arXiv subjects

Guangzheng Zuo

Publications and source records attributed to Guangzheng Zuo.

4 recordsLinked to original sources

arXiv2026

Homojunction-induced thermopower enhancement in polymer films

It has been more than twenty years since conductive polymers began to receive attention as an emerging thermoelectric material. However, the trade-off between electrical conductivity (σ) and thermopower (S) has proven to be a major challenge that has obstructed their use in actual devices. Here we report the discovery that the thermopower of the p- and n-type legs of organic thermogenerators can be substantially enhanced, without significant deterioration of σ, by constructing an in-plane segmented structure consisting of a homojunction with different doping levels on either side. In such segmented layers, the S is abnormally higher than the average value of the constituent parts when applying a forward temperature gradient (heating the heavily doped counterpart), while it is lower upon a reverse temperature gradient. Typically, for a two-stage segmented film of p-type PDPP-Se, an abnormally large S of 210 uV K-1 and σ of 2.5*10^4 S m-1 are obtained, resulting in a large power factor (PF) of 1100 uW m-1 K-2 and a record ZT of 1.36 at room temperature. The enhanced thermopower is attributed to an additional voltage developed at the homojunction under heating as explained by kinetic Monte Carlo simulations. This finding provides a breakthrough approach to the modulation of thermoelectric transport properties of conductive polymers.

cond-mat.mtrl-sci↗

arXiv2025

Soft Coulomb Gap Limits the Performance of Organic Thermoelectrics

Although consensus exists that the thermoelectric properties of doped organic semiconductors result from a complex interplay between a large number of mutually dependent factors, there is no consensus on which of these are dominant, or even on how to best describe the charge and energy transport. This holds particularly in the intermediate doping regime where the optimal performance is typically observed at the roll-off in the Seebeck coefficient - conductivity (S-σ correlation, fundamentally limiting the rational advancement of organic thermoelectric materials. Here, we combine experiments on a board set of conjugated polymers with kinetic Monte Carlo simulations across varying doping levels to uncover a general transport framework. We demonstrate that the optimal thermoelectric power factor (PF_max) consistently occurs at the transition between conventional variable-range hopping (VRH) and VRH in a density of states in which a soft Coulomb gap forms at the Fermi level, as described by Efros and Shklovskii (ES-VRH). This suggests the use of high dielectric constant materials or the promotion of charge delocalization as an avenue to shift the roll-off of the S-σ} curve, which constrains PF_max, to higher doping levels and accordingly higher PF.

cond-mat.mtrl-sci↗

arXiv2025

Eu-doped CsSrCl$_3$ Large Nanocrystal Clusters with Self-Reduction Effect and Near-Unity Quantum Yield

Europium halide perovskites have emerged as promising candidates for environmental-friendly blue-emitting materials. However, their development is hindered by relative low photoluminescence quantum yields (PLQY, e.g. ~2-5% for intrinsic CsEuCl3) and poor stability against air. Here, we introduce a one-step-procedure for synthesizing Eu$^{2+}$-doped CsSrCl$_3$ large nanocrystal clusters (LNCs) with the effect of self-reduction, therefore eliminating the use of conventional reductant oleylamine (OAm) and ensuring phase purity. The CsSrCl$_3$:Eu LNCs shows photoluminescence emission centered at 430 nm with a full width at half-maximum (FWHM) of 25 nm and a PLQY of ~40%, which can be further enhanced to ~97% after passivating the surface defects by adding trioctylphosphine (TOP), the highest among all reported lead-free blue-emitting perovskite nanocrystals. The stability of CsSrCl$_3$:Eu can also be improved significantly by epitaxially growing ZnS shell on the surface. This work will shed more light on lanthanide and alkaline-earth metal (AEM)-based perovskites for nontoxic light-emitting materials.

cond-mat.mtrl-sci↗

arXiv2021

General Rules for the Impact of Energetic Disorder and Mobility on Nongeminate Recombination in Phase-Separated Organic Solar Cells

State of the art organic solar cells exhibit power conversion efficiencies of 18 % and above. These devices benefit from the suppression of free charge recombination with regard to the Langevin-limit of charge encounter in a homogeneous medium. It has been recognized that the main cause of suppressed free charge recombination is the reformation and resplitting of charge transfer states at the interface between donor and acceptor domains. Here, we use kinetic Monte Carlo simulations to understand the interplay between free charge motion and recombination in an energetically-disordered phase-separated donor-acceptor blend. We identify conditions for encounter-dominated and resplitting-dominated recombination. In the former regime, recombination is proportional to mobility for all parameters tested and only slightly reduced with respect to the Langevin limit. In contrast, mobility is not the decisive parameter determining the non-geminate recombination coefficient k_2in the latter case where k_2 is a sole function of the morphology, CT and CS energetics and CT states decay properties. Our simulations also show that free charge encounter in the phase-separated disordered blend is determined by the average mobility of all carriers, while CT reformation and resplitting involves mostly states near the transport energy. Therefore, charge encounter is more affected by increased disorder than the resplitting of the CT state. As a consequence, for a given mobility, larger energetic disorder in combination with a higher hopping rate is preferred. These findings have important implications for the understanding of suppressed recombination in solar cells with non-fullerene acceptors which are known to exhibit lower energetic disorder than fullerenes.

physics.app-ph↗