Abstract:The light-emitting electrochemical cell (LEC) is an area-emitting device, which features a complex turn-on process that ends with the formation of a p-n junction doping structure within the active material. This in-situ doping transformation is attractive in that it promises to pave the way for an unprecedented low-cost fabrication of thin and light-weight devices that present efficient light emission at low applied voltage. In this review, we present recent insights regarding the operational mechanism, breakt… Show more
“…In order to realize an optimum doping structure over the entire device area, it is therefore desirable that the electrolyte and the emitter are intimately mixed within the active material. If not, it is probable that the ion‐rich regions will exhibit a too high doping concentration that results in severe exciton quenching and self‐absorption, while the ion‐poor regions will suffer from a too low doping concentration with concomitant poor injection and transport . In this context, we note that previous studies on ether‐based electrolytes[9b,c,13b,d] have arrived at the same conclusion, viz., that an oligomeric ion transporter outperforms a structurally similar polymeric ion transporter in LEC devices.…”
The light-emitting electrochemical cell (LEC) is fundamentally dependent on mobile ions for its operation. In polymer LECs, the mobile ions are commonly provided by dissolving a salt in an ion transporter, with the latter almost invariably being an ether-based compound. Here, the synthesis, characterization, and application of a new class of carbonate-based ion transporters are reported. A polymer LEC, comprising a star-branched oligocarbonate endowed with aliphatic side groups as the ion transporter, features a current efficacy of 13.8 cd A −1 at a luminance of 1060 cd m −2 , which is a record-high efficiency/luminance combination for a singlet-emitting LEC. It is further established that the design principles of a high-performance carbonate ion transporter constitute the selection of an oligomeric structure over a corresponding polymeric structure and the endowment of the oligomer with functional side chains to render it compatible with the polymeric emitter.
“…In order to realize an optimum doping structure over the entire device area, it is therefore desirable that the electrolyte and the emitter are intimately mixed within the active material. If not, it is probable that the ion‐rich regions will exhibit a too high doping concentration that results in severe exciton quenching and self‐absorption, while the ion‐poor regions will suffer from a too low doping concentration with concomitant poor injection and transport . In this context, we note that previous studies on ether‐based electrolytes[9b,c,13b,d] have arrived at the same conclusion, viz., that an oligomeric ion transporter outperforms a structurally similar polymeric ion transporter in LEC devices.…”
The light-emitting electrochemical cell (LEC) is fundamentally dependent on mobile ions for its operation. In polymer LECs, the mobile ions are commonly provided by dissolving a salt in an ion transporter, with the latter almost invariably being an ether-based compound. Here, the synthesis, characterization, and application of a new class of carbonate-based ion transporters are reported. A polymer LEC, comprising a star-branched oligocarbonate endowed with aliphatic side groups as the ion transporter, features a current efficacy of 13.8 cd A −1 at a luminance of 1060 cd m −2 , which is a record-high efficiency/luminance combination for a singlet-emitting LEC. It is further established that the design principles of a high-performance carbonate ion transporter constitute the selection of an oligomeric structure over a corresponding polymeric structure and the endowment of the oligomer with functional side chains to render it compatible with the polymeric emitter.
“…The efficient operation of a LEC is dependent on that the electroactive compound can be both p‐type doped and n‐type doped 1a,14. As the observed oxidation and reduction reactions in CV are good indicators of electrochemical p‐type doping and n‐type doping, respectively, there are good reasons to believe that these host:guest compounds might function as the electroactive compound in LEC devices.…”
It has recently been demonstrated that light‐emitting electrochemical cells (LECs) can be designed to deliver strong emission with high efficiency when the charge transport is effectuated by a majority host and the emission is executed by a minority guest. A relevant question is then: should the guest be physically blended with or chemically incorporated into the host? A systematic study is presented that establishes that for near‐infrared‐(NIR‐) emitting LECs based on poly(indacenodithieno[3,2‐b]thiophene) (PIDTT) as the host and 4,7‐bis(4,4‐bis(2‐ethylhexyl)‐4H‐silolo[3,2‐b:4,5‐b′]dithiophen‐2‐yl)benzo[c][1,2,5]‐thiadiazole (SBS) as the guest the chemical‐incorporation approach is preferable. The host‐to‐guest energy transfer in LEC devices is highly efficient at a low guest concentration of 0.5%, whereas guest aggregation and ion redistribution during device operation severly inhibits this transfer in the physical‐blend devices. The chemical‐incorporation approach also results in a redshifted emission with a somewhat lowered photoluminescence quantum yield, but the LEC performance is nevertheless very good. Specifically, an NIR‐LEC device comprising a guest‐dilute (0.5 molar%) PIDTT‐SBS copolymer delivers highly stabile operation at a high radiance of 263 µW cm−2 (peak wavelength = 725 nm) and with an external quantum efficiency of 0.214%, which is close to the theoretical limit for this particular emitter and device geometry.
“…The research field of the LEC devices has been mainly classified by these two primary light‐emitting materials. For a detailed overview of LEC devices, the reader is referred to previously published review articles . In the following, we will briefly introduce the emission mechanism and properties of LECs and highlight some recent progress related to fiber‐based LEC devices.…”
Section: Materials and Architecture Design Of Fiber Shaped Lighting Dmentioning
confidence: 99%
“…i) Photographs of an operating stretchable fabric‐based PLEC. a) Reproduced with permission . Copyright 2016, Springer International Publishing Switzerland.…”
Section: Materials and Architecture Design Of Fiber Shaped Lighting Dmentioning
Advances in material science and nanotechnology have fostered the miniaturization of devices. Over the past two decades, the form‐factor of these devices has evolved from 3D rigid, volumetric devices through 2D film‐based flexible electronics, finally to 1D fiber electronics (fibertronics). In this regard, fibertronic strategies toward wearable applications (e.g., electronic textiles (e‐textiles)) have attracted considerable attention thanks to their capability to impart various functions into textiles with retaining textiles' intrinsic properties as well as imperceptible irritation by foreign matters. In recent years, extensive research has been carried out to develop various functional devices in the fiber form. Among various features, lighting and display features are the highly desirable functions in wearable electronics. This article discusses the recent progress of materials, architectural designs, and new fabrication technologies of fiber‐shaped lighting devices and the current challenges corresponding to each device's operating mechanism. Moreover, opportunities and applications that the revolutionary convergence between the state‐of‐the‐art fibertronic technology and age‐long textile industry will bring in the future are also discussed.
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