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原位构建具有增强界面电荷转移的CsSnI钙钛矿纳米晶体/SnS纳米片异质结

In Situ Construction of a CsSnI Perovskite Nanocrystal/SnS Nanosheet Heterojunction with Boosted Interfacial Charge Transfer.

作者信息

Wang Xu-Dong, Huang Yu-Hua, Liao Jin-Feng, Jiang Yong, Zhou Lei, Zhang Xiao-Yan, Chen Hong-Yan, Kuang Dai-Bin

机构信息

MOE Key Laboratory of Bioinorganic and Synthetic Chemistry, Lehn Institute of Functional Materials, School of Chemistry , Sun Yat-sen University , Guangzhou 510275 , P. R. China.

出版信息

J Am Chem Soc. 2019 Aug 28;141(34):13434-13441. doi: 10.1021/jacs.9b04482. Epub 2019 Aug 15.

Abstract

Heterojunction engineering has played an indispensable role in the exploitation of innovative artificial materials with exceptional properties and has consequently triggered a new revolution in achieving high-performance optoelectronic devices. Herein, an intriguing halide perovskite (PVK) and metal dichalcogenide (MD) heterojunction, i.e., a lead-free CsSnI perovskite nanocrystal/SnS nanosheet hybrid, was fabricated in situ for the first time. Comprehensive investigations with experimental characterizations and theoretical calculations demonstrate that cosharing of the Sn atom enables intimate contact in the CsSnI/SnS hybrid together with a type II band alignment structure. Additionally, ultrafast carrier separation between SnS and CsSnI has been observed in the CsSnI/SnS hybrid by transient absorption measurements, which efficiently prolongs the lifetime of the photogenerated electrons in SnS (from 1290 to 3080 ps). The resultant spatial charge separation in the CsSnI/SnS hybrid evidenced by Kelvin probe force microscopy (KPFM) significantly boosts the photocatalytic activity toward CO reduction and the photoelectrochemical performance, with 5.4-fold and 10.6-fold enhancements compared with unadorned SnS. This work provides a facile and effective method for the in situ preparation of PVK-MD heterojunctions, which may significantly stimulate the synthesis of various perovskite-based hybrid materials and their further optoelectronic applications.

摘要

异质结工程在开发具有优异性能的创新人工材料方面发挥了不可或缺的作用,从而引发了一场实现高性能光电器件的新革命。在此,首次原位制备了一种引人关注的卤化物钙钛矿(PVK)与金属二硫属化物(MD)异质结,即无铅CsSnI钙钛矿纳米晶/SnS纳米片杂化材料。通过实验表征和理论计算进行的全面研究表明,Sn原子的共用使得CsSnI/SnS杂化材料中能够实现紧密接触,并形成II型能带排列结构。此外,通过瞬态吸收测量在CsSnI/SnS杂化材料中观察到了SnS和CsSnI之间的超快载流子分离,这有效地延长了SnS中光生电子的寿命(从1290皮秒延长至3080皮秒)。通过开尔文探针力显微镜(KPFM)证明,CsSnI/SnS杂化材料中产生的空间电荷分离显著提高了对CO还原的光催化活性和光电化学性能,与未修饰的SnS相比,分别提高了5.4倍和10.6倍。这项工作为原位制备PVK-MD异质结提供了一种简便有效的方法,这可能会极大地促进各种基于钙钛矿的杂化材料的合成及其进一步的光电子应用。

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