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Publications [#330217] of Michael J. Therien

Papers Published

  1. Bai, Y; Olivier, J-H; Yoo, H; Polizzi, NF; Park, J; Rawson, J; Therien, MJ, Molecular Road Map to Tuning Ground State Absorption and Excited State Dynamics of Long-Wavelength Absorbers., Journal of the American Chemical Society, vol. 139 no. 46 (November, 2017), pp. 16946-16958 [doi]
    (last updated on 2018/06/22)

    Abstract:
    Realizing chromophores that simultaneously possess substantial near-infrared (NIR) absorptivity and long-lived, high-yield triplet excited states is vital for many optoelectronic applications, such as optical power limiting and triplet-triplet annihilation photon upconversion (TTA-UC). However, the energy gap law ensures such chromophores are rare, and molecular engineering of absorbers having such properties has proven challenging. Here, we present a versatile methodology to tackle this design issue by exploiting the ethyne-bridged (polypyridyl)metal(II) (M; M = Ru, Os)-(porphinato)metal(II) (PM'; M' = Zn, Pt, Pd) molecular architecture (M-(PM')n-M), wherein high-oscillator-strength NIR absorptivity up to 850 nm, near-unity intersystem crossing (ISC) quantum yields (ΦISC), and triplet excited-state (T1) lifetimes on the microseconds time scale are simultaneously realized. By varying the extent to which the atomic coefficients of heavy metal d orbitals contribute to the one-electron excitation configurations describing the initially prepared singlet and triplet excited-state wave functions, we (i) show that the relative magnitudes of fluorescence (k0F), S1 → S0 nonradiative decay (knr), S1 → T1 ISC (kISC), and T1 → S0 relaxation (kT1→S0) rate constants can be finely tuned in M-(PM')n-M compounds and (ii) demonstrate designs in which the kISC magnitude dominates singlet manifold relaxation dynamics but does not give rise to T1 → S0 conversion dynamics that short-circuit a microseconds time scale triplet lifetime. Notably, the NIR spectral domain absorptivities of M-(PM')n-M chromophores far exceed those of classic coordination complexes and organic materials possessing similarly high yields of triplet-state formation: in contrast to these benchmark materials, this work demonstrates that these M-(PM')n-M systems realize near unit ΦISC at extraordinarily modest S1-T1 energy gaps (∼0.25 eV). This study underscores the photophysical diversity of the M-(PM')n-M platform and presents a new library of long-wavelength absorbers that efficiently populate long-lived T1 states.


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