4.6 Article

The relationship between the boron dipyrromethene (BODIPY) structure and the effectiveness of homogeneous and heterogeneous solar hydrogen-generating systems as well as DSSCs

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PHYSICAL CHEMISTRY CHEMICAL PHYSICS
卷 17, 期 15, 页码 9716-9729

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ROYAL SOC CHEMISTRY
DOI: 10.1039/c5cp00732a

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资金

  1. National Natural Science Foundation of China [21201066]
  2. Natural Science Foundation of Fujian Province [2011J01047]
  3. outstanding Youth Scientific Research Cultivation Plan of Colleges and Universities of Fujian Province [JA13008]
  4. Young and Middle-aged Teacher in Science and Technology Research of Huaqiao University [ZQN-PY104]
  5. National Innovative Foundation Project [20140385003]

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A series of boron dipyrromethene (BODIPY) dyes (B1-B5) having H atoms at 2,6-positions or heavy-atom I at 2-/2,6-positions, and an ortho-or a para-COOH substituted phenyl moiety at the 8-position on the BODIPY core were synthesized and characterized. These organic dyes were applied for investigating the relationship between the BODIPY structure and the effectiveness of homogeneous and heterogeneous visible-light-driven hydrogen production as well as dye-sensitized solar cells (DSSCs). For the homogeneous photocatalytic hydrogen production systems with a cobaloxime catalyst, the efficiency of hydrogen production could be tuned by substituting with heavy atoms and varying carboxyl group orientations of BODIPYs. As a result, B5 containing two I atoms and an ortho-COOH anchoring group was the most active one (TONs = 197). The activity of hydrogen generation followed the order B5 > B3 > B2 > B1 = B4 = 0. An interesting ortho-position effect'' was observed in the present homogeneous systems, i.e., substitution groups were located at the ortho-position and higher hydrogen production activities were obtained. For the heterogeneous hydrogen production systems with a platinized TiO2 catalyst, the effectiveness of hydrogen evolution was highly influenced by the intersystem crossing efficiency, molar absorptivity and positions of the anchoring group of dyes. Thus, B3 having two core iodine atoms and a para-COOH group with TONs of 70 excelled other BODIPYs and the TONs of hydrogen generation showed the trend of B3 > B5 > B2 > B1 = B4 = 0. The results demonstrate that the present photocatalytic H-2 production proceeds with higher efficiency and stability in the homogeneity than in the heterogeneity. In the case of DSSCs, the overall cell performance of BODIPY chromophores was highly dependent on both the absence or the presence of iodine atoms on the BODIPY core and -COOH anchoring positions. The B1-TiO2 system showed the best cell performance, because the most effective surface binding mode is allowed with this structure. This is also in contrast with the case of dye-sensitized solar H-2 generation, in which B3 was the most efficient chromophore. The differences between dye-sensitized hydrogen-generating systems and DSSCs may be due to rates of electron transfer and the dye aggregation tendency.

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