Origin of the Exclusive Ternary Electroluminescent Behavior of BN‐Doped Nanographenes in Efficient Single‐Component White Light‐Emitting Electrochemical Cells

White-light-emitting electrochemical cells (WLECs) still represent a significant milestone, since only a few examples with moderate performances have been reported. Particularly, multiemissive white emitters are highly desired, as a paradigm to circumvent phase separation and voltage-dependent emission color issues that are encountered following host:guest and multilayered approaches. Herein, the origin of the exclusive white ternary electroluminescent behavior of BN-doped nanographenes with a B3N3 doping pattern (hexa-perihexabenzoborazinocoronene) is rationalized, leading to one of the most efficient (approximate to 3 cd A(-1)) and stable-over-days single-component and single-layered WLECs. To date, BN-doped nanographenes have featured blue thermally activated delayed fluorescence (TADF). This doping pattern provides, however, white electroluminescence spanning the whole visible range (x/y CIE coordinates of 0.29-31/0.31-38 and average color rendering index (CRI) of 87) through a ternary emission involving fluorescence and thermally activated dual phosphorescence. This temperature-dependent multiemissive mechanism is operative for both photo- and electroluminescence processes and holds over the device lifespan, regardless of the device architecture, active layer composition, and operating conditions. As such, this work represents a new stepping-stone toward designing a new family of multiemissive white emitters based on BN-doped nanographenes that realizes one of the best-performing single-component white-emitting devices compared to the prior-art

Subpicosecond photoinduced Stark spectroscopy in fullerene-based devices

Published versio

Photoinduced transient stark spectroscopy in organic semiconductors: a method for charge mobility determination in the picosecond regime.

Published versio

Assembly-Induced Bright-Light Emission from Solution-Processed Platinum(II) Inorganic Polymers

Synthesis, processing, and characterization are reported for a series of tetracyanoplatinate Magnus' salt (TCN-MS) derivatives-soluble derivatives of the generally intractable Magnus' green salt-that feature the general structure [Pt(NH2R)(4)] [Pt(CN)(4)] where R is a branched alkyl group or a w-phenylalkyl group. In solutions, these coordination compounds generally dissolve on the level of individual ion pairs as shown by X-ray diffraction analysis. To enable the formation of quasi-one-dimensional linear stacks of Pt(II) atoms in thin films, the matrix-assisted assembly is employed, whereby the compounds are codissolved with poly(ethylene oxide) (PEO), followed by film casting, thermally activated assembly, and eventual removal of PEO. Remarkably, assembled TCN-MS inorganic polymers exhibit bright blue-green photoluminescence. A detailed investigation of the assembly process and simultaneously modified solid-state optical properties is performed using a range of microscopy, optical and vibrational spectroscopy, and thermal analysis techniques. Given their unusual combination of optical properties, namely, transparency in the visible region, high photoluminescence quantum efficiencies (up to 13% in first-demonstration samples), and large Stokes shifts (up to 1 eV), TCN-MS derivatives are proposed as a promising class of light-emitting materials for emerging applications in molecular optoelectronics, the potential and challenges of which are discussed.The work in Barcelona was financially supported by the Ministerio de Economía y Competitividad of Spain through the Severo Ochoa Programme for Centres of Excellence in R&D (SEV-2015-0496) and project MAT2015-70850-P and the European Research Council (ERC) under grant agreement no. 648901. The work in Madrid and Valencia was supported by the Spanish Ministerio de Economía y Competitividad (MINECO-FEDER project CTQ2017-87054); the work in Madrid was further supported by the Severo Ochoa Programme for Centers of Excellence in R&D program of the MINECO (SEV-2016-0686) and by the Campus of International Excellence (CEI) UAM + CSIC.Peer reviewe