The development of sustainable, high-safety, and low-cost energy storage systems has recently stimulated growing interest in ammonium-ion batteries (AIBs) as a promising option^[1]. Benefiting from their unique non-metal characteristic, appropriate hydrated ionic radius, rapid diffusion kinetics, and unique hydrogen-bond-mediated intercalation mechanism, the NH₄⁺ charge carrier exhibits distinct advantages in aqueous environments for energy storage^[2]. However, the rational design of anode host materials that simultaneously enable rapid ion transport and efficient electron transfer remains a critical challenge. In particular, most widely reported covalent organic frameworks (COFs) suffer from intrinsically low electrical conductivity, low electron delocalization, and less electron redox, which severely restrict the reversible capacity and cycling stability in AIBs^[3,4].

In a recent work published in Science Advances, entitled “Rigid-flexible heptazine-biguanide frameworks enable fast electron delocalization and low-steric-hindrance ammonium-ion storage”, Prof. Liu and co-workers developed a novel rigid–flexible polymeric heptazine–biguanide framework (HBF) as a high-performance anode for NH₄⁺ storage, as illustrated in Figure 1^[5]. By integrating planar π-conjugated heptazine units with rotational biguanide linkers, the authors constructed a unique framework that synergistically combines fast electron delocalization with reduced steric hindrance. The rigid heptazine domains provide extended π-conjugation for rapid charge transport, while the flexible biguanide chains effectively expose redox-active C=N sites and facilitate ion coordination. This cooperative design overcomes the intrinsic trade-off between conductivity and active-site utilization in COFs.

Beyond materials design, the research provides fundamental insights into the NH₄⁺ storage mechanism in COFs. The electrochemical energy-storage process is governed by reversible NH₄⁺ transport within the electrode, confirming NH₄⁺ is the dominant charge carrier rather than H⁺. As presented in Figure 1, the HBFs architecture enables a highly reversible multi-electron storage process involving a seven-electron transfer, governed by synergistic hydrogen-bond interactions and coordination with imine sites. Specifically, NH₄⁺ storage proceeds via a stepwise binding process, where four NH₄⁺ ions are initially accommodated by the four C=N sites of the biguanide unit, followed by the binding of three additional NH₄⁺ ions to the three C=N sites of the heptazine unit. The mechanism not only stabilizes NH₄⁺ within the framework but also facilitates rapid ion transport through dynamic hydrogen-bond networks. Meanwhile, the extended π-conjugation significantly lowers the activation energy (0.15 eV) and ensures efficient electron delocalization^[5], while the flexible molecular chains minimize steric hindrance and enable nearly complete utilization of redox-active sites (up to 99.6%). Consequently, the HBFs anode delivers an exceptional reversible capacity of 314 mAh·g^-1, and ultralong cycling stability exceeding 120,000 cycles. More importantly, this work establishes a new design paradigm by integrating rigid π-conjugated units with flexible coordination motifs, providing a viable pathway toward high-performance organic electrode materials in COFs.

Overall, this work highlights a promising strategy for advancing AIBs through rational conjugation engineering in COFs. By simultaneously enabling multi-electron redox chemistry and efficient charge transport, such rigid-flexible architectures effectively bridge the gap between molecular-level design and device-level performance. Future efforts may focus on tailoring electronic structures, optimizing ion-framework interactions, and extending this design principle to other COF systems. These advances are expected to accelerate the development of next-generation sustainable energy storage technologies.