Search arXiv⌕ Search

arXiv subjects

Stefaan De Wolf

Publications and source records attributed to Stefaan De Wolf.

3 recordsLinked to original sources

High-Throughput Imaging of Degradation-Inducing Microscopic Impurities in Perovskite Solar Cells

The scalable fabrication of high-quality, large-area perovskite thin films is hindered by microscopic inhomogeneities, particularly residual compositional impurities formed during processing. Identifying these impurities, understanding their impact on device operation, and enabling their rapid detection are essential for upscaling perovskite solar cells (PSCs). Here, nano-Fourier transform infrared spectroscopy combined with high-resolution optical and scanning probe techniques was used to identify detrimental impurities in wide-bandgap perovskite films relevant to tandem solar cells. Photo-stress experiments revealed that degradation of the perovskite layer initiates at impurity-perovskite interfaces, demonstrating that impurities act as failure nucleation sites. Leveraging these insights, a rapid, non-invasive, and high-throughput framework based on high-resolution reflected light microscopy and machine learning-supported image analysis was developed, enabling detection and quantification of harmful impurities in as-prepared films within seconds. Films with higher impurity density show accelerated early degradation, establishing this parameter as an early-warning metric for stability screening. Extending this framework to degradation tracking further reveals coupled photo- and thermo-chemical contributions to impurity-mediated instability. Overall, this work establishes a practical chemically-validated diagnostic imaging framework for rapid pre-screening of perovskite films to enable stable and scalable PSCs.

cond-mat.mtrl-sci↗

Lessons from Chalcopyrites for Scaling Thin Film Perovskite Photovoltaic Technology

The growing demand for photovoltaic (PV) technologies that are lightweight, flexible, and seamlessly integrated into diverse applications has propelled interest in thin-film solar cells. Among these, Cu(In,Ga)(S,Se)2 (CIGS) and metal halide perovskites have garnered significant attention in the past and present, respectively. While CIGS reached commercial readiness after decades of refinement, their large-scale deployment was hindered by manufacturing complexity, scale-up challenges, and a lack of coordination between materials, device design, and production systems. Perovskite solar cells, despite setting record efficiencies at an unprecedented pace, now face similar challenges on their path to commercialization: ensuring long-term stability, translating laboratory performance to scalable architectures, and aligning with industrial realities. In this perspective, we revisit the CIGS experience not as a benchmark, but as a blueprint, highlighting how its successes and failures can inform a more deliberate and durable trajectory for perovskite PV. Bridging this historical perspective with the current frontier, we propose that the future of perovskites depends not only on continued innovation, but on learning from past thin-film PV experience to avoid its repetition.

physics.app-ph↗

Impact of TCO Microstructure on the Electronic Properties of Carbazole-based Self-Assembled Monolayers

Carbazole-based self-assembled monolayers (PACz-SAMs), anchored via their phosphonic acid group on a transparent conductive oxide (TCO) have demonstrated excellent performance as hole-selective layers in inverted perovskite solar cells. However, the influence of the TCO microstructure on the work function (WF) shift after SAM anchoring as well as the WF variations at the micro/nanoscale have not been extensively studied yet. Herein, we investigate the effect of the Sn-doped In2O3 (ITO) microstructure on the WF distribution upon 2PACz-SAMs and NiOx/2PACz-SAMs application. For this, ITO substrates with amorphous and polycrystalline (featuring either nanoscale or microscale-sized grains) microstructures are studied. A correlation between the ITO grain orientation and 2PACz-SAMs local potential distribution was found via Kelvin probe force microscopy and electron backscatter diffraction. These variations vanish for amorphous ITO or when adding an amorphous NiOx buffer layer, where a homogeneous surface potential distribution is mapped. Ultraviolet photoelectron spectroscopy confirmed the ITO WF increase after 2PACz-SAMs deposition. Considering the importance of polycrystalline TCOs as high mobility and broadband transparent electrodes, we provide insights to ensure uniform WF distribution upon application of hole transport SAMs, which is critical towards enhanced device performance.

cond-mat.mtrl-sci↗