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Poor kinetics of hole transportation at the electrode/electrolyte interface is regarded as a primary cause for the mediocre performance of n-type TiO photoelectrodes. By adopting nanotubes as the electrode backbone, light absorption and carrier collection can be spatially decoupled, allowing n-type TiO, with its short hole diffusion length, to maximize the use of the available photoexcited charge carriers during operation in photoelectrochemical (PEC) water splitting. Here, we presented a delicate electrochemical anodization process for the preparation of quaternary Ti-Nb-Ta-Zr-O mixed-oxide (denoted as TNTZO) nanotube arrays and demonstrated their utility in PEC water splitting. The charge-transfer dynamics for the electrodes was investigated using time-resolved photoluminescence, electrochemical impedance spectroscopy, and the decay of open-circuit voltage analysis. Data reveal that the superior photoactivity of TNTZO over pristine TiO originated from the introduction of Nd, Ta, and Zr elements, which enhanced the amount of accessible charge carriers, modified the electronic structure, and improved the hole injection kinetics for expediting water splitting. By modulating the water content of the electrolyte employed in the anodization process, the wall thickness of the grown TNTZO nanotubes can be reduced to a size smaller than that of the depletion layer thickness, realizing a fully depleted state for charge carriers to further advance the PEC performance. Hydrogen evolution tests demonstrate the practical efficacy of TNTZO for realizing solar hydrogen production. Furthermore, with the composition complexity and fully depleted band structure, the present TNTZO nanotube arrays may offer a feasible and universal platform for the loading of other semiconductors to construct a sophisticated heterostructure photoelectrode paradigm, in which the photoexcited charge carriers can be entirely utilized for efficient solar-to-fuel conversion.
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http://dx.doi.org/10.1021/acsami.8b00727 | DOI Listing |
Adv Mater
September 2025
College of Smart Materials and Future Energy, and State Key Laboratory of Photovoltaic Science and Technology, Fudan University, Shanghai, 200438, China.
Nonfullerene acceptor-based organic solar cells have recently taken a milestone leap with power conversion efficiencies approaching 20%. A key to further boost the efficiencies up to the Shockley-Queisser limit rests upon attaining a delicate balance between exciton dissociation and charge transport. This perspective presents two seminal and reciprocal strategies developed by our group and others to reconcile the intricacy of charge carrier dynamics, spanning from intrinsic molecular structure design to extrinsic dopant exploitation.
View Article and Find Full Text PDFSmall
September 2025
Key Laboratory of Luminescence Analysis and Molecular Sensing, Ministry of Education, School of Chemistry and Chemical Engineering, Southwest University, Chongqing, 400715, P. R. China.
Perovskites have a large number of intrinsic defects and interface defects, which often lead to non-radiative recombination, and thus affect the efficiency of perovskite solar cells (PSCs). Introducing appropriate passivators between the perovskite layer and the transport layer for defect modification is crucial for improving the performance of PSCs. Herein, two positional isomers, 1-naphthylmethylammonium iodide (NMAI) and 2-naphthylmethylammonium iodide (NYAI) are designed.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
National Laboratory of Solid State Microstructures, School of Physics, and Collaborative Innovation Center of Advanced Microstructures, Nanjing University, Nanjing 210093, China.
For optoelectronic devices based on lead-halide perovskites and other semiconductors, a comprehensive understanding of the electric field influences on the carrier transport characteristics is critical to the optimization of their practical performances. To fulfill this challenging goal, here we have employed photoluminescence spatial image and transient absorption microscopy measurements on an individual CsPbBr microplate biased at external voltages in an Au/CsPbBr/Au device. At the subpicosecond time scale, some photogenerated excitons are dissociated into free electrons and holes that drift toward the electrodes to leave behind unfilled defect sites, which are capable of scattering the residual excitons to yield a reduced diffusion coefficient.
View Article and Find Full Text PDFChem Sci
August 2025
Department of Chemistry and Biochemistry, Auburn University Auburn Alabama 36849 USA
Organic mixed ionic-electronic conducting polymers remain at the forefront of materials development for bioelectronic device applications. During electrochemical operation, structural dynamics and variations in electrostatic interactions in the polymer occur, which affect dual transport of the ions and electronic charge carriers. Such effects remain unclear due to a lack of spectroscopic methods capable of capturing these dynamics, which hinders the rational design of higher-performance polymers.
View Article and Find Full Text PDFACS Omega
September 2025
Institut de Chimie et Procédés pour l'Energie, l'Environnement et la Santé (ICPEES), UMR-7515 CNRS-Université de Strasbourg, 25 rue Becquerel, 67087 Strasbourg, France.
For photodetection applications using 3D hybrid perovskites (HPs), dense and thick films or compacted powders in wafer form are needed and generally require large amounts of HPs. HPs are also often combined with a graphene/carbon layer to improve their conductivity. Among HP synthesis methods, mechanosynthesis, a green synthesis method, provides a large amount of powders, which are furthermore easily densified in compact wafers due to their mechanical activation.
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