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A High Dielectric N-Type Small Molecular Acceptor Containing Oligoethyleneglycol Side-Chains for Organic Solar Cellst

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Chinese Journal of Chemistry 2018年第3期36卷 199-205页

作者： Bomee Jang changyeon lee Young Woong lee Donguk Kim Mohammad Afsar Uddin Felix Sunjoo Kim Bumjoon J. Kim Han Young Woo Department of Chemistry Korea University Seoul 02841 Republic of Korea Department of Chemical and Biornolecular Engineering Korea Advanced Institute of Science and Technology (KAIST) Daejeon 34141 Republic of Korea School of Chemical Engineering and Materials Science Chung-Ang UniversitySeoul 06974 Republic of Korea

We report a new small molecular acceptor, ITIC-OEG, which is based on indacenodithieno[3,2-b]thiophene and 1,1-（dicyanomethylene）-3- indanone including oligoethyleneglycol （OEG） side-chains. ITIC-OEG was found to have higher dielectric constant （ε1=5.6} than that of a reference molecule of ITIC with normal alkyl substituents （ε1=3.9）. The dielectric constant of medium influences significantly the exciton binding energy and the resulting charge separation and recombination. The optical, electrochemical and morphological properties of ITIC-OEG and its photovoltaic characteristics were investigated by blending with a semi-crystalline donor polymer, PPDT2FBT, with comparison to those of ITIC. ITIC-OEG shows more red-shifted absorption and stronger crystalline packing than ITIC. However, the lower photovoltaic performance （with 1.58% power conversion efficiency, PCE） was measured for PPDT2FBT-ITIC-OEG, compared to PPDT2FBT：ITIC （5..52% PCE）. The incompatibility between PPDT2FBT and ITIC-OEG （due to high hydrophilic nature of OEG chains） resulted in poor intermixing with large domain separation over 300 nm, showing inefficient charge separation and significant charge recombination. Therefore, to investigate the effect of dielectric constant of the materials on the charge separation and recombination, the blend morphology of the PPDT2FBT：ITIC-OEG should be optimized first by improving their miscibility and phase separation.

关键词： N-type small molecule dielectric constant morphology organic solar cells

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Direct Synthesis of Molybdenum Phosphide Nanorods on Silicon Using Graphene at the Heterointerface for Efficient Photoelectrochemical Water Reduction

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Nano-Micro Letters 2021年第5期13卷 135-150页

作者： Sang Eon Jun Seokhoon Choi Shinyoung Choi Tae Hyung lee changyeon Kim Jin Wook Yang Woon‑Oh Choe In‑Hyuk Im Cheol‑Joo Kim Ho Won Jang Department of Materials Science and Engineering Research Institute of Advanced MaterialsSeoul National UniversitySeoul 08826Republic of Korea Department of Chemical Engineering Pohang University of Science and TechnologyPohang 37673Republic of Korea

Transition metal phosphides(TMPs)and transition metal dichalcogenides(TMDs)have been widely investigated as photoelectrochemical(PEC)catalysts for hydrogen evolution reaction(HER).Using high-temperature processes to get crystallized compounds with large-area uniformity,it is still challenging to directly synthesize these catalysts on silicon photocathodes due to chemical incompatibility at the ***,a graphene interlayer is applied between p-Si and MoP nanorods to enable fully engineered interfaces without forming a metallic secondary compound that absorbs a parasitic light and provides an inefficient electron path for hydrogen ***,the graphene facilitates the photogenerated electrons to rapidly transfer by creating Mo-O-C covalent bondings and energetically favorable band *** a bridging role of graphene,numerous active sites and anti-reflectance of MoP nanorods lead to significantly improved PEC-HER performance with a high photocurrent density of 21.8 mA cm−2 at 0 V versus RHE and high ***,low dependence on pH and temperature is observed with MoP nanorods incorporated photocathodes,which is desirable for practical use as a part of PEC *** results indicate that the direct synthesis of TMPs and TMDs enabled by graphene interlayer is a new promising way to fabricate Si-based photocathodes with high-quality interfaces and superior HER performance.

关键词： Photoelectrochemical water splitting Silicon Molybdenum phosphide Hydrogen evolution Graphene

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