Fons Paul, Tampo Hiroshi, Kolobov Alexander V, Ohkubo Masataka, Niki Shigeru, Tominaga Junji, Carboni Roberta, Boscherini Federico, Friedrich Stephan
National Institute of Advanced Industrial Science & Technology, Tsukuba Central 4, Higashi 1-1-1, Tsukuba, Ibaraki, 305-8562, Japan.
Phys Rev Lett. 2006 Feb 3;96(4):045504. doi: 10.1103/PhysRevLett.96.045504. Epub 2006 Feb 2.
ZnO is a wide band gap, naturally n-type semiconductor with great promise for optoelectronic applications; the main obstacle yet to be overcome is p-type doping. Nitrogen, the most promising candidate currently being pursued as a dopant, has been predicted to preferentially incorporate into the ZnO lattice in the form of a N-2 molecule at an O site when a plasma source is used, leading to compensation rather than p-type doping. We demonstrate this to be incorrect by using N K-edge x-ray absorption spectra and comparing them with first-principles calculations showing that nitrogen, in fact, incorporates substitutionally at O sites where it is expected to act as an acceptor. We also detect the formation of molecular nitrogen upon annealing. These results suggest that effective p-type doping of ZnO with N may be possible only for low-temperature growth processes.
氧化锌是一种宽带隙的天然n型半导体,在光电子应用方面极具潜力;然而,有待克服的主要障碍是p型掺杂。氮是目前最有希望用作掺杂剂的候选元素,据预测,当使用等离子体源时,氮会优先以N₂分子的形式掺入氧化锌晶格中的氧位点,导致补偿而非p型掺杂。我们通过使用N K边x射线吸收光谱并将其与第一性原理计算结果进行比较,证明这是不正确的,结果表明,事实上,氮以替代方式掺入氧位点,预计在该位点它会作为受主起作用。我们还检测到退火后分子氮的形成。这些结果表明,只有对于低温生长过程,才可能实现用氮对氧化锌进行有效的p型掺杂。