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Wenjie Mai

Publications and source records attributed to Wenjie Mai.

3 recordsLinked to original sources

Carbon Layer Orientation and Closed-Pore Construction Achieving Ultra-Low Specific Surface Area Hard Carbon for High-Performance Na-ion Storage

Addressing the critical trade-off between initial Coulombic efficiency (ICE) and reversible capacity in hard carbon anodes for Na-ion batteries (NIBs), we introduce a novel coupling strategy that combines carbon layer orientation reconstruction with closed-pore construction to produce hard carbon with an ultra-low specific surface area. We demonstrate that the nanographite domains within the hard carbon precursor undergo entropy-driven orientation reconstruction through the synergistic regulation of heteroatom doping and medium-temperature carbonization. This process not only increases interlayer spacing and promotes structural disorder but also enables the formation of dense, closed pores and ultramicropores at domain boundaries via confined atomic migration, while simultaneously encapsulating surface open pores within internal closed ones. Due to this unique pore architecture, our hard carbon exhibits an ultra-low specific surface area of 1.89 m2 g-1 with a markedly higher proportion of closed pores. As a result, our hard carbon achieves a remarkable reversible capacity of 342.3 mAh g-1 at 20 mA g-1, with an exceptional ICE of 90.4% and a dominant plateau capacity of 262.3 mAh g-1 (76.6%) for NIBs. We believe this coupling strategy provides a new paradigm for the structural engineering of high-ICE anode materials in advanced NIBs.

cond-mat.mtrl-sci↗

Robust, High-Contrast, Recyclable Zinc-Based Dynamic Windows via Synergistic Electrolyte and Interfacial Engineering

Zinc-based electrochromic devices offer a sustainable route for dynamic optical management but are plagued by poor cycling stability due to irreversible zinc plating/stripping and side reactions. Herein, we report a robust, high-contrast, and recyclable zinc-based dynamic window enabled by a synergistic electrolyte and interfacial engineering strategy. Molecular dynamics simulations and electrochemical analyses reveal a dual-ion cooperative mechanism that governs the reversibility: anions with the strongest binding affinity guide uniform Zn deposition by stabilizing the inner solvation shell, while formate anions co-enriched at the interface facilitate smooth stripping via protonation during the oxidation process. This orchestrated interplay effectively eliminates "dead Zn" accumulation and dendrite growth. Consequently, the device demonstrates a record-high lifespan of 15,000 cycles with negligible degradation and maintains a large optical modulation of >50%, along with multiple optical states (transparent, gray, black, and mirror). Furthermore, it achieves a large reflectance modulation (>50%) stable for over 2,000 cycles. This work establishes the recyclable zinc-based dynamic window as a scalable, high-performance alternative to conventional electrochromic systems, advancing the feasibility of solution-processed energy-saving windows in sustainable buildings.

cond-mat.mtrl-sci↗

Precise phase control of large-scale inorganic perovskites via vapor-phase anion-exchange strategy

Anion exchange offers great flexibility and high precision in phase control, compositional engineering and optoelectronic property tuning. Different from previous successful anion exchange process in liquid solution, herein, we develop a vapor-phase anion-exchange strategy to realize the precise phase and bandgap control of large-scale inorganic perovskites by using gas injection cycle, produing some perovskites such as CsPbCl3 which has never been reported in thin film morphology. Ab-initio calculations also provide the insightful mechanism to understand the impact of anion exchange on tuning the electronic properties and optimizing the structural stability. Furthermore, because of precise control of specific atomic concentrations, intriguing tunable photoluminsecence is observed and photodetectors with tunable photoresponse edge from green to ultraviolet light can be realized accurately with an ultrahigh spectral resolution of 1 nm. Therefore, we offer a new, universal vapor-phase anion exchange method for inorganic perovskite with fine-tunable optoelectronic properties.

physics.app-ph↗