Excited-State Charge Transfer in Covalently Functionalized MoS2 with a Zinc Phthalocyanine Donor-Acceptor Hybrid

被引:47
作者
Canton-Vitoria, Ruben [1 ]
Gobeze, Habtom B. [2 ]
Blas-Ferrando, Vicente M. [3 ]
Ortiz, Javier [3 ]
Jang, Youngwoo [2 ]
Fernandez-Lazaro, Fernando [3 ]
Sastre-Santos, Angela [3 ]
Nakanishi, Yusuke [4 ]
Shinohara, Hisanori [4 ]
D'Souza, Francis [2 ]
Tagmatarchis, Nikos [1 ,4 ]
机构
[1] Natl Hellen Res Fdn, Inst Theoret & Phys Chem, GR-11635 Athens, Greece
[2] Univ North Texas, Dept Chem, Denton, TX 76203 USA
[3] Univ Miguel Hernandez, Inst Bioingn, Area Quim Organ, Elche 03202, Spain
[4] Nagoya Univ, Dept Chem, Nagoya, Aichi 4648602, Japan
基金
欧盟地平线“2020”; 美国国家科学基金会;
关键词
charge transfer; functionalization; phthalocyanines; spectroelectrochemistry; transition-metal dichalcogenides; MONOLAYER MOS2; DYNAMICS;
D O I
10.1002/anie.201900101
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The functionalization of MoS2 is of paramount importance for tailoring its properties towards optoelectronic applications and unlocking its full potential. Zinc phthalocyanine (ZnPc) carrying an 1,2-dithiolane oxide linker was used to functionalize MoS2 at defect sites located at the edges. The structure of ZnPc-MoS2 was fully assessed by complementary spectroscopic, thermal, and microscopy imaging techniques. An energy-level diagram visualizing different photochemical events in ZnPc-MoS2 was established and revealed a bidirectional electron transfer leading to a charge separated state ZnPc center dot+-MoS2 center dot-. Markedly, evidence of the charge transfer in the hybrid material was demonstrated using fluorescence spectroelectrochemistry. Systematic studies performed by femtosecond transient absorption revealed the involvement of excitons generated in MoS2 in promoting the charge transfer, while the transfer was also possible when ZnPc was excited, signifying their potential in light-energy-harvesting devices.
引用
收藏
页码:5712 / 5717
页数:6
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