Abstract:Uncontrollable dendrite growth and sluggish ion‐transport kinetics are considered as the main obstacles for the further development of high‐performance aqueous zinc ion batteries (AZIBs). Here, a nature‐inspired separator (ZnHAP/BC) is developed to tackle these issues via the hybridization of the biomass‐derived bacterial cellulose (BC) network and nano‐hydroxyapatite particles (HAP). The as‐prepared ZnHAP/BC separator not only regulates the desolvation process of the hydrated Zn2+ ions (Zn(H2O)62+) by suppres… Show more
“…The desolvation activation energies (E a ) of Zn 2+ species in different electrolyte environments were calculated according to EIS data of Zn∥Zn symmetric cells (Figure S13). Based on the Arrhenius equation, 40 the activation energies were calculated, summarized in Figure 4c. The [Zn(H 2 O) 6 ] 2+ species constitute a high energy barrier for a solvated Zn 2+ to desolvate and deposit, thus requiring the highest E a value of 41.4 kJ mol −1 .…”
Zn−Mn batteries with two-electron conversion reactions simultaneously on the cathode and anode harvest a high voltage plateau and high energy density. However, the zinc anode faces dendrite growth and parasitic side reactions while the Mn 2+ / MnO 2 reaction on the cathode involves oxygen evolution and possesses poor reversibility. Herein, a novel nanomicellar electrolyte using methylurea (Mu) has been developed that can encapsulate ions in the nanodomain structure to guide the homogeneous deposition of Zn 2+ /Mn 2+ in the form of controlled release under an external electric field. Consecutive hydrogen bonding network is broken and a favorable local hydrogen bonding system is established, thus inhibiting the water-splitting-derived side reactions. Concomitantly, the solid−electrolyte interface protective layer is in situ generated on the Zn anode, further circumventing the corrosion issue resulting from the penetration of water molecules. The reversibility of the Mn 2+ /MnO 2 conversion reaction is also significantly enhanced by regulating interfacial wettability and improving nucleation kinetics. Accordingly, the modified electrolyte endows the symmetric Zn∥Zn cell with extended cyclic stability of 800 h with suppressed dendrites growth at an areal capacity of 1 mAh cm −2 . The assembled Zn−Mn electrolytic battery also demonstrates an exceptional capacity retention of nearly 100% after 800 cycles and a superior energy density of 800 Wh kg −1 at an areal capacity of 0.5 mAh cm −2 .
“…The desolvation activation energies (E a ) of Zn 2+ species in different electrolyte environments were calculated according to EIS data of Zn∥Zn symmetric cells (Figure S13). Based on the Arrhenius equation, 40 the activation energies were calculated, summarized in Figure 4c. The [Zn(H 2 O) 6 ] 2+ species constitute a high energy barrier for a solvated Zn 2+ to desolvate and deposit, thus requiring the highest E a value of 41.4 kJ mol −1 .…”
Zn−Mn batteries with two-electron conversion reactions simultaneously on the cathode and anode harvest a high voltage plateau and high energy density. However, the zinc anode faces dendrite growth and parasitic side reactions while the Mn 2+ / MnO 2 reaction on the cathode involves oxygen evolution and possesses poor reversibility. Herein, a novel nanomicellar electrolyte using methylurea (Mu) has been developed that can encapsulate ions in the nanodomain structure to guide the homogeneous deposition of Zn 2+ /Mn 2+ in the form of controlled release under an external electric field. Consecutive hydrogen bonding network is broken and a favorable local hydrogen bonding system is established, thus inhibiting the water-splitting-derived side reactions. Concomitantly, the solid−electrolyte interface protective layer is in situ generated on the Zn anode, further circumventing the corrosion issue resulting from the penetration of water molecules. The reversibility of the Mn 2+ /MnO 2 conversion reaction is also significantly enhanced by regulating interfacial wettability and improving nucleation kinetics. Accordingly, the modified electrolyte endows the symmetric Zn∥Zn cell with extended cyclic stability of 800 h with suppressed dendrites growth at an areal capacity of 1 mAh cm −2 . The assembled Zn−Mn electrolytic battery also demonstrates an exceptional capacity retention of nearly 100% after 800 cycles and a superior energy density of 800 Wh kg −1 at an areal capacity of 0.5 mAh cm −2 .
“…Therefore, rising temperature strongly affects the phenomenon that occurs at the semiconductor/electrolyte interface. Below 30 °C, the change-transfer resistance was expected to follow the Arrhenius equation 1R2=A−EakBTwhere A is a proportionality constant, E a is the activation energy, k B is the Boltzmann constant, and T is the temperature. Since the catalyst does not change, the temperature is inversely proportional to the transfer resistance, which is taken for the resistance of electrons through the electrode/electrolyte interface.…”
GeSe photovoltaic thin films are very promising for photoelectrochemical
(PEC) hydrogen evolution. The GeSe-based PEC water splitting device
is a system containing a photoelectrode, electrolyte, and other packages,
and the performance of the GeSe photoelectrode inside the system is
very sensitive to the PEC system environment, such as the electrolyte
temperature, pH, and concentration. Here, we reveal how the electrolyte
environment at the electrolyte/photoelectrode interface influences
the optoelectronic/PEC properties of GeSe photoelectrodes. It was
found that the photocurrent density of the GeSe photoelectrode increased
with temperature between 10 and 50 °C but decreased when the
temperature was over 50 °C. In addition, the pH values of the
electrolyte were inversely proportional to the photocurrent density
of the GeSe photoelectrode. Moreover, the PEC performance improved
as the sodium ion concentration of the electrolyte increased. The
results in this work should provide a new direction for further optimizing
the performance of photoelectrodes.
“…Cellulose, particularly bacterial cellulose (BC) with a highpurity cellulose content (84-89%), shows promise in resolving the issues outlined above. [25,[28][29][30] The hydroxyl groups of the fibrillated cellulose provide adequate aqueous electrolyte uptake and good wettability while strengthening cellulose's mechanical properties through van der Waals interactions and intramolecular hydrogen bonds within the fibrils. BC separators are easily prepared through industrial methods.…”
Aqueous zinc‐ion batteries (AZIBs) offer promising prospects for large‐scale energy storage due to their inherent abundance and safety features. However, the growth of zinc dendrites remains a primary obstacle to the practical industrialization of AZIBs, especially under harsh conditions of high current densities and elevated temperatures. To address this issue, we developed a Janus separator with an exceptionally ultrathin thickness of 29 μm. This Janus separator features the bacterial cellulose (BC) layer on one side and Ag nanowires/bacterial cellulose (AgNWs/BC) layer on the other side. The high zincophilic property and excellent electric/thermal conductivity of AgNWs make them ideal for serving as an ion pump to accelerate Zn2+ transport in the electrolyte, resulting in the greatly improved Zn2+ conductivity, the deposition of homogeneous Zn nuclei, and dendrite‐free Zn. Consequently, the Zn||Zn symmetrical cells with the Janus separator exhibit a stable cycle life of over 1000 hours under 80 mA cm−2 and sustain over 600 hours at 10 mA cm−2 under 50°C. Furthermore, the Janus separator enables excellent cycling stability in AZIBs, aqueous zinc‐ion capacitors (AZICs), and scaled‐up flexible soft‐packaged batteries. Our study demonstrates the potential of functional separators in promoting the application of aqueous zinc batteries, particularly under harsh conditions.This article is protected by copyright. All rights reserved
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