State-of-the-art external quantum efficiencies (EQEs) have exceeded 20% for near-infrared, red, and green perovskite light-emitting diodes (PeLEDs) so far. Nevertheless, the cutting-edge blue counterparts demonstrate an inferior device performance, which impedes the commercialization and industrialization of PeLEDs in ultrahigh-definition displays. As the most popular hole transport layer, poly­(3,4-ethylenedioxythiophene):polystyrenesulfonate (PEDOT:PSS) bears the acidic and hygroscopic drawbacks, which deteriorates the device efficiency and long-term stability of blue PeLEDs. In this work, the basic amino acids with zwitterionic characteristics are proposed to modulate the pH of PEDOT:PSS, which are arginine, lysine, and histidine. It is found that they play a triple function to the blue perovskite films: modulating the acidity of PEDOT:PSS, controlling the crystalline process, and passivating the defects at the PEDOT:PSS/perovskite interface. As a result, the utilization of neutral PEDOT:PSS leads to a significant enhancement in stability and photoluminescence quantum yield. Eventually, the pure-blue PeLEDs achieve a record EQE of 5.6% with the emission peak at 467 nm. This research proves that the interfacial engineering of hole transport layers is a reliable strategy to enhance the device efficiency and operation stability of blue PeLEDs.

Poly­(3,4-ethylenedioxythiophene):poly­(styrenesulfonate) (PEDOT:PSS) is one of the most prospering transparent conductive materials for flexible optoelectronic devices, which arises from its nonpareil features of low-cost solution processability, tunable conductivity, high transparency, and superior mechanical flexibility. However, acidity and hygroscopicity of PSS chains cause a decrease in conductivity, substrate corrosion, and device degradation. This work proposes a facile and effective direct doping strategy of sodium 3-methylsalicylate to enhance the conductivity, alleviate the acidity, and improve the stability of PEDOT:PSS electrodes, simultaneously. Owing to the formation of weaker acid and PSS-Na, PSS chains are disentangled from the coiled PEDOT:PSS complexes, leading to the phase separation of PEDOT:PSS and the formation of fibril-like PEDOT domains. Eventually, the sodium 3-methylsalicylate-modified PEDOT:PSS electrode is employed in flexible organic light-emitting diodes with an outstanding external quantum efficiency of up to 25%. The improved performance is attributed to the more matched work function and the as-formed interfacial dipole. The sodium 3-methylsalicylate-modified PEDOT:PSS electrode with high conductivity and transmittance, superior stability in the air as well as good mechanical flexibility has the potential to be the most promising transparent conductive material for flexible optoelectronic device applications.

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Perovskite light-emitting diodes (PeLEDs) have demonstrated rapid development during the past decade, whereas the inferior device performance of blue ones impedes the application in full-color display and lighting. Low-dimensional perovskites turn out to be the most promising blue-emitters owing to their superior stability. In this work, a multidentate zwitterionic l-arginine is proposed to achieve blue emission from pure bromide-based perovskites by in situ-forming low-dimensional nanosheets. First, l-arginine can promote the formation of perovskite nanosheets due to the strong interaction between the peripheral guanidinium cations and [PbBr6]4– octahedral layers, enabling a significant blue-shift. Second, the carboxyl group within l-arginine can passivate uncoordinated Pb2+ ions, improving the device performance. Finally, a blue PeLED is successfully constructed on the basis of the l-arginine-modulated perovskite film, demonstrating a peak luminance of 2152 cd/m2, an external quantum efficiency of 5.4%, and operation lifetime of 13.81 min. Further, the enlightenment from this work is hopefully to be applied in rationally designing spacer cations for low-dimensional perovskite optoelectronic devices.