Organic and inorganic clusteroluminescence have attracted great attention while the underlying mechanisms is still not well understood.Here,we employed a series of ancient inorganic complexes platinocyanides with aggr...Organic and inorganic clusteroluminescence have attracted great attention while the underlying mechanisms is still not well understood.Here,we employed a series of ancient inorganic complexes platinocyanides with aggregation-induced emission property to elucidate the mechanism of clusteroluminescence including how does the chromophore form and how does the solid structures influence the luminescence behaviors.The results indicate that the isolated platinocyanide cannot work as a chromophore to emit visible light,while their clusterization at aggregate state can trigger the d-orbitals coupling of the platinum atoms to facilitate the electron exchange and delocalization to form a new chromophore to emit visible light.Furthermore,the counter ions and H2O ligands help to rigidify the three-dimensional network structure of the platinocyanides to suppress the excited state nonradiative decay,resulting in the high quantum yield of up to 96%.This work fundamentally helps understanding both the organic and inorganic clusteroluminescence phenomenon.展开更多
基金National Natural Science Foundation of China,Grant/Award Numbers:21788102,52003228Science and Technology Plan of Shenzhen,Grant/Award Number:JCYJ20180306174910791+2 种基金Natural Science Foundation of Guangdong Province,Grant/Award Number:2019B121205002Research Grants Council of Hong Kong,Grant/Award Numbers:N_HKUT609/19,16305518,A-HKUST605/16,C6009-17GInnovation and Technology Commission,Grant/Award Numbers:ITC-CNERC14SC01,ITCPD/17-9。
文摘Organic and inorganic clusteroluminescence have attracted great attention while the underlying mechanisms is still not well understood.Here,we employed a series of ancient inorganic complexes platinocyanides with aggregation-induced emission property to elucidate the mechanism of clusteroluminescence including how does the chromophore form and how does the solid structures influence the luminescence behaviors.The results indicate that the isolated platinocyanide cannot work as a chromophore to emit visible light,while their clusterization at aggregate state can trigger the d-orbitals coupling of the platinum atoms to facilitate the electron exchange and delocalization to form a new chromophore to emit visible light.Furthermore,the counter ions and H2O ligands help to rigidify the three-dimensional network structure of the platinocyanides to suppress the excited state nonradiative decay,resulting in the high quantum yield of up to 96%.This work fundamentally helps understanding both the organic and inorganic clusteroluminescence phenomenon.
