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Over the past 20 years, a revolution has been seen in battery research culminating with a much‐awaited Nobel Prize in Chemistry in 2019 for the development of Li‐ion batteries. New Li‐ion battery materials have been developed recently with improvements in performance. New Li battery chemistries have also emerged, exhibiting high energy density such as Li‐S, Li‐O2, Li‐metal with solid state electrolytes as well as zero‐excess Li anode metal batteries. This is tremendous progress and batteries are becoming more efficient and cheaper each year. Yet, most research in batteries is entirely focused on performance while the sustainability of all battery components making up the cell, as well as the battery chemistry itself are much overlooked. In this essay some perspectives are discussed and opinion is provided on the advancement of sustainability in battery research. [ABSTRACT FROM AUTHOR]

Nature has vast experience in optimising systems to perform adaptively to their environment. Bio-organisms are intrinsically dynamic: as they react to stimuli, their components work synergistically to achieve the appropriate response to the range of conditions of the environment they are in. Due to this singular specificity, achieved with exquisite tailoring of function and structure from the nanoscopic to the macroscopic level, biological systems have been an inspiration not only for materials design but for many engineering-related applications, including energy storage devices, in particular batteries, which are covered in this review. Bioinspiration is explored as a tool to unlock new materials, hierarchical architectures, and chemistries to achieve specific functions that will be key to addressing the complex range of performance and sustainability requirements for future batteries. Many excellent examples of biomimicry and bioinspiration can be found in the literature, yet the conceptualization of fully biomimetic batteries has not been accomplished. In this review we analyse the possibilities by which batteries could expand beyond structure replication of individual materials, components or chemistries found in nature and provide a broader perspective on their integration. We place battery systems at the interface between green chemistry, nanotechnology, and bioengineering to analyse their basic requirements and contrast how nature has achieved these needs in biological systems. [ABSTRACT FROM AUTHOR]

Sodium‐ion batteries (SIBs) and potassium‐ion batteries (PIBs) are prospective candidates for large‐scale energy storage systems cause of their abundant resources. However, unsatisfactory rate and cycling performance of carbon‐based anodes present a bottleneck for the applications of SIBs/PIBs due to the large sizes of sodium/potassium ions. Herein, oxygen‐doped vertically aligned carbon aerogels (VCAs) with hierarchically tailored channels are synthesized as anodes in SIBs/PIBs via a controllable unidirectional ice‐templating technique. VCA‐3 (cooling rate of 3 K min−1) delivers the highest reversible capacity of ≈298 mAh g−1 at 0.1 C with an excellent cycling performance over 2000 cycles at 0.5 C for SIBs, while VCA‐5 manifests a superior capacity of ≈258 mAh g−1 at 0.1 C with an 82.7% retention over 1000 cycles at 0.5 C for PIBs. Moreover, their full cells demonstrate the promising potential of VCAs in applications. This novel controllable ice‐templating strategy opens unique avenues to tune the construction of hollow aligned channels for shortening ion‐transport pathways and ensuring structural integrity. New insights into structure‐performance correlations regulated by the cooling rates of an ice‐templating strategy and design guidelines for electrodes applicable in multiple energy storage technologies are reported. [ABSTRACT FROM AUTHOR]

Heteroatom doping has been proved to effectively enhance the sloping capacity, nevertheless, the high sloping capacity almost encounters a conflict with the disappointing initial Coulombic efficiency (ICE). Herein, we propose a heteroatom configuration screening strategy by introducing a secondary carbonization process for the phosphate‐treated carbons to remove the irreversible heteroatom configurations but with the reversible ones and free radicals remaining, achieving a simultaneity between the high sloping capacity and ICE (≈250 mAh g−1 and 80 %). The Na storage mechanism was also studied based on this "slope‐dominated" carbon to reveal the reason for the absence of the plateau. This work could inspire to distinguish and filter the irreversible heteroatom configurations and facilitate the future design of practical "slope‐dominated" carbon anodes towards high‐power Na‐ion batteries. [ABSTRACT FROM AUTHOR]

Heteroatom doping has been proved to effectively enhance the sloping capacity, nevertheless, the high sloping capacity almost encounters a conflict with the disappointing initial Coulombic efficiency (ICE). Herein, we propose a heteroatom configuration screening strategy by introducing a secondary carbonization process for the phosphate‐treated carbons to remove the irreversible heteroatom configurations but with the reversible ones and free radicals remaining, achieving a simultaneity between the high sloping capacity and ICE (≈250 mAh g−1 and 80 %). The Na storage mechanism was also studied based on this "slope‐dominated" carbon to reveal the reason for the absence of the plateau. This work could inspire to distinguish and filter the irreversible heteroatom configurations and facilitate the future design of practical "slope‐dominated" carbon anodes towards high‐power Na‐ion batteries. [ABSTRACT FROM AUTHOR]

Hard carbons (HCs) are a significantly promising anode material for alkali metal-ion batteries. However, long calcination time and much energy consumption are required for the traditional fabrication way, resulting in an obstacle for high-throughput synthesis and structure regulation of HCs. Herein, we report an emerging sintering method to rapidly fabricate HCs from different carbon precursors at an ultrafast heating rate (300 to 500 °C min-1) under one minute by a multifield-regulated spark plasma sintering (SPS) technology. HCs prepared via the SPS possess significantly fewer defects, lower porosity, and less oxygen content than those pyrolyzed in traditional sintering ways. The molecular dynamics simulations are employed to elucidate the mechanism of the remarkably accelerated pyrolysis from the quickly increased carbon sp² content under the multifield effect. As a proof of concept, the SPSderived HC exhibits an improved initial Coulombic efficiency (88.9%), a larger reversible capacity (299.4 mAh⋅g-1), and remarkably enhanced rate capacities (136.6 mAh⋅g-1 at 5 A⋅g-1) than anode materials derived from a traditional route for Na-ion batteries. [ABSTRACT FROM AUTHOR]

Reversibly intercalating ions into host materials for electrochemical energy storage is the essence of the working principle of rocking-chair type batteries. The most relevant example is the graphite anode for rechargeable Li-ion batteries which has been commercialized in 1991 and still represents the benchmark anode in Li-ion batteries 30 years later. Learning from past lessons on alkali metal intercalation in graphite, recent breakthroughs in sodium and potassium intercalation in graphite have been demonstrated for Na-ion batteries and K-ion batteries. Interestingly, some significant differences proved to exist for the intercalation of Na+ and K+ into graphite compared with the Li+ case. Such different host–guest interactions are unique depending on the host materials and electrolytes, which greatly contribute to a deeper understanding of intercalation-type electrode materials for next generation alkali metal ion batteries. This review summarizes significant advances from both experimental and theoretical calculations with a focus on comparing the intercalation of three alkali metal ions (Li+, Na+, K+) into graphite and aims to clarify the intimate host–guest relationships and the underlying mechanisms. New approaches developed to achieve favorable intercalation coupled with the challenges in this field are also discussed. We also extrapolate alkali metal ion intercalation in graphite to mono-/multi-valent ions in layered electrode materials, which will deepen the understanding of intercalation chemistry and provide guidance to explore new guests and hosts. [ABSTRACT FROM AUTHOR]

Highlights from the article: Sodium-Ion Batteries: Hard-Soft Carbon Composite Anodes with Synergistic Sodium Storage Performance (Adv. Funct. Keywords: closed pores; hard carbon; sodium-ion batteries; soft carbon; synergistic effect Closed pores, hard carbon, sodium-ion batteries, soft carbon, synergistic effect.