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含氧化钴纳米片、卟啉和甲基紫精的逐层固体薄膜中的光致电子转移

Photoinduced electron transfer in layer-by-layer thin solid films containing cobalt oxide nanosheets, porphyrin, and methyl viologen.

作者信息

Sasai R, Kato Y, Soontornchaiyakul W, Usami H, Masumori A, Norimatsu W, Fujimura T, Takagi S

机构信息

Department of Physics and Materials Sciences, Interdisciplinary Graduate School of Science and Engineering, Shimane University, 1060, Nishi-kawatsu-cho, Matsue 690-8504, Japan.

Department of Fine Materials Engineering, Faculty of Textile Science and Technology, Shinshu University, 3-15-1 Tokida, Ueda 386-8567, Japan.

出版信息

Phys Chem Chem Phys. 2017 Feb 15;19(7):5611-5616. doi: 10.1039/c6cp07250j.

Abstract

The well-known layer-by-layer (LbL) method can be used to prepare solid thin films with a controlled electron transfer direction by appropriately stacking metal oxide nanosheets and functional organic ions. In this study, we prepared thin solid films consisting of cobalt oxide nanosheets (CoNSs) as the electron transfer medium, α,β,γ,δ-tetrakis(1-methylpyridinium-4-yl)porphyrin (TMPyP) as the electron donor, and 1,1'-dimethyl-4,4'-bipyridinium or methyl viologen (MV) as the electron acceptor. We investigated the photoinduced electron transfer phenomenon in these films by irradiating them with 450 nm light. Irradiating the LbL thin solid films prepared with the CoNS/TMPyP/CoNS/MV/CoNS sequence under reduced pressure led to the production of a one-electron reduction compound of MV. Hence, photoinduced electron transfer from TMPyP to MV bound to CoNSs occurred in these LbL thin solid films. However, the conduction band of CoNSs, as determined by the photoabsorption spectral and photoelectrochemical measurements, was much higher than the lowest unoccupied molecular orbital level of TMPyP. Our findings indicate that the observed equipotential photoinduced electron transfer was caused by the metallic electron conductivity of CoNSs, which show a unique charge arrangement of Co and Co. Moreover, it was also found that the observed photoinduced charge separation state has a longer life-time (>5 h) under the reduced conditions.

摘要

众所周知的层层(LbL)方法可用于通过适当堆叠金属氧化物纳米片和功能性有机离子来制备具有可控电子转移方向的固体薄膜。在本研究中,我们制备了由氧化钴纳米片(CoNSs)作为电子转移介质、α,β,γ,δ-四(1-甲基吡啶-4-基)卟啉(TMPyP)作为电子供体以及1,1'-二甲基-4,4'-联吡啶鎓或甲基紫精(MV)作为电子受体组成的固体薄膜。我们通过用450 nm光照射这些薄膜来研究其中的光致电子转移现象。在减压条件下照射以CoNS/TMPyP/CoNS/MV/CoNS序列制备的LbL固体薄膜会导致产生MV的单电子还原化合物。因此,在这些LbL固体薄膜中发生了从TMPyP到与CoNSs结合的MV的光致电子转移。然而,通过光吸收光谱和光电化学测量确定的CoNSs的导带远高于TMPyP的最低未占据分子轨道能级。我们的研究结果表明,观察到的等势光致电子转移是由CoNSs的金属电子导电性引起的,CoNSs显示出Co和Co独特的电荷排列。此外,还发现在还原条件下观察到的光致电荷分离态具有更长的寿命(>5小时)。

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