric internal field and the amorphous Ni–B acid salt thin layer during photogenerated charge separation were extensively explored in this paper, including the introduction of a port for pyroelectric polarization.</p><h3>Graphical Abstract</h3>\n<div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":508,"journal":{"name":"Catalysis Letters","volume":"154 12","pages":"6241 - 6253"},"PeriodicalIF":2.3000,"publicationDate":"2024-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Catalysis Letters","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s10562-024-04798-5","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

Abstract

The decomposition mechanism of dyes under the synergistic effect of pyroelectric catalysis and photocatalysis was systematically investigated using a BaTiO3/NiB catalyst in this paper, and the degradation efficiency of BaTiO3/NiB was 97.5% under light and 24 cycles of hot and cold at 25 ~ 65 °C, showing high pyroelectroic catalytic RhB decomposition activity and excellent recoverability. The degradation rate constants of RhB chromophore degradation by Pyro-photocatalytic coupled were 3.2 times as high as those of photocatalysis and 11.8 times as high as those of pyroelectric catalysis. In this study, we used light-assisted electrodeposition to deposit a thin layer of amorphous NiB acid salts onto the surface of a BaTiO3 photoelectrode aiming to explore its influence on photocharge separation and the catalytic mechanism of NiB in the context of pollutant degradation. The synergies between the pyroelectric internal field and the amorphous Ni–B acid salt thin layer during photogenerated charge separation were extensively explored in this paper, including the introduction of a port for pyroelectric polarization.

Graphical Abstract

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
在可见光和冷热循环驱动下增强 BaTiO3/NiB 催化剂的热释光催化作用以降解染料
本文利用BaTiO3/NiB催化剂系统研究了热电催化和光催化协同作用下染料的分解机理,在光照和25~65 ℃冷热循环24次的条件下,BaTiO3/NiB的降解效率为97.5%,显示出较高的热电催化RhB分解活性和优异的可回收性。热光催化耦合降解 RhB 发色团的降解速率常数是光催化的 3.2 倍,是热电催化的 11.8 倍。在本研究中,我们利用光辅助电沉积技术在 BaTiO3 光电极表面沉积了一薄层无定形 NiB 酸盐,旨在探索其对光电分离的影响以及 NiB 在污染物降解方面的催化机理。本文广泛探讨了热释电内场与无定形镍硼酸盐薄膜在光生电荷分离过程中的协同作用,包括热释电极化端口的引入。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Catalysis Letters
Catalysis Letters 化学-物理化学
CiteScore
5.70
自引率
3.60%
发文量
327
审稿时长
1 months
期刊介绍: Catalysis Letters aim is the rapid publication of outstanding and high-impact original research articles in catalysis. The scope of the journal covers a broad range of topics in all fields of both applied and theoretical catalysis, including heterogeneous, homogeneous and biocatalysis. The high-quality original research articles published in Catalysis Letters are subject to rigorous peer review. Accepted papers are published online first and subsequently in print issues. All contributions must include a graphical abstract. Manuscripts should be written in English and the responsibility lies with the authors to ensure that they are grammatically and linguistically correct. Authors for whom English is not the working language are encouraged to consider using a professional language-editing service before submitting their manuscripts.
期刊最新文献
Visible Light Induced Eosin Y Catalysed Green Synthesis of Substituted Pyrroles Correction to: In Silico Models for Prediction of Methanol Yield in CO2 Hydrogenation Reaction Using CuBased Catalysts Promotional Catalytic Activity of Bifunctional Ru-Ce-Zr Catalysts forNH3-SCO by Deposition Order of Dual Active Components Palladium-Based Catalyst on L-Histidine-Modified Boron Nitride Nanosheets: A Novel, Stable, and Highly Efficient Heterogeneous Catalyst for Suzuki–Miyaura Reaction M-BTC as Efficient Catalyst for the Synthesis of Cyclic Organic Carbonates Assisted Tandem by Olefin Epoxidation and CO2 Cycloaddition
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1