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Chemical structures of natural dye pigments (a) chlorophyll, (b) flavonoid, (c) anthocyanin, (d) carotenoid. 

Chemical structures of natural dye pigments (a) chlorophyll, (b) flavonoid, (c) anthocyanin, (d) carotenoid. 

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Dye-sensitized solar cells (DSSCs) have become a topic of significant research in the last two decades because of their scientific importance in the area of energy conversion. Currently, DSSC is using inorganic ruthenium (Ru)-based, metal-free organic dyes, quantum-dot sensitizer, perovskite-based sensitizer, and natural dyes as sensitizer. The use...

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... are a large family (over 600 members) of isoprenoids that provide many fruits and flowers with dis- tinctive red, orange, and yellow colors. Carotenoids are Sensitizers for DSSC S. Shalini et al. distinguished by the presence of C 40 hydrocarbon back- bone that induces structural and oxygenic modifications [99]. Figure 7d shows the chemical structure of carotenoid. The light absorption is achieved by a photo-induced trans- formation of 'p' delocalized electrons of carotenoid mole- cules. This in turn transfers the absorbed energy to the chlorophyll molecules to form a singlet chlorophyll state with a slightly higher energy. This transfer of energy from carotenoids to chlorophyll molecules is facilitated by phys- ical structure of chlorophyll [108]. Experimental procedure for synthesis of natural sen- sitizers starts with collection of fresh flowers and extrac- tion of dyes with suitable solvent. Fresh rosella or blue pea flower of 1 g was extracted in 100 ml of water and ethanol at different temperatures for 30 min. Solid resi- dues were filtered out to obtain clear dye solutions [59]. Fresh spinach and ipomoea leaves of 10 g are sep- arately put into 200 ml of alcohol. Through indirect hy- dronic heating in boiling water, they were heated for 20 min to extract their chlorophyll. The solid dregs in the solution were filtered by filter paper to acquire a pure and natural dye solution [61]. Table III summarizes the photoelectrochemical pa- rameters of the different natural dyes extracted from leaves, seeds, flowers, fruits, vegetables, and tree ...
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... belong to natural photosynthetic pigments [101,102] that give plants green color. The two major types of chlorophylls are chlorophyll 'a' and chlorophyll 'b'. Chlorophylls and their derivatives are employed as sensi- tizers in DSSC because of their tendency to absorb blue and red lights. The most efficient is the derivative of chlo- rophyll 'a' (methyl trans-32-carboxy-pyropheophorbide) [99]. The absorbance spectrum of chlorophyll 'b' shows a characteristic blue tinge and has a red shift when com- pared with chlorophyll 'a'. Chemical structure of chloro- phyll 'a' and chlorophyll 'b' is shown in Figure ...
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... are the most widespread and physiologi- cally active group of natural constituents with a basic C 6 - C 3 -C 6 skeleton. Flavone consists of two benzene rings, joined together by a γ ring that distinguishes one flavonoid compound from the other [99]. Figure 7b shows the basic chemical structure of commonly occurring ...
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... are glycoside salts of phenyl-2- benzopyrilium based on a C 15 skeleton with a chromane ring bearing a second aromatic ring B in position 2 (C 6 - C 3 -C 6 ) [104,105]. Basic chemical structure of anthocyanin is shown in Figure ...
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... are a large family (over 600 members) of isoprenoids that provide many fruits and flowers with dis- tinctive red, orange, and yellow colors. Carotenoids are Sensitizers for DSSC S. Shalini et al. distinguished by the presence of C 40 hydrocarbon back- bone that induces structural and oxygenic modifications [99]. Figure 7d shows the chemical structure of carotenoid. The light absorption is achieved by a photo-induced trans- formation of 'p' delocalized electrons of carotenoid mole- cules. This in turn transfers the absorbed energy to the chlorophyll molecules to form a singlet chlorophyll state with a slightly higher energy. This transfer of energy from carotenoids to chlorophyll molecules is facilitated by phys- ical structure of chlorophyll [108]. Experimental procedure for synthesis of natural sen- sitizers starts with collection of fresh flowers and extrac- tion of dyes with suitable solvent. Fresh rosella or blue pea flower of 1 g was extracted in 100 ml of water and ethanol at different temperatures for 30 min. Solid resi- dues were filtered out to obtain clear dye solutions [59]. Fresh spinach and ipomoea leaves of 10 g are sep- arately put into 200 ml of alcohol. Through indirect hy- dronic heating in boiling water, they were heated for 20 min to extract their chlorophyll. The solid dregs in the solution were filtered by filter paper to acquire a pure and natural dye solution [61]. Table III summarizes the photoelectrochemical pa- rameters of the different natural dyes extracted from leaves, seeds, flowers, fruits, vegetables, and tree ...
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... belong to natural photosynthetic pigments [101,102] that give plants green color. The two major types of chlorophylls are chlorophyll 'a' and chlorophyll 'b'. Chlorophylls and their derivatives are employed as sensi- tizers in DSSC because of their tendency to absorb blue and red lights. The most efficient is the derivative of chlo- rophyll 'a' (methyl trans-32-carboxy-pyropheophorbide) [99]. The absorbance spectrum of chlorophyll 'b' shows a characteristic blue tinge and has a red shift when com- pared with chlorophyll 'a'. Chemical structure of chloro- phyll 'a' and chlorophyll 'b' is shown in Figure ...
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... are the most widespread and physiologi- cally active group of natural constituents with a basic C 6 - C 3 -C 6 skeleton. Flavone consists of two benzene rings, joined together by a γ ring that distinguishes one flavonoid compound from the other [99]. Figure 7b shows the basic chemical structure of commonly occurring ...
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... are glycoside salts of phenyl-2- benzopyrilium based on a C 15 skeleton with a chromane ring bearing a second aromatic ring B in position 2 (C 6 - C 3 -C 6 ) [104,105]. Basic chemical structure of anthocyanin is shown in Figure ...

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