Strain and Surface Engineering of Multicomponent Metallic Nanomaterials with Unconventional Phases.

Multicomponent metallic nanomaterials with unconventional phases show great prospects in electrochemical energy storage and conversion, owing to unique crystal structures and abundant structural effects. In this review, we emphasize the progress in the strain and surface engineering of these novel nanomaterials. We start with a brief introduction of the structural configurations of these materials, based on the interaction types between the components. Next, the fundamentals of strain, strain effect in relevant metallic nanomaterials with unconventional phases, and their formation mechanisms are discussed. Then the progress in surface engineering of these multicomponent metallic nanomaterials is demonstrated from the aspects of morphology control, crystallinity control, surface modification, and surface reconstruction. Moreover, the applications of the strain- and surface-engineered unconventional nanomaterials mainly in electrocatalysis are also introduced, where in addition to the catalytic performance, the structure-performance correlations are highlighted. Finally, the challenges and opportunities in this promising field are prospected.

Alkylamine-Confined Thickness-Tunable Synthesis of Co(OH)2-CoO Nanosheets toward Oxygen Evolution Catalysis.

Thickness regulation of transition metal hydroxides/oxides nanosheets with superior catalytic properties represents a promising strategy to enhance catalytic performance, but it remains an enormous challenge to achieve precise control, especially when it comes to the ultrathin limit (several atomic layers). In this work, a facile strategy of alkylamine-confined growth is proposed for the synthesis of thickness-tunable metal hydroxide/oxide nanosheets. Specifically, ultrathin cobalt hydroxide and cobaltous oxide hybrid (Co(OH)2-CoO) nanosheets (Co-O NSs) with a thickness in the range of 2-6 nm (5-13 atomic layers) are synthesized by using alkylamines with different carbon chain lengths as the ligand to modulate vertical coordination ability. Co-O NSs with a thickness of 2 nm (Co-O NSs-2 nm) exhibit excellent oxygen evolution reaction (OER) performance with an overpotential of 278 mV at 10 mA/cm2. The maximized number of active sites including oxygen vacancies, optimal adsorption strength, and the highest electrical conductivity are considered as the potential factors contributing to the excellent OER performance of Co-O NSs-2 nm. This work holds great significance for the precise thickness-tunable synthesis of transition metal layered hydroxide nanosheets with modulated and improved catalytic performance.

Highly Selective CO2 Electroreduction to C2+ Products over Cu2O-Decorated 2D Metal-Organic Frameworks with Rich Heterogeneous Interfaces.

The electroreduction of carbon dioxide into high-value-added products is an effective approach to alleviating the energy crisis and pollution issues. However, there are still significant challenges for multicarbon (C2+) product production due to the lack of efficient catalysts with high selectivity. Herein, a Cu-rich electrocatalyst, where Cu2O nanoparticles are decorated on two-dimensional (2D) Cu-BDC metal-organic frameworks (MOFs) with abundant heterogeneous interfaces, is synthesized for highly selective CO2 electroreduction into C2+ products. A high C2+ Faradaic efficiency of 72.1% in an H-type cell and 58.2% in a flow cell are obtained, respectively. The heterogeneous interfaces of Cu2O/Cu-BDC can optimize the adsorption energy of reaction intermediates during CO2 electroreduction. An in situ infrared spectroscopy study indicates that the constructed interfaces can maintain the particular distribution of Cu valence states, where the C-C coupling is promoted to efficiently produce C2+ products owing to the stabilization of *CHO and *COH intermediates.

Medium/High-Entropy Amalgamated Core/Shell Nanoplate Achieves Efficient Formic Acid Catalysis for Direct Formic Acid Fuel Cell.

High-entropy alloys (HEAs) have been attracting extensive research interests in designing advanced nanomaterials, while their precise control is still in the infancy stage. Herein, we have reported a well-defined PtBiPbNiCo hexagonal nanoplates (HEA HPs) as high-performance electrocatalysts. Structure analysis decodes that the HEA HP is constructed with PtBiPb medium-entropy core and PtBiNiCo high-entropy shell. Significantly, the HEA HPs can reach the specific and mass activities of 27.2 mA cm-2 and 7.1 A mgPt -1 for formic acid oxidation reaction (FAOR), being the record catalyst ever achieved in Pt-based catalysts, and can realize the membrane electrode assembly (MEA) power density (321.2 mW cm-2 ) in fuel cell. Further experimental and theoretical analyses collectively evidence that the hexagonal intermetallic core/atomic layer shell structure and multi-element synergy greatly promote the direct dehydrogenation pathway of formic acid molecule and suppress the formation of CO*.

Phase Engineering of a Ruthenium Nanostructure toward High-Performance Bifunctional Hydrogen Catalysis.

The physicochemical properties and catalytic performance of transition metals are highly phase-dependent. Ru-based nanomaterials are superior catalysts toward hydrogen evolution reaction (HER) and hydrogen oxidation reaction (HOR), but studies are mostly limited to conventional hexagonal-close-packed (hcp) Ru, mainly arising from the difficulty in synthesizing Ru with pure face-centered-cubic (fcc) phase. Herein, we report a crystal-phase-dependent catalytic study of MoOx-modified Ru (MoOx-Ru fcc and MoOx-Ru hcp) for bifunctional HER and HOR. MoOx-Ru fcc is proven to outperform MoOx-Ru hcp in catalyzing both HER and HOR with much higher catalytic activity and more durable stability. The modification effect of MoOx gives rise to optimal adsorption of H and OH especially on fcc Ru, which thus has resulted in the superior catalytic performance. This work highlights the significance of phase engineering in constructing superior electrocatalysts and may stimulate more efforts on phase engineering of other metal-based materials for diversified applications.

Single-site Pt-doped RuO2 hollow nanospheres with interstitial C for high-performance acidic overall water splitting.

Realizing stable and efficient overall water splitting is highly desirable for sustainable and efficient hydrogen production yet challenging because of the rapid deactivation of electrocatalysts during the acidic oxygen evolution process. Here, we report that the single-site Pt-doped RuO2 hollow nanospheres (SS Pt-RuO2 HNSs) with interstitial C can serve as highly active and stable electrocatalysts for overall water splitting in 0.5 M H2SO4. The performance toward overall water splitting have surpassed most of the reported catalysts. Impressively, the SS Pt-RuO2 HNSs exhibit promising stability in polymer electrolyte membrane electrolyzer at 100 mA cm-2 during continuous operation for 100 hours. Detailed experiments reveal that the interstitial C can elongate Ru-O and Pt-O bonds, and the presence of SS Pt can readily vary the electronic properties of RuO2 and improve the OER activity by reducing the energy barriers and enhancing the dissociation energy of *O species.

Reducing leakage current and enhancing polarization in multiferroic 3D super-nanocomposites by microstructure engineering.

Multiferroic materials have generated great interest due to their potential as functional device materials. Nanocomposites have been increasingly used to design and generate new functionalities by pairing dissimilar ferroic materials, though the combination often introduces new complexity and challenges unforeseeable in single-phase counterparts. The recently developed approaches to fabricate 3D super-nanocomposites (3D-sNC) open new avenues to control and enhance functional properties. In this work, we develop a new 3D-sNC with CoFe2O4(CFO) short nanopillar arrays embedded in BaTiO3(BTO) film matrix via microstructure engineering by alternatively depositing BTO:CFO vertically-aligned nanocomposite layers and single-phase BTO layers. This microstructure engineering method allows encapsulating the relative conducting CFO phase by the insulating BTO phase, which suppress the leakage current and enhance the polarization. Our results demonstrate that microstructure engineering in 3D-sNC offers a new bottom-up method of fabricating advanced nanostructures with a wide range of possible configurations for applications where the functional properties need to be systematically modified.

Compensating Electronic Effect Enables Fast Site-to-Site Electron Transfer over Ultrathin RuMn Nanosheet Branches toward Highly Electroactive and Stable Water Splitting.

To improve the electroactivity and stability of electrocatalysts, various modulation strategies have been applied in nanocatalysts. Among different methods, heteroatom doping has been considered as an effective method, which modifies the local bonding environments and the electronic structures. Meanwhile, the design of novel two-dimensional (2D) nanostructures also offers new opportunities for achieving efficient electrocatalysts. In this work, Mn-doped ultrathin Ru nanosheet branches (RuMn NSBs), a newly reported 2D nanostructure, is synthesized. With the ultrathin and naturally abundant edges, the RuMn NSBs have exhibited bifunctionalities of hydrogen evolution reaction and oxygen evolution reaction with high electroactivity and durability in different electrolytes. Experimental characterizations have revealed that RuO bonds are shortened due to Mn doping, which is the key factor that leads to improved electrochemical performances. Density functional theory (DFT) calculations have confirmed that the introduction of Mn enables flexible modulations on the valence states of Ru sites. The inversed redox state evolutions of Ru and Mn sites not only improve the electroactivity for the water splitting but also the long-term stability due to the pinning effect of Ru sites. This work has provided important inspirations for the design of future advanced Ru-based electrocatalysts with high performances and durability.

Highly Surface-Distorted Pt Superstructures for Multifunctional Electrocatalysis.

Platinum (Pt) catalysts play a key role in energy conversion and storage processes, but the realization of further performance enhancement remains challenging. Herein, we report a new class of Pt superstructures (SSs) with surface distortion engineering by electrochemical leaching of PtTex SSs that can largely boost the oxygen reduction reaction (ORR), the methanol oxidation reaction (MOR), and the hydrogen evolution reaction (HER). In particular, the high-distortion (H)-Pt SSs achieve a mass activity of 2.24 A mg-1 at 0.90 VRHE for the ORR and 2.89 A mg-1 for the MOR as well as a low overpotential of 25.3 mV at 10 mA cm-2 for the HER. Moreover, the distorted surface features of Pt SSs can be preserved by mitigating the detrimental effects of agglomeration/degradation during long-time electrocatalysis. A multiscale modeling demonstrates that surface compressions, defects, and nanopores act in synergy for the enhanced ORR performance. This work highlights the advances of stable superstructure and distortion engineering for realizing high-performance Pt nanostructures.

A Top-Down Strategy to Realize Surface Reconstruction of Small-Sized Platinum-Based Nanoparticles for Selective Hydrogenation.

Over the past decades, despite the substantial efforts that have been devoted to the modifications of Pt nanoparticles (NPs) to tailor their selectivities for hydrogenation reactions, there are still a lack of facile strategies for precisely regulation of the surface properties of NPs, especially for those with small sizes. In this work, we propose a top-down thermal annealing strategy for tuning the surface properties of Pt-based NPs (≈4 nm) without the occurrence of aggregation. Compared to conventional bottom-up methods, the present top-down strategy can precisely regulate the surface compositions of Pt-Cd NPs and other ternary Pt-Cd-M NPs (M=Fe, Ni, Co, Mn, and Sn). The optimized Pt-Cd NPs exhibit excellent selectivity toward phenylacetylene and 4-nitrostyrene hydrogenations with a styrene selectivity and 4-aminophenyl styrene selectivity of 95.2 % and 94.5 %, respectively. This work provides a general strategy for the surface reconstructions of Pt-based NPs, and promotes fundamental research on catalyst design for heterogeneous catalysis.

Recent Progress in Advanced Electrocatalyst Design for Acidic Oxygen Evolution Reaction.

Proton exchange membrane (PEM) water electrolyzers hold great significance for renewable energy storage and conversion. The acidic oxygen evolution reaction (OER) is one of the main roadblocks that hinder the practical application of PEM water electrolyzers. Highly active, cost-effective, and durable electrocatalysts are indispensable for lowering the high kinetic barrier of OER to achieve boosted reaction kinetics. To date, a wide spectrum of advanced electrocatalysts has been designed and synthesized for enhanced acidic OER performance, though Ir and Ru based nanostructures still represent the state-of-the-art catalysts. In this Progress Report, recent research progress in advanced electrocatalysts for improved acidic OER performance is summarized. First, fundamental understanding about acidic OER including reaction mechanisms and atomic understanding to acidic OER for rational design of efficient electrocatalysts are discussed. Thereafter, an overview of the progress in the design and synthesis of advanced acidic OER electrocatalysts is provided in terms of catalyst category, i.e., metallic nanostructures (Ir and Ru based), precious metal oxides, nonprecious metal oxides, and carbon based nanomaterials. Finally, perspectives to the future development of acidic OER are provided from the aspects of reaction mechanism investigation and more efficient electrocatalyst design.

Self-Assembled BaTiO3-AuxAg1-x Low-Loss Hybrid Plasmonic Metamaterials with an Ordered "Nano-Domino-like" Microstructure.

Metallic plasmonic hybrid nanostructures have attracted enormous research interest due to the combined physical properties coming from different material components and the broad range of applications in nanophotonic and electronic devices. However, the high loss and narrow range of property tunability of the metallic hybrid materials have limited their practical applications. Here, a metallic alloy-based self-assembled plasmonic hybrid nanostructure, i.e., a BaTiO3-AuxAg1-x (BTO) vertically aligned nanocomposite, has been integrated by a templated growth method for low-loss plasmonic systems. Comprehensive microstructural characterizations including high-resolution scanning transmission electron microscopy (HRSTEM), energy-dispersive X-ray spectroscopy (EDS), and three-dimensional (3D) electron tomography demonstrate the formation of an ordered "nano-domino-like" morphology with Au0.4Ag0.6 nanopillars as cylindrical cores and BTO as square shells. By comparing with the BTO-Au hybrid thin film, the BTO-Au0.4Ag0.6 alloyed film exhibits much broader plasmon resonance, hyperbolic dispersion, low-loss, and thermally robust features in the UV-vis-NIR wavelength region. This study provides a feasible platform for a complex alloyed plasmonic hybrid material design with low-loss and highly tunable optical properties toward all-optical integrated devices.

Grain-Boundary-Engineered La2CuO4 Perovskite Nanobamboos for Efficient CO2 Reduction Reaction.

Electroreduction of carbon dioxide (CO2RR) has been regarded as a promising approach to realize the production of useful fuels and to decrease greenhouse gas levels simultaneously, where high-efficiency catalysts are required. Herein, we report La2CuO4 nanobamboo (La2CuO4 NBs) perovskite with rich twin boundaries showing a high Faraday efficiency (FE) of 60% toward ethylene (C2H4), whereas bulk La2CuO4 exhibits a FECO of 91%. X-ray absorption spectroscopy (XAS) reveals that the Cu in La2CuO4 NBs is in the Cu2+ state, and no obvious change can be observed during the catalytic process, as monitored by in situ XAS. Density functional theory calculations reveal that the superior FEC2H4 of La2CuO4 NBs originates from the active (113) surfaces with intrinsic strain. The formation of gap states annihilates the electron transfer barrier of C-C coupling, resulting in the high FEC2H4. This work provides a new perspective for developing efficient perovskite catalysts via grain boundary engineering.

Te-Doped Pd Nanocrystal for Electrochemical Urea Production by Efficiently Coupling Carbon Dioxide Reduction with Nitrite Reduction.

The renewable electricity-driven reduction of carbon dioxide (CO2RR) is a promising technology for carbon utilization. However, it is still a challenge to broaden the application of CO2RR. Herein, we report a Te-doped Pd nanocrystals (Te-Pd NCs) for promoting urea synthesis by coupling CO2RR with electrochemical reduction of nitrite. The electrochemical synthesis of urea has been achieved with nearly 12.2% Faraday efficiency (FE) and 88.7% N atom efficiency (NE) at -1.1 V versus reversible hydrogen electrode (vs RHE), much higher than those of pure Pd NCs (4.2% FE and 21.8% NE). Significantly, an FE of ∼10.2% and an NE of ∼82.3% for urea solution production via an optimized flow cell system have been realized, where a solution with up to 0.95 wt % of urea has been obtained. Mechanistic insights show that Te-doping not only optimizes the CO2/CO adsorption but also promotes NH3 production, fully meeting the requirements of urea synthesis.

Induced ferroelectric phases in SrTiO3 by a nanocomposite approach.

Inducing new phases in thick films via vertical lattice strain is one of the critical advantages of vertically aligned nanocomposites (VANs). In SrTiO3 (STO), the ground state is ferroelastic, and the ferroelectricity in STO is suppressed by the orthorhombic transition. Here, we explore whether vertical lattice strain in three-dimensional VANs can be used to induce new ferroelectric phases in SrTiO3:MgO (STO:MgO) VAN thin films. The STO:MgO system incorporates ordered, vertically aligned MgO nanopillars into a STO film matrix. Strong lattice coupling between STO and MgO imposes a large lattice strain in the STO film. We have investigated ferroelectricity in the STO phase, existing up to room temperature, using piezoresponse force microscopy, phase field simulation and second harmonic generation. We also serendipitously discovered the formation of metastable TiO nanocores in MgO nanopillars embedded in the STO film matrix. Our results emphasize the design of new phases via vertical epitaxial strain in VAN thin films.

Cation Exchange Strategy to Single-Atom Noble-Metal Doped CuO Nanowire Arrays with Ultralow Overpotential for H2O Splitting.

Single-atom site catalysts (SACs) have aroused enormous attention and brought about new opportunities for many applications. Herein, we report a versatile strategy to rhodium (Rh) SAC by a facile cation exchange reaction. Remarkably, the Rh SAC modified CuO nanowire arrays on copper foam (Rh SAC-CuO NAs/CF) show unprecedented alkaline oxygen evolution reaction (OER) activity with a high current density of 84.5 mA cm-2@1.5 V vs reversible hydrogen electrode (RHE), 9.7 times that of Ir/C/CF. More strikingly, when used as an anode and a cathode for overall water splitting, the Rh SAC-CuO NAs/CF can achieve 10 mA cm-2 at only 1.51 V. Density functional theory calculations reveal that the high OER and HER intrinsic catalytic activities result from moderate adsorption energy of intermediates on Rh SAC. Finally, we demonstrate the general synthesis of different single-atom noble-metal catalysts on CuO NAs (M SAC-CuO NAs/CF, where M = Ru, Ir, Os, and Au).

Metallic nanostructures with low dimensionality for electrochemical water splitting.

Metallic nanostructures with low dimensionality (one-dimension and two-dimension) possess unique structural characteristics and distinctive electronic and physicochemical properties including high aspect ratio, high specific surface area, high density of surface unsaturated atoms and high electron mobility. These distinctive features have rendered them remarkable advantages over their bulk counterparts for surface-related applications, for example, electrochemical water splitting. In this review article, we highlight the recent research progress in low-dimensional metallic nanostructures for electrochemical water splitting including hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). Fundamental understanding of the electrochemistry of water splitting including HER and OER is firstly provided from the aspects of catalytic mechanisms, activity descriptors and property evaluation metrics. Generally, it is challenging to obtain low-dimensional metallic nanostructures with desirable characteristics for HER and OER. We hereby introduce several typical methods for synthesizing one-dimensional and two-dimensional metallic nanostructures including organic ligand-assisted synthesis, hydrothermal/solvothermal synthesis, carbon monoxide confined growth, topotactic reduction, and templated growth. We then put emphasis on the strategies adopted for the design and fabrication of high-performance low-dimensional metallic nanostructures for electrochemical water splitting such as alloying, structure design, surface engineering, interface engineering and strain engineering. The underlying structure-property correlation for each strategy is elucidated aiming to facilitate the design of more advanced electrocatalysts for water splitting. The challenges and perspectives for the development of electrochemical water splitting and low-dimensional metallic nanostructures are also proposed.

Novel layered Bi3MoMTO9 (MT = Mn, Fe, Co and Ni) thin films with tunable multifunctionalities.

Bi3MoMTO9 (BMoMTO; MT, transition metals of Mn, Fe, Co and Ni) thin films with a layered supercell structure have been deposited on LaAlO3 (001) substrates by pulsed laser deposition. Microstructural analysis suggests that pillar-like domains with higher transition metal concentration (e.g., Mn, Fe, Co and Ni) are embedded in the Mo-rich matrix with layered supercell structures. The layered supercell structure of the BMoMTO thin films accounts for the anisotropic multifunctionalities such as the magnetic easy axis along the in-plane direction, and the anisotropic optical properties. Ferroelectricity and ferromagnetism have been demonstrated in the thin films at room temperature, which confirms the multiferroic nature of the system. By varying the transition metal MT in the film, the band gaps of the BMoMTO films can be effectively tuned from 2.44 eV to 2.82 eV, while the out-of-plane dielectric constant of the thin films also varies. The newly discovered layered nanocomposite systems present their potential in ferroelectrics, multiferroics and non-linear optics.

Surface-Regulated Rhodium-Antimony Nanorods for Nitrogen Fixation.

Surface regulation is an effective strategy to improve the performance of catalysts, but it has been rarely demonstrated for nitrogen reduction reaction (NRR) to date. Now, surface-rough Rh2 Sb nanorod (RNR) and surface-smooth Rh2 Sb NR (SNR) were selectively created, and their performance for NRR was investigated. The high-index-facet bounded Rh2 Sb RNRs/C exhibit a high NH3 yield rate of 228.85±12.96 µg h-1 mg-1 Rh at -0.45 V versus reversible hydrogen electrode (RHE), outperforming the Rh2 Sb SNRs/C (63.07±4.45 µg h-1 mg-1 Rh ) and Rh nanoparticles/C (22.82±1.49 µg h-1 mg-1 Rh ), owing to the enhanced adsorption and activation of N2 on high-index facets. Rh2 Sb RNRs/C also show durable stability with negligible activity decay after 10 h of successive electrolysis. The present work demonstrates that surface regulation plays an important role in promoting NRR activity and provides a new strategy for creating efficient NRR electrocatalysts.

Tunable physical properties in BiAl1-x Mn x O3 thin films with novel layered supercell structures.

Morphological control in oxide nanocomposites presents enormous opportunities for tailoring the physical properties. Here, we demonstrate the strong tunability of the magnetic and optical properties of Bi-based layered supercell (LSC) multiferroic structures, i.e., BiAl1-x Mn x O3, by varying the Al : Mn molar ratio. The microstructure of the LSC structure evolves from a supercell structure to Al-rich pillars in the supercell structure as the Al molar ratio increases. The LSC structures present excellent multiferroic properties with preferred in-plane magnetic anisotropy, a tunable band gap and anisotropic dielectric permittivity, all attributed to the microstructure evolution and their anisotropic microstructure. Three different strain relaxation mechanisms are identified that are active during thin film growth. This study provides opportunities for microstructure and physical property tuning which can also be explored in other Bi-based LSC materials with tailorable multiferroic and optical properties.