Organic Electronics最新文献

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Biodegradable TMCM-CdCl3/polylactic acid composites for piezoelectric energy harvesting 可生物降解TMCM-CdCl3/聚乳酸压电能量收集复合材料
IF 2.6 4区 工程技术
Organic Electronics Pub Date : 2025-12-01 Epub Date: 2025-09-04 DOI: 10.1016/j.orgel.2025.107331
Meng Guo, Guan-Zhi Wang, Yunchao Miao, Hai-Run Yang, Chen Zhao, Zhi-Gang Li
{"title":"Biodegradable TMCM-CdCl3/polylactic acid composites for piezoelectric energy harvesting","authors":"Meng Guo,&nbsp;Guan-Zhi Wang,&nbsp;Yunchao Miao,&nbsp;Hai-Run Yang,&nbsp;Chen Zhao,&nbsp;Zhi-Gang Li","doi":"10.1016/j.orgel.2025.107331","DOIUrl":"10.1016/j.orgel.2025.107331","url":null,"abstract":"<div><div>Hybrid organic-inorganic perovskites (HOIPs) have attracted extensive attention due to their unique piezoelectric properties, mild synthesis conditions, and structural flexibility. However, the intrinsic rigidity and poor biodegradability of HOIPs limit their applications in flexible wearable devices. In this work, we integrate HOIPs (TMCM-CdCl<sub>3</sub>) (TMCM, trimethylchloromethyl ammonium; Cd, Cadmium; Cl, chloride) with biodegradable polylactic acid (PLA) to fabricate flexible composite films that simultaneously maintain excellent piezoelectric properties, provide the mechanical flexibility needed for wearable devices, and overcome the environmental limitations of conventional non-degradable polymers. The composite film exhibits optimal properties, achieving a short-circuit current (<em>I</em><sub>SC</sub>) of 1.74 μA, an open-circuit voltage (<em>V</em><sub>OC</sub>) of 4.35 V, and a peak power density of 1.47 × 10<sup>−6</sup> W/cm<sup>2</sup> under a 5 N force. Furthermore, the composite film exhibits robust mechanical flexibility and cyclic stability, maintaining stability over 10,000 bending cycles, which positions it as a promising candidate for flexible wearable devices with broad application prospects.</div></div>","PeriodicalId":399,"journal":{"name":"Organic Electronics","volume":"147 ","pages":"Article 107331"},"PeriodicalIF":2.6,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145020849","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Improved performance of small molecule based organic photovoltaic cells enabled by fine-tuning side chains on terminal units 通过微调末端单元侧链,提高了基于小分子的有机光伏电池的性能
IF 2.6 4区 工程技术
Organic Electronics Pub Date : 2025-12-01 Epub Date: 2025-09-15 DOI: 10.1016/j.orgel.2025.107339
Wang Ni , Ruochen Wang , Zhaochen Lv , Miaomiao Li
{"title":"Improved performance of small molecule based organic photovoltaic cells enabled by fine-tuning side chains on terminal units","authors":"Wang Ni ,&nbsp;Ruochen Wang ,&nbsp;Zhaochen Lv ,&nbsp;Miaomiao Li","doi":"10.1016/j.orgel.2025.107339","DOIUrl":"10.1016/j.orgel.2025.107339","url":null,"abstract":"<div><div>Achieving proper film morphology and microstructures via molecular engineering remains a long-standing challenge for small-molecule-based organic photovoltaics. Herein, we designed and synthesized a small molecule donor, namely DAR3TBDT with allyl substituted rhodanine as terminal units. Compared to molecule DR3TBDT with ethyl groups on the terminus, DAR3TBDT in film showed similar optical bandgap and frontier molecular orbital energy levels, but more ordered molecular packing. Moreover, DAR3TBDT:PC<sub>71</sub>BM blend film exhibited better morphology with more defined phase separation in comparison to DR3TBDT:PC<sub>71</sub>BM counterpart. Owing to efficient exciton dissociation, charge transport and charge collection, the photovoltaic devices based on DAR3TBDT:PC<sub>71</sub>BM achieved a power conversion efficiency (PCE) of 9.05 % under one sun (AM 1.5G, 100 mW cm<sup>−2</sup>), outperforming the DR3TBDT:PC<sub>71</sub>BM-based counterparts (7.94 %). Furthermore, the DAR3TBDT:PC<sub>71</sub>BM-based devices are applied as the laser power converter under 532 nm laser irradiation, and achieved a high PCE of 23.11 %. This study opens a promising avenue to develop high-performance photovoltaic materials from the view of side chain engineering.</div></div>","PeriodicalId":399,"journal":{"name":"Organic Electronics","volume":"147 ","pages":"Article 107339"},"PeriodicalIF":2.6,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145097072","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Solution-processed NiO tailoring hole injection and enhancing photoluminescence in light-emitting diodes 溶液处理NiO裁剪孔注入和增强发光二极管的光致发光
IF 2.6 4区 工程技术
Organic Electronics Pub Date : 2025-12-01 Epub Date: 2025-09-18 DOI: 10.1016/j.orgel.2025.107341
Lingyu Huo , Muci Li , Hao Sun , Xiaocui Wang , Bingyu Wang , Xiaowen Zhang
{"title":"Solution-processed NiO tailoring hole injection and enhancing photoluminescence in light-emitting diodes","authors":"Lingyu Huo ,&nbsp;Muci Li ,&nbsp;Hao Sun ,&nbsp;Xiaocui Wang ,&nbsp;Bingyu Wang ,&nbsp;Xiaowen Zhang","doi":"10.1016/j.orgel.2025.107341","DOIUrl":"10.1016/j.orgel.2025.107341","url":null,"abstract":"<div><div>Solution-processed NiO mediating light-emitting diodes (LEDs) performance have been demonstrated. Using NiO-doped poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) tailoring hole injection, fantastic UV organic LEDs with maximum external quantum efficiency of 4.24 %, radiance of 3.9 mW/cm<sup>2</sup>, and 375 nm short-wavelength emission are demonstrated. Using hybrid NiO-quantum dots/carbon dots dispersed in poly(methyl methacrylate) as composite fluorescence film, the 365-nm (and 395-nm) excited photoluminescent LEDs show high luminance of 22014 (and 23937) cd/m<sup>2</sup> at 100 mA (and 110 mA), power efficiency of 13.86 (and 13.00) lm/W, and yellow-green emission with spectra peak of about 555 nm and wide full width at half maximum of about 140 nm. Atomic force microscope, transmission electron microscope, X-ray/ultraviolet photoelectron spectroscopy, current-voltage, photoluminescence, impedance spectroscopy, and conductivity measurements confirm that NiO-doped poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) promotes hole injection in organic LEDs, NiO incorporation enhances photoluminescence of carbon dots, and accordingly contributing to superior device performance. Our experiments provide alternative methods for constructing fascinating LEDs and boosting NiO applications.</div></div>","PeriodicalId":399,"journal":{"name":"Organic Electronics","volume":"147 ","pages":"Article 107341"},"PeriodicalIF":2.6,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145097073","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Interfacial defect mitigation in bilayer organic photovoltaics via low-temperature annealing for enhanced indoor light performance 通过低温退火降低双层有机光伏电池的界面缺陷以增强室内光性能
IF 2.6 4区 工程技术
Organic Electronics Pub Date : 2025-12-01 Epub Date: 2025-09-29 DOI: 10.1016/j.orgel.2025.107342
Dogyeong Kim , Jinwook Jung , Yoohan Ma , Gyuwan Hwang , Jae-Seung Roh , Jongbok Kim , Dongwook Ko
{"title":"Interfacial defect mitigation in bilayer organic photovoltaics via low-temperature annealing for enhanced indoor light performance","authors":"Dogyeong Kim ,&nbsp;Jinwook Jung ,&nbsp;Yoohan Ma ,&nbsp;Gyuwan Hwang ,&nbsp;Jae-Seung Roh ,&nbsp;Jongbok Kim ,&nbsp;Dongwook Ko","doi":"10.1016/j.orgel.2025.107342","DOIUrl":"10.1016/j.orgel.2025.107342","url":null,"abstract":"<div><div>Organic photovoltaics (OPVs) are promising for indoor energy harvesting due to their lightweight, and tunable absorption. However, bulk heterojunction (BHJ) structures suffer from severe recombination losses under low-intensity illumination, limiting device efficiency. In contrast, planar bilayer OPVs mitigate these losses by providing well-defined donor–acceptor interfaces and direct charge transport pathways. Here, bilayer OPVs were fabricated using a water-assisted lamination method, enabling the transfer of the donor polymer PTB7 onto a PC71BM acceptor layer without intermixing. To mitigate interfacial trap states caused by oxygen adsorption, we applied low-temperature annealing at 40 °C. Bilayer OPVs annealed for 1 min achieved the highest power conversion efficiency of 2.36 % under 1000 lux compact fluorescent lamp (CFL) illumination. Angle-resolved X-ray photoelectron spectroscopy confirmed the removal of surface-bound oxygen, while photoluminescence and contact angle measurements revealed suppressed trap states and preserved π–conjugation. Optical absorption and XPS depth-profile analyses further verified that the bilayer morphology remained intact without donor–acceptor interdiffusion. In addition, light-intensity-dependent open-circuit voltage analysis indicated reduced trap-assisted recombination in optimally annealed devices. These findings demonstrate that low-temperature annealing is an effective strategy to enhance the efficiency of bilayer OPVs by eliminating interfacial adsorbed traps while maintaining structural stability under indoor illumination.</div></div>","PeriodicalId":399,"journal":{"name":"Organic Electronics","volume":"147 ","pages":"Article 107342"},"PeriodicalIF":2.6,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145217514","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Organic–inorganic hybrid injection layers for efficient charge injection in organic transistors 用于有机晶体管高效电荷注入的有机-无机杂化注入层
IF 2.6 4区 工程技术
Organic Electronics Pub Date : 2025-12-01 Epub Date: 2025-09-04 DOI: 10.1016/j.orgel.2025.107332
Walid Boukhili , Kunfang Chen , Xiang Wan , Chee Leong Tan , Huabin Sun , Zhihao Yu , Swelm Wageh , Yong Xu , Dongyoon Khim
{"title":"Organic–inorganic hybrid injection layers for efficient charge injection in organic transistors","authors":"Walid Boukhili ,&nbsp;Kunfang Chen ,&nbsp;Xiang Wan ,&nbsp;Chee Leong Tan ,&nbsp;Huabin Sun ,&nbsp;Zhihao Yu ,&nbsp;Swelm Wageh ,&nbsp;Yong Xu ,&nbsp;Dongyoon Khim","doi":"10.1016/j.orgel.2025.107332","DOIUrl":"10.1016/j.orgel.2025.107332","url":null,"abstract":"<div><div>Exploring suitable injection layer architectures, whether simple or hybrid organic–inorganic bilayers, that ensure efficient charge injection, favorable interfacial properties, and low-cost fabrication is of great technological significance for advancing inorganic and organic electronic devices. In this study, a series of tetracene-based organic thin-film transistors (tetracene-OTFTs) were fabricated, characterized, and systematically investigated, including reference devices with bare Au source/drain (S/D) electrodes and devices incorporating injection layers such as MoO<sub>3</sub>, pentacene (P5), and a hybrid P5/MoO<sub>3</sub> bilayer beneath the Au S/D electrodes. Among all configurations, devices employing the P5/MoO<sub>3</sub> injection bilayer demonstrated the highest performance, achieving a hole mobility of 2.5 × 10<sup>−2</sup> cm<sup>2</sup> V<sup>−1</sup> s<sup>−1</sup>, a reduced threshold voltage of −0.65 V, near-zero onset voltage, a high on/off current ratio of 5.6 × 10<sup>4</sup>, a low contact resistance of 1.2 × 10<sup>3</sup> kΩ, and reduced trap densities. The enhanced electrical performance of devices with the hybrid P5/MoO<sub>3</sub> injection bilayer is attributed to its synergistic function: MoO<sub>3</sub> enables favorable energy level alignment for efficient hole injection, while the ultrathin P5 layer acts as a diffusion barrier and forms a coherent organic/organic interface that enhances morphological compatibility with the tetracene active layer. These findings highlight the significant potential of hybrid injection bilayer architectures to simultaneously optimize charge injection, interfacial energetics, and device performance, thereby paving the way toward next-generation high-performance hybrid electronic devices.</div></div>","PeriodicalId":399,"journal":{"name":"Organic Electronics","volume":"147 ","pages":"Article 107332"},"PeriodicalIF":2.6,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145005037","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Interface-Engineered polymer nanocomposite RRAM with enhanced switching reliability and performance 具有增强开关可靠性和性能的界面工程聚合物纳米复合RRAM
IF 2.6 4区 工程技术
Organic Electronics Pub Date : 2025-12-01 Epub Date: 2025-09-19 DOI: 10.1016/j.orgel.2025.107340
Yu-Kyung Kim , Min-Guen Kim , Jea-Young Choi
{"title":"Interface-Engineered polymer nanocomposite RRAM with enhanced switching reliability and performance","authors":"Yu-Kyung Kim ,&nbsp;Min-Guen Kim ,&nbsp;Jea-Young Choi","doi":"10.1016/j.orgel.2025.107340","DOIUrl":"10.1016/j.orgel.2025.107340","url":null,"abstract":"<div><div>In this study, non-volatile resistive random access memory (RRAM) devices were fabricated using polymer nanocomposites (NCs) consisting of polyvinyl alcohol (PVA) and copper oxide (CuO) nanoparticles (NPs). The fabricated ITO/CuO:PVA/Al devices demonstrated bipolar resistive switching (RS) behavior, primarily driven by the charge trapping/de-trapping dynamics associated with the CuO NPs. However, excessive defect densities within the NC layer limited device reliability and switching performance. To address this issue, a hydroquinone-modified PEDOT:PSS (HQ-PEDOT:PSS) interfacial buffer layer was introduced to enhance interfacial properties. Electrical impedance spectroscopy (EIS) analysis confirmed that HQ-PEDOT:PSS effectively suppressed trap-assisted charge recombination and improved charge transfer efficiency at the interface. As a result, HQ-PEDOT:PSS-incorporated devices (HQ-NC-RRAM) demonstrated a significantly enhanced ON/OFF ratio of ∼10<sup>4</sup> and a remarkably low data dispersion variance (VDD ≈ 0.01) during endurance measurements. Compared to devices with conventional pristine-PEDOT:PSS or no buffer layer, the HQ-NC-RRAM demonstrated notably improved switching performance and device reliability. These findings highlight the effectiveness of HQ-PEDOT:PSS in interface engineering for high-performance NC-RRAMs.</div></div>","PeriodicalId":399,"journal":{"name":"Organic Electronics","volume":"147 ","pages":"Article 107340"},"PeriodicalIF":2.6,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145119329","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
H+-triggered solid-state fluorescence of carbon dots for dual anti-counterfeiting 氢离子触发碳点固态荧光双重防伪
IF 2.6 4区 工程技术
Organic Electronics Pub Date : 2025-11-01 Epub Date: 2025-08-26 DOI: 10.1016/j.orgel.2025.107328
Pengkun Xia , Nouman Ahmad , Chao Tang , Zhaolin Na , Xiaohui Gao , Shengxiang Huang , Lianwen Deng
{"title":"H+-triggered solid-state fluorescence of carbon dots for dual anti-counterfeiting","authors":"Pengkun Xia ,&nbsp;Nouman Ahmad ,&nbsp;Chao Tang ,&nbsp;Zhaolin Na ,&nbsp;Xiaohui Gao ,&nbsp;Shengxiang Huang ,&nbsp;Lianwen Deng","doi":"10.1016/j.orgel.2025.107328","DOIUrl":"10.1016/j.orgel.2025.107328","url":null,"abstract":"<div><div>Developing luminescent materials with tunable and reversible fluorescence remains challenging, as it requires stable, responsive, and versatile systems capable of switching emission states under precise stimuli. Herein, we prepared carbon quantum dots (CDs) by using 2-aniline-3-methyl-6-(dibutylamine) fluoroalkane as raw material. The optical characterization showed the parent CDs presented a cyan fluorescence resulted from the surface oxidative functional groups dominating the low-energy transitions. Interestingly, stimulated by various acids, this fluorescence phenomenon can be changed into yellow, no matter in aqueous solution or solid state. It can be explained by the fact that H<sup>+</sup> reduces oxidized surface groups such as nitro to amino groups, creating new emissive traps. Based on this, a reversible dual-switch mode luminescent ink was demonstrated for advanced anti-counterfeiting and dual encryption.</div></div>","PeriodicalId":399,"journal":{"name":"Organic Electronics","volume":"146 ","pages":"Article 107328"},"PeriodicalIF":2.6,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144908429","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Enhanced photovoltaic performance of organic solar cells with low cost azomethine-based non-fullerene acceptors 低成本偶氮胺基非富勒烯受体增强有机太阳能电池的光电性能
IF 2.6 4区 工程技术
Organic Electronics Pub Date : 2025-11-01 Epub Date: 2025-08-19 DOI: 10.1016/j.orgel.2025.107326
Lu Zhou , Chao Zuo , Bin Du , Jie Min , Yang Wang , Xiangchun Li , Wen-Yong Lai
{"title":"Enhanced photovoltaic performance of organic solar cells with low cost azomethine-based non-fullerene acceptors","authors":"Lu Zhou ,&nbsp;Chao Zuo ,&nbsp;Bin Du ,&nbsp;Jie Min ,&nbsp;Yang Wang ,&nbsp;Xiangchun Li ,&nbsp;Wen-Yong Lai","doi":"10.1016/j.orgel.2025.107326","DOIUrl":"10.1016/j.orgel.2025.107326","url":null,"abstract":"<div><div>Most of non-fullerene acceptors used in organic solar cells are synthesized through cross-coupling reactions, which require expensive transition metal catalysts, harsh reaction conditions and complex purification processes, making large-scale production high cost. Here, two azomethine-based perylene diimides (PDIs) are designed and synthesized through a simple and economical Schiff base condensation reaction with water as the only by-product. As the non-fullerene acceptors for organic solar cells, power conversion efficiencies exceeding 4.3 % were reached. Furthermore, the cost estimations show that the material cost of azomethine-based PDIs is about two orders of magnitude lower. In addition, the synthesis of azomethine-based PDIs also reduces the toxic chemical waste, thus greatly reducing the environmental impact. Our results pave the way for low-cost, environmentally friendly and efficient non-fullerene acceptors.</div></div>","PeriodicalId":399,"journal":{"name":"Organic Electronics","volume":"146 ","pages":"Article 107326"},"PeriodicalIF":2.6,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144887416","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Benzothiadiazole-thiophene based conjugated Polymers: Impact of conjugated chain length on electrochromic performance 苯并噻唑-噻吩基共轭聚合物:共轭链长度对电致变色性能的影响
IF 2.6 4区 工程技术
Organic Electronics Pub Date : 2025-11-01 Epub Date: 2025-08-18 DOI: 10.1016/j.orgel.2025.107324
Kaiwen Lin , Zhaoji Xin , Guiliang Tan , Yeyi Lei , Yufei Zhao , Xiaoge Liu , Yulian Liu , Dong Yuan , Hao Liu , Liangying Wang
{"title":"Benzothiadiazole-thiophene based conjugated Polymers: Impact of conjugated chain length on electrochromic performance","authors":"Kaiwen Lin ,&nbsp;Zhaoji Xin ,&nbsp;Guiliang Tan ,&nbsp;Yeyi Lei ,&nbsp;Yufei Zhao ,&nbsp;Xiaoge Liu ,&nbsp;Yulian Liu ,&nbsp;Dong Yuan ,&nbsp;Hao Liu ,&nbsp;Liangying Wang","doi":"10.1016/j.orgel.2025.107324","DOIUrl":"10.1016/j.orgel.2025.107324","url":null,"abstract":"<div><div>In this work, two donor-acceptor-donor (D-A-D) type electrochromic conjugated polymers were prepared upon electrochemical oxidation through their precursors employed thiophenes as the donor units and benzothiazole as the acceptor unit. The conjugated chain length effects of the polymers’ electrochemical and electrochromic properties were carefully examined. As the conjugated chain length increases, both precursors exhibited reduced the HOMO-LUMO energy gap and red-shifted UV–Vis absorption and fluorescence spectra. Both polymers displayed n-doping and p-doping process with excellent redox stability, PBT-4T retained 94.17 % of its original electroactivity, which is higher than that of PBT-2T (92.86 %). Meanwhile, both polymers exhibited reversible changes in UV–Vis absorption spectra under voltage drive of 0 V–1.8 V, accompanied by color changes from light pink to black-gray (PBT-2T) and from purple to dark brown (PBT-4T). PBT-2T showed highest optical contrast of 41 % at 750 nm and fastest response time of 0.2 s for the oxidation process at 528 nm because of porous structure, which undoubtedly facilitates the ingress and egress of ions. The varying the π-conjugated chain length from bithiophene to quaterthiophene strategy may provide a new research idea to achieve high-performance electrochromic conjugated polymers.</div></div>","PeriodicalId":399,"journal":{"name":"Organic Electronics","volume":"146 ","pages":"Article 107324"},"PeriodicalIF":2.6,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144867020","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Research progress in small-molecule donor-polymer acceptor organic photovoltaic cells 小分子给体-聚合物受体有机光伏电池的研究进展
IF 2.6 4区 工程技术
Organic Electronics Pub Date : 2025-11-01 Epub Date: 2025-08-20 DOI: 10.1016/j.orgel.2025.107325
Beining Wang , Tianyu Huang , Junhao Song , Chenghuan Chen , Yuxuan Wang , István Bíró , Gusztáv Fekete , Hai-Qiao Wang
{"title":"Research progress in small-molecule donor-polymer acceptor organic photovoltaic cells","authors":"Beining Wang ,&nbsp;Tianyu Huang ,&nbsp;Junhao Song ,&nbsp;Chenghuan Chen ,&nbsp;Yuxuan Wang ,&nbsp;István Bíró ,&nbsp;Gusztáv Fekete ,&nbsp;Hai-Qiao Wang","doi":"10.1016/j.orgel.2025.107325","DOIUrl":"10.1016/j.orgel.2025.107325","url":null,"abstract":"<div><div>Organic solar cells (OSCs), characterized by their lightweight, flexibility, solution-processability for large-area fabrication, and low cost, exhibit significant complementary advantages to silicon-based photovoltaics, positioning them as a cutting-edge research frontier in clean energy. Among emerging architectures, small-molecule donor/polymer acceptor (SDPA)-based OSCs have attracted considerable attention due to their unique active layer stability, particularly their ability to maintain optimized phase-separated morphology under high-temperature conditions (&gt;85 °C), offering potential to overcome the stability bottleneck in organic photovoltaic industrialization. However, the current record power conversion efficiency (PCE) of SDPA-OSCs remains at 12.1 %, significantly lagging behind mainstream bulk heterojunction systems (PCE &gt;20 %). To advance the efficiency of SDPA-OSCs, extensive efforts have been devoted to optimizing materials, device engineering, and processing techniques. This review systematically summarizes recent progress in SDPA-OSCs from the perspectives of device architecture and active layer processing. Key focus areas include the impact of device structure engineering (conventional vs. inverted configurations) and active layer fabrication strategies (bulk heterojunction solution-coating and layer-by-layer deposition techniques) on charge carrier transport and device performance. By establishing robust \"material structure–morphology–device performance\" correlations, this work provides critical insights and technical references for developing high-efficiency SDPA-OSCs. Furthermore, future research directions and challenges in material innovation, morphology control, and scalable manufacturing are discussed to guide the advancement of SDPA-based organic photovoltaics.</div></div>","PeriodicalId":399,"journal":{"name":"Organic Electronics","volume":"146 ","pages":"Article 107325"},"PeriodicalIF":2.6,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144887415","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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