Peng Zhang, Xin Chen, Jing Li, Lei Fang, Xiangying Sun
{"title":"Dynamic room-temperature phosphorescence enabled by boronic acid group-mediated 2D perovskite heterojunctions for time-resolved multidimensional anti-counterfeiting and encryption","authors":"Peng Zhang, Xin Chen, Jing Li, Lei Fang, Xiangying Sun","doi":"10.1039/d5qi01664a","DOIUrl":null,"url":null,"abstract":"Dynamic room-temperature phosphorescence (RTP) materials with color-tunable afterglow characteristics hold great promise for advanced anti-counterfeiting and multidimensional encryption applications. In this work, we successfully synthesized a novel two-dimensional phenylammonium cadmium chloride perovskite (B-PACC) with enhanced RTP efficiency <em>via</em> boronic acid group-assisted crystallization. Furthermore, a precise doping strategy was employed to introduce Mn<small><sup>2+</sup></small>, which assembled into Mn<small><sup>2+</sup></small> pairs forming a Mn<small><sup>2+</sup></small>-based inorganic layer. This layer, together with B-PACC, constructed a heterojunction structure with different interlayer spacings, enabling dynamic afterglow emission color modulation from red to blue. Moreover, tuning the Mn<small><sup>2+</sup></small> concentration enables precise modulation of the energy transfer rates from the singlet and triplet states of the organic moieties to the Mn<small><sup>2+</sup></small> layer, thereby allowing fine control over the dynamic RTP behavior. Benefiting from the minimal background interference and large chromaticity contrast associated with the red-to-blue phosphorescence transition, the system exhibited high visual detectability. Based on this dynamic afterglow behavior, we successfully developed time-resolved anti-counterfeiting patterns and constructed dynamic room-temperature phosphorescence-based four-dimensional (4D) codes, providing new insights into the design of dynamic RTP materials and highly secure encryption strategies.","PeriodicalId":79,"journal":{"name":"Inorganic Chemistry Frontiers","volume":"44 1","pages":""},"PeriodicalIF":6.4000,"publicationDate":"2025-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Inorganic Chemistry Frontiers","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d5qi01664a","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
引用次数: 0
Abstract
Dynamic room-temperature phosphorescence (RTP) materials with color-tunable afterglow characteristics hold great promise for advanced anti-counterfeiting and multidimensional encryption applications. In this work, we successfully synthesized a novel two-dimensional phenylammonium cadmium chloride perovskite (B-PACC) with enhanced RTP efficiency via boronic acid group-assisted crystallization. Furthermore, a precise doping strategy was employed to introduce Mn2+, which assembled into Mn2+ pairs forming a Mn2+-based inorganic layer. This layer, together with B-PACC, constructed a heterojunction structure with different interlayer spacings, enabling dynamic afterglow emission color modulation from red to blue. Moreover, tuning the Mn2+ concentration enables precise modulation of the energy transfer rates from the singlet and triplet states of the organic moieties to the Mn2+ layer, thereby allowing fine control over the dynamic RTP behavior. Benefiting from the minimal background interference and large chromaticity contrast associated with the red-to-blue phosphorescence transition, the system exhibited high visual detectability. Based on this dynamic afterglow behavior, we successfully developed time-resolved anti-counterfeiting patterns and constructed dynamic room-temperature phosphorescence-based four-dimensional (4D) codes, providing new insights into the design of dynamic RTP materials and highly secure encryption strategies.