The altering of electronic states of metal oxides offers a promising opportunity to realize high‐efficiency surface catalysis, which play a key role in regulating polysulfides (PS) redox in lithium–sulfur (Li–S) batteries. However, little effort has been devoted to understanding the relationship between the electronic state of metal oxides and a catalyst's properties in Li–S cells. Herein, defect‐rich heterojunction electrocatalysts composed of ultrathin TiO2‐x nanosheets and carbon nanotubes (CNTs) for Li–S batteries are reported. Theoretical simulations indicate that oxygen vacancies and heterojunction can enhance electronic conductivity and chemical adsorption. Spectroscopy and electrochemical techniques further indicate that the rich surface vacancies in TiO2‐x nanosheets result in highly activated trapping sites for LiPS and lower energy barriers for fast Li ion mobility. Meanwhile, the redistribution of electrons at the heterojunction interfaces realizes accelerated surface electron exchange. Coupled with a polyacrylate terpolymer (LA132) binder, the CNT@TiO2‐x–S electrodes exhibit a long cycle life of more than 300 cycles at 1 C and a high area capacity of 5.4 mAh cm−2. This work offers a new perspective on understanding catalyst design in energy storage devices through band engineering.
Construction of ultrafine ZnSe nanoparticles on/in amorphous carbon hollow nanospheres with high-power-density sodium storage, Nano Energy (2019), doi:
Phase engineering of nanomaterials (PEN) is critically important for the preparation of nanomaterials with new phases, which are key for the investigation of phase‐dependent physicochemical properties and applications. This essay presents the state‐of‐the‐art development of PEN for the unique properties of nanomaterials with unconventional phases and their applications in energy storage and conversion and catalytic reactions. Finally, personal perspectives on the challenges and future opportunities of PEN in various applications are also provided.
Lithium ion conductivity and mechanical strength of a PEO based composite solid polymer electrolyte are improved by adding h-BN.
Metrics & MoreArticle Recommendations CONSPECTUS: Gold (Au), a transition metal with an atomic number of 79 in the periodic table of elements, was discovered in approximately 3000 B.C. Due to the ultrahigh chemical stability and brilliant golden color, Au had long been thought to be a most inert material and was widely utilized in art, jewelry, and finance. However, it has been found that Au becomes exceptionally active as a catalyst when its size shrinks to the nanometer scale.With continuous efforts toward the exploration of catalytic applications over the past decades, Au nanomaterials show critical importance in many catalytic processes. Besides catalysis, Au nanomaterials also possess other promising applications in plasmonics, sensing, biology and medicine, due to their unique localized surface plasmon resonance, intriguing biocompatibility, and superior stability. Unfortunately, the practical applications of Au nanomaterials could be limited because of the scarce reserves and high price of Au. Therefore, it is quite essential to further explore novel physicochemical properties and functions of Au nanomaterials so as to enhance their performance in different types of applications.Recently, phase engineering of nanomaterials (PEN), which involves the rearrangement of atoms in the unit cell, has emerged as a fantastic and effective strategy to adjust the intrinsic physicochemical properties of nanomaterials. In this Account, we give an overview of the recent progress on crystal phase control of Au nanomaterials using wet-chemical synthesis. Starting from a brief introduction of the research background, we first describe the development history of wet-chemical synthesis of Au nanomaterials and especially emphasize the key research findings. Subsequently, we introduce the typical Au nanomaterials with untraditional crystal phases and heterophases that have been observed, such as 2H, 4H, body-centered phases, and crystal-phase heterostructures. Importantly, crystal phase control of Au nanomaterials by wet-chemical synthesis is systematically described. After that, we highlight the importance of crystal phase control in Au nanomaterials by demonstrating the remarkable effect of crystal phases on their physicochemical properties (e.g., electronic and optical properties) and potential applications (e.g., catalysis). Finally, after a concise summary of recent advances in this emerging research field, some personal perspectives are provided on the challenges, opportunities, and research directions in the future.
Crystal phase engineering of noble-metal-based alloy nanomaterials paves a new way to the rational synthesis of high-performance catalysts for various applications. However, the controlled preparation of noble-metal-based alloy nanomaterials with unconventional crystal phases still remains a great challenge due to their thermodynamically unstable nature. Herein, we develop a robust and general seeded method to synthesize PdCu alloy nanomaterials with unconventional hexagonal close-packed (hcp, 2H type) phase and also tunable Cu contents. Moreover, galvanic replacement of Cu by Pt can be further conducted to prepare unconventional trimetallic 2H-PdCuPt nanomaterials. Impressively, 2H-Pd67Cu33 nanoparticles possess a high mass activity of 0.87 A mg–1 Pd at 0.9 V (vs reversible hydrogen electrode (RHE)) in electrochemical oxygen reduction reaction (ORR) under alkaline condition, which is 2.5 times that of the conventional face-centered cubic (fcc) Pd69Cu31 counterpart, revealing the important role of crystal phase on determining the ORR performance. After the incorporation of Pt, the obtained 2H-Pd71Cu22Pt7 catalyst shows a significantly enhanced mass activity of 1.92 A mg–1 Pd+Pt at 0.9 V (vs RHE), which is 19.2 and 8.7 times those of commercial Pt/C and Pd/C, placing it among the best reported Pd-based ORR electrocatalysts under alkaline conditions.
Stretchable ionic conductors with multiple functions provide new opportunities for flexible electronics, soft robots, and wearable devices. However, the practical applications of the existing stretchable ionic conductors are hampered greatly due to their poor stability. In this research, we prepared a novel organogel ionic conductor (OIC) via a simple photocuring method of 4-acryloylmorpholine in propylene carbonate. After being carefully optimized, the asdesigned OICs demonstrate many unique advantages including high transparency (93%) in the visible region, extremetemperature tolerance (from −100 to 100 °C), superb stretchability (elongation at break of 1219%), high ionic conductivity (7.9 × 10 −4 S cm −1 at 25 °C), wide voltage window (5.0 V), and perfect chemical stability; these properties are not simultaneously available in hydrogels. When used as ionic conductors for stress sensors and electrolytes for LiCoO 2 /Li batteries, such novel OICs deliver rapid current responses and excellent electrochemical stability. OICs present the extensive potential applications in flexible and wearable devices.
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