Uniaxiality‐Induced Reduced‐Pressure Synthesis of Ultrahard Paracrystalline Diamond

Synthesizing fully sp<sup>3</sup>-bonded non-crystalline carbon remains a long-standing challenge due to the intrinsic instability of the sp<sup>3</sup> bond at ambient pressure. Recently, paracrystalline diamond, a new-form sp<sup>3</sup>-bonded non-crystalline carbon consisting of sub-nanometer-sized paracrystallites, has been synthesized from face-centered cubic C<sub>60</sub> at 30 GPa, which has attracted attention due to its unique structural features and excellent physical properties. However, the ultrahigh synthesis pressure of paracrystalline diamond poses an obstacle to its large-scale production and applications. In this study, paracrystalline diamond is synthesized at an exceptionally low pressure (16 GPa) via inducing uniaxiality at high-pressure and high-temperature conditions, thereby breaking through the temperature-pressure phase diagram of C<sub>60</sub>. By combining structural characteristics and advanced molecular dynamics simulation, the remarkable reduction of synthesis pressure is attributed to the fact that the symmetry of the C<sub>60</sub> cage is broken due to the uniaxiality, which further allows the C<sub>60</sub> cage to collapse at much lower pressures. This work reveals the critical role of uniaxiality in the reduced-pressure synthesis of paracrystalline diamond, which may provide a potent methodological strategy for the development of novel low-cost high-pressure materials.

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Publication Details

Journal
Advanced Materials
Published
2025-04-14
DOI
https://doi.org/10.1002/adma.202500037
Citations
2
Primary Topic
Diamond and Carbon-based Materials Research
Type
article
Field-Weighted Citation Impact
1.04

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article

Uniaxiality‐Induced Reduced‐Pressure Synthesis of Ultrahard Paracrystalline Diamond

Yong Cheng, Baoyin Xu, Hu Tang, Zhi-Tong Wang et al.
2 citations
Advanced Materials
Diamond and Carbon-based Materials Research
1.04
article

Uniaxiality‐Induced Reduced‐Pressure Synthesis of Ultrahard Paracrystalline Diamond

Yong Cheng, Baoyin Xu, Hu Tang, Zhi-Tong Wang, Xiaohong Yuan, Kuo Hu, Shengcai Zhu, Zhaodong Liu, Bingbing Liu, Ming‐Sheng Wang, Yue Pan, Shida Wang, Quanjun Li, Shucheng Liu
article en
2 citations

Abstract

Synthesizing fully sp<sup>3</sup>-bonded non-crystalline carbon remains a long-standing challenge due to the intrinsic instability of the sp<sup>3</sup> bond at ambient pressure. Recently, paracrystalline diamond, a new-form sp<sup>3</sup>-bonded non-crystalline carbon consisting of sub-nanometer-sized paracrystallites, has been synthesized from face-centered cubic C<sub>60</sub> at 30 GPa, which has attracted attention due to its unique structural features and excellent physical properties. However, the ultrahigh synthesis pressure of paracrystalline diamond poses an obstacle to its large-scale production and applications. In this study, paracrystalline diamond is synthesized at an exceptionally low pressure (16 GPa) via inducing uniaxiality at high-pressure and high-temperature conditions, thereby breaking through the temperature-pressure phase diagram of C<sub>60</sub>. By combining structural characteristics and advanced molecular dynamics simulation, the remarkable reduction of synthesis pressure is attributed to the fact that the symmetry of the C<sub>60</sub> cage is broken due to the uniaxiality, which further allows the C<sub>60</sub> cage to collapse at much lower pressures. This work reveals the critical role of uniaxiality in the reduced-pressure synthesis of paracrystalline diamond, which may provide a potent methodological strategy for the development of novel low-cost high-pressure materials.

Advanced MaterialsVol. 37(27)
Sun Yat-sen University (CN), Xiamen University (CN), Jilin University (CN), Center for High Pressure Science & Technology Advanced Research (CN)
National Natural Science Foundation of China, Natural Science Foundation of Guangdong Province, National Key Research and Development Program of China
Openalex Percentile: Top 26%
Diamond and Carbon-based Materials Research
1.04
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