Direct observation of the distribution of impurity in phosphorous/boron co-doped Si nanocrystals

被引:2
作者
Li, Dongke [1 ,2 ]
Han, Junnan [1 ]
Sun, Teng [1 ]
Chen, Jiaming [1 ]
Talbot, Etienne [3 ]
Demoulin, Remi [3 ]
Chen, Wanghua [4 ]
Pi, Xiaodong [2 ]
Xu, Jun [1 ]
Chen, Kunji [1 ]
机构
[1] Nanjing Univ, Collaborat Innovat Ctr Adv Microstruct, Jiangsu Prov Key Lab Adv Photon & Elect Mat, Sch Elect Sci & Engn,Natl Lab Solid State Microst, Nanjing 210000, Peoples R China
[2] Zhejiang Univ, ZJU Hangzhou Global Sci & Technol Innovat Ctr, Sch Mat Sci & Engn, Hangzhou 311200, Peoples R China
[3] Univ Rouen Normandie, INSA Rouen Normandie, CNRS, GPM UMR 6634, F-76000 Rouen, France
[4] Ningbo Univ, Sch Phys Sci & Technol, Ningbo 315211, Peoples R China
基金
中国国家自然科学基金;
关键词
Si nanocrystals; phosphorous and boron; co-doping; impurity distribution; 61.72.uf; 61.82.Rx; 61.72.U-; 61.72.sh; SILICON NANOCRYSTALS; BORON; TEMPERATURE;
D O I
10.1088/1674-1056/acd7cf
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
Doping in Si nanocrystals is an interesting topic and directly studying the distribution of dopants in phosphorous/boron co-doping is an important issue facing the scientific community. In this study, atom probe tomography is performed to study the structures and distribution of impurity in phosphorous/boron co-doped Si nanocrystals/SiO2 multilayers. Compared with phosphorous singly doped Si nanocrystals, it is interesting to find that the concentration of phosphorous in co-doped samples can be significantly improved. Theoretical simulation suggests that phosphorous-boron pairs are formed in co-doped Si nanocrystals with the lowest formation energy, which also reduces the formation energy of phosphorous in Si nanocrystals. The results indicate that co-doping can promote the entry of phosphorous impurities into the near-surface and inner sites of Si nanocrystals, which provides an interesting way to regulate the electronic and optical properties of Si nanocrystals such as the observed enhancement of conductivity and sub-band light emission.
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页数:5
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