Self-assembly of particle-like dissipative solitons,in the presence of mutual interactions,emphasizes the vibrant concept of soliton molecules in varieties of laser resonators.Controllable manipulation of the molecula...Self-assembly of particle-like dissipative solitons,in the presence of mutual interactions,emphasizes the vibrant concept of soliton molecules in varieties of laser resonators.Controllable manipulation of the molecular patterns,held by the degrees of freedom of internal motions,still remains challenging to explore more efficient and subtle tailoring approaches for the increasing demands.Here,we report a new phase-tailored quaternary encoding format based on the controllable internal assembly of dissipative soliton molecules.Artificial manipulation of the energy exchange of soliton-molecular elements stimulates the deterministic harnessing of the assemblies of internal dynamics.Self-assembled soliton molecules are tailored into four phase-defined regimes,thus constituting the phase-tailored quaternary encoding format.Such phase-tailored streams are endowed with great robustness and are resistant to significant timing jitter.All these results experimentally demonstrate the programmable phase tailoring and exemplify the application of the phase-tailored quaternary encoding,prospectively promoting high-capacity all-optical storage.展开更多
Due to the electronic bottleneck limited real-time measurement speed of common temporal-spectral detection and the particle-like nature of optical soliton enabled nonrepeatable transient behaviors, capturing the ultra...Due to the electronic bottleneck limited real-time measurement speed of common temporal-spectral detection and the particle-like nature of optical soliton enabled nonrepeatable transient behaviors, capturing the ultrafast laser pulses with unknown times of arrival and synchronously characterizing their temporal-spectral dynamic evolution is still a challenge. Here, using the Raman soliton frequency shift based temporal magnifier and dispersive Fourier transform based spectral analyzer, we demonstrate a self-synchronized, ultrafast temporal-spectral characterization system with a resolution of 160 fs and 0.05 nm, and a recording length above milliseconds. The synchronized nonlinear process makes it possible to image full-filled temporal sub-picosecond pulse trains regardless of their arrival times and without extra pump lasers and photoelectric conversion devices. To demonstrate the significance of this improvement, a buildup dynamic process of a soliton laser with a complex breakup and collisions of multisolitons is visually displayed in the spectral and temporal domains. The soliton dynamic evolution processes observed by our characterization system are in one-to-one correspondence with the numerical simulation results. We believe this work provides a new multidimensional technique to break the electronic bottleneck to gain additional insight into the dynamics of ultrafast lasers and nonlinear science.展开更多
The evolution of soliton molecules emphasizes the complex soliton dynamics akin to matter molecules.Beyond the simplest soliton molecule-a soliton pair constituted by two bound pulses-soliton molecules with more const...The evolution of soliton molecules emphasizes the complex soliton dynamics akin to matter molecules.Beyond the simplest soliton molecule-a soliton pair constituted by two bound pulses-soliton molecules with more constituents have more degrees of freedom because of the temporal pulse separations and relative phases.Here we detailedly characterize the transient dynamics of soliton triplets in fiber lasers by using the dispersive Fourier transform measurement.A particular form of leading,central,and tailing pulses is constructed to shed new light on more intriguing scenarios and fuel the molecular analogy.Especially the vibrating dynamics of the central and tailing pulses are captured near the regime of equally spaced soliton triplets,which is reminiscent of the recurrent timing jitters within multi-pulse structures.Further insights enable acess into a universal form of unequally spaced soliton triplets interpreted as 2+1 soliton molecules.Different binding strengths of intramo-lecular and intermolecular bonds are validated with respect to the diverse internal motions involved in this soliton triplet molcule.All these findings unveil the transient dynamics with more degrees of freedom as well as highlight the possible application for all-optical bit storage.展开更多
基金This work is supported by the National Natural Science Foundation of China(U22A20206,61922033,62275097)Open Project Program of Wuhan National Laboratory for Optoelectronics(2022WNLOKF007)China Postdoctoral Science Foundation(2022M711243).
文摘Self-assembly of particle-like dissipative solitons,in the presence of mutual interactions,emphasizes the vibrant concept of soliton molecules in varieties of laser resonators.Controllable manipulation of the molecular patterns,held by the degrees of freedom of internal motions,still remains challenging to explore more efficient and subtle tailoring approaches for the increasing demands.Here,we report a new phase-tailored quaternary encoding format based on the controllable internal assembly of dissipative soliton molecules.Artificial manipulation of the energy exchange of soliton-molecular elements stimulates the deterministic harnessing of the assemblies of internal dynamics.Self-assembled soliton molecules are tailored into four phase-defined regimes,thus constituting the phase-tailored quaternary encoding format.Such phase-tailored streams are endowed with great robustness and are resistant to significant timing jitter.All these results experimentally demonstrate the programmable phase tailoring and exemplify the application of the phase-tailored quaternary encoding,prospectively promoting high-capacity all-optical storage.
基金National Natural Science Foundation of China(61635004,62075021)National Science Fund for Distinguished Young Scholars(61825501)Chongqing Natural Science Foundation of Innovative Research Groups(CSTC2020JCYJ,CXTTX0005)
文摘Due to the electronic bottleneck limited real-time measurement speed of common temporal-spectral detection and the particle-like nature of optical soliton enabled nonrepeatable transient behaviors, capturing the ultrafast laser pulses with unknown times of arrival and synchronously characterizing their temporal-spectral dynamic evolution is still a challenge. Here, using the Raman soliton frequency shift based temporal magnifier and dispersive Fourier transform based spectral analyzer, we demonstrate a self-synchronized, ultrafast temporal-spectral characterization system with a resolution of 160 fs and 0.05 nm, and a recording length above milliseconds. The synchronized nonlinear process makes it possible to image full-filled temporal sub-picosecond pulse trains regardless of their arrival times and without extra pump lasers and photoelectric conversion devices. To demonstrate the significance of this improvement, a buildup dynamic process of a soliton laser with a complex breakup and collisions of multisolitons is visually displayed in the spectral and temporal domains. The soliton dynamic evolution processes observed by our characterization system are in one-to-one correspondence with the numerical simulation results. We believe this work provides a new multidimensional technique to break the electronic bottleneck to gain additional insight into the dynamics of ultrafast lasers and nonlinear science.
基金National Natural Science Foundation of China(61775067,61775072)Ministry of Education-Singapore(MOE2019-T1-001-111)National Research Foundation Singapore(NRF-CRP-18-2017-02).
文摘The evolution of soliton molecules emphasizes the complex soliton dynamics akin to matter molecules.Beyond the simplest soliton molecule-a soliton pair constituted by two bound pulses-soliton molecules with more constituents have more degrees of freedom because of the temporal pulse separations and relative phases.Here we detailedly characterize the transient dynamics of soliton triplets in fiber lasers by using the dispersive Fourier transform measurement.A particular form of leading,central,and tailing pulses is constructed to shed new light on more intriguing scenarios and fuel the molecular analogy.Especially the vibrating dynamics of the central and tailing pulses are captured near the regime of equally spaced soliton triplets,which is reminiscent of the recurrent timing jitters within multi-pulse structures.Further insights enable acess into a universal form of unequally spaced soliton triplets interpreted as 2+1 soliton molecules.Different binding strengths of intramo-lecular and intermolecular bonds are validated with respect to the diverse internal motions involved in this soliton triplet molcule.All these findings unveil the transient dynamics with more degrees of freedom as well as highlight the possible application for all-optical bit storage.