Abstract
Ångström-scale polygonal rings in monolayer amorphous carbon (MAC) enhance its electronic and mechanical properties while providing unique ångström pores for precise subatomic species separation, essential for advancements in catalysis, energy and medicine. However, the absence of an industrial-scale synthesis method for intrinsic MAC has limited its technological applications compared with graphene and bulk amorphous materials. Herein, we report an industry-compatible disorder-to-disorder synthesis approach to achieve wafer-scale ultraclean MAC (UC-MAC) within a timescale of seconds, featuring optimized ångström polygons without detectable metal contamination, and nanosized pores. In contrast to metal-contaminated MAC, UC-MAC allows atomic-scale characterization of intrinsic electronic properties and functions as an ångström-scale membrane, facilitating the splitting of high-flux H2+ ions into a high-precision proton beam with minimal detrimental fragment-proton scattering events, about half and 40 times less than those from single-crystal graphene and commercial carbon thin films, respectively. The minimum possible membrane material thickness that can yield a highly sharpened proton beam with accurately modulated beam current is desired for proton therapy. © The Author(s), under exclusive licence to Springer Nature Limited 2025
| Original language | English |
|---|---|
| Pages (from-to) | 1431-1438 |
| Number of pages | 18 |
| Journal | Nature Nanotechnology |
| Volume | 20 |
| Online published | 28 Jul 2025 |
| DOIs | |
| Publication status | Published - Oct 2025 |
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RGC Funding Information
- RGC-funded
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