Herein, a novel dual single-atom catalyst comprising adjacent Fe-N4 and Mn-N4 sites on 2D ultrathin N-doped carbon nanosheets with porous structure (FeMn-DSAC) was constructed as the cathode for a flexible low-temperature Zn-air battery (ZAB). FeMn-DSAC exhibits remarkable bifunctional activities for oxygen reduction reaction (ORR) and oxygen evolution reaction (OER). Control experiments and density functional theory calculations reveal that the catalytic activity arises from the cooperative effect of the Fe/Mn dual-sites aiding *OOH dissociation as well as the porous 2D nanosheet structure promoting active sits exposure and mass transfer during the reaction process. The excellent bifunctional activity of FeMn-DSAC enables the ZAB to operate efficiently at ultra-low temperature of -40 °C, delivering 30 mW cm-2 peak power density and retaining up to 86 % specific capacity from the room temperature counterpart. 

Engineering Dual Single‐Atom Sites on 2D Ultrathin N‐doped Carbon Nanosheets Attaining Ultra‐Low Temperature Zn‐Air Battery

The new‐generation flexible aqueous zinc‐ion batteries require enhanced mechanical properties and ionic conductivities at low temperature for practical applications. This fundamentally means that it is desired that the hydrogel electrolyte possesses antifreezing merits to resist flexibility loss and performance decrease at subzero temperatures. Herein, a highly flexible polysaccharide hydrogel is realized in situ and is regulated in zinc‐ion batteries through the Hofmeister effect with low‐concentration Zn(ClO4)2 salts to satisfy the abovementioned requirements. The chaotropic ClO4− anions, water, and polymer chains can form ternary and weak hydrogen bonding (HB), which enables the polymer chains to have improved mechanical properties, breaks the HB of water to remarkably decrease the electrolyte freezing point, and reduces the amounts of free water for effective side reactions and dendrite inhibition. Consequently, even at −30 °C, the Zn(ClO4)2 in situ optimized hydrogel electrolyte features a high ionic conductivity of 7.8 mS cm−1 and excellent flexibility, which enables a Zn/polyaniline (PANI) battery with a reversible capacity of 70 mA h g−1 under 5 A g−1 for 2500 cycles, and renderd the flexible full battery with excellent cycling performances under different bending angles. This work provides a new pathway for designing high‐performance antifreezing flexible batteries via the Hofmeister effect.

Antifreezing Hydrogel Electrolyte with Ternary Hydrogen Bonding for High‐Performance Zinc‐Ion Batteries

The practical application of the Zn‐metal anode for aqueous batteries is greatly restricted by catastrophic dendrite growth, intricate hydrogen evolution, and parasitic surface passivation. Herein, a polyanionic hydrogel film is introduced as a protective layer on the Zn anode with the assistance of a silane coupling agent (denoted as Zn–SHn). The hydrogel framework with zincophilic –SO3− functional groups uniformizes the zinc ions flux and transport. Furthermore, such a hydrogel layer chemically bonded on the Zn surface possesses an anti‐catalysis effect, which effectively suppresses both the hydrogen evolution reaction and formation of Zn dendrites. As a result, stable and reversible Zn stripping/plating at various currents and capacities is achieved. A full cell by pairing the Zn–SHn anode with a NaV3O8·1.5 H2O cathode shows a capacity of around 176 mAh g−1 with a retention around 67% over 4000 cycles at 10 A g−1. This polyanionic hydrogel film protection strategy paves a new way for future Zn‐anode design and safe aqueous batteries construction.

Stable Zinc Anodes Enabled by a Zincophilic Polyanionic Hydrogel Layer

Flexible zinc-ion hybrid capacitors (ZIHCs) based on hydrogel electrolytes are an up-and-coming and highly promising candidate for potential large-scale energy storage due to their combined complementary advantages of zinc batteries and capacitors. However, the freezing induces a sharp drop in conductivity and mechanical property with tremendous compromise of the interfacial adhesion, thereby severely impeding the low-temperature application of such flexible ZIHCs. To achieve the flexible ZIHCs with excellent low-temperature adaptability, an antifreezing and self-adhesive polyzwitterionic hydrogel electrolyte (PZHE) is engineered via a self-catalytic nano-reinforced strategy, affording unparalleled conductivity and robust interfacial adhesion, together with superhigh mechanical strength over a broad temperature ranging from 25 to -60 °C. Meanwhile, the water-in-salt-type PZHE filled with ZnCl2 can provide ion migration channels to enhance the reversibility of Zn metal electrodes, thus greatly reducing side reactions and extending the cycling life. With distinctive integrated merits of the water-in-salt type PZHE, the as-built ZIHCs deliver a high-level energy density of 80.5 Wh kg-1, a desired specific capacity of 81.5 mAh g-1, along with a long-duration cycling lifespan (100 000 cycles) with 84.6% capacity retention at -40 °C, even outperforming the state-of-the-art ZIHCs at room temperature. More encouragingly, the extraordinary temperature-adaptability for both electrochemical and mechanical performance under severe mechanical challenges is achieved for the flexible ZIHCs at extremely low temperature. Noticeably, the ZIHC is also capable of operating in an ice-water bath and vacuum. It is believed that this strategy makes contributions to inspire the design and application of high-performance PZHEs in fields of flexible and wearable electronics that can work in extremely cold environments.

Engineering Self-Adhesive Polyzwitterionic Hydrogel Electrolytes for Flexible Zinc-Ion Hybrid Capacitors with Superior Low-Temperature Adaptability

Won the Third Prize (Category: Innovation ) in the "Challenge Cup" National Competition – Hong Kong Regional Final, Hong Kong University Student Innovation and Entrepreneurship Competition 2017 organized by the Hong Kong New Generation Cultural Association.

Lingchao Xia

Papers

Multi-Functional Hydrogels for Flexible Zinc-Based Batteries Working under Extreme Conditions

Optimization of gas diffusion layer in high temperature PEMFC with the focuses on thickness and porosity

Thermo-electrochemical modelling of high temperature methanol-fuelled solid oxide fuel cells

Numerical study of high temperature proton exchange membrane fuel cell (HT-PEMFC) with a focus on rib design

Effects of cathode thickness and microstructural properties on the performance of protonic ceramic fuel cell (PCFC): A 3D modelling study