Publications by authors named "Huanran Zheng"

Article Synopsis
  • Reducing the charging voltage is crucial for enhancing the performance and efficiency of zinc-air batteries (ZABs), with Fe facilitating electron transfer from cobalt sites during charging.
  • The study shows that liquid ZABs operate at a charging voltage of about 1.94 V with a minimal increase over 180 hours, while quasi-solid-state ZABs maintain around 1.87 V under similar conditions.
  • The research highlights that the interactions between oxygen and iron sites are weaker than those with cobalt, with iron proving more effective for boosting the oxygen evolution reaction and improving battery performance.
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Due to the slow dynamics of mass and charge transfer at Zn|electrolyte interface, the stable operation of Zn-air batteries (ZABs) is challenging, especially at low temperature. Herein, inspired by cell membrane, a hydrophilic-hydrophobic dual modulated Zn|electrolyte interface is constructed. This amphiphilic design enables the quasi-solid-state (QSS) ZABs to display a long-term cyclability of 180 h@50 mA cm at 25 °C.

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The bifunctional oxygen electrocatalyst is the Achilles' heel of achieving robust reversible Zn-air batteries (ZABs). Herein, durable bifunctional oxygen electrocatalysis in alkaline media is realized on atomic Fe-N-C sites reinforced by NiCoO (NiCoO@Fe/NC). Compared with that of pristine Fe/NC, the stability of the oxygen evolution reaction (OER) is increased 10 times and the oxygen reduction reaction (ORR) performance is also improved.

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Single-metal atomic sites and vacancies can accelerate the transfer of photogenerated electrons and enhance photocatalytic performance in photocatalysis. In this study, a series of nickel hydroxide nanoboards (Ni(OH) NBs) with different loadings of single-atomic Ru sites (w-SA-Ru/Ni(OH)) were synthesized via a photoreduction strategy. In such catalysts, single-atomic Ru sites are anchored to the vacancies surrounding the pits.

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The unsatisfactory adsorption and activation of CO suppress electrochemical reduction over a wide potential window. Herein, the built-in electric field (BIEF) at the CeO/InO n-n heterostructure realizes the C (CO and HCOO) selectivity over 90.0% in a broad range of potentials from -0.

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It is an urgent need to improve the depth of discharge (DOD) of Zn-air batteries (ZABs), considering that most reported ZABs with long cycle life are realized at low DOD (<1%). In this work, our solid-state ZABs achieved a long cycle life of more than 220 h at 3.2% DOD (the discharge capacity of 10 mA h cm per cycle).

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Electrochemical CO reduction (ECOR) with renewable electricity is an advanced carbon conversion technology. At present, copper is the only metal to selectively convert CO into multicarbon (C) products. Among them, atomically dispersed (AD) Cu catalysts have received great attention due to the relatively single chemical environment, which are able to minimize the negative impact of morphology, valence state, and crystallographic properties, etc.

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