Dhruba B. Khadka*, Yan-Chen Kuo, Yi Zhen Li, Muhammad Waqas, You-Jia Xu, Masatoshi Yanagida, Hiroshi Nishihara, Kazuhito Tsukagoshi, Mitch M. C. Chou, Yasuhiro Shirai and Ying-Chiao Wang*,
{"title":"配位纳米片稳定高效锡基钙钛矿太阳能电池","authors":"Dhruba B. Khadka*, Yan-Chen Kuo, Yi Zhen Li, Muhammad Waqas, You-Jia Xu, Masatoshi Yanagida, Hiroshi Nishihara, Kazuhito Tsukagoshi, Mitch M. C. Chou, Yasuhiro Shirai and Ying-Chiao Wang*, ","doi":"10.1021/acsami.5c0501110.1021/acsami.5c05011","DOIUrl":null,"url":null,"abstract":"<p >Tin-based perovskites, characterized by their advantageous bandgap and much lower toxicity, have emerged as a promising alternative to lead-based perovskites in solar cell applications. However, the efficiency and stability of tin-based perovskite solar cells (Sn-PSCs) are still limited by defects resulting from the easy oxidation of Sn<sup>2+</sup> to Sn<sup>4+</sup>. Herein, an approach to enhance the optoelectronic performance of Sn-PSCs by incorporating terpyridine-zinc(II) (ZnTPY) coordination nanosheets (CONASHs), synthesized via liquid–liquid interfacial polymerization, into tin-based perovskites is delivered. Following physical fragmentation, ZnTPY CONASHs, enriched with unsaturated terpyridine groups, undergo multidentate chelation with SnI<sub>2</sub>, forming ZnTPY:SnI<sub>2</sub> heterogeneous nuclei. This process effectively enhances the crystallization of tin-based perovskites while mitigating recombination and defect chemistry related to Sn<sup>2+</sup> oxidation. As a result of superior crystal quality, the ZnTPY CONASHs-modified tin perovskite exhibits a longer photoluminescence lifetime. Consequently, the Sn-PSC incorporating ZnTPY complex achieves a power conversion efficiency of 11.59%, compared to 9.14% for the control device, along with improved operational stability with encapsulation. Thus, this work underscores the critical role of coordination nanosheets for regulating coordination in the precursor solution to achieve high-quality tin-based perovskite films, offering a pathway to more efficient and stable Sn-PSCs.</p>","PeriodicalId":5,"journal":{"name":"ACS Applied Materials & Interfaces","volume":"17 18","pages":"26813–26822 26813–26822"},"PeriodicalIF":8.2000,"publicationDate":"2025-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.acs.org/doi/epdf/10.1021/acsami.5c05011","citationCount":"0","resultStr":"{\"title\":\"Coordination Nanosheets Stabilizing Efficient Tin-Based Perovskite Solar Cells\",\"authors\":\"Dhruba B. Khadka*, Yan-Chen Kuo, Yi Zhen Li, Muhammad Waqas, You-Jia Xu, Masatoshi Yanagida, Hiroshi Nishihara, Kazuhito Tsukagoshi, Mitch M. C. Chou, Yasuhiro Shirai and Ying-Chiao Wang*, \",\"doi\":\"10.1021/acsami.5c0501110.1021/acsami.5c05011\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Tin-based perovskites, characterized by their advantageous bandgap and much lower toxicity, have emerged as a promising alternative to lead-based perovskites in solar cell applications. However, the efficiency and stability of tin-based perovskite solar cells (Sn-PSCs) are still limited by defects resulting from the easy oxidation of Sn<sup>2+</sup> to Sn<sup>4+</sup>. Herein, an approach to enhance the optoelectronic performance of Sn-PSCs by incorporating terpyridine-zinc(II) (ZnTPY) coordination nanosheets (CONASHs), synthesized via liquid–liquid interfacial polymerization, into tin-based perovskites is delivered. Following physical fragmentation, ZnTPY CONASHs, enriched with unsaturated terpyridine groups, undergo multidentate chelation with SnI<sub>2</sub>, forming ZnTPY:SnI<sub>2</sub> heterogeneous nuclei. This process effectively enhances the crystallization of tin-based perovskites while mitigating recombination and defect chemistry related to Sn<sup>2+</sup> oxidation. As a result of superior crystal quality, the ZnTPY CONASHs-modified tin perovskite exhibits a longer photoluminescence lifetime. Consequently, the Sn-PSC incorporating ZnTPY complex achieves a power conversion efficiency of 11.59%, compared to 9.14% for the control device, along with improved operational stability with encapsulation. 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Coordination Nanosheets Stabilizing Efficient Tin-Based Perovskite Solar Cells
Tin-based perovskites, characterized by their advantageous bandgap and much lower toxicity, have emerged as a promising alternative to lead-based perovskites in solar cell applications. However, the efficiency and stability of tin-based perovskite solar cells (Sn-PSCs) are still limited by defects resulting from the easy oxidation of Sn2+ to Sn4+. Herein, an approach to enhance the optoelectronic performance of Sn-PSCs by incorporating terpyridine-zinc(II) (ZnTPY) coordination nanosheets (CONASHs), synthesized via liquid–liquid interfacial polymerization, into tin-based perovskites is delivered. Following physical fragmentation, ZnTPY CONASHs, enriched with unsaturated terpyridine groups, undergo multidentate chelation with SnI2, forming ZnTPY:SnI2 heterogeneous nuclei. This process effectively enhances the crystallization of tin-based perovskites while mitigating recombination and defect chemistry related to Sn2+ oxidation. As a result of superior crystal quality, the ZnTPY CONASHs-modified tin perovskite exhibits a longer photoluminescence lifetime. Consequently, the Sn-PSC incorporating ZnTPY complex achieves a power conversion efficiency of 11.59%, compared to 9.14% for the control device, along with improved operational stability with encapsulation. Thus, this work underscores the critical role of coordination nanosheets for regulating coordination in the precursor solution to achieve high-quality tin-based perovskite films, offering a pathway to more efficient and stable Sn-PSCs.
期刊介绍:
ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.