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CMP
Credit: Jack Hobhouse

Prof Henry Snaith FRS

Professor of Physics

Sub department

  • Condensed Matter Physics

Research groups

  • Snaith group
  • Advanced Device Concepts for Next-Generation Photovoltaics
Henry.Snaith@physics.ox.ac.uk
Robert Hooke Building, room G21
  • About
  • Publications

Compositional Transformation and Impurity‐Mediated Optical Transitions in Co‐Evaporated Cu2AgBiI6 Thin Films for Photovoltaic Applications

Advanced Energy Materials Wiley 14:8 (2024)

Authors:

Benjamin WJ Putland, Marcello Righetto, Heon Jin, Markus Fischer, Alexandra J Ramadan, Karl‐Augustin Zaininger, Laura M Herz, Harry C Sansom, Henry J Snaith
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Minimizing Interfacial Recombination in 1.8 eV Triple-Halide Perovskites for 27.5% Efficient All-Perovskite Tandems.

Advanced materials (Deerfield Beach, Fla.) 36:6 (2024) e2307743

Authors:

Fengjiu Yang, Philipp Tockhorn, Artem Musiienko, Felix Lang, Dorothee Menzel, Rowan Macqueen, Eike Köhnen, Ke Xu, Silvia Mariotti, Daniele Mantione, Lena Merten, Alexander Hinderhofer, Bor Li, Dan R Wargulski, Steven P Harvey, Jiahuan Zhang, Florian Scheler, Sebastian Berwig, Marcel Roß, Jarla Thiesbrummel, Amran Al-Ashouri, Kai O Brinkmann, Thomas Riedl, Frank Schreiber, Daniel Abou-Ras, Henry Snaith, Dieter Neher, Lars Korte, Martin Stolterfoht, Steve Albrecht

Abstract:

All-perovskite tandem solar cells show great potential to enable the highest performance at reasonable costs for a viable market entry in the near future. In particular, wide-bandgap (WBG) perovskites with higher open-circuit voltage (VOC ) are essential to further improve the tandem solar cells' performance. Here, a new 1.8 eV bandgap triple-halide perovskite composition in conjunction with a piperazinium iodide (PI) surface treatment is developed. With structural analysis, it is found that the PI modifies the surface through a reduction of excess lead iodide in the perovskite and additionally penetrates the bulk. Constant light-induced magneto-transport measurements are applied to separately resolve charge carrier properties of electrons and holes. These measurements reveal a reduced deep trap state density, and improved steady-state carrier lifetime (factor 2.6) and diffusion lengths (factor 1.6). As a result, WBG PSCs achieve 1.36 V VOC , reaching 90% of the radiative limit. Combined with a 1.26 eV narrow bandgap (NBG) perovskite with a rubidium iodide additive, this enables a tandem cell with a certified scan efficiency of 27.5%.
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Multifunctional ytterbium oxide buffer for perovskite solar cells

Nature Springer Nature 625:7995 (2024) 516-522

Authors:

Peng Chen, Yun Xiao, Juntao Hu, Shunde Li, Deying Luo, Rui Su, Pietro Caprioglio, Pascal Kaienburg, Xiaohan Jia, Nan Chen, Jingjing Wu, Yanping Sui, Pengyi Tang, Haoming Yan, Tianyu Huang, Maotao Yu, Qiuyang Li, Lichen Zhao, Cheng-Hung Hou, Yun-Wen You, Jing-Jong Shyue, Dengke Wang, Xiaojun Li, Qing Zhao, Qihuang Gong, Zheng-Hong Lu, Henry J Snaith, Rui Zhu

Abstract:

Perovskite solar cells (PSCs) comprise a solid perovskite absorber sandwiched between several layers of different charge-selective materials, ensuring unidirectional current flow and high voltage output of the devices. A ‘buffer material’ between the electron-selective layer and the metal electrode in p-type/intrinsic/n-type (p-i-n) PSCs (also known as inverted PSCs) enables electrons to flow from the electron-selective layer to the electrode. Furthermore, it acts as a barrier inhibiting the inter-diffusion of harmful species into or degradation products out of the perovskite absorber. Thus far, evaporable organic molecules and atomic-layer-deposited metal oxides have been successful, but each has specific imperfections. Here we report a chemically stable and multifunctional buffer material, ytterbium oxide (YbOx), for p-i-n PSCs by scalable thermal evaporation deposition. We used this YbOx buffer in the p-i-n PSCs with a narrow-bandgap perovskite absorber, yielding a certified power conversion efficiency of more than 25%. We also demonstrate the broad applicability of YbOx in enabling highly efficient PSCs from various types of perovskite absorber layer, delivering state-of-the-art efficiencies of 20.1% for the wide-bandgap perovskite absorber and 22.1% for the mid-bandgap perovskite absorber, respectively. Moreover, when subjected to ISOS-L-3 accelerated ageing, encapsulated devices with YbOx exhibit markedly enhanced device stability.
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DATASET FOR: Disentangling the origin of degradation in perovskite solar cells via optical imaging and Bayesian inference.

University of Oxford (2024)

Authors:

Akash Dasgupta, Robert Oliver, Yen Lin, Manuel Kober-Czerny, Alexandra Ramadan, Henry Snaith

Abstract:

Here we deposit the data and code necessary to generate the analysis found in our work. We have included: Simulation output from drift diffusion simulations; Photoluminescence imaging data (in a semi-raw and processed format); Outputs from our Bayesian analysis combining the two; and a clone of the code (from our public git repo) used to generate the analysis.
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Buried-Metal-Grid Electrodes for Efficient Parallel-Connected Perovskite Solar Cells.

Advanced materials (Deerfield Beach, Fla.) 36:2 (2024) e2305238

Authors:

Lei Li, Peng Chen, Rui Su, Hongyu Xu, Qiuyang Li, Qixuan Zhong, Haoming Yan, Xiaoyu Yang, Juntao Hu, Shunde Li, Tianyu Huang, Yun Xiao, Bin Liu, Yongqiang Ji, Dengke Wang, Huiliang Sun, Xugang Guo, Zheng-Hong Lu, Henry J Snaith, Qihuang Gong, Lichen Zhao, Rui Zhu

Abstract:

The limited conductivity of existing transparent conducting oxide (TCO) greatly restricts the further performance improvement of perovskite solar cells (PSCs), especially for large-area devices. Herein, buried-metal-grid tin-doped indium oxide (BMG ITO) electrodes are developed to minimize the power loss caused by the undesirable high sheet resistance of TCOs. By burying 140-nm-thick metal grids into ITO using a photolithography technique, the sheet resistance of ITO is reduced from 15.0 to 2.7 Ω sq-1 . The metal step of BMG over ITO has a huge impact on the charge carrier transport in PSCs. The PSCs using BMG ITO with a low metal step deliver power conversion efficiencies (PCEs) significantly better than that of their counterparts with higher metal steps. Moreover, compared with the pristine ITO-based PSCs, the BMG ITO-based PSCs show a smaller PCE decrease when scaling up the active area of devices. The parallel-connected large-area PSCs with an active area of 102.8 mm2 reach a PCE of 22.5%. The BMG ITO electrodes are also compatible with the fabrication of inverted-structure PSCs and organic solar cells. The work demonstrates the great efficacy of improving the conductivity of TCO by BMG and opens up a promising avenue for constructing highly efficient large-area PSCs.
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