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In recent years, significant attention has been directed toward advancing compact, point-of-care testing (POCT) devices to better deliver patient care and alleviate the burden on the medical care system. Common POCTs, such as blood oxygen sensors, leverage electrochemical sensing in their design. However, conventional electrochemical devices typically use Ag/AgCl reference electrodes, which are likely to release trace amounts of silver ions that contaminate the working electrode, causing rapid deterioration of the devices. This study proposes an effective reference electrode using graphene-coated porous silica spheres (G/PSS) with embedded Prussian blue (PB), denoted PB/G/PSS, designed specifically for small oxygen sensors. PB is a redox species that is an improvement over Ag/AgCl since it is significantly less water-soluble than AgCl. Since PB is an insulator, we dispersed PB in G/PSS, well-conductive mesoporous matrices, to ensure contact between PB clusters and the electrolytes. Moreover, the monodispersed, spherically shaped PB/G/PSS is an advantageous medium for fabricating POCT devices by screen printing. In this study, the open-circuit potential of the PB/G/PSS electrode remained stable within 30 mV for 31 days. The small oxygen sensor assembled through screen printing using PB/G/PSS demonstrated stable operation for several days or more. In contrast, a similar sensor with Ag/AgCl reference electrode rapidly deteriorated within a day. This PB/G/PSS reference electrode with improved stability is expected to be an excellent alternative to the Ag/AgCl system for small electrochemical-based POCT devices.

Supported metal single atom catalysis is a dynamic research area in catalysis science combining the advantages of homogeneous and heterogeneous catalysis. Understanding the interactions between metal single atoms and the support constitutes a challenge facing the development of such catalysts, since these interactions are essential in optimizing the catalytic performance. For conventional carbon supports, two types of surfaces can contribute to single atom stabilization: the basal planes and the prismatic surface; both of which can be decorated by defects and surface oxygen groups. To date, most studies on carbon-supported single atom catalysts focused on nitrogen-doped carbons, which, unlike classic carbon materials, have a fairly well-defined chemical environment. Herein we report the synthesis, characterization and modeling of rhodium single atom catalysts supported on carbon materials presenting distinct concentrations of surface oxygen groups and basal/prismatic surface area. The influence of these parameters on the speciation of the Rh species, their coordination and ultimately on their catalytic performance in hydrogenation and hydroformylation reactions is analyzed. The results obtained show that catalysis itself is an interesting tool for the fine characterization of these materials, for which the detection of small quantities of metal clusters remains a challenge, even when combining several cutting-edge analytical methods., (© 2024 Wiley-VCH GmbH.)

Porous materials synthesized through bottom-up approaches, such as metal-organic frameworks and covalent organic frameworks, have attracted attention owing to their design flexibility for functional materials. However, achieving the chemical and thermal stability of these materials for various applications is challenging considering the reversible coordination bonds and irreversible covalent bonds in their frameworks. Thus, ordered carbonaceous frameworks (OCFs) emerge as a promising class of bottom-up materials with good periodicity, thermal and chemical stability, and electrical conductivity. However, a few OCFs have been reported owing to the limited range of precursor molecules. Herein, we designed a hexaazatrinaphthylene-based molecule with enediyne groups as a precursor molecule for synthesizing an OCF. The solid-state Bergman cyclization of enediyne groups at a low temperature formed a microporous polymer and an OCF, exhibiting redox activity and demonstrating their potential for electrochemical applications. The microporous polymer was used as an active material in sodium-ion batteries, while the OCF was used as an electrochemical capacitor. These findings illustrate the utility of the Bergman cyclization reaction for synthesizing microporous polymers and OCFs with a customizable functionality for broad applications.

Nitrogen (N) doping of perovskite-type oxides is an effective method for enhancing their photocatalytic performance. Quantitative and qualitative analyses of the doped N species are essential for a deeper understanding of the catalytic activity enhancement mechanism. However, examining the N environment in perovskite-type oxides, particularly in the bulk, using conventional analytical techniques, such as X-ray photoelectron spectroscopy (XPS), is challenging. In this study, we propose a new analytical technique, advanced temperature-programmed desorption (TPD) up to 1600 °C, to complement the conventional methods. TPD can quantify all N species in bulk oxides. Moreover, it facilitates chemical speciation of N environments, such as substitutional and interstitial N species. This is verified by XPS, CHN elemental analysis, X-ray absorption spectroscopy, and in situ diffuse reflectance infrared Fourier-transform spectroscopy. This study demonstrates the feasibility of advanced TPD as a new analytical method that offers comprehensive information on the N species within N-doped oxide materials at the bulk level., Competing Interests: The authors declare that they have no competing financial interests or personal relationships that may have influenced the work reported in this study., (This journal is © The Royal Society of Chemistry.)

Microporous molecular crystals are promising materials because of their designable porosity as well as their resistance to chemical and other stimuli. Here, we developed microporous molecular cocrystals by taking advantage of the specific interactions between porphyrins and fullerene molecules. Single-crystal X-ray diffraction analysis revealed that one nickel(II) porphyrin interacts with two fullerene molecules to form a two-dimensional honeycomb network with an eclipsed stacking mode, providing one-dimensional void channels. After the pores were activated by heat treatment or mechanical grinding, the prepared cocrystal can incorporate gas and solvent molecules reversibly while maintaining its single-crystallinity. Also, it retained its single-crystallinity in the presence of water, acid-base, or high pressure. These findings in this study expand the availability of molecular crystals based on intermolecular interactions as porous materials, which are expected to work under conditions that have not been applicable to other molecule-based porous materials., Competing Interests: The authors declare no competing financial interest., (© 2024 The Authors. Co-published by University of Science and Technology of China and American Chemical Society.)

Porous carbons are important electrode materials for supercapacitors. One of the challenges associated with supercapacitors is improving their energy density without relying on pseudocapacitance, which is based on fast redox reactions that often shorten device lifetimes. A possible solution involves achieving high total capacitance (C tot ), which comprises Helmholtz capacitance (C H ) and possibly quantum capacitance (C Q ), in high-surface carbon materials comprising minimally stacked graphene walls. In this work, a templating method is used to synthesize 3D mesoporous graphenes with largely identical pore structures (≈2100 m 2 g -1 with an average pore size of ≈7 nm) but different concentrations of oxygen-containing functional groups (0.3-6.7 wt.%) and nitrogen dopants (0.1-4.5 wt.%). Thus, the impact of the heteroatom functionalities on C tot is systematically investigated in an organic electrolyte excluding the effect of pore structures. It is found that heteroatom functionalities determine C tot , resulting in the cyclic voltammetry curves being rectangular or butterfly-shaped. The nitrogen functionalities are found to significantly enhance C tot owing to increased C Q ., (© 2023 The Authors. Small published by Wiley‐VCH GmbH.)

Hierarchically porous carbon microlattices (HPCMLs) fabricated by using a composite photoresin and stereolithography (SLA) 3D printing is reported. Containing magnesium oxide nanoparticles (MgO NPs) as porogens and multilayer graphene nanosheets as UV-scattering inhibitors, the composite photoresin is formed to simple cubic microlattices with digitally designed porosity of 50%. After carbonization in vacuum at 1000 °C and chemical removal of MgO NPs, it is realized that carbon microlattices possessing hierarchical porosity are composed of the lattice architecture (≈100 µm), macropores (≈5 µm), mesopores (≈50 nm), and micropores (≈1 nm). The linear shrinkage after pyrolysis is as small as 33%. Compressive strength of 7.45 to 10.45 MPa and Young's modulus of 375 to 736 MPa are achieved, proving HPCMLs a robust mechanical component among reported carbon materials with a random pore structure. Having a few millimeters in thickness, the HPCMLs can serve as thick supercapacitor electrodes that demonstrate gravimetric capacitances 105 and 13.8 F g -1 in aqueous and organic electrolyte, reaching footprint areal capacitances beyond 10 and 1 F cm -2 , respectively. The results present that the composite photoresin for SLA can yield carbon microarchitectures that integrate structural and functional properties for structural energy storages ., (© 2023 Wiley-VCH GmbH.)

The structural evolution of highly mesoporous templated carbons is examined from temperatures of 1173 to 2873 K to elucidate the optimal conditions for facilitating graphene-zipping reactions whilst minimizing graphene stacking processes. Mesoporous carbons comprising a few-layer graphene wall display excellent thermal stability up to 2073 K coupled with a nanoporous structure and three-dimensional framework. Nevertheless, advanced temperature-programmed desorption (TPD), X-ray diffraction, and Raman spectroscopy show graphene-zipping reactions occur at temperatures between 1173 and 1873 K. TPD analysis estimates zipping reactions lead to a 1100 fold increase in the average graphene-domain, affording the structure a superior chemical stability, electrochemical stability, and electrical conductivity, while increasing the bulk modulus of the framework. At above 2073 K, the carbon framework shows a loss of porosity due to the development of graphene-stacking structures. Thus, a temperature range between 1873 and 2073 K is preferable to balance the developed graphene domain size and high porosity. Utilizing a neutron pair distribution function and soft X-ray emission spectra, we prove that these highly mesoporous carbons already consist of a well-developed sp 2 -carbon network, and the property evolution is governed by the changes in the edge sites and stacked structures., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

Three-dimensionally ordered nanoporous structures were generated in carbon materials doped with metals and nitrogen as catalytically active sites for electrochemical reactions. Free-base and metal phthalocyanines with a strategically designed molecular structure were used as carbon sources to obtain an ordered porous structure via homogeneous self-assembly with Fe 3 O 4 nanoparticles as the pore template and the prevention of melting away during carbonization. The doping of Fe and nitrogen was achieved by a reaction between the free-base phthalocyanine and Fe 3 O 4 through carbonization at 550 °C, while Co and Ni were doped using the corresponding metal phthalocyanines. The preference of these three types of ordered porous carbon materials for catalytic reactions was distinctly determined by the doped metals. Fe-N-doped carbon showed the highest activity for O 2 reduction. Additional heat treatment at 800 °C enhanced this activity. CO 2 reduction and H 2 evolution were preferred by the Ni- and Co-N-doped carbon materials, respectively. A change in the template particle size was capable of controlling the pore size to enhance mass transfer and improve performance. The technique presented in this study enabled systematic metal doping and pore size control in the ordered porous structures of carbonaceous catalysts.

The rational design of a stable and catalytic carbon cathode is crucial for the development of rechargeable lithium-oxygen (LiO 2 ) batteries. An edge-site-free and topological-defect-rich graphene-based material is proposed as a pure carbon cathode that drastically improves LiO 2 battery performance, even in the absence of extra catalysts and mediators. The proposed graphene-based material is synthesized using the advanced template technique coupled with high-temperature annealing at 1800 °C. The material possesses an edge-site-free framework and mesoporosity, which is crucial to achieve excellent electrochemical stability and an ultra-large capacity (>6700 mAh g -1 ). Moreover, both experimental and theoretical structural characterization demonstrates the presence of a significant number of topological defects, which are non-hexagonal carbon rings in the graphene framework. In situ isotopic electrochemical mass spectrometry and theoretical calculations reveal the unique catalysis of topological defects in the formation of amorphous Li 2 O 2 , which may be decomposed at low potential (∼ 3.6 V versus Li/Li + ) and leads to improved cycle performance. Furthermore, a flexible electrode sheet that excludes organic binders exhibits an extremely long lifetime of up to 307 cycles (>1535 h), in the absence of solid or soluble catalysts. These findings may be used to design robust carbon cathodes for LiO 2 batteries., (© 2023 The Authors. Advanced Science published by Wiley-VCH GmbH.)

Ordered carbonaceous frameworks (OCFs) are a new class of carbon materials with a three-dimensional ordered structure synthesized by simple carbonization of metalloporphyrin crystals with polymerizable moieties. Carbonization via solid-state polymerization results in the formation of graphene-based ordered frameworks in which regularly aligned single-atomic metals are embedded. These unique structural features afford molecular-level designability like organic-based frameworks together with high electrical conductivity, thermal/chemical stability, and mechanical flexibility, towards a variety of applications including electrocatalysis and force-driven phase transition. This feature article summarizes the synthetic strategies and characteristics of OCFs in comparison with conventional organic-based frameworks and porous carbons, to discuss the potential applications and further development of the OCF family.

While the functions of carbon materials with precisely controlled nanostructures have been reported in many studies, their chiral discriminating abilities have not been reported yet. Herein, chiral discrimination is achieved using helical carbon materials devoid of chiral attachments. A Fe 3 O 4 nanoparticle template with ethyl cellulose (carbon source) is self-assembled on dispersed multiwalled carbon nanotubes (MWCNTs) fixed in a lamellar structure, with helical nanoparticle alignment induced by the addition of a binaphthyl derivative. Carbonization followed by template removal produces helically aligned fused carbon hollow nanospheres (CHNSs) with no chiral molecules left. Helicity is confirmed using vacuum-ultraviolet circular dichroism spectroscopy. Chiral discrimination, as revealed by the electrochemical reactions of binaphthol and a chiral ferrocene derivative in aqueous and nonaqueous electrolytes, respectively, is attributable to the chiral space formed between the CHNS and MWCNT surfaces.

Force-responsive ordered carbonaceous frameworks (OCFs) are synthesized for the first time. Carbonization of Ni porphyrin monomers having eight polymerizable ethynyl groups yields OCFs with atomically dispersed divalent Ni species and developed micropores. The highest specific surface area (673 m 2 g -1 ) among the OCFs has been achieved. The OCFs thus synthesized comprise non-stacked graphene sheets, affording a unique mechanical flexibility that enables force-driven reversible phase transition.

A new type of pyrene-thiol derivative-modified Pd nanoparticle (NP) catalyst on a carbon black support for the efficient semihydrogenation of alkynes to alkenes is reported herein. Colloidal Pd NPs surrounded by pyrene-thiol modifiers were prepared using the two-phase Brust method followed by impregnation of carbon black materials. Based on the structural characterization of the prepared catalyst (PyC 12 S-Pd/VC) by NMR, UV-vis, FT-IR, TEM, HAADF-STEM, Pd K-edge XAFS, XRD, N 2 adsorption, and XPS, we show that highly dispersed Pd NPs are immobilized on the catalysts via π-π interaction between pyrene groups bound to the Pd NPs and carbon black supports. PyC 12 S-Pd/VC efficiently catalyzes the alkyne semihydrogenation reaction while maintaining high alkene selectivity; an alkene selectivity of 94% is attained at 98% conversion after 5 h of reaction, and the selectivity was retained around 80% in 10 h of reaction. This performance is superior to that of a catalyst without pyrene groups and that of a commercial Lindlar catalyst. The steric hindrance of pyrene groups restricts access of the substrates to Pd NP surfaces, suppressing the unfavorable overhydrogenation of alkenes to alkanes, which is revealed by the solvent and substrate dependency on the catalytic performance and a DFT calculation study. Furthermore, the high selectivity and stability of PyC 12 S-Pd/VC are caused by the strong interaction between pyrene groups and carbon supports, which prevents the separation of pyrene modifiers and the leaching or sintering of Pd NPs during the catalytic reaction. It is demonstrated that the combination of Pd NPs, pyrene-thiol modifiers, and carbon supports offers high activity, alkene selectivity, and stability in the semihydrogenation reaction.

Metal organic frameworks (MOFs) are a class of porous organic-inorganic crystalline materials that have attracted much attention as H 2 storage devices and catalytic supports. In this paper, the synthesis of highly-dispersed Ni nanoparticles (NPs) for the hydrogenation of olefins was achieved by employing Ni-MOF-74 as a precursor. Investigations of the structural transformation of Ni species derived from Ni-MOF-74 during heat treatment were conducted. The transformation was monitored in detail by a combination of XRD, in situ XAFS, and XPS measurements. Ni NPs prepared from Ni-MOF-74 were easily reduced by the generation of reducing gases accompanied by the decomposition of Ni-MOF-74 structures during heat treatment at over 300 °C under N 2 flow. Ni-MOF-74-300 exhibited the highest activity for the hydrogenation of 1-octene due to efficient suppression of excess agglomerated Ni species during heat treatment. Moreover, Ni-MOF-74-300 showed not only high activity for the hydrogenation of olefins but also high size-selectivity because of the selective formation of Ni NPs covered by MOFs and the MOF-derived carbonaceous layer., (© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Realizing accurate control of catalytically active centers on solid surfaces is one of the most essential goals in the development of functionalized heterogeneous catalysts. Controlled synthesis of carbon-supported Co catalysts from single-site to nanoparticles can be successfully achieved by the structural transformation of the deposited Co(salen) complex precursor under heat treatment. The obtained structures were characterized using techniques such as XRD, in situ XAFS, and TEM. The first decomposition of the Co(salen) complex is initiated by the dissociation of Co-O-C bonds at around 250 °C, which produces isolated single-atom Co species while retaining the Co-N-C bonds even up to 400 °C. When the heat treatment temperature exceeds 450 °C, the second decomposition of the Co-N-C bonds occurs to form Co oxide nanoclusters followed by the growth of Co NPs upon further increase of the heat treatment temperature. The single-site catalyst is highly dispersed and electronically deficient owing to the interaction with the carbon support, and shows activity and selectivity for the oxidation of ethylbenzene, as compared to the inherent Co(salen) complex and nanoparticle catalysts.