Clean graphene transfer has received widespread research attention, where most methods are focused on cleaning the upper surface of graphene to improve the transfer technique. However, the residue formation on the bot...Clean graphene transfer has received widespread research attention, where most methods are focused on cleaning the upper surface of graphene to improve the transfer technique. However, the residue formation on the bottom surface of graphene is also inevitable;therefore, cleaning the bottom surface is crucial. In this study, we proposed an improved graphene wet transfer method using an ultrasonic processing(UP) step for etching copper(Cu). Using this method, the bottom surface can be cleaned efficiently. The results of atomic force microscopy(AFM)and Raman spectroscopy mapping revealed that the graphene films transferred with UP had smoother and cleaner surfaces, less contamination, and higher quality than those transferred without UP.展开更多
The transfer of graphene from metallic substrates onto application-specific substrates is usually inevitable for the applications of high-quality graphene films derived from chemical vapour deposition(CVD)approaches.C...The transfer of graphene from metallic substrates onto application-specific substrates is usually inevitable for the applications of high-quality graphene films derived from chemical vapour deposition(CVD)approaches.Commonly used to support the graphene films during the transfer,the coating of the polymer would produce the surface contaminations and hinder the industrially compatible transfer.In this work,through the thermal imidization of polyamide acid(PAA)to polyimide(PI)and tuning of the concentration of dangling chains,we achieved the ultraclean and crack-free transfer of graphene wafers with high electronic quality.The resulting contamination-free and hydrophilic surface also enabled the observed improved cell viability in a biomedical applications.By avoiding aqueous etching or the usage of strong bases,our proposed transfer method is industrially compatible for batch transfer of graphene films towards the real applications.展开更多
Noble metals such as Pt are a perfect substrate for the catalytic growth of monolayer graphene. However, the requirements of the subsequent transfer process are not compatible with the traditional etching method. In t...Noble metals such as Pt are a perfect substrate for the catalytic growth of monolayer graphene. However, the requirements of the subsequent transfer process are not compatible with the traditional etching method. In this work, we find that the interaction of graphene with Pt foil can be weakened through the intercalation of carbon monoxide (CO) under ambient pressure. This intercalation process occurs on both hexagonal-shape graphene islands and irregular graphene patches on changing the CO partial pressure from 0 to 0.6 MPa, as observed by scanning electron microscopy (SEM), Raman spectroscopy and X-ray photoemission spectroscopy. We demonstrate that, on a practical timescale, the intercalation ratio is proportional to the partial pressure of CO. Furthermore, we develop a clean transfer method of CO-intercalated graphene with water as a peeling agent. We show that this method enables the transfer of tens of micrometer-scale graphene patches onto SiO2/Si, which are free from metal or oxide particle contamination. This transfer method should be a significant step towards the dean transfer of graphene, as well as the recydable use of noble metal substrates.展开更多
In this work, we developed a novel triboelectricity-assisted polymer-free method for the transfer of large-area chemical vapor deposited graphene films. With the assistance of electrostatic forces from friction-genera...In this work, we developed a novel triboelectricity-assisted polymer-free method for the transfer of large-area chemical vapor deposited graphene films. With the assistance of electrostatic forces from friction-generated charges, graphene sheets were successfully transferred from copper foils to flexible polymer substrates. Characterization results confirmed the presence of high quality graphene with less defects and contaminations, compared to graphene transferred by conventional poly(methyl rnethacrylate)-mediated processes. In addition, the graphene samples possessed outstanding electrical transport capabilities and mechanical stability, when studied as electron transfer matrixes in graphene/ZnO hybrid flexible photodetectors. Our results showed a broad application potential for this transfer method in future flexible electronics and optoelectronics.展开更多
Based on thermoacoustic theory, a coupled thermal-mechanical model for graphene films is established, and the analytical solutions for thermal-acoustic radiation from a graphene thin film are obtained. The sound press...Based on thermoacoustic theory, a coupled thermal-mechanical model for graphene films is established, and the analytical solutions for thermal-acoustic radiation from a graphene thin film are obtained. The sound pressure of the graphene film generator on different substrates is measured, and the measurement data is compared with the theoretical results. The frequency response from the experimental results is consistent with the theoretical ones, while the measured values are slightly lower than the theoretical ones. Therefore, the accuracy of the proposed theoretical model is verified. It is shown that thermal-acoustic radiation from a graphene thin film reveals a wide frequency response. The sound pressure level increases with the frequency in the low frequency range, while the sound pressure varies smoothly with frequency in the high frequency range. Thus it can be used as excellent thermal generator. When the thermal effusivity of the substrate is smaller, then the sound pressure of grapheme films will be higher. Furthermore, the sound pressure decreases with the increase of heat capacity per unit area of grapheme films. Results will contribute to the mechanism of graphene films generator and its applications in the design of loudspeaker and other related areas.展开更多
基金supported by the National Key Research and Development Program of China under Grants No.2017YFA0701000and No.2020YFA0714001the National Natural Science Foundation of China under Grants No.61988102,No.61921002,and No.62071108the Fundamental Research Funds for the Central Universities under Grants No.ZYGX2020J003 and No.ZYGX2020ZB007。
文摘Clean graphene transfer has received widespread research attention, where most methods are focused on cleaning the upper surface of graphene to improve the transfer technique. However, the residue formation on the bottom surface of graphene is also inevitable;therefore, cleaning the bottom surface is crucial. In this study, we proposed an improved graphene wet transfer method using an ultrasonic processing(UP) step for etching copper(Cu). Using this method, the bottom surface can be cleaned efficiently. The results of atomic force microscopy(AFM)and Raman spectroscopy mapping revealed that the graphene films transferred with UP had smoother and cleaner surfaces, less contamination, and higher quality than those transferred without UP.
基金supported by the National Natural Science Foundation of China(Nos.T2188101 and 52372038)the National Key Research and Development Program of China(No.2022YFA1204900)the China Postdoctoral Science Foundation(No.2023M740030).
文摘The transfer of graphene from metallic substrates onto application-specific substrates is usually inevitable for the applications of high-quality graphene films derived from chemical vapour deposition(CVD)approaches.Commonly used to support the graphene films during the transfer,the coating of the polymer would produce the surface contaminations and hinder the industrially compatible transfer.In this work,through the thermal imidization of polyamide acid(PAA)to polyimide(PI)and tuning of the concentration of dangling chains,we achieved the ultraclean and crack-free transfer of graphene wafers with high electronic quality.The resulting contamination-free and hydrophilic surface also enabled the observed improved cell viability in a biomedical applications.By avoiding aqueous etching or the usage of strong bases,our proposed transfer method is industrially compatible for batch transfer of graphene films towards the real applications.
基金Acknowledgements This work was financially supported by the Ministry of Science and Technology of China (Grant Nos. 2011CB921903, 2012CB921404, 2012CB933404, 2013CB932603, and 2011CB933003), and the National Natural Science Foundation of China (Grant Nos. 21073003, 51222201, 51290272, 51121091, and 51072004).
文摘Noble metals such as Pt are a perfect substrate for the catalytic growth of monolayer graphene. However, the requirements of the subsequent transfer process are not compatible with the traditional etching method. In this work, we find that the interaction of graphene with Pt foil can be weakened through the intercalation of carbon monoxide (CO) under ambient pressure. This intercalation process occurs on both hexagonal-shape graphene islands and irregular graphene patches on changing the CO partial pressure from 0 to 0.6 MPa, as observed by scanning electron microscopy (SEM), Raman spectroscopy and X-ray photoemission spectroscopy. We demonstrate that, on a practical timescale, the intercalation ratio is proportional to the partial pressure of CO. Furthermore, we develop a clean transfer method of CO-intercalated graphene with water as a peeling agent. We show that this method enables the transfer of tens of micrometer-scale graphene patches onto SiO2/Si, which are free from metal or oxide particle contamination. This transfer method should be a significant step towards the dean transfer of graphene, as well as the recydable use of noble metal substrates.
基金This work was supported by the National Basic Research Program of China (No. 2013CB932602), the Program of Introducing Talents of Discipline to Universities (No. B14003), National Natural Science Foundation of China (Nos. 51527802 and 51232001), Beijing Municipal Science & Technology Commission, the Fundamental Research Funds for Central Universities.
文摘In this work, we developed a novel triboelectricity-assisted polymer-free method for the transfer of large-area chemical vapor deposited graphene films. With the assistance of electrostatic forces from friction-generated charges, graphene sheets were successfully transferred from copper foils to flexible polymer substrates. Characterization results confirmed the presence of high quality graphene with less defects and contaminations, compared to graphene transferred by conventional poly(methyl rnethacrylate)-mediated processes. In addition, the graphene samples possessed outstanding electrical transport capabilities and mechanical stability, when studied as electron transfer matrixes in graphene/ZnO hybrid flexible photodetectors. Our results showed a broad application potential for this transfer method in future flexible electronics and optoelectronics.
基金supported by the National Natural Science Foundation of China(51375321)Soochow University "Soochow Scholars" program(R513300116)
文摘Based on thermoacoustic theory, a coupled thermal-mechanical model for graphene films is established, and the analytical solutions for thermal-acoustic radiation from a graphene thin film are obtained. The sound pressure of the graphene film generator on different substrates is measured, and the measurement data is compared with the theoretical results. The frequency response from the experimental results is consistent with the theoretical ones, while the measured values are slightly lower than the theoretical ones. Therefore, the accuracy of the proposed theoretical model is verified. It is shown that thermal-acoustic radiation from a graphene thin film reveals a wide frequency response. The sound pressure level increases with the frequency in the low frequency range, while the sound pressure varies smoothly with frequency in the high frequency range. Thus it can be used as excellent thermal generator. When the thermal effusivity of the substrate is smaller, then the sound pressure of grapheme films will be higher. Furthermore, the sound pressure decreases with the increase of heat capacity per unit area of grapheme films. Results will contribute to the mechanism of graphene films generator and its applications in the design of loudspeaker and other related areas.