Solid-solution-induced lattice hardening reinforces perovskite stiffness for stable solar cell

Clicks: 21
ID: 326374
2026
Article Quality & Performance Metrics
Overall Quality
Not rated
Combines reader engagement with the AI quality analysis. This article has not been analysed, so there is no overall score — reader engagement is measured and shown alongside.
AI Quality Assessment
Not analyzed
Readership in this journal
Steady

Ranked #150 of 416 articles by views in national science review

Most read Least read

Bar heights use a square-root scale. Only the 120 most-read articles are drawn; the journal has 416 in total.

Mint this article as an NFT
Not yet minted

Create a permanent, verifiable on-chain record of this article on the Scimatic Network. The NFT is held in your Journament account, and you can withdraw it to your own wallet at any time.

5 SUSD one-off · no wallet required
Abstract
Abstract The operational instability of perovskite photovoltaics is mainly attributed to the soft, ionic nature of its lattice. However, the quantification and intrinsic tuning strategy of perovskite lattice stiffness, and its correlation with device performance and stability has not been well explored. Here, we propose a solid-solution-induced lattice hardening (SSILH) strategy to enhance the stiffness of perovskite through partial substitution of lead ions with lanthanum ions. The reinforcement mechanism stems from the beneficial lattice contraction and bond-strengthening induced by lanthanum dopant with smaller ionic radius and stronger chemical interaction, which collectively yield a denser and more rigid framework. Consequently, the strategy obviously enhances the perovskite stiffness with Young’s modulus increasing from 27.96 to 35.71 GPa. The enhanced lattice stiffness reduces the thermal expansion coefficient, suppresses defect formation and ion migration, thereby mitigating non-radiative recombination and structural degradation under external stress. By employing 4-Isopropyl-4’-methyldiphenyliodonium tetrakis(pentafluorophenyl) borate as a stable p-dopant for the hole transport layer, the resulting device achieves a champion power conversion efficiency (PCE) of 26.54% and a certified steady-state efficiency of 26.03%. The optimized devices retain >95% and >90% of their initial efficiencies after 1000 hours of continuous 1-sun illumination at 65°C and under damp-heat conditions, respectively.
Reference Key
openalex_W7204186209 Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors
Journal national science review
Year 2026
DOI
10.1093/nsr/nwag484
URL
Keywords Keywords not found

Citations

No citations found. To add a citation, contact the admin at info@scimatic.org

No comments yet. Be the first to comment on this article.