CsPtI is a promising photoabsorber with a direct bandgap of 1.4 eV and a high carrier lifetime; however, the cost of Pt inhibits its commercial viability. Here, we performed a cost analysis and experimentally explored the effect of replacing Pt with earth-abundant Ni in solution-processed Cs(PtNi)(I,Cl) thin films on the properties and stability of the perovskite material. Films fabricated with CsI and PtI precursors result in a perovskite phase with a bandgap of 2.13 eV which transitions into stable CsPtI with a bandgap of 1.6 eV upon annealing. The complete substitution of PtI in films with CsI + NiCl precursors results in a wider bandgap of 2.35 eV and SEM shows two phases-a rod-like structure identified as CsNi(I,Cl) and residual white particles of CsI, also confirmed by XRD and Raman spectra. Upon extended thermal annealing, the bandgap reduces to 1.65 eV and transforms to CsNiCl with a peak shift to higher 2-theta. The partial substitution of PtI with NiCl in mixed 50-50 Pt-Ni-based films produces a bandgap of 1.9 eV, exhibiting a phase of Cs(Pt,Ni)(I,Cl) composition. A similar bandgap of 1.85 eV and the same diffraction pattern with improved crystallinity is observed after 100 h of annealing, confirming the formation of a stable mixed Pt-Ni phase.
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http://dx.doi.org/10.3390/ma17246196 | DOI Listing |
Materials (Basel)
December 2024
School of Mechanical Engineering, Purdue University, West Lafayette, IN 47907, USA.
CsPtI is a promising photoabsorber with a direct bandgap of 1.4 eV and a high carrier lifetime; however, the cost of Pt inhibits its commercial viability. Here, we performed a cost analysis and experimentally explored the effect of replacing Pt with earth-abundant Ni in solution-processed Cs(PtNi)(I,Cl) thin films on the properties and stability of the perovskite material.
View Article and Find Full Text PDFAdv Mater
January 2023
Key Laboratory of Materials Physics, Ministry of Education, School of Physics and Microelectronics, Zhengzhou University, Zhengzhou, 450052, China.
Pt nanocatalysts play a critical role in direct methanol fuel cells (DMFCs) due to their appropriate adsorption/desorption energy, yet suffer from an unbalanced relationship between size-dependent activity and stability. Herein, mixed-dimensional Pt-Ni alloy polyhedral nanochains (Pt-Ni PNCs) with an ordered assembly of a nanopolyhedra-nanowire-nanopolyhedra architecture are fabricated as bifunctional electrocatalysts for DMFCs, effectively alleviating the size effect. The Pt-Ni PNCs exhibit 7.
View Article and Find Full Text PDFMolecules
August 2021
Department für Chemie, Institut für Anorganische Chemie, Universität zu Köln, Greinstraße 6, D-50939 Köln, Germany.
The three complexes [M(Medpb)Cl] (M = Ni, Pd, Pt) containing the tridentate ,,-cyclometalating 3,5-dimethyl-1,5-dipyridyl-phenide ligand (Medpb) were synthesised using a base-assisted C‒H activation method. Oxidation potentials from cyclic voltammetry increased along the series Pt < Ni < Pd from 0.15 to 0.
View Article and Find Full Text PDFACS Appl Mater Interfaces
June 2021
Joint Key Laboratory of the Ministry of Education, Institute of Applied Physics and Materials Engineering, University of Macau, Avenida da Universidade, Taipa, Macau SAR 999078, China.
It is challenging to develop highly efficient and stable multifunctional electrocatalysts for improving the hydrogen evolution reaction (HER), the oxygen evolution reaction (OER), and the oxygen reduction reaction (ORR) for sustainable energy conversion and storage systems such as water-alkali electrolyzers (WAEs) and hybrid sodium-air batteries (HSABs). In this work, sub-nm Pt nanoclusters (NCs) on defective NiFe layered double hydroxide nanosheets (NiFe LDHs) are synthesized by a facile electrodeposition method. Due to the synergistic effect between Pt NCs and abundant atomic (II) defects, along with hierarchical porous nanostructures, the Pt/NiFe LDHs catalysts exhibit superior trifunctional electrocatalytic activity and durability toward the HER/OER/ORR.
View Article and Find Full Text PDFChem Asian J
January 2020
Department of Materials Science WW4-LKO, University of Erlangen-Nuremberg, Martensstrasse 7, Erlangen, 91058, Germany.
Pt nanoparticles are typically decorated as co-catalyst on semiconductors to enhance the photocatalytic performance. Due to the low abundance and high cost of Pt, reaching a high activity with minimized co-catalyst loadings is a key challenge in the field. We explore a dewetting-dealloying strategy to fabricate on TiO nanotubes nanoporous Pt nanoparticles, aiming at improving the co-catalyst mass activity for H generation.
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