2021
DOI: 10.1002/adma.202103708
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Fully Bottom‐Up Waste‐Free Growth of Ultrathin Silicon Wafer via Self‐Releasing Seed Layer

Abstract: The fabrication of ultrathin silicon wafers at low cost is crucial for advancing silicon electronics toward stretchability and flexibility. However, conventional fabrication techniques are inefficient because they sacrifice a large amount of substrate material. Thus, advanced silicon electronics that have been realized in laboratories cannot move forward to commercialization. Here, a fully bottom‐up technique for producing a self‐releasing ultrathin silicon wafer without sacrificing any of the substrate is pre… Show more

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Cited by 13 publications
(10 citation statements)
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“…At the end of this process, surface oxides were removed by dipping the wafers in a diluted hydrofluoric acid (HF, 5%) solution for 45 s. These wafers were then immediately transferred to the vacuum chamber, and the wafers were passivated on both sides by an i-layer (hereafter, I) using radio frequency (RF, 13.56 MHz) capacitively coupled PECVD using SiH 4 diluted in H 2 . 31 For the doped a-Si:H layers, dopant gases, namely, PH 3 and B 2 H 6 , were added for electron-and hole-passivating contacts, respectively. An I layer was deposited using the following conditions: R({[SiH 4 ]/([H 2 ] + [SiH 4 ])} × 100) = 6.86%, a pressure (P) of 1800 mTorr, interelectrode distance (D i ) of 2 cm, RF power of 50 W, and substrate temperature of 220 °C.…”
Section: Methodsmentioning
confidence: 99%
“…At the end of this process, surface oxides were removed by dipping the wafers in a diluted hydrofluoric acid (HF, 5%) solution for 45 s. These wafers were then immediately transferred to the vacuum chamber, and the wafers were passivated on both sides by an i-layer (hereafter, I) using radio frequency (RF, 13.56 MHz) capacitively coupled PECVD using SiH 4 diluted in H 2 . 31 For the doped a-Si:H layers, dopant gases, namely, PH 3 and B 2 H 6 , were added for electron-and hole-passivating contacts, respectively. An I layer was deposited using the following conditions: R({[SiH 4 ]/([H 2 ] + [SiH 4 ])} × 100) = 6.86%, a pressure (P) of 1800 mTorr, interelectrode distance (D i ) of 2 cm, RF power of 50 W, and substrate temperature of 220 °C.…”
Section: Methodsmentioning
confidence: 99%
“…Interestingly, PECVD‐induced surface porosity can be further transformed into nanogaps with a post hydrogen annealing at 900 °C for 10 min, [ 40 ] as shown in Figure . The key point of this method is to use plasma‐epitaxial Si as the self‐releasing seed layer of a high‐temperature epitaxial (HTE) film of high quality deposited at a higher rate than in the case of low‐temperature epitaxy.…”
Section: “Bottom‐up” Approachesmentioning
confidence: 99%
“…Reproduced with permission. [ 40 ] Copyright 2021, Wiley‐VCH. b) Deposition and lift‐off of epitaxial Si based on porous Si substrates and fabrication of solar cells.…”
Section: Introductionmentioning
confidence: 99%
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“…On the other hand, epitaxial Silicon (epi-Si) films are receiving increased attention for the fabrication of novel devices, where c-Si films can be grown or etched in a selective way to produce 3D structures on the surface of the c-Si wafer, in addition to the production of ultrathin c-Si films [16][17][18] on foreign substrates [19], and epi-Si on metallic surfaces [20,21], crystalline semiconductors surfaces such as (100) c-Si [22] and gallium arsenide (c-GaAs) [23]. Moreover, the crystallization process using PECVD, which has been discussed in terms of the impact of silicon clusters [24] opens the possibility to produce novel devices at low substrate temperatures.…”
Section: Introductionmentioning
confidence: 99%