Self-Supporting Hierarchical Carbon Network Loaded with NiW Nanoparticles for Efficient Hydrogen Evolution.

Water splitting technology can convert renewable energies such as solar and wind into hydrogen energy, which is key to achieving a low-carbon hydrogen economy cycle. However, Pt-based catalysts for hydrogen evolution reaction (HER) are too expensive, thus it needs to develop efficient non-noble metal catalysts as alternatives. Herein, Ni-BDC-loaded carbon cloth (CC) is co-pyrolyzed with urea to obtain a composite structure of carbon nanotubes (CNT) and porous carbon (PC) embedded with W-doped Ni nanoparticles on CC, resulting in NiW-CNT/PC/CC. Benefiting from the synergistic effect between Ni and W, the high conductivity of CNT, and the high mass transfer rate of PC, NiW-CNT/PC/CC exhibits excellent HER activity in KOH, which only requires a low overpotential of 45 mV to drive a current density of 10 mA cm-2 with stability exceeding 40 h. Simulation calculations confirm that the W doping in metal Ni can optimize its electronic structure by lowering the d-band center and weakening hydrogen adsorption, thus reducing its HER barrier.

Design and Advanced Manufacturing of NU-1000 Metal-Organic Frameworks with Future Perspectives for Environmental and Renewable Energy Applications.

Metal-organic frameworks (MOFs) represent a relatively new family of materials that attract lots of attention thanks to their unique features such as hierarchical porosity, active metal centers, versatility of linkers/metal nodes, and large surface area. Among the extended list of MOFs, Zr-based-MOFs demonstrate comparably superior chemical and thermal stabilities, making them ideal candidates for energy and environmental applications. As a Zr-MOF, NU-1000 is first synthesized at Northwestern University. A comprehensive review of various approaches to the synthesis of NU-1000 MOFs for obtaining unique surface properties (e.g., diverse surface morphologies, large surface area, and particular pore size distribution) and their applications in the catalysis (electro-, and photo-catalysis), CO2 reduction, batteries, hydrogen storage, gas storage/separation, and other environmental fields are presented. The review further outlines the current challenges in the development of NU-1000 MOFs and their derivatives in practical applications, revealing areas for future investigation.

Electrical-Driven Directed-Evolution of Copper Nanowires Catalysts for Efficient Nitrate Reduction to Ammonia.

The electrocatalytic conversion of nitrate (NO3 -) to NH3 (NO3RR) at ambient conditions offers a promising alternative to the Haber-Bosch process. The pivotal factors in optimizing the proficient conversion of NO3 - into NH3 include enhancing the adsorption capabilities of the intermediates on the catalyst surface and expediting the hydrogenation steps. Herein, the Cu/Cu2O/Pi NWs catalyst is designed based on the directed-evolution strategy to achieve an efficient reduction of NO3‾. Benefiting from the synergistic effect of the OV-enriched Cu2O phase developed during the directed-evolution process and the pristine Cu phase, the catalyst exhibits improved adsorption performance for diverse NO3RR intermediates. Additionally, the phosphate group anchored on the catalyst's surface during the directed-evolution process facilitates water electrolysis, thereby generating Hads on the catalyst surface and promoting the hydrogenation step of NO3RR. As a result, the Cu/Cu2O/Pi NWs catalyst shows an excellent FE for NH3 (96.6%) and super-high NH3 yield rate of 1.2 mol h-1 gcat. -1 in 1 m KOH and 0.1 m KNO3 solution at -0.5 V versus RHE. Moreover, the catalyst's stability is enhanced by the stabilizing influence of the phosphate group on the Cu2O phase. This work highlights the promise of a directed-evolution approach in designing catalysts for NO3RR.

Hierarchical Superhydrophilic/Superaerophobic Ni(OH)2@NiFe-PBA Nanoarray Supported on Nickel Foam for Boosting the Oxygen Evolution Reaction.

The design of hierarchical electrocatalysts with plentiful active sites and high mass transfer efficiency is critical to efficiently and sustainably carrying out the oxygen evolution reaction (OER), which presents a challenging and pressing need. In this study, a hierarchical Ni(OH)2@NiFe-Prussian blue analogue nanoarray grown on nickel foam (NF) [labeled as Ni(OH)2@NiFe-PBA/NF] was synthesized by combining a mild electrodeposition method with an ion-exchange strategy. The resultant Ni(OH)2@NiFe-PBA/NF displays superhydrophilic/superaerophobic properties that optimize the contact with the electrolyte, improve mass transfer efficiency, and expedite detachment of O2 bubbles during the electrocatalytic OER. Specifically, Ni(OH)2@NiFe-PBA/NF exhibits exceptional capability in the OER with low overpotentials of 224 and 240 mV at the current densities of 50 and 100 mA cm-2, respectively, accompanied by a low Tafel slope of 37.1 mV dec-1 and outstanding stability over 100 h at a fixed potential of 1.78 V vs reversible hydrogen electrode (RHE). Furthermore, Ni(OH)2@NiFe-PBA/NF demonstrates remarkable OER performance even in alkaline simulated seawater. During the OER process, active metal-OOH intermediates were formed by the partial self-reconstruction of NiFe-PBA in the heterostructure, as revealed by in situ Raman spectroscopy.

Tuning Morphologies of Metal-Organic Framework-Derived Ni3P/Ni Carbon Nanocomposites for Water Oxidation.

The oxygen evolution reaction (OER) frequently acts as a kinetic bottleneck in various energy storage and conversion systems. Effective electrocatalysts for the OER play a crucial role in reducing the reaction barrier and expediting the reaction. Multicomponent transition metal phosphides (TMPs) have garnered an extensive amount of attention as a result of their exceptional performance in the OER. Here, we present a direct method for preparing two intrinsic morphologies of metal-organic frameworks (MOFs), barrel-like BMM-10 and pancake-like BMM-10(Ac), achieved by establishing a protonation/deprotonation equilibrium with varying NO3-/Ac- ratios. The BMM-10(Ac)-C catalyst was synthesized via heat treatment of the BMM-10(Ac) precursor, exhibiting superior OER performance. It realized an overpotential of 286 mV at a current density of 10 mA cm-2, with a Tafel slope of 111.17 mV decade-1 and a current retention of 98.03%. This improvement arises from the synergistic interaction between Ni3P/Ni nanoparticles and the partially graphitic carbon layer, augmenting the exposure of active sites. Furthermore, alterations in the morphological features of MOF-derived Ni3P/Ni carbon nanocomposites adjusted the active electrochemical surface area, thereby modulating the overall OER performance of the corresponding TMP carbon nanocomposites. This methodology can be extended to control the morphology of other MOFs and their derivatives, providing innovative avenues for the design and synthesis of new MOF-based TMP nanomaterials.

Copper-Based Bio-MOF/GO with Lewis Basic Sites for CO2 Fixation into Cyclic Carbonates and C-C Bond-Forming Reactions.

Several measures, including crude oil recovery improvement and carbon dioxide (CO2) conversion into valuable chemicals, have been considered to decrease the greenhouse effect and ensure a sustainable low-carbon future. The Knoevenagel condensation and CO2 fixation have been introduced as two principal solutions to these challenges. In the present study for the first time, bio-metal-organic frameworks (MOF)(Cu)/graphene oxide (GO) nanocomposites have been used as catalytic agents for these two reactions. In view of the attendance of amine groups, biological MOFs with NH2 functional groups as Lewis base sites protruding on the channels' internal surface were used. The bio-MOF(Cu)/20%GO performs efficaciously in CO2 fixation, leading to more than 99.9% conversion with TON = 525 via a solvent-free reaction under a 1 bar CO2 atmosphere. It has been shown that these frameworks are highly catalytic due to the Lewis basic sites, i.e., NH2, pyrimidine, and C═O groups. Besides, the Lewis base active sites exert synergistic effects and render bio-MOF(Cu)/10%GO nanostructures as highly efficient catalysts, significantly accelerating Knoevenagel condensation reactions of aldehydes and malononitrile as substrates, thanks to the high TOF (1327 h-1) and acceptable reusability. Bio-MOFs can be stabilized in reactions using GO with oxygen-containing functional groups that contribute as efficient substitutes, leading to an expeditious reaction speed and facilitating substrate absorption.

In-based coordination polymer-derived carbon nanoribbons with abundant CoP nanoparticles in carbon nanotubes for water oxidation.

The sluggish oxygen evolution reaction (OER) in overall electrocatalytic water splitting poses a significant challenge in hydrogen production. A series of transition metal phosphides are emerging as promising electrocatalysts, effectively modulating the charge distribution of surrounding atoms for OER. In this study, a highly efficient OER electrocatalyst (CoP-CNR-CNT) was successfully synthesized through the pyrolysis and phosphatization of a Co-doped In-based coordination polymer, specifically InOF-25. This process resulted in evenly dispersed CoP nanoparticles encapsulated in coordination polymer-derived carbon nanoribbons. The synthesized CoP-CNR-CNT demonstrated a competitive OER activity with a smaller overpotential (η10) of 295.7 mV at 10 mA cm-2 and a satisfactory long-term stability compared to the state-of-the-art RuO2 (η10 = 353.7 mV). The high OER activity and stability can be attributed to the high conductivity of the carbon network, the abundance of CoP particles, and the intricate nanostructure of nanoribbons/nanotubes. This work provides valuable insights into the rational design and facile preparation of efficient non-precious metal-based OER electrocatalysts from inorganic-organic coordination polymers, with potential applications in various energy conversion and storage systems.

Interfacial Engineering of Heterogeneous Reactions for MOF-on-MOF Heterostructures.

Metal-organic frameworks (MOFs), as a subclass of porous crystalline materials with unique structures and multifunctional properties, play a pivotal role in various research domains. In recent years, significant attention has been directed toward composite materials based on MOFs, particularly MOF-on-MOF heterostructures. Compared to individual MOF materials, MOF-on-MOF structures harness the distinctive attributes of two or more different MOFs, enabling synergistic effects and allowing for the tailored design of diverse multilayered architectures to expand their application scope. However, the rational design and facile synthesis of MOF-on-MOF composite materials are in principle challenging due to the structural diversity and the intricate interfaces. Hence, this review primarily focuses on elucidating the factors that influence their interfacial growth, with a specific emphasis on the interfacial engineering of heterogeneous reactions, in which MOF-on-MOF hybrids can be conveniently obtained by using pre-fabricated MOF precursors. These factors are categorized as internal and external elements, encompassing inorganic metals, organic ligands, lattice matching, nucleation kinetics, thermodynamics, etc. Meanwhile, these intriguing MOF-on-MOF materials offer a wide range of advantages in various application fields, such as adsorption, separation, catalysis, and energy-related applications. Finally, this review highlights current complexities and challenges while providing a forward-looking perspective on future research directions.

Metal-Organic Frameworks for Greenhouse Gas Applications.

Using petrol to supply energy for a car or burning coal to heat a building generates plenty of greenhouse gas (GHG) emissions, including carbon dioxide (CO2 ), water vapor (H2 O), methane (CH4 ), nitrous oxide (N2 O), ozone (O3 ), fluorinated gases. These up-and-coming metal-organic frameworks (MOFs) are structurally endowed with rigid inorganic nodes and versatile organic linkers, which have been extensively used in the GHG-related applications to improve the lives and protect the environment. Porous MOF materials and their derivatives have been demonstrated to be competitive and promising candidates for GHG separation, storage and conversions as they shows facile preparation, large porosity, adjustable nanostructure, abundant topology, and tunable physicochemical property. Enormous progress has been made in GHG storage and separation intrinsically stemmed from the different interaction between guest molecule and host framework from MOF itself in the recent five years. Meanwhile, the use of porous MOF materials to transform GHG and the influence of external conditions on the adsorption performance of MOFs for GHG are also enclosed. In this review, it is also highlighted that the existing challenges and future directions are discussed and envisioned in the rational design, facile synthesis and comprehensive utilization of MOFs and their derivatives for practical applications.

En Route to High-Density Chiral Single-walled Carbon Nanotube Arrays using Solid Trojan Catalysts.

Solid catalyst is widely recognized as an effective strategy to control the chirality of single-walled carbon nanotubes (SWNTs). However, it is still not compatible with high density in horizontal arrays. "Trojan" catalysts strategy is one of the most effective methods to realize SWNTs with high density and has great potential in chirality control. Here, the co-realization of high density and chirality controlling for SWNTs in a low-temperature growth process is reported based on the developed solid "Trojan" catalyst. High temperature "Trojan" catalyst formation process provides sufficient catalyst number to acquire high density. These liquid "Trojan" catalysts are cooled to solid state by adopting low growth temperature (540 °C), which can be good template to realize the chirality controlling of SWNTs with exposing six-fold symmetry face, (111). Finally, (9, 6) and (13, 1) SWNTs enriched horizontal array with the purity of ≈90% and density of 4 tubes µm-1 is realized. The comparison between the distribution of initial catalysts and the density of as-grown tubes indicates no sacrificing on catalysts number to improve chirality selectivity. This work opens a new avenue on the catalyst's design and chirality controlling in SWNTs growth.

Rhenium Suppresses Iridium (IV) Oxide Crystallization and Enables Efficient, Stable Electrochemical Water Oxidation.

IrO2 as benchmark electrocatalyst for acidic oxygen evolution reaction (OER) suffers from its low activity and poor stability. Modulating the coordination environment of IrO2 by chemical doping is a methodology to suppress Ir dissolution and tailor adsorption behavior of active oxygen intermediates on interfacial Ir sites. Herein, the Re-doped IrO2 with low crystallinity is rationally designed as highly active and robust electrocatalysts for acidic OER. Theoretical calculations suggest that the similar ionic sizes of Ir and Re impart large spontaneous substitution energy and successfully incorporate Re into the IrO2 lattice. Re-doped IrO2 exhibits a much larger migration energy from IrO2 surface (0.96 eV) than other dopants (Ni, Cu, and Zn), indicating strong confinement of Re within the IrO2 lattice for suppressing Ir dissolution. The optimal catalysts (Re: 10 at%) exhibit a low overpotential of 255 mV at 10 mA cm-2 and a high stability of 170 h for acidic OER. The comprehensive mechanism investigations demonstrate that the unique structural arrangement of the Ir active sites with Re-dopant imparts high performance of catalysts by minimizing Ir dissolution, facilitating *OH adsorption and *OOH deprotonation, and lowering kinetic barrier during OER. This study provides a methodology for designing highly-performed catalysts for energy conversion.

Fluorinated Metal-Organic Frameworks with Dual-Functionalized Linkers to Enhance Photocatalytic H2 Evolution and High Water Adsorption.

Photocatalytic H2 evolution has recently attracted much attention due to the reduction of nonrenewable energy sources and the increasing demand for renewable sustainable energies. Meanwhile, metal-organic frameworks (MOFs) are emerging potential photocatalysts due to their structural adaptability, porous configuration, several active sites, and a wide range of performance. Nevertheless, there are still limitations in the photocatalytic H2 evolution reaction of MOFs with higher charge recombination rates. Herein, a copper-organic framework with dual-functionalized linkers {[Cu2(L)(H2O)2]·(5DMF)(4H2O)}n (fluorinated MOF(Cu)-NH2; H4L = 3,5-bis(2,4-dicarboxylic acid)-4-(trifluoromethyl)aniline) and with a rare 2-nodal 4,12-connected shp topology has been synthesized by a ligand-functionalization strategy and evaluated for the photocatalytic production of H2 to overcome this issue. According to the photocatalytic H2 evolution results, fluorinated MOF(Cu)-NH2 showed a hydrogen evolution rate of 63.64 mmol·g-1·h-1 exposed to light irradiation, indicating values 12 times that of the pure ligand when cocatalyst Pt and photosensitizer Rhodamine B were present. In addition, this MOF showed a maximum water absorption of 205 cm3·g-1. When dual-functionalized linkers are introduced to the structure of this MOF, its visible-light absorption increases considerably, which can be associated with nearly narrower energy band gaps (2.18 eV). More importantly, this MOF contributes to water absorption and electron collection and transport, acting as a bridge that helps to separate and transfer photogenerated charges while shortening the electron migration path because of the functional group in its configuration. The current paper seeks to shed light on the design of advanced visible-light photocatalysts with no MOF calcination for H2 photocatalytic production.

Abundant Surface Defects in Cobalt Hydroxides/Oxyhydroxides Induced by Zinc Species Facilitate Water Oxidation.

The complex process of the anodic oxygen evolution reaction (OER) severely hinders overall water splitting, which further limits the large-scale production and application of hydrogen energy. In this work, one type of bimetallic coordination polymer of ZnCoBTC using the MOF-on-MOF strategy has been synthesized where both Co(II) and Zn(II) cations exhibit the same coordination environment. By applying an electric potential, the predesigned bimetallic MOF precursor can be conveniently degraded into CoOxHy as an active species for efficient OER. Owing to the dissolution of ZnOxHy species, in situ formed disordered defects on the external surface of the catalyst increase the specific surface area as well as expose abundant active materials. Therefore, the ZnCoOxHy nanosheet shows excellent OER performance and reaches an overpotential of only 334 mV at 10 mA cm-2 with a Tafel slope of 66.4 mV dec-1, indicating fast reaction kinetics. The results demonstrate that metals with the same coordination environment can undergo in situ replacement or secondary growth on the pristine MOF, and they can be electrochemically degraded into highly efficient catalysts for future energy applications.

Partially Oxidized Carbon Nanomaterials with Ni/NiO Heterostructures as Durable Glucose Sensors.

Conventional enzyme-based glucose biosensors have limited extensive applications in daily life because glucose oxidase is easily inactivated and is expensive. In this paper, we propose a strategy to prepare a new type of cost-effective, efficient, and robust nonenzymatic Ni-CNT-O for electrochemical glucose sensing. It is first followed by the pyrolysis of Ni-ABDC nanostrips using melamine to grow carbon nanotubes (CNTs) to give an intermediate product of Ni-CNT, which is further accompanied by partial oxidation to enable the facile formation of hierarchical carbon nanomaterials with improved hydrophilicity. A series of physicochemical characterizations have fully proved that Ni-CNT-O is a carbon-coated heterostructure of Ni and NiO nanoparticles embedded into coordination polymer-derived porous carbons. The obtained Ni-CNT-O exhibits a better electrocatalytic activity for glucose oxidation stemming from the synergistic effect of a metal element and a metal oxide than unoxidized Ni-CNT, which also shows high performance with a wide linear range from 1 to 3000 µM. It also offers a high sensitivity of 79.4 µA mM-1 cm-2, a low detection limit of 500 nM (S/N = 3), and a satisfactory long-term durability. Finally, this glucose sensor exhibits good reproducibility, high selectivity, as well as satisfactory results by comparing the current response of simulated serum within egg albumen.

MOF-Derived Pt/ZrO2 Carbon Electrocatalyst for Efficient Hydrogen Evolution.

One type of porous carbon nanomaterial decorated by abundant Pt/ZrO2 nanoparticles can be conveniently prepared, which is pyrolyzed from flower-shaped Zr-based UiO-67 precursor with a small amount of H2PtCl6 molecules in its large pores. In addition, the obtained Pt/ZrO2 carbon electrocatalyst can bring efficient electrocatalytic hydrogen evolution performance and long-term stability.

MOF-on-MOF Strategy to Construct a Nitrogen-Doped Carbon-Incorporated CoP@Fe-CoP Core-Shelled Heterostructure for High-Performance Overall Water Splitting.

The design and preparation of efficient and low-cost catalysts for water electrolysis are crucial and highly desirable to produce eco-friendly and sustainable hydrogen fuel. Herein, we prepared nitrogen-doped carbon-incorporated CoP@Fe-CoP core-shelled nanorod arrays grown on Ni foam (CoP@Fe-CoP/NC/NF) through phosphorization of ZIF-67@Co-Fe Prussian blue analogue (ZIF-67@CoFe-PBA). The hierarchical nanorod arrays combined with the core-shelled structure offer favorable mass/electron transport capacity and maximize the active sites, thus enhancing the electrochemically active surface area. The synergistic effect of the bimetallic components and the nitrogen-doped carbon matrix endow the composite with an optimized electronic structure. Benefiting from the above superiorities of morphological and chemical compositions, this self-supported CoP@Fe-CoP/NC/NF heterostructure can drive alkaline hydrogen evolution reaction and oxygen evolution reaction with overpotentials of 97 and 270 mV to yield 100 mA cm-2, respectively. The two-electrode alkaline electrolyzer constructed by this heterostructure shows a low cell voltage of 1.58 V to yield 10 mA cm-2, superior to the precious-metal-based electrocatalyst apparatus (IrO2∥Pt/C). This study offers a feasible and facile approach to develop efficient electrocatalysts for water electrolysis, which applies to other electrochemical energy conversion and storage applications.

Morphologically Controlled Metal-Organic Framework-Derived FeNi Oxides for Efficient Water Oxidation.

The complex oxygen evolution reaction (OER) is recognized as the most studied and explored electrochemical conversion, which plays a crucial role in energy-related applications. In this work, a series of metal-organic framework (MOF)-derived FeNi oxides from a barrel-shaped Ni-based BMM-10 precursor are conveniently obtained to show an excellent OER performance. Under mild Fe(III) etching, a type of core-shell Fe0.5-BMM-10 can be well preserved and the coordination bond of the middle frame structure is decomposed. Furthermore, the Fex-BMM-10-T series is successfully synthesized with a well-preserved morphology compared to precursors after direct oxidation. Finally, followed by initial electrochemical activation, the decomposition of FeNi oxides generates active Fe-doped nickel oxyhydroxides for efficient water oxidation. The improved OER performance stems from the high specific surface area and abundant exposed active centers, as well as the significant synergistic effect between iron and nickel, which is further verified by the theoretical calculation. This approach can be extended to precisely adjust the morphology of MOFs and their derivatives that can result in superior electrocatalytic properties in terms of energy conversion and storage applications.

Size-Selective Suzuki-Miyaura Coupling Reaction over Ultrafine Pd Nanocatalysts in a Water-Stable Indium-Organic Framework.

Metal nanoparticles stabilized by crystalline metal-organic frameworks (MOFs) are highly promising for green heterogeneous catalysis. In this work, in situ formed ultrafine Pd nanocatalysts with an average size of 3.14 nm have been successfully immobilized into the mesopores or defects of a water-stable indium-based MOF by the double-solvent method and subsequent reduction. Significantly, the obtained Pd@InOF-1 displays an obvious and satisfactory size-selective effect in the Suzuki-Miyaura coupling reaction between arylboronic acids and aryl bromides. On the basis of the synergistic effect, microporous InOF-1 nanorods afford a confined space for improving the selectivity of target products while Pd nanoparticles endow abundant active sites for catalysis. Herein, choosing the smallest size reactant with only one benzene ring gives the highest isolated yield of 90%, and if the size is larger, the yield is obviously reduced or even the target product could not be collected. Looking forward, this demonstrated study not only assembles a well-designed Pd@MOF composite with unique micro-nanostructures but also delivers an impressive option for cross-coupling reaction, which has implications for the further development of MOF hybrids for sustainable applications.

Rational Design and Growth of MOF-on-MOF Heterostructures.

Multiporous metal-organic frameworks (MOFs) have emerged as a subclass of highly crystalline inorganic-organic materials, which are endowed with high surface areas, tunable pores, and fascinating nanostructures. Heterostructured MOF-on-MOF composites are recently becoming a research hotspot in the field of chemistry and materials science, which focus on the assembly of two or more different homogeneous or heterogeneous MOFs with various structures and morphologies. Compared with one single MOF, the dual MOF-on-MOF composites exhibit unprecedented tunability, hierarchical nanostructure, synergistic effect, and enhanced performance. Due to the difference of inorganic metals and organic ligands, the lattice parameters in a, b, and c directions in the single crystal cells could bring about subtle or large structural difference. It will result in the composite material with distinct growth methods to obtain secondary MOF grown from the initial MOF. In this review, the authors wish to mainly outline the latest synthetic strategies of heterostructured MOF-on-MOFs and their derivatives, including ordered epitaxial growth, random epitaxial growth, etc., which show the tutorial guidelines for the further development of various MOF-on-MOFs.

Confined Fe Catalysts for High-Density SWNT Arrays Growth: a New Territory for Catalyst-Substrate Interaction Engineering.

Great efforts have been devoted to searching for efficient catalytic systems to produce ultra-high density single-walled carbon nanotube (SWNT) arrays, which lay the foundation for future electronic devices. However, one major obstacle for realizing high-density surface-aligned SWNT arrays is the poor stability of metal nanoparticles in chemical vapor deposition catalytic processes. Recently, Trojan catalyst has been reported to yield unprecedented high-density SWNT arrays with 130 SWNTs per µm on the a-plane (11-20) of the sapphire substrate. Herein, a concept of catalyst confinement effect is put forward to revealing the secret of remarkable growth efficiency of SWNT arrays by Trojan catalyst. Combined experimental and theoretical studies indicate that confinement of catalyst nanoparticles on discrete a-plane strips plays a key role in stabilizing the small nanoparticles. The highly dispersive and active states of catalysts are maintained, which promote the growth of super-dense SWNT arrays. By rationally designing the substrate reconstruction process, large areas of dense SWNT arrays (130 SWNTs per µm) covering the entire substrate are obtained. This approach may provide novel ideas for the synthesis of various high-density 1D nanomaterials.