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Hydrogen Passivation of Interstitial Zn Defects in Heteroepitaxial InP Cell Structures and Influence on Device Characteristics

机译:异质外延InP细胞结构中间隙Zn缺陷的氢钝化及其对器件特性的影响

摘要

Hydrogen passivation of heteroepitaxial InP solar cells is of recent interest for deactivation of dislocations and other defects caused by the cell/substrate lattice mismatch that currently limit the photovoltaic performance of these devices. In this paper we present strong evidence that, in addition to direct hydrogen-dislocation interactions, hydrogen forms complexes with the high concentration of interstitial Zn defects present within the p(+) Zn-doped emitter of MOCVD-grown heteroepitaxial InP devices, resulting in a dramatic increase of the forward bias turn-on voltage by as much as 280 mV, from ~680 mV to ~960 mV. This shift is reproducible and thermally reversible and no such effect is observed for either n(+)p structures or homoepitaxial p(+)n structures grown under identical conditions. A combination of photoluminescence (PL), electrochemical C-V dopant profiling, SIMS and I-V measurements were performed on a set of samples having undergone a matrix of hydrogenation and post-hydrogenation annealing conditions to investigate the source of this voltage enhancement and confirm the expected role of interstitial Zn and hydrogen. A precise correlation between all measurements is demonstrated which indicates that Zn interstitials within the p(+) emitter and their interaction with hydrogen are indeed responsible for this device behavior.
机译:异质外延InP太阳能电池的氢钝化最近对于使位错失活和由电池/衬底晶格失配引起的其他缺陷产生了兴趣,目前这些缺陷限制了这些器件的光伏性能。在本文中,我们提供有力的证据表明,除了直接的氢位错相互作用外,氢还形成了具有高浓度的间隙Zn缺陷的复合物,这些缺陷存在于MOCVD生长的异质外延InP器件的p(+)Zn掺杂发射极中,从而导致正向偏置导通电压从〜680 mV急剧增加至〜960 mV,幅度高达280 mV。这种位移是可重现的,并且是热可逆的,对于在相同条件下生长的n(+)p结构或同质外延p(+)n结构,均未观察到这种影响。对一组经历了加氢和加氢后退火条件的样品进行了光致发光(PL),电化学CV掺杂物分析,SIMS和IV测量的组合,以研究这种电压增强的来源并确认其预期的作用锌和氢。证实了所有测量值之间的精确相关性,这表明p(+)发射极内的Zn间隙及其与氢的相互作用确实是造成此器件行为的原因。

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    Chatterjee B.; Ringel S. A.;

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  • 年度 2004
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