Unzipping hBN with ultrashort mid-infrared pulses

Author:

Chen Cecilia Y.1ORCID,Moore Samuel L.2ORCID,Maiti Rishi34,Ginsberg Jared S.3,Jadidi M. Mehdi3,Li Baichang5ORCID,Chae Sang Hoon567ORCID,Rajendran Anjaly1ORCID,Patwardhan Gauri N.38ORCID,Watanabe Kenji9ORCID,Taniguchi Takashi10ORCID,Hone James5ORCID,Basov D. N.2ORCID,Gaeta Alexander L.13ORCID

Affiliation:

1. Department of Electrical Engineering, Columbia University, New York, NY 10027, USA.

2. Department of Physics, Columbia University, New York, NY 10027, USA.

3. Department of Applied Physics and Applied Mathematics, Columbia University, New York, NY 10027, USA.

4. Department of Physics, Indian Institute of Technology Guwahati, Assam 781039, India.

5. Department of Mechanical Engineering, Columbia University, New York, NY 10027, USA.

6. School of Electrical and Electronic Engineering, Nanyang Technological University, Singapore 639798, Singapore.

7. School of Materials Science and Engineering, Nanyang Technological University, Singapore 639798, Singapore.

8. School of Applied and Engineering Physics, Cornell University, Ithaca, NY 14853, USA.

9. Research Center for Functional Materials, National Institute for Materials Science, 1-1 Namiki, Tsukuba 305-0044, Japan.

10. International Center for Materials Nanoarchitectonics, National Institute for Materials Science, 1-1 Namiki, Tsukuba 305-0044, Japan.

Abstract

Manipulating the nanostructure of materials is critical for numerous applications in electronics, magnetics, and photonics. However, conventional methods such as lithography and laser writing require cleanroom facilities or leave residue. We describe an approach to creating atomically sharp line defects in hexagonal boron nitride (hBN) at room temperature by direct optical phonon excitation with a mid-infrared pulsed laser from free space. We term this phenomenon “unzipping” to describe the rapid formation and growth of a crack tens of nanometers wide from a point within the laser-driven region. Formation of these features is attributed to the large atomic displacement and high local bond strain produced by strongly driving the crystal at a natural resonance. This process occurs only via coherent phonon excitation and is highly sensitive to the relative orientation of the crystal axes and the laser polarization. Its cleanliness, directionality, and sharpness enable applications such as polariton cavities, phonon-wave coupling, and in situ flake cleaving.

Publisher

American Association for the Advancement of Science (AAAS)

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