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Janne Halme

Researcher at Aalto University

Publications -  84
Citations -  3331

Janne Halme is an academic researcher from Aalto University. The author has contributed to research in topics: Dye-sensitized solar cell & Solar cell. The author has an hindex of 29, co-authored 81 publications receiving 2942 citations. Previous affiliations of Janne Halme include Helsinki University of Technology.

Papers
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Device physics of dye solar cells.

TL;DR: The model parameters can be determined from complete DSCs by current dependent EIS and incident-photon-to-collected-electron (IPCE) measurements, supplemented by optical characterization, and used to quantify performance losses in D SCs.
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Review of stability for advanced dye solar cells

TL;DR: In this article, the current status of the long-term stability of dye solar cells and factors affecting it are reviewed, and the authors conclude that techniques giving chemical information are needed for the stability investigations of DSCs to reveal possible ways to improve their lifetime.
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Review of materials and manufacturing options for large area flexible dye solar cells

TL;DR: In this article, the current state of the art related to up-scaling and commercialization of dye solar cells (DSC) is reviewed. But, the main focus of this work is to identify the best materials and preparation techniques suitable for an ideal roll-to-roll process of flexible dye solar module fabrication as well as the areas where further development is needed.
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Spectral Characteristics of Light Harvesting, Electron Injection, and Steady-State Charge Collection in Pressed TiO2 Dye Solar Cells

TL;DR: In this paper, the factors that limit photocurrent in dye solar cells (DSC) were studied by incident-photon-to-collected-electron efficiency (IPCE), optical, and photovoltaic measurements.
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Scalability and feasibility of photoelectrochemical H2 evolution: the ultimate limit of Pt nanoparticle as an HER catalyst

TL;DR: In this paper, the authors investigate ultra-low Pt loadings for use in photoelectrochemical H2 evolution using TiO2-Ti-pn+Si photocathodes and find that the overpotentials were dominated by mass transfer effects, rather than catalysis unless catalyst loadings were less than 1000 ng cm−2.