| 1. |
- Dong, Jiajun, et al.
(författare)
-
Decompression-Induced Diamond Formation from Graphite Sheared under Pressure
- 2020
-
Ingår i: Physical Review Letters. - : American Physical Society. - 0031-9007 .- 1079-7114. ; 124:6
-
Tidskriftsartikel (refereegranskat)abstract
- Graphite is known to transform into diamond under dynamic compression or under combined high pressure and high temperature, either by a concerted mechanism or by a nucleation mechanism. However, these mechanisms fail to explain the recently reported discovery of diamond formation during ambient temperature compression combined with shear stress. Here we report a new transition pathway for graphite to diamond under compression combined with shear, based on results from both theoretical simulations and advanced experiments. In contrast to the known model for thermally activated diamond formation under pressure, the shear-induced diamond formation takes place during the decompression process via structural transitions. At a high pressure with large shear, graphite transforms into ultrastrong sp3 phases whose structures depend on the degree of shear stress. These metastable sp3 phases transform into either diamond or graphite upon decompression. Our results explain several recent experimental observations of low-temperature diamond formation. They also emphasize the importance of shear stress for diamond formation, providing new insight into the graphite-diamond transformation mechanism.
|
|
| 2. |
- Yin, Xiu, et al.
(författare)
-
Doping of charge-transfer molecules in cocrystals for the design of materials with novel piezo-activated luminescence
- 2023
-
Ingår i: Chemical Science. - : Royal Society of Chemistry. - 2041-6520 .- 2041-6539. ; 14:6, s. 1479-1484
-
Tidskriftsartikel (refereegranskat)abstract
- A novel piezo-activated luminescent material with wide range modulation of the luminescence wavelength and a giant intensity enhancement upon compression was prepared using a strategy of molecular doping. The doping of THT molecules into TCNB-perylene cocrystals results in the formation of a weak but pressure-enhanced emission center in the material at ambient pressure. Upon compression, the emissive band from the undoped component TCNB-perylene undergoes a normal red shift and emission quenching, while the weak emission center shows an anomalous blue shift from 615 nm to 574 nm and a giant luminescence enhancement up to 16 GPa. Further theoretical calculations show that doping by THT could modify intermolecular interactions, promote molecular deformation, and importantly, inject electrons into the host TCNB-perylene upon compression, which contributes to the novel piezochromic luminescence behavior. Based on this finding, we further propose a universal approach to design and regulate the piezo-activated luminescence of materials by using other similar dopants.
|
|
| 3. |
- Zhang, Ying, et al.
(författare)
-
Capture of novel sp3 hybridized Z-BN by compressing boron nitride nanotubes with small diameter
- 2022
-
Ingår i: Diamond and related materials. - : Elsevier. - 0925-9635 .- 1879-0062. ; 130
-
Tidskriftsartikel (refereegranskat)abstract
- Experimental synthesis of new sp3 hybridized carbon/boron nitride structures remains challenging despite that numerous sp3 structures have been proposed in theory. Here, we showed that compressed multi-walled boron nitride nanotubes (MWBNNTs) and boron nitride peapods (C60@BNNTs) with small diameters could transform into a new sp3 hybridized boron nitride allotrope (Z-BN). This strategy is considered from the topological transition point of view in boron nitride nanotubes upon compression. Due to the increased curvature in compressed small-diameter MWBNNTs, the uncommon 4- and 8-membered rings in Z-BN could be more favorably formed. And the irreversible tube collapse is proved to be a critical factor for the capture of the formed Z-BN, because of the competition between the resilience of tube before collapse and the stress limitation for the lattice stabilization of Z-BN upon decompression. In this case, Z-BN starts to form above 19.0 GPa, which is fully reversible below 45 GPa and finally becomes quenchable at 93.5 GPa. This collapse-induced capture of the high-pressure phase could also be extended to other tubular materials for quenching novel sp3 structures.
|
|
| 4. |
- Zhang, Ying, et al.
(författare)
-
Negative Volume Compressibility in Sc3N@C-80-Cubane Cocrystal with Charge Transfer
- 2020
-
Ingår i: Journal of the American Chemical Society. - : American Chemical Society (ACS). - 0002-7863 .- 1520-5126. ; 142:16, s. 7584-7590
-
Tidskriftsartikel (refereegranskat)abstract
- According to the laws of thermodynamics, materials normally exhibit contraction or expansion along the directions of the applied pressure or tension. Here, we show that a man-made cocrystal of a metallofullerene and highly energetic cubane, with strained sp(3) bonding, may exhibit an anomalous negative volume compressibility. In this cocrystal, the freely rotating fullerene Sc3N@C-80 acts as a structural building block while static cubane molecules fill the lattice interstitial sites. Under high pressure, Sc3N@C-80 keeps stable and preserves the crystalline framework of the materials, while the cubane undergoes a progressive configurational transformation above 6.5 GPa, probably promoted by charge transfer from fullerene to cubane. A further configurational change of the cubane into a low-density configuration at higher pressure results in an anomalous pressure-driven lattice expansion of the cocrystal (similar to 1.8% volume expansion). Such unusual negative compressibility has previously only been predicted by theory and suggested to appear in mechanical metamaterials.
|
|
| 5. |
- Shang, Yuchen, et al.
(författare)
-
Enhancement of short/medium-range order and thermal conductivity in ultrahard sp3 amorphous carbon by C70 precursor
- 2023
-
Ingår i: Nature Communications. - : Springer Nature. - 2041-1723. ; 14:1
-
Tidskriftsartikel (refereegranskat)abstract
- As an advanced amorphous material, sp3 amorphous carbon exhibits exceptional mechanical, thermal and optical properties, but it cannot be synthesized by using traditional processes such as fast cooling liquid carbon and an efficient strategy to tune its structure and properties is thus lacking. Here we show that the structures and physical properties of sp3 amorphous carbon can be modified by changing the concentration of carbon pentagons and hexagons in the fullerene precursor from the topological transition point of view. A highly transparent, nearly pure sp3−hybridized bulk amorphous carbon, which inherits more hexagonal-diamond structural feature, was synthesized from C70 at high pressure and high temperature. This amorphous carbon shows more hexagonal-diamond-like clusters, stronger short/medium-range structural order, and significantly enhanced thermal conductivity (36.3 ± 2.2 W m−1 K−1) and higher hardness (109.8 ± 5.6 GPa) compared to that synthesized from C60. Our work thus provides a valid strategy to modify the microstructure of amorphous solids for desirable properties.
|
|
| 6. |
- Shang, Yuchen, et al.
(författare)
-
Ultrahard bulk amorphous carbon from collapsed fullerene
- 2021
-
Ingår i: Nature. - : Nature Publishing Group. - 0028-0836 .- 1476-4687. ; 599:7886, s. 599-604
-
Tidskriftsartikel (refereegranskat)abstract
- Amorphous materials inherit short- and medium-range order from the corresponding crystal and thus preserve some of its properties while still exhibiting novel properties1,2. Due to its important applications in technology, amorphous carbon with sp2 or mixed sp2–sp3 hybridization has been explored and prepared3,4, but synthesis of bulk amorphous carbon with sp3 concentration close to 100% remains a challenge. Such materials inherit the short-/medium-range order of diamond and should also inherit its superior properties5. Here, we successfully synthesized millimetre-sized samples—with volumes 103–104 times as large as produced in earlier studies—of transparent, nearly pure sp3 amorphous carbon by heating fullerenes at pressures close to the cage collapse boundary. The material synthesized consists of many randomly oriented clusters with diamond-like short-/medium-range order and possesses the highest hardness (101.9 ± 2.3 GPa), elastic modulus (1,182 ± 40 GPa) and thermal conductivity (26.0 ± 1.3 W m−1 K−1) observed in any known amorphous material. It also exhibits optical bandgaps tunable from 1.85 eV to 2.79 eV. These discoveries contribute to our knowledge about advanced amorphous materials and the synthesis of bulk amorphous materials by high-pressure and high-temperature techniques and may enable new applications for amorphous solids.
|
|
| 7. |
- Wu, Bingze, et al.
(författare)
-
Significant electron-phonon coupling in nanographene confined in single-walled carbon nanotubes due to the large amplitude of radial breathinglike vibrations
- 2024
-
Ingår i: Physical Review B. - : American Physical Society. - 2469-9950 .- 2469-9969. ; 109:19
-
Tidskriftsartikel (refereegranskat)abstract
- One-dimensional (1D) van der Waals heterostructures (vdWHs) exhibit many properties, but many of these are difficult to understand because of their complicated structures and host-guest couplings that remain challenging to understand. Here, we observe a significant electron-phonon coupling (EPC) in 1D armchair graphene nanoribbons (AGNRs) confined in single-walled carbon nanotubes (SWNTs) via resonance Raman spectroscopy combined with theoretical calculation. A strong coupling between radial breathinglike mode (RBLM) phonons and the host nanotubes occurs due to the large vibration amplitude of RBLMs of the guest AGNRs. This results in unique deformation potential interactions in the heterostructure, contributing to the observed EPC enhancement. The EPC could be further modulated and strengthened by high pressure through tuning the RBLM-nanotube interactions. In this paper, we discover a mechanism governing the EPC in vdWHs and pave the way for manipulating the host-guest EPC for further control of the physical properties and potential device applications.
|
|
| 8. |
- Yang, Zhenxing, et al.
(författare)
-
Anomalous phonon softening of G-band in compressed graphitic carbon nitride due to strong electrostatic repulsion
- 2021
-
Ingår i: Applied Physics Letters. - : American Institute of Physics (AIP). - 0003-6951 .- 1077-3118. ; 118:2
-
Tidskriftsartikel (refereegranskat)abstract
- Graphitic carbon nitride (C2N and C3N) with various p electron distributions on layers have been studied under pressure through acombined theoretical and experimental approach and a comparison with graphite. It is found that as these materials transform into lowcompressibility phases in the pressure range from 15 to 45 GPa, strong electrostatic repulsion between p electrons and in-plane sp2 electronsmay distort and soften the sp2 bonds, leading to anomalous pressure evolutions of the intralayer phonon vibrations, such as a plateau-likebehavior of E2g mode (G-band) in C2N and C3N. This also causes a slow increase in the resistivity/resistance of C2N and C3N as pressureincreases, and the gradual interlayer bonding leads to an abrupt increase in resistance of the materials but with different pressure responsesdue to their different p electron distributions. Moreover, the intensity enhancement of the G band in both CN materials may be related totheir electronic structure changes. The results deepen our understanding of the effects of p electron distribution on the structural transitionof graphitic materials and may explain some unexplained in previous studies.
|
|
| 9. |
- Zhai, Chunguang, et al.
(författare)
-
Molecular insertion regulates the donor-acceptor interactions in cocrystals for the design of piezochromic luminescent materials
- 2021
-
Ingår i: Nature Communications. - : Nature Publishing Group. - 2041-1723. ; 12:1
-
Tidskriftsartikel (refereegranskat)abstract
- Developing a universal strategy to design piezochromic luminescent materials with desirable properties remains challenging. Here, we report that insertion of a non-emissive molecule into a donor (perylene) and acceptor (1,2,4,5-tetracyanobezene) binary cocrystal can realize fine manipulation of intermolecular interactions between perylene and 1,2,4,5-tetracyanobezene (TCNB) for desirable piezochromic luminescent properties. A continuous pressure-induced emission enhancement up to 3 GPa and a blue shift from 655 to 619 nm have been observed in perylene-TCNB cocrystals upon THF insertion, in contrast to the red-shifted and quenched emission observed when compressing perylene-TCNB cocrystals and other cocrystals reported earlier. By combining experiment with theory, it is further revealed that the inserted non-emissive THF forms blue-shifting hydrogen bonds with neighboring TCNB molecules and promote a conformation change of perylene molecules upon compression, causing the blue-shifted and enhanced emission. This strategy remains valid when inserting other molecules as non-emissive component into perylene-TCNB cocrystals for abnormal piezochromic luminescent behaviors.
|
|
