Underpotential Deposition of Cadmium on Colloidal CdSe Quantum Dots: Effect of Particle Size and Surface Ligands

被引:10
作者
Aniskevich, Yauhen [1 ,2 ]
Antanovich, Artsiom [1 ]
Prudnikau, Anatol [1 ,4 ]
Artemyev, Mikhail V. [1 ]
Mazanik, Alexander V. [3 ]
Ragoisha, Genady [1 ]
Streltsov, Eugene A. [2 ]
机构
[1] Belarusian State Univ, Res Inst Phys Chem Problems, Minsk 220006, BELARUS
[2] Belarusian State Univ, Fac Chem, Minsk 220030, BELARUS
[3] Belarusian State Univ, Energy Phys Dept, Fac Phys, Minsk 220030, BELARUS
[4] Tech Univ Dresden, Phys Chem, Bergstr 66b, D-01062 Dresden, Germany
关键词
ELECTROCHEMICAL PROPERTIES; SOLAR-CELLS; ELECTROPHORETIC DEPOSITION; ELECTRONIC-STRUCTURE; BAND ALIGNMENT; SHAPE CONTROL; THIN-FILMS; NANOCRYSTALS; ENERGY; RAMAN;
D O I
10.1021/acs.jpcc.8b10318
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Electrochemistry of quantum dots (QDs) can provide useful information on their redox behavior and energy states. Here, we present a study of the surface-limited electrochemical deposition of cadmium adatoms (underpotential deposition or upd) on electro-phoretically formed films of CdSe QDs of different sizes (2.4-6.3 nm) capped with different ligands (oleate and sulfide). Oleate-capped QD films were shown to have a weak electrochemical response in upd reaction, whereas sulfide-capped QDs demonstrated a significant increase in cathodic current that was attributed to enhanced surface accessibility and improved interparticle electron transfer. Cadmium upd onset potential in sulfide-treated QD films was found to be markedly size dependent. The increase of QD size results in the positive shift of upd onset potential which is in agreement with the change in lowest unoccupied molecular orbital position. The results imply that the proposed method utilizing electrochemical surface-limited reaction on QDs can be applied to probe energy states of chalcogenide semiconductor nanoparticles.
引用
收藏
页码:931 / 939
页数:9
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