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Integrating molecular photon upconversion via triplet–triplet annihilation (TTA-UC) directly into a solar cell offers a means of harnessing sub-bandgap, near infrared (NIR) photons and surpassing the Shockley–Queisser limit. However, all integrated TTA-UC solar cells to date only harness visible light. Here, we incorporate an osmium polypyridal complex (Os) as the triplet sensitizer in a metal ion linked multilayer photoanode that is capable of harnessing NIR light via S 0 to T 1 * excitation, triple energy transfer to a phosphonated bis(9,10-diphenylethynyl)anthracene annihilator (A), TTA-UC, and electron injection into TiO 2 from the upcoverted state. The TiO 2 -A-Zn-Os devices have five-fold higher photocurrent (∼3.5 μA cm −2 ) than the sum of their parts. IPCE data and excitation intensity dependent measurements indicate that the NIR photons are harvested through a TTA-UC mechanism. Transient absorption spectroscopy is used to show that the low photocurrent, as compared to visible light harnessing TTA-UC solar cells, can be atributed to: (1) slow sensitizer to annihilator triplet energy transfer, (2) a low injection yield for the annihilator, and (3) fast back energy transfer from the upconverted state to the sensitizer. Regardless, these results serve as a proof-of-concept that NIR photons can be harnessed via an S 0 to T 1 * sensitizer excited, integrated TTA-UC solar cell and that further improvements can readily be made by remedying the performance limiting processes noted above.
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Triplet Fusion Upconversion for Photocuring 3D‐Printed Particle‐Reinforced Composite Networks
Abstract High energy photons (λ < 400 nm) are frequently used to initiate free radical polymerizations to form polymer networks, but are only effective for transparent objects. This phenomenon poses a major challenge to additive manufacturing of particle‐reinforced composite networks since deep light penetration of short‐wavelength photons limits the homogeneous modification of physicochemical and mechanical properties. Herein, the unconventional, yet versatile, multiexciton process of triplet–triplet annihilation upconversion (TTA‐UC) is employed for curing opaque hydrogel composites created by direct‐ink‐write (DIW) 3D printing. TTA‐UC converts low energy red light (λmax = 660 nm) for deep penetration into higher‐energy blue light to initiate free radical polymerizations within opaque objects. As proof‐of‐principle, hydrogels containing up to 15 wt.% TiO2filler particles and doped with TTA‐UC chromophores are readily cured with red light, while composites without the chromophores and TiO2loadings as little as 1–2 wt.% remain uncured. Importantly, this method has wide potential to modify the chemical and mechanical properties of complex DIW 3D‐printed composite polymer networks.
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- PAR ID:
- 10396017
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- Advanced Materials
- Volume:
- 35
- Issue:
- 11
- ISSN:
- 0935-9648
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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