The authors report on carrier transport properties and spectral sensitivities of hydrogenated microcrystalline silicon-germanium (μc-Si1−xGex:H) alloys fabricated by low-temperature (∼200°C) plasma-enhanced chemical vapor deposition over the wide compositional range. Hall-effect and conductivity measurements reveal a change from weak n-type to strong p-type conduction for x>0.75 and a monotonic decrease in photoconductivity upon Ge incorporation. In a p-i-n diode structure, the Ge incorporation into i layer reduces quantum efficiencies in the short wavelengths, indicating an increased photocarrier recombination at p∕i interface. Nevertheless, under reverse biased condition, a 0.9-μm-thick μc-Si0.6Ge0.4:H absorber yields a large photocurrent of >27mA∕cm2 (air mass 1.5 global) with spectral sensitivities extending into infrared wavelengths, offering a potential advantage over conventional microcrystalline silicon solar cells.

In the design of electron-transport layers (ETLs) to enhance the efficiency of planar perovskite solar cells (PSCs), facile electron extraction and transport are important features. Here, we consider the effects of different titanium oxide (TiO2) polymorphs, anatase and brookite. We design and fabricate high-phase-purity, single-crystalline, highly conductive, and low-temperature (<180 °C)-processed brookite-based TiO2 heterophase junctions on fluorine-doped tin oxide (FTO) as the substrate. We test and compare single-phase anatase (A) and brookite (B) and heterophase anatase–brookite (AB) and brookite–anatase (BA) as ETLs in PSCs. The power-conversion efficiencies (PCEs) of PSCs with low-temperature-processed single-layer FTO-B as the ETL were as high as 14.92%, which is the highest reported efficiency of FTO-B-based single-layer PSC. This implies that FTO-B serves as an active phase and can be a potential candidate as an n-type ETL scaffold in planar PSCs. Moreover, the surface of highly crystalline brookite TiO2 exhibits a tendency toward interparticle necking, leading to the formation of compact scaffolds. Furthermore, PSCs with heterophase junction FTO-AB ETLs exhibited PCEs as high as 16.82%, which is superior to those of PSCs with single-phase anatase (FTO-A) and brookite (FTO-B) as the ETLs (13.86% and 14.92%, respectively). In addition, the PSCs with FTO-AB exhibited improved efficiency and decreased hysteresis compared with those with FTO-BA (13.45%) due to the suitable band alignment with the perovskite layer, which resulted in superior photogenerated charge-carrier extraction and reduced charge accumulation at the interface between the heterophase junction and perovskite. Thus, the present work presents an effective strategy by which to develop heterophase junction ETLs and manipulate the interfacial energy band to further improve the performance of planar PSCs and enable the clean and eco-friendly fabrication of low-cost mass production.

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The influence of the Si-H2 bond on light-induced degradation and the thermal recovery of a-Si films and a-Si solar cells were studied. The influence of the Si-H2 bond on light-induced degradation depends on the impurity content in a-Si films, and light-induced degradation can be reduced by decreasing the Si-H2 bond density in a-Si films with impurity content of 1018 cm-3. The activation energy of the thermal recovery process was about 1.0 eV, and it did not depend on the Si-H2 bond density. However, an irreversible phenomenon was observed in film properties and solar cell characteristics with high Si-H2 bond density. It is thought that the structural flexibility of the Si-H2 bond is related to this irreversible phenomenon.

Electron-transport layer (ETL)/perovskite interface modification plays a key task for producing efficient planar perovskite solar cells (PSCs). In this study, interfacial modification of compact TiO2 using novel, one-step hydrothermally synthesized single-crystalline anatase (AT) titania nanoparticles (TiO2 NPs) (average diameter = 6–10 nm) was applied as an ETL bilayer to enhance the efficient charge generation and extraction and eliminate the electron–hole recombination ratio. We report here an easy approach for enhancing the performance of planar PSCs by introducing a compact TiO2/AT TiO2 NPs bilayer through spray pyrolysis (SP) deposition and spin-coating (SC) techniques, respectively. The enhanced performance of the devices with an SP-TiO2/SC-AT TiO2 NPs bilayer facilitated more efficient electron transport, charge extraction, and low interfacial recombination. Ultimately, the best device had a 17.05% power conversion efficiency resulting from the significant decrease in J–V hysteresis, presenting almost a 12% performance improvement compared to the TiO2 only layer-based counterpart. Thus, the present study provides an important advance to the design of photovoltaic devices with respect to charge transport and electron–hole recombination.