Figures & data
This paper provides a perspective that theory and experiment are best used in tandem to study DSC devices
![This paper provides a perspective that theory and experiment are best used in tandem to study DSC devices](/cms/asset/62454d72-aa4f-44c4-b0df-91a6fa5ee3fd/tsta_a_1492858_uf0001_c.jpg)
Figure 1. Schematic of DSC device showing key steps for device operation (in black) and competing processes (in red).
![Figure 1. Schematic of DSC device showing key steps for device operation (in black) and competing processes (in red).](/cms/asset/f3cd5c3e-bab1-4974-aac2-358d33b8f409/tsta_a_1492858_f0001_c.jpg)
Figure 2. Schematic of DSC components illustrating dye co-sensitization: C, dye chromophore; BAC, bulky alkyl chain; D, donor; A, acceptor; AG, anchoring group; I, TiO2/dye interface. Red, O; light grey, Ti; blue, N; grey, C; white, H.
![Figure 2. Schematic of DSC components illustrating dye co-sensitization: C, dye chromophore; BAC, bulky alkyl chain; D, donor; A, acceptor; AG, anchoring group; I, TiO2/dye interface. Red, O; light grey, Ti; blue, N; grey, C; white, H.](/cms/asset/efa6327e-d7bc-49cc-b074-85613a2a2cb3/tsta_a_1492858_f0002_c.jpg)
Figure 3. Possible binding modes for a carboxylate anchor group binding to a metal oxide surface. Reproduced with permission from [Citation85].
![Figure 3. Possible binding modes for a carboxylate anchor group binding to a metal oxide surface. Reproduced with permission from [Citation85].](/cms/asset/81eb8866-e16c-470a-a7d3-bc36a4d27d9d/tsta_a_1492858_f0003_b.gif)
Table 1. DSC device parameters for triphenylamine dyes with 1,2 or 3 linkers. Errors in brackets. Reproduced with permission from [Citation57].
Figure 4. Dye anchoring points A, B, C and D on a half-squaraine chromophore. Reproduced with permission from [Citation7].
![Figure 4. Dye anchoring points A, B, C and D on a half-squaraine chromophore. Reproduced with permission from [Citation7].](/cms/asset/473021ba-18e9-4654-a532-69eafa3c7b84/tsta_a_1492858_f0004_c.jpg)
Figure 5. Molecular structures of (a) N3, (b) HSQ1 and (c) SQ1. Reproduced with permission from [Citation68].
![Figure 5. Molecular structures of (a) N3, (b) HSQ1 and (c) SQ1. Reproduced with permission from [Citation68].](/cms/asset/ec0c6a12-ba49-4b6a-8ef0-4233f2cb5cee/tsta_a_1492858_f0005_b.gif)
Figure 6. Shift in HOMO caused by the addition of sulphur atom to half-squaraine sensitizer. EF = Fermi level, (i) dye injection overpotential and (ii) dye regeneration overpotential. D = ground state dye, D* = excited state dye, D+; = oxidized dye, CB =conduction band, hν = sunlight and Voc = open circuit voltage.
![Figure 6. Shift in HOMO caused by the addition of sulphur atom to half-squaraine sensitizer. EF = Fermi level, (i) dye injection overpotential and (ii) dye regeneration overpotential. D = ground state dye, D* = excited state dye, D+; = oxidized dye, CB =conduction band, hν = sunlight and Voc = open circuit voltage.](/cms/asset/53fb51ed-4501-4bd0-ba93-941a0715c881/tsta_a_1492858_f0006_c.jpg)