Two-dimensional transition metal dichalcogenides （2D TMDs） possess a tunable excitonic light emission that is sensitive to external conditions such as electric field, strain, and chemical doping. In this work, we re...Two-dimensional transition metal dichalcogenides （2D TMDs） possess a tunable excitonic light emission that is sensitive to external conditions such as electric field, strain, and chemical doping. In this work, we reveal the interactions between DNA nucleobases, i.e., adenine （A）, guanine （G）, cytosine （C）, and thymine （T） and monolayer WS2 by investigating the changes in the photoluminescence （PL） emissions of the monolayer WS2 after coating with nucleobase solutions. We found that adenine and guanine exert a clear effect on the PL profile of the monolayer WS2 and cause different PL evolution trends. In contrast, cytosine and thymine have little effect on the PL behavior. To obtain information on the interactions between the DNA bases and WS2, a series of measurements were conducted on adenine-coated WS2 monolayers, as a demonstration. The p-type doping of the WS2 monolayers on the introduction of adenine is clearly shown by both the evolution of the PL spectra and the electrical transport response. Our findings open the door for the development of label-free optical sensing approaches in which the detection signals arise from the tunable excitonic emission of the TMD itself rather than the fluorescence signals of label molecules. This dopant-selective optical response to the DNA nucleobases fills the gaps in previously reported optical biosensing methods and indicates a potential new strategy for DNA sequencing.展开更多
基金This work is supported by the Singapore National Research Foundation NRF RF Award No. NRFRF2010- 07, MOE Tier 2 MOE2012-T2-2-049, A＇Star SERC PSF grant No. 1321202101, and MOE Tier 1 MOE2013- T1-2-235. W. Huang acknowledges the support of the National Basic Research Program of China （973 Program） （No. 2015CB932200）, the National Natural Science Foundation of China （NSFC） （Grant Nos. 21144004, 20974046, 21101095, 21003076, 20774043, 51173081, 50428303, 61136003, and 50428303）, the Ministry of Education of China （No. IRT1148）, the NSF of Jiangsu Province （Grant Nos. SBK201122680, 11KJB510017, BK2008053, 11KJB510017, BK2009025, 10KJB510013, and BZ2010043）, and NUPT （Nos. NY210030 and NY211022）. J. R Wang is grateful for the NSFC （No. 11474164）, NSF of Jiangsu province （No. BK20131413）, and the Jiangsu Specially-Appointed Professor program. Y. L. Wang thanks Luqing Wang, Dr. Xiaolong Zou, and Dr. Alex Kutana for the constructive discussion.
基金This work is supported by the Singapore Ministry of Education under MOE Tier 1 RG178/15 and MOE Tier 1 RG100/15. C. X. C. thanks the support by the National Young 1000 Talent Plan of China and the Shanghai Municipal Natural Science Foundation （No. 16ZR1402500）. M. E. appreciates the support by National Synergetic Innovation Center for Advanced Materials （SICAM）, the start-up fund by Nanjing Tech University, and Jiangsu 100 Talent.
文摘Two-dimensional transition metal dichalcogenides （2D TMDs） possess a tunable excitonic light emission that is sensitive to external conditions such as electric field, strain, and chemical doping. In this work, we reveal the interactions between DNA nucleobases, i.e., adenine （A）, guanine （G）, cytosine （C）, and thymine （T） and monolayer WS2 by investigating the changes in the photoluminescence （PL） emissions of the monolayer WS2 after coating with nucleobase solutions. We found that adenine and guanine exert a clear effect on the PL profile of the monolayer WS2 and cause different PL evolution trends. In contrast, cytosine and thymine have little effect on the PL behavior. To obtain information on the interactions between the DNA bases and WS2, a series of measurements were conducted on adenine-coated WS2 monolayers, as a demonstration. The p-type doping of the WS2 monolayers on the introduction of adenine is clearly shown by both the evolution of the PL spectra and the electrical transport response. Our findings open the door for the development of label-free optical sensing approaches in which the detection signals arise from the tunable excitonic emission of the TMD itself rather than the fluorescence signals of label molecules. This dopant-selective optical response to the DNA nucleobases fills the gaps in previously reported optical biosensing methods and indicates a potential new strategy for DNA sequencing.
