Xu Huajun, Elder Delwin L, Johnson Lewis E, Heni Wolfgang, de Coene Yovan, De Leo Eva, Destraz Marcel, Meier Norbert, Vander Ghinst Wouter, Hammond Scott R, Clays Koen, Leuthold Juerg, Dalton Larry R, Robinson Bruce H
Department of Chemistry, University of Washington, Seattle, WA 98195, USA.
Nonlinear Materials Corporation, Seattle, WA 98109, USA.
Mater Horiz. 2022 Jan 4;9(1):261-270. doi: 10.1039/d1mh01206a.
This study demonstrates enhancement of in-device electro-optic activity a series of theory-inspired organic electro-optic (OEO) chromophores based on strong (diarylamino)phenyl electron donating moieties. These chromophores are tuned to minimize trade-offs between molecular hyperpolarizability and optical loss. Hyper-Rayleigh scattering (HRS) measurements demonstrate that these chromophores, herein described as BAH, show >2-fold improvement in standard chromophores such as JRD1, and approach that of the recent BTP and BAY chromophore families. Electric field poled bulk devices of neat and binary BAH chromophores exhibited significantly enhanced EO coefficients () and poling efficiencies (/) compared with state-of-the-art chromophores such as JRD1. The neat BAH13 devices with charge blocking layers produced very large poling efficiencies of 11.6 ± 0.7 nm V and maximum value of 1100 ± 100 pm V at 1310 nm on hafnium dioxide (HfO). These results were comparable to that of our recently reported BAY1 but with much lower loss (extinction coefficient, ), and greatly exceeding that of other previously reported OEO compounds. 3 : 1 BAH-FD : BAH13 blends showed a poling efficiency of 6.7 ± 0.3 nm V and an even greater reduction in . 1 : 1 BAH-BB : BAH13 showed a higher poling efficiency of 8.4 ± 0.3 nm V, which is approximately a 2.5-fold enhancement in poling efficiency JRD1. Neat BAH13 was evaluated in plasmonic-organic hybrid (POH) Mach-Zehnder modulators with a phase shifter length of 10 μm and slot widths of 80 and 105 nm. In-device BAH13 achieved a maximum of 208 pm V at 1550 nm, which is ∼1.7 times higher than JRD1 under equivalent conditions.
本研究展示了基于强(二芳基氨基)苯基供电子基团的一系列受理论启发的有机电光(OEO)发色团在器件内电光活性的增强。这些发色团经过调整,以尽量减少分子超极化率与光学损耗之间的权衡。超瑞利散射(HRS)测量表明,这些在此称为BAH的发色团,与标准发色团如JRD1相比,改善超过2倍,接近最近的BTP和BAY发色团家族的水平。与诸如JRD1等最先进的发色团相比,纯BAH发色团和二元BAH发色团的电场极化块状器件表现出显著增强的电光系数()和极化效率(/)。具有电荷阻挡层的纯BAH13器件在二氧化铪(HfO)上于1310 nm处产生了非常大的极化效率,为11.6±0.7 nm V,最大值为1100±100 pm V。这些结果与我们最近报道的BAY1相当,但损耗(消光系数,)要低得多,大大超过了其他先前报道的OEO化合物。3∶1的BAH - FD∶BAH13共混物表现出6.7±0.3 nm V的极化效率,并且在方面有更大程度的降低。1∶1的BAH - BB∶BAH13表现出更高的极化效率,为8.4±0.3 nm V,这大约是JRD1极化效率的2.5倍。在相移器长度为10μm、狭缝宽度为80和105 nm的等离子体 - 有机混合(POH)马赫 - 曾德尔调制器中对纯BAH13进行了评估。器件内的BAH13在1550 nm处实现了最大为208 pm V,这在等效条件下比JRD1高约1.7倍。