Perovskite solar cells-TiO2 tandem assembly for photoelectrocatalytic degradation of organic pollutants

Perovskite solar cells-TiO2 tandem assembly for photoelectrocatalytic degradation of organic pollutants
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钙钛矿太阳能电池-TiO2串联组装用于光电催化降解有机污染物

DOI:
10.1016/j.jpcs.2019.03.025
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发表时间:
2019-09
影响因子:
4
通讯作者:
Tao Xia
Tao Xia
中科院分区:
材料科学3区
文献类型:
--
作者:
Chen Dong;Lu Yanting;Wu Jiaojiao;Li Nan;Zheng Yan-Zhen;Tao Xia

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以多壁碳纳米管(CNTs)和甲胺(CH 3 NH 2)修饰的钙钛矿太阳能电池(PSCs)为电源,CNT/TiO 2为光阳极,设计了一种自供电光电催化(PEC)装置。在PSCs中,碳纳米管和CH 3 NH 2被用来修饰钙钛矿和碳电极之间的界面,以提高光电性能。特别地,CH 3 NH 2诱导的CH 3 NH3 PbI 3钙钛矿薄膜的表面愈合和CNT充当单个钙钛矿纳米颗粒之间的电荷传输路径,以促进由碳电极收集光生空穴。在用碳纳米管和CH 3 NH 2修饰后,实现了10.39%的功率转换效率。在光阳极中,CNT修饰的TiO 2电极加速了电子-空穴的分离和传输,从而提高了降解性能。将CNT和CH 3 NH 2修饰的PSC与CNT/TiO 2组装后,太阳能驱动的PEC体系对罗丹明B(RhB)表现出较高的PEC降解率。串联装置对RhB的最佳降解效率在80 min后接近100%。这种低成本的串联装置在污染物降解研究中具有很好的应用前景。
In this study, a self-powered photoelectrocatalytic (PEC) device was designed using multi-walled carbon nanotubes (CNTs) and methylamine (CH3NH2) modified perovskite solar cells (PSCs) as the power source and CNT/TiO2as the photoanodes. In the PSCs, CNTs and CH3NH2were used to modify the interface between the perovskite and carbon electrode to improve the photoelectronic performance. In particular, CH3NH2induced surface-healing of the CH3NH3PbI3perovskite thin films and the CNTs acted as a charge transport pathway among individual perovskite nanoparticles to facilitate the collection of photogenerated holes by the carbon electrode. A power conversion efficiency of 10.39% was achieved after modification with the CNTs and CH3NH2. In the photoanodes, the CNT-modified TiO2electrode accelerated the electron–hole separation and transportation, thereby improving the degradation performance. After assembling the PSCs modified using CNT and CH3NH2with CNT/TiO2, the solar-driven PEC system exhibited a high PEC degradation rate with rhodamine B (RhB). The optimal degradation efficiency for RhB with the tandem device was close to 100% after 80 min. This low-cost tandem assembly has promising applications in pollutant degradation research.
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