• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

通过增强界面载流子分离提高C介导的NH-MIL-125(Ti)/Zn Cd S S型异质结上的H产量

Boosting H Production over C -Mediated NH -MIL-125(Ti)/Zn Cd S S-Scheme Heterojunction via Enhanced Interfacial Carrier Separation.

作者信息

Li Chunxue, Liu Xiaoteng, Huo Pengwei, Yan Yongsheng, Liao Guangfu, Ding Guixiang, Liu Chunbo

机构信息

Institute of Green Chemistry and Chemical Technology, Advanced Chemical Engineering Laboratory of Green Materials and Energy of Jiangsu Province, School of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang, 212013, China.

Engineering Research Center of Nano-Geomaterials of Ministry of Education, China University of Geosciences, Wuhan, 430074, China.

出版信息

Small. 2021 Oct;17(39):e2102539. doi: 10.1002/smll.202102539. Epub 2021 Aug 18.

DOI:10.1002/smll.202102539
PMID:34405940
Abstract

Improving greatly the separation efficiency of interfacial charge carrier is a major challenge in photocatalysis. Herein, a new class of C -mediated NH -MIL-125(Ti)/Zn Cd S S-scheme heterojunction with enhanced interfacial charge carrier separation is designed and synthesized. The constructed S-scheme heterojunction thermodynamically favors photocatalytic H evolution because of the large driving force resulting from its strong redox abilities. As a consequence, the optimum proportion of C -mediated NH -MIL-125(Ti)/Zn Cd S S-scheme heterojunction displays comparable H evolution activity with a rate of 7825.20 µmol h g under visible light irradiation, which is about 93.05 times, 6.38 times and 2.65 times higher than that of 2% C /NH -MIL-125(Ti), Zn Cd S and 45% NH -MIL-125(Ti)/Zn Cd S, and outperforms the majority of the previously reported MOFs-based photocatalysts. Spectroscopic characterizations and theory calculations indicate that the S-scheme heterojunction can powerfully promote the separation of photogenerated carriers. This work offers a new insight for future design and development of highly active MOFs-based photocatalysts.

摘要

大幅提高界面电荷载流子的分离效率是光催化领域的一项重大挑战。在此,设计并合成了一类新型的具有增强界面电荷载流子分离能力的C介导的NH -MIL-125(Ti)/Zn Cd S S型异质结。所构建的S型异质结由于其强大的氧化还原能力所产生的大驱动力,在热力学上有利于光催化析氢。因此,C介导的NH -MIL-125(Ti)/Zn Cd S S型异质结的最佳比例在可见光照射下表现出相当的析氢活性,析氢速率为7825.20 µmol h g,分别比2% C /NH -MIL-125(Ti)、Zn Cd S和45% NH -MIL-125(Ti)/Zn Cd S高约93.05倍、6.38倍和2.65倍,并且优于大多数先前报道的基于金属有机框架(MOF)的光催化剂。光谱表征和理论计算表明,该S型异质结能够有力地促进光生载流子的分离。这项工作为未来设计和开发高活性的基于MOF的光催化剂提供了新的见解。

相似文献

1
Boosting H Production over C -Mediated NH -MIL-125(Ti)/Zn Cd S S-Scheme Heterojunction via Enhanced Interfacial Carrier Separation.通过增强界面载流子分离提高C介导的NH-MIL-125(Ti)/Zn Cd S S型异质结上的H产量
Small. 2021 Oct;17(39):e2102539. doi: 10.1002/smll.202102539. Epub 2021 Aug 18.
2
Construction of CoS /Zn Cd S S-Scheme Heterojunction for Enhancing H Evolution Activity Under Visible Light.构建用于增强可见光下析氢活性的CoS/Zn Cd S S型异质结
Chemistry. 2021 Nov 11;27(63):15795-15805. doi: 10.1002/chem.202102811. Epub 2021 Oct 6.
3
Construction of NH-MIL-125(Ti)/CdS Z-scheme heterojunction for efficient photocatalytic H evolution.构建用于高效光催化析氢的NH-MIL-125(Ti)/CdS Z型异质结
J Hazard Mater. 2021 Mar 5;405:124128. doi: 10.1016/j.jhazmat.2020.124128. Epub 2020 Oct 6.
4
In Situ Decoration of Zn Cd S with FeP for Efficient Photocatalytic Generation of Hydrogen under Irradiation with Visible Light.用FeP原位修饰Zn Cd S以在可见光照射下高效光催化产氢
Chempluschem. 2018 Sep;83(9):825-830. doi: 10.1002/cplu.201800316.
5
An Efficient and Stable MoS /Zn Cd S Nanocatalyst for Photocatalytic Hydrogen Evolution.一种用于光催化析氢的高效稳定的MoS /Zn Cd S纳米催化剂。
Chemistry. 2020 Sep 21;26(53):12206-12211. doi: 10.1002/chem.202000821. Epub 2020 Aug 25.
6
Engineering of Ultra-Thin Layer of MIL-125(Ti) Nanosheet\Zn-Tetracarboxy-Phthalocyanine S-Scheme Heterojunction as Photocatalytic CO Reduction Catalyst.MIL-125(Ti)纳米片/锌-四羧基酞菁S型异质结超薄层作为光催化CO还原催化剂的工程设计
Small. 2024 Jun;20(24):e2309094. doi: 10.1002/smll.202309094. Epub 2024 Jan 4.
7
Kinetically and Thermodynamically Favorable Ni-Al Layered Double Hydroxide/Ni-Doped ZnCdS S-Scheme Heterojunction Triggering Photocatalytic H Evolution.动力学和热力学有利的镍铝层状双氢氧化物/镍掺杂硫化锌镉硫S型异质结引发光催化析氢
Inorg Chem. 2023 May 1;62(17):6843-6850. doi: 10.1021/acs.inorgchem.3c00613. Epub 2023 Apr 20.
8
Unique CdZnS/WO direct -scheme heterojunction with S, O vacancies and twinning superlattices for efficient photocatalytic water-splitting.具有硫、氧空位和孪晶超晶格的独特CdZnS/WO直接型异质结用于高效光催化水分解。
Dalton Trans. 2022 Jan 17;51(3):1150-1162. doi: 10.1039/d1dt03561d.
9
Enhanced photocatalytic performance over PANI/NH-MIL-101(Fe) with tight interfacial contact.通过紧密的界面接触提高PANI/NH-MIL-101(Fe)的光催化性能。
Dalton Trans. 2022 Oct 11;51(39):15080-15088. doi: 10.1039/d2dt01680j.
10
Novel hollow core-shell ZnCdS@ZnInS/MoS nanocages with Z-scheme heterojunction for enhanced photocatalysis of hydrogen generation.具有Z型异质结的新型中空核壳结构ZnCdS@ZnInS/MoS纳米笼用于增强光催化产氢
J Colloid Interface Sci. 2024 May 15;662:928-940. doi: 10.1016/j.jcis.2024.02.082. Epub 2024 Feb 13.

引用本文的文献

1
Challenges in Photocatalytic Carbon Dioxide Reduction.光催化二氧化碳还原面临的挑战。
Precis Chem. 2024 Jan 17;2(2):49-56. doi: 10.1021/prechem.3c00112. eCollection 2024 Feb 26.
2
In situ and bio-green synthesis of silver nanoparticles immobilized on zeolite as a recyclable catalyst for the degradation of OPDs.原位及生物绿色合成负载于沸石上的银纳米颗粒作为可循环催化剂用于氧化偶氮苯类化合物的降解
Sci Rep. 2024 Jan 11;14(1):1143. doi: 10.1038/s41598-024-51271-9.
3
Recent Advances in Carbon Nitride-Based S-scheme Photocatalysts for Solar Energy Conversion.
用于太阳能转换的氮化碳基S型光催化剂的最新进展
Materials (Basel). 2023 May 15;16(10):3745. doi: 10.3390/ma16103745.
4
3D/2D Heterojunction of CeO/Ultrathin MXene Nanosheets for Photocatalytic Hydrogen Production.用于光催化产氢的CeO/超薄MXene纳米片的3D/2D异质结
ACS Omega. 2022 Jun 16;7(25):21684-21693. doi: 10.1021/acsomega.2c01674. eCollection 2022 Jun 28.