Hydrogen economy has emerged as a very promising alternative to the current hydrocarbon economy, which involves the process of harvesting renewable energy to split water into hydrogen and oxygen and ...then further utilization of clean hydrogen fuel. The production of hydrogen by water electrolysis is an essential prerequisite of the hydrogen economy with zero carbon emission. Among various water electrolysis technologies, alkaline water splitting has been commercialized for more than 100 years, representing the most mature and economic technology. Here, the historic development of water electrolysis is overviewed, and several critical electrochemical parameters are discussed. After that, advanced nonprecious metal electrocatalysts that emerged recently for negotiating the alkaline oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) are discussed, including transition metal oxides, (oxy)hydroxides, chalcogenides, phosphides, and nitrides for the OER, as well as transition metal alloys, chalcogenides, phosphides, and carbides for the HER. In this section, particular attention is paid to the catalyst synthesis, activity and stability challenges, performance improvement, and industry‐relevant developments. Some recent works about scaled‐up catalyst synthesis, novel electrode designs, and alkaline seawater electrolysis are also spotlighted. Finally, an outlook on future challenges and opportunities for alkaline water splitting is offered, and potential future directions are speculated.
The hydrogen economy has emerged as a very promising alternative to the current hydrocarbon economy, which involves the process of harvesting renewable energy to split water into hydrogen and oxygen and then further utilization of hydrogen fuel. Alkaline water splitting represents the most mature and economic technology for clean hydrogen production, making high potential for successful implementation of hydrogen economy.
It remains highly desired but a great challenge to achieve atomically dispersed metals in high loadings for efficient catalysis. Now porphyrinic metal–organic frameworks (MOFs) have been synthesized ...based on a novel mixed‐ligand strategy to afford high‐content (1.76 wt %) single‐atom (SA) iron‐implanted N‐doped porous carbon (FeSA‐N‐C) via pyrolysis. Thanks to the single‐atom Fe sites, hierarchical pores, oriented mesochannels and high conductivity, the optimized FeSA‐N‐C exhibits excellent oxygen reduction activity and stability, surpassing almost all non‐noble‐metal catalysts and state‐of‐the‐art Pt/C, in both alkaline and more challenging acidic media. More far‐reaching, this MOF‐based mixed‐ligand strategy opens a novel avenue to the precise fabrication of efficient single‐atom catalysts.
Iron islands: Based on a mixed‐ligand strategy, a porphyrinic MOF was pyrolyzed to afford high‐content single‐atom iron‐implanted N‐doped porous carbon (FeSA‐N‐C). Thanks to the FeSA sites, hierarchical pores, oriented mesochannels, and high conductivity, FeSA‐N‐C exhibits excellent oxygen reduction activity and stability, surpassing almost all non‐noble‐metal catalysts and Pt/C, in both alkaline and the more challenging acidic media.
A high efficiency and great tunability of bandwidth and absorption‐range electromagnetic wave absorber is proposed without precedent. A series of 2D carbon‐based nanocomposites with the loading of ...cerium oxide (CN‐Ce) and other types of rare earth oxides (CN‐REOs) can be successfully synthesized by a simple solvothermal‐sintering method. As‐synthesized 2D nanocomposites with local graphite‐like C3N4 structure and trace N‐doped are identified by transmission electron microscopy, X‐ray photoelectron spectroscopy, X‐ray powder diffraction, Fourier transform infrared spectroscopy, and Raman spectroscopy. The CN‐REOs and polyvinylidene fluoride composite absorbers with reflection loss values above −40 dB are obtained in C‐band, X‐band, and Ku‐band, respectively. The empirical rules on effective bandwidth and frequency range are discovered and summarized, which can be successfully realized by simply tuning the doping amount or type of REO. The mechanism is explained by enhanced attenuation and tunable impedance matching. In addition co‐filled samples by two types of CN‐REOs nanocomposites are prepared to support these findings and inspire the preparation of absorber with desirable frequency band in the range of 2–18 GHz.
In the system of composites of PVDF and trace n‐doped carbon nanocomposites loaded with rare earth oxide, a high‐performance electromagnetic wave‐absorbing composite with adjustable electromagnetic wave absorption frequency range and adjustable effective absorption width is obtained. Regular performance is found based on extensive experimental data and analysis of intrinsic performance. In addition, the empirical conclusions are well‐validated by co‐filled (CN‐Ce+CN‐Eu)/PVDF samples.
Bimetallic metal–organic frameworks are rationally synthesized as templates and employed for porous carbons with retained morphology, high graphitization degree, hierarchical porosity, high surface ...area, CoNx moiety and uniform N/Co dopant by pyrolysis. The optimized carbon with additional phosphorus dopant exhibits excellent electrocatalytic performance for the oxygen reduction reaction, which is much better than the benchmark Pt/C in alkaline media.
Oil sorbents play a very important part in the remediation processes of oil spills. To enhance the oil‐sorption properties and simplify the oil‐recovery process, various advanced oil sorbents and ...oil‐collecting devices based on them have been proposed recently. Here, we firstly discuss the design considerations for the fabrication of oil sorbents and describe recently developed oil sorbents based on modification strategy. Then, recent advances regarding oil sorbents mainly based on carbon materials and swellable oleophilic polymers are also presented. Subsequently, some additional properties are emphasized, which are required by oil sorbents to cope with oil spills under extreme conditions or to facilitate the oil‐collection processes. Furthermore, some oil‐collection devices based on oil sorbents that have been developed recently are shown. Finally, an outlook and challenges for the next generation of oil‐spill‐remediation technology based on oil‐sorbents materials are given.
Hydrophobic and oleophilic sorbent materials are demonstrated as promising candidates for the cleanup of oil spills. An overview of the latest developments and advances in the fabrication of oil sorbents through modification strategy, carbon‐based oil sorbents, and polymer‐based oil sorbents, as well as some smart oil sorbents and oil‐collecting devices based on oil‐sorbent materials are presented.
The anode oxygen evolution reaction (OER) is known to largely limit the efficiency of electrolyzers owing to its sluggish kinetics. While crystalline metal oxides are promising as OER catalysts, ...their amorphous phases also show high activities. Efforts to produce amorphous metal oxides have progressed slowly, and how an amorphous structure benefits the catalytic performances remains elusive. Now the first scalable synthesis of amorphous NiFeMo oxide (up to 515 g in one batch) is presented with homogeneous elemental distribution via a facile supersaturated co‐precipitation method. In contrast to its crystalline counterpart, amorphous NiFeMo oxide undergoes a faster surface self‐reconstruction process during OER, forming a metal oxy(hydroxide) active layer with rich oxygen vacancies, leading to superior OER activity (280 mV overpotential at 10 mA cm−2 in 0.1 m KOH). This opens up the potential of fast, facile, and scale‐up production of amorphous metal oxides for high‐performance OER catalysts.
Amorphous NiFeMo oxide (up to 515 g one batch) with homogeneous elemental distribution was synthesized through a facile supersaturated co‐precipitation method. The amorphous NiFeMo oxide undergoes rapid surface self‐reconstruction during OER that forms a metal oxy(hydroxide) active layer with oxygen vacancies, enabling efficient OER catalysis.
The exploitation of photocatalysts that harvest solar spectrum as broad as possible remains a high‐priority target yet grand challenge. In this work, for the first time, metal–organic framework (MOF) ...composites are rationally fabricated to achieve broadband spectral response from UV to near‐infrared (NIR) region. In the core–shell structured upconversion nanoparticles (UCNPs)‐Pt@MOF/Au composites, the MOF is responsive to UV and a bit visible light, the plasmonic Au nanoparticles (NPs) accept visible light, whereas the UCNPs absorb NIR light to emit UV and visible light that are harvested by the MOF and Au once again. Moreover, the MOF not only facilitates the generation of “bare and clean” Au NPs on its surface and realizes the spatial separation for the Au and Pt NPs, but also provides necessary access for catalytic substrates/products to Pt active sites. As a result, the optimized composite exhibits excellent photocatalytic hydrogen production activity (280 µmol g−1 h−1) under simulated solar light, and the involved mechanism of photocatalytic H2 production under UV, visible, and NIR irradiation is elucidated. Reportedly, this is an extremely rare study on photocatalytic H2 production by light harvesting in all UV, visible, and NIR regions.
Novel broadband spectrum‐responsive metal–organic framework (MOF) composites, upconversion nanoparticles‐Pt@MOF/Au, are fabricated based on plasmonic and upconversion effects. Strikingly, the composites exhibit considerable photocatalytic hydrogen production activities under UV, visible, or even near‐infrared light irradiation, which represents the first work reporting hydrogen production photocatalysts with considerable activity toward all these three regions of light irradiation.
In addition to a high specific capacitance, a large stretchability and self‐healing properties are also essential to improve the practicality and reliability of supercapacitors in portable and ...wearable electronics. However, the integration of multiple functions into one device remains challenging. Here, the construction of a highly stretchable and real‐time omni‐healable supercapacitor is demonstrated by sandwiching the polypyrrole‐incorporated gold nanoparticle/carbon nanotube (CNT)/poly(acrylamide) (GCP@PPy) hydrogel electrodes with a CNT‐free GCP (GP) hydrogel as the electrolyte and chemically soldering an Ag nanowire film to the hydrogel electrode as the current collector. The newly developed dynamic metal‐thiolate (M‐SR, M = Au, Ag) bond‐induced integrated configuration, with an intrinsically powerful electrode and electrolyte, enables the assembled supercapacitor to deliver an areal capacitance of 885 mF cm−2 and an energy density of 123 µWh cm−2, which are among the highest‐reported values for stretchable supercapacitors. Notably, the device exhibits a superhigh stretching strain of 800%, rapid optical healing capability, and significant real‐time healability during the charge–discharge process. The exceptional performance combined with the facile assembly method confirms this multifunctional device as the best performer among all the flexible supercapacitors reported to date.
A highly stretchable and real‐time omni‐healable supercapacitor is constructed by synergistically designing the entire device from the microstructures of the hydrogel electrode and electrolyte, to the interfacial interactions among the current collector, electrode, and electrolyte, and further to all‐in‐one device configuration via dynamic metal‐thiolate coordination chemistry. This supercapacitor shows great potential in the field of next‐generation flexible/wearable electronics.
Inspired by smart biological tissues, artificial muscle-like actuators offer fascinating prospects due to their distinctive shape transformation and self-healing function under external stimuli. ...However, further practical application is hindered by the lack of simple and general routes to fabricate ingenious soft materials with anisotropic responsiveness. Here, we describe a general in situ polymerization strategy for the fabrication of anisotropic hydrogels composed of highly-ordered lamellar network crosslinked by the metal nanostructure assemblies, accompanied with remarkably anisotropic performances on mechanical, optical, de-swelling and swelling behaviors. Owing to the dynamic thiolate-metal coordination as healing motifs, the composites exhibit rapid and efficient multi-responsive self-healing performance under NIR irradiation and low pH condition. Dependent on well-defined anisotropic structures, the hydrogel presents controllable solvent-responsive mechanical actuating performance. Impressively, the integrated device through a healing-induced assembly way can deliver more complicated, elaborate forms of actuation, demonstrating its great potentials as superior soft actuators like smart robots.
SiOx is proposed as one of the most promising anodes for Li‐ion batteries (LIBs) for its advantageous capacity and stable Li uptake/release electrochemistry, yet its practical application is still a ...big challenge. Here encapsulation of SiOx nanoparticles into conductive graphene bubble film via a facile and scalable self‐assembly in solution is shown. The SiOx nanoparticles are closely wrapped in multilayered graphene to reconstruct a flake‐graphite‐like macrostructure, which promises uniform and agglomeration‐free distribution of SiOx in the carbon while ensures a high mechanical strength and a high tap density of the composite. The composites present unprecedented cycling stability and excellent rate capabilities upon Li storage, rendering an opportunity for its anode use in the next‐generation high‐energy LIBs.
SiOx nanoparticles are closely wrapped in multilayered graphene to reconstruct a macrostructure resembling flake graphite, which promises agglomeration‐free distribution of SiOx in the bulk while ensuring a high mechanical strength and a high tap density of the bubble film. By taking the advantages of the graphene network, the composites present unprecedented cycling stability and excellent rate capabilities upon Li storage.
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