首页> 外文期刊>Journal of Materials Chemistry, C. materials for optical and electronic devices >A mono(carboxy)porphyrin-triazine-(bodipy)(2) triad as a donor for bulk heterojunction organic solar cells
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A mono(carboxy)porphyrin-triazine-(bodipy)(2) triad as a donor for bulk heterojunction organic solar cells

机译:单(羧基)卟啉-三嗪-(bodipy)(2)三重态作为体异质结有机太阳能电池的供体

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In the present article bulk heterojunction (BHJ) solution processed organic solar cells have been prepared using a mono(carboxy)porphyrin-triazine-(bodipy)(2) triad (PorCOOH)(BDP)(2) as a donor and ([6,6]-phenyl C-71 butyric acid methyl ester) (PC71BM) as an acceptor. This donor-acceptor system aims to increase the light capturing process efficiency of the device. The solution processed BHJ organic solar cell with an optimized weight ratio of 1 : 1 (PorCOOH)(BDP)(2) : PC71BM processed with THF as a solvent showed an overall power conversion efficiency (PCE) of 3.48% with short circuit current J(sc) = 8.04 mA cm(-2), open circuit voltage V-oc = 0.94 V and fill factor FF = 0.46. The relatively high value of V-oc was attributed to the deeper highest occupied molecular orbital energy level of (PorCOOH)(BDP)(2). When the active layer of the solar cell was processed using a mixture of 4% v/v of pyridine in THF solvent, it achieved a PCE value of 5.29% with J(sc) = 10.48 mA cm(-2), V-oc = 0.90 V and FF = 0.56. This was ascribed to the enhancement of both the J(sc) and the FF values. The higher value of J(sc) is explained by the increased absorption profile of the blend, the stronger incident photon to current efficiency (IPCE) response and the higher crystallinity of the active layer, induced by the solvent additive while the enhancement of FF may be due to the better charge transport capability and the charge collection efficiency in the later device.
机译:在本文中,已使用单(羧基)卟啉-三嗪-(bodipy)(2)三单元组(PorCOOH)(BDP)(2)作为供体和([6]制备了本体异质结(BHJ)溶液处理的有机太阳能电池。 ,6]-苯基C-71丁酸甲酯(PC71BM)作为受体。该供体-受体系统旨在提高装置的光捕获过程效率。溶液处理的BHJ有机太阳能电池的最佳重量比为1:1(PorCOOH)(BDP)(2):用THF作为溶剂处理的PC71BM在短路电流J下的总功率转换效率(PCE)为3.48% (sc)= 8.04 mA cm(-2),开路电压V-oc = 0.94 V,填充系数FF = 0.46。 V-oc值相对较高是由于(PorCOOH)(BDP)(2)的最高占据分子轨道能级更深。当使用4%v / v吡啶在THF溶剂中的混合物处理太阳能电池的活性层时,其J(sc)= 10.48 mA cm(-2),V-oc的PCE值达到5.29% = 0.90 V和FF = 0.56。这归因于J(sc)和FF值的增强。 J(sc)的较高值是由共混物的吸收曲线增加,入射光子对电流效率(IPCE)的响应更强以及由溶剂添加剂引起的活性层的较高结晶度所解释的,而FF的增强可能这是因为后面的设备具有更好的电荷传输能力和电荷收集效率。

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