Hydrogen-Driven Phase Differentiation in BN Nucleation on Diamond

IF 5.1 Q1 POLYMER SCIENCE
Ting Cheng, Ksenia V. Bets, Boris I. Yakobson
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引用次数: 0

Abstract

Boron nitride has attracted scientific interest in recent years due to its potential use in electronics, both as hexagonal (hBN) and cubic (cBN) phases. While both are successfully realized through chemical vapor deposition, the heteroepitaxial growth of cBN on another iconic semiconductor, diamond is plagued with mixed-phase formation. Employing first-principles computations and a nanoreactor approach, the BN phase preferences are explored on diamond (001) controlled—as it is discovered—by the hydrogen gas concentration. In a limited-hydrogen environment, the initial BN-island expands along the diamond surface, forming a 3D metastable cubic phase that grows in the direction normal to the basal plane through kinetically-limited nucleation, thus overcoming the thermodynamic preference toward the hBN phase. Comparatively, the amorphous phase is favored in the absence of hydrogen, while the hexagonal phase dominates at its high levels, elucidating numerous experimental observations. A obtained kinetic phase diagram connects the phase with hydrogen chemical potential to facilitate targeted phase selection. The results suggest that gas-mediated nucleation kinetics provide feasible control for the precise synthesis. It also offers valuable guidance for the controllable synthesis of desired BN phases and advances research toward potential BN electronics.

Abstract Image

金刚石上 BN 成核过程中的氢驱动相分化
近年来,氮化硼因其在电子学中的潜在用途而引起了科学界的兴趣,包括六方氮化硼(hBN)和立方氮化硼(cBN)。虽然两者都能通过化学气相沉积成功实现,但在另一种标志性半导体--金刚石上的立方氮化硼异质外延生长却受到混相形成的困扰。利用第一原理计算和纳米反应器方法,我们探索了金刚石 (001) 上的 BN 相偏好,发现它受氢气浓度的控制。在有限的氢气环境中,初始 BN 岛沿金刚石表面扩展,形成三维可转移立方相,该相通过动力学限制成核在基底面的法线方向上生长,从而克服了热力学对 hBN 相的偏好。相对而言,无定形相在没有氢的情况下更受青睐,而六方相在氢含量较高的情况下则占主导地位,这解释了大量的实验观察结果。所获得的动力学相图将相与氢化学势联系起来,便于进行有针对性的相选择。结果表明,气体介导的成核动力学为精确合成提供了可行的控制。它还为所需 BN 相的可控合成提供了有价值的指导,并推动了对潜在 BN 电子学的研究。
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来源期刊
CiteScore
10.40
自引率
3.40%
发文量
209
审稿时长
1 months
期刊介绍: ACS Macro Letters publishes research in all areas of contemporary soft matter science in which macromolecules play a key role, including nanotechnology, self-assembly, supramolecular chemistry, biomaterials, energy generation and storage, and renewable/sustainable materials. Submissions to ACS Macro Letters should justify clearly the rapid disclosure of the key elements of the study. The scope of the journal includes high-impact research of broad interest in all areas of polymer science and engineering, including cross-disciplinary research that interfaces with polymer science. With the launch of ACS Macro Letters, all Communications that were formerly published in Macromolecules and Biomacromolecules will be published as Letters in ACS Macro Letters.
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