Enhanced Photocatalytic Hydrogen Production Activity Driven by TiO2/(MoP/CdS): Insights from Powder Particles to Thin Films

IF 3.9 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Langmuir Pub Date : 2024-09-26 DOI:10.1021/acs.langmuir.4c02635
Jiajia Wang, Jinfeng Tian, Peng Han, Lingxiao Song, Wei Wang, Keying Lin, Dong Feng, Baojun Ma
{"title":"Enhanced Photocatalytic Hydrogen Production Activity Driven by TiO2/(MoP/CdS): Insights from Powder Particles to Thin Films","authors":"Jiajia Wang, Jinfeng Tian, Peng Han, Lingxiao Song, Wei Wang, Keying Lin, Dong Feng, Baojun Ma","doi":"10.1021/acs.langmuir.4c02635","DOIUrl":null,"url":null,"abstract":"Transitioning from powder photocatalysts to thin film photocatalysts is one of the necessary steps toward industrializing photocatalytic hydrogen production. Herein, we reported the integration of non-noble metal cocatalyst MoP decorated with TiO<sub>2</sub> and CdS, forming TiO<sub>2</sub>/(MoP/CdS) for ultraviolet–visible light utilization. The designed powder TiO<sub>2</sub>/(MoP/CdS) composites achieved a superior hydrogen production rate of 42.2 mmol g<sup>–1</sup> h<sup>–1</sup>, which is 30.1 times that of TiO<sub>2</sub>/CdS, performing the highest activity among the TiO<sub>2</sub>-CdS-based composite photocatalysts. Moreover, we fabricated a thin film from TiO<sub>2</sub>/(MoP/CdS) powder, which exhibited comparable photocatalytic activity for hydrogen production, achieving 35.5 mmol g<sup>–1</sup> h<sup>–1</sup> and maintaining long-term stability for 150 h. The outstanding performance was attributed to the ability of the TiO<sub>2</sub>/(MoP/CdS) composite photocatalysts to absorb both visible and ultraviolet light. Additionally, the heterojunction formed between TiO<sub>2</sub> and CdS also played a significant role in the overall photocatalyst activity. This cost-effective catalyst holds promise for future large-scale industrial applications.","PeriodicalId":50,"journal":{"name":"Langmuir","volume":"51 1","pages":""},"PeriodicalIF":3.9000,"publicationDate":"2024-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Langmuir","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acs.langmuir.4c02635","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

Transitioning from powder photocatalysts to thin film photocatalysts is one of the necessary steps toward industrializing photocatalytic hydrogen production. Herein, we reported the integration of non-noble metal cocatalyst MoP decorated with TiO2 and CdS, forming TiO2/(MoP/CdS) for ultraviolet–visible light utilization. The designed powder TiO2/(MoP/CdS) composites achieved a superior hydrogen production rate of 42.2 mmol g–1 h–1, which is 30.1 times that of TiO2/CdS, performing the highest activity among the TiO2-CdS-based composite photocatalysts. Moreover, we fabricated a thin film from TiO2/(MoP/CdS) powder, which exhibited comparable photocatalytic activity for hydrogen production, achieving 35.5 mmol g–1 h–1 and maintaining long-term stability for 150 h. The outstanding performance was attributed to the ability of the TiO2/(MoP/CdS) composite photocatalysts to absorb both visible and ultraviolet light. Additionally, the heterojunction formed between TiO2 and CdS also played a significant role in the overall photocatalyst activity. This cost-effective catalyst holds promise for future large-scale industrial applications.

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
TiO2/(MoP/CdS)增强光催化制氢活性:从粉末颗粒到薄膜的启示
从粉末光催化剂过渡到薄膜光催化剂是实现光催化制氢工业化的必要步骤之一。在此,我们报告了将非贵金属协同催化剂 MoP 与 TiO2 和 CdS 进行装饰,形成 TiO2/(MoP/CdS),用于紫外-可见光的利用。所设计的粉末 TiO2/(MoP/CdS)复合材料的产氢率高达 42.2 mmol g-1 h-1,是 TiO2/CdS 的 30.1 倍,在基于 TiO2-CdS 的复合光催化剂中活性最高。此外,我们还利用 TiO2/(MoP/CdS)粉末制备了一层薄膜,该薄膜在制氢方面表现出了相当的光催化活性,达到了 35.5 mmol g-1 h-1,并能保持 150 h 的长期稳定性。此外,TiO2 和 CdS 之间形成的异质结在整个光催化剂活性中也发挥了重要作用。这种具有成本效益的催化剂有望在未来大规模工业应用。
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
Langmuir
Langmuir 化学-材料科学:综合
CiteScore
6.50
自引率
10.30%
发文量
1464
审稿时长
2.1 months
期刊介绍: Langmuir is an interdisciplinary journal publishing articles in the following subject categories: Colloids: surfactants and self-assembly, dispersions, emulsions, foams Interfaces: adsorption, reactions, films, forces Biological Interfaces: biocolloids, biomolecular and biomimetic materials Materials: nano- and mesostructured materials, polymers, gels, liquid crystals Electrochemistry: interfacial charge transfer, charge transport, electrocatalysis, electrokinetic phenomena, bioelectrochemistry Devices and Applications: sensors, fluidics, patterning, catalysis, photonic crystals However, when high-impact, original work is submitted that does not fit within the above categories, decisions to accept or decline such papers will be based on one criteria: What Would Irving Do? Langmuir ranks #2 in citations out of 136 journals in the category of Physical Chemistry with 113,157 total citations. The journal received an Impact Factor of 4.384*. This journal is also indexed in the categories of Materials Science (ranked #1) and Multidisciplinary Chemistry (ranked #5).
期刊最新文献
In Situ Characterization of the Hydration Structure at the Silica-Water Interface. A Bifunctional Cellulose/MIL-53(Fe) Paper-Based Material for Selective Fluorescent Sensing of Cr(VI) and Wastewater Treatment. Soft Magnetism Meets Self-Assembly: Molecularly Engineered Magnetic Ionic Liquid Nanomicelles for the Solubilization, Sustained Release, and Anticancer Activity of Quercetin. Synergistic Engineering of Electron Structure and Interface in BiVO4 Photoelectrodes for Efficient PEC Water Splitting and Self-Powered Photodetectors. Self-Assembly Mechanism of pH-Responsive Wormlike Micelles and Their Structure-Property Correlation with Macroscopic Viscoelasticity.
×
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学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
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