In situ inward epitaxial growth of bulk macroporous single crystals

被引:24
作者
Chen, Chenlong [1 ]
Sun, Shujing [1 ]
Chou, Mitch M. C. [2 ]
Xie, Kui [3 ]
机构
[1] Chinese Acad Sci, Fujian Inst Res Struct Matter, Key Lab Optoelect Mat Chem & Phys, Fuzhou 350002, Fujian, Peoples R China
[2] Natl Sun Yat Sen Univ, Dept Mat & Optoelect Sci, MOST Taiwan Consortium Emergent Crystalline Mat T, Kaohsiung 80424, Taiwan
[3] Chinese Acad Sci, Fujian Inst Res Struct Matter, Key Lab Design & Assembly Funct Nanostruct, Fuzhou 350002, Fujian, Peoples R China
关键词
TRANSITION-METAL OXIDES; MESOPOROUS MATERIALS; MATERIALS CHEMISTRY; NITRIDE MATERIALS; GAN NANOWIRES; LIGAO2; FILMS; NANOSTRUCTURES; EVOLUTION; MOBILITY;
D O I
10.1038/s41467-017-02197-6
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The functionalities of porous materials could be significantly enhanced if the materials themselves were in single-crystal form, which, owing to structural coherence, would reduce electronic and optical scattering effects. However, growing macroporous single crystals remains a fundamental challenge, let alone manufacturing crystals large enough to be of practical use. Here we demonstrate a straightforward, inexpensive, versatile method for creating macroporous gallium nitride single crystals on a centimetre scale. The synthetic strategy is built upon a disruptive crystal growth mechanism that utilises direct nitridation of a parent LiGaO2 single crystal rendering an inward epitaxial growth process. Strikingly, the resulting single crystals exhibit electron mobility comparable to that for bulk crystals grown by the conventional sodium flux method. This approach not only affords control of both crystal and pore size through synthetic modification, but proves generic, thus opening up the possibility of designing macroporous crystals in a wealth of other materials.
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页数:8
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