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Professor Chia-Kuang (Frank) Tsung made his scientific impact primarily through the atomic-level design of nanoscale materials for application in heterogeneous catalysis. He approached this challenge from two directions: above and below the material surface. Below the surface, Prof. Tsung synthesized finely controlled nanoparticles, primarily of noble metals and metal oxides, tailoring their composition and surface structure for efficient catalysis. Above the surface, he was among the first to leverage the tunability and stability of metal-organic frameworks (MOFs) to improve heterogeneous, molecular, and biocatalysts. This article, written by his former students, seeks first to commemorate Prof. Tsung's scientific accomplishments in three parts: (1) rationally designing nanocrystal surfaces to promote catalytic activity; (2) encapsulating nanocrystals in MOFs to improve catalyst selectivity; and (3) tuning the host-guest interaction between MOFs and guest molecules to inhibit catalyst degradation. The subsequent discussion focuses on building on the foundation laid by Prof. Tsung and on his considerable influence on his former group members and collaborators, both inside and outside of the lab.

An elevated level of anthropogenic CO2 has been the major cause of global warming, and significant efforts are being made around the world towards the development of CO2 capture, storage and reuse technologies. Among various CO2 conversion technologies, electrochemical CO2 reduction (CO2 RR) by nanocrystals is one of the most promising strategies as it is facile, quick, and can be integrated with other renewable energy techniques. Judiciously designed catalytic nanomaterials promise to be the next generation of electrochemical electrodes that offer cutting-edge performance, low energy consumption and aid in reducing overall carbon footprint. In this minireview, we highlight the recent developments related to the bimetallic Cu-based nanocatalysts and discuss their structure-property relationships. We focus on the design principles and parameters required for the enhancement of CO2 conversion efficiency, selectivity, and stability.

Advances in new systems of organic–inorganic hybrid nanocomposites are less prevalent, owing to a lack of facile strategies for precise control of their structures, compositions, and, hence, their properties. In this work, Au-BINOL hybrid nanocomposites with eccentric and concentric nanostructures were produced. The hybrid nanocomposites containing two distinct moieties of inorganic Au nanocrystals and organic BINOL nanospheres were applied to the catalytic hydrogenation of 4-nitrophenol with NaBH4 in the aqueous phase with and without the illumination of visible light. Here, we demonstrate that the existence of Au–BINOL interfaces offers benefits to their performance. The eccentric nanostructures made with CTAC show the superior activity from large Au–BINOL interfaces formed between the BINOL nanospheres and the faces of Au nanoplates. They further exhibit a high Au localized surface plasmon resonance (LSPR)-enhancement effect on the photoreduction of 4-nitrophenol, which is attributed to the strong LSPR...

Controlling the surface composition of shaped bimetallic nanoparticles could offer precise tunability of geometric and electronic surface structure for new nanocatalysts. To achieve this goal, a platform for studying the intermixing process in a shaped nanoparticle was designed, using multilayered Pd-Ni-Pt core-shell nanocubes as precursors. Under mild conditions, the intermixing between Ni and Pt could be tuned by changing layer thickness and number, triggering intermixing while preserving nanoparticle shape. Intermixing of the two metals is monitored using transmission electron microscopy. The surface structure evolution is characterized using electrochemical methanol oxidation. DFT calculations suggest that the low-temperature mixing is enhanced by shorter diffusion lengths and strain introduced by the layered structure. The platform and insights presented are an advance toward the realization of shape-controlled multimetallic nanoparticles tailored to each potential application.

The combined functionality of components in organic–inorganic hybrid nanomaterials render them efficient nanoreactors. However, the development in this field is limited due to a lack of synthetic avenues and systematic control of the growth kinetics of hybrid structures. In this work, we take advantage of an ionic switch for regio-control of Au-BINOL(1,1′-Bi-2-naphthol) hybrid nanostructures. Aromatic BINOL molecules assemble into nanospheres, concomitant with the growth of the Au nanocrystals. The morphological evolution of Au nanocrystals is solely controlled by the presence of halides in the synthetic system. Here we show that quaternary ammonium surfactants (CTAB or CTAC), not only bridging Au and BINOL, but also contributing to the formation of concentric or eccentric structures when their concentrations are tuned to the range of 10–5 to 10–3 M. This facile strategy offers the potential advantage of scalable production, with diverse functional organic–inorganic hybrid nanocomposites being produced ba...

Conventional gas sensors work upon changes in mechanical or conductive properties of sensing materials during a chemical process, which may limit availabilities of size miniaturization and design simplification. However, fabrication of miniaturized sensors with superior sensitivities in real-time and label-free probing of chemical reactions or catalytic processes remains highly challenging, in particular with regard to integration of materials into a desired smaller volume without losing the recyclability of sensing properties. Here, we demonstrate a unique bimetallic nanostructure, the Au–Pd–Au core–shell–frame nanobrick, as a promising archetype for fabrication of miniaturized sensors at nanoscale. Upon analysis of the aqueous synthesis, both ex situ and in situ, the formation of Au frames is consistent with selective deposition and aggregation of NaBH4-reduced Au nanoparticles at the corners and edges of cubic Pd shells, where the {100} surfaces, capped by iodide ions, are growth-limited. By virtue of ...

Platinum was coated on the surfaces of copper nanocubes to form Cu–CuPt core–alloy–frame nanocrystals with a rhombic dodecahedral (RD) shape. Co-reduction of Pt2+ ions and residual Cu+ ions in the supernatant of the Cu nanocube solution followed by the interdiffusion of Cu and Pt atoms over the core–shell interface allowed their formation. Growth in the ⟨100⟩ directions of the {100}-terminated Cu nanocubes resulted in the {110}-faceted rhombic dodecahedra. By the introduction of additional Pt precursor, the {100} vertices of the Cu–CuPt RD nanocrystals could be selectively extended to form spiny CuPt RD nanocrystals. After removing the Cu core template, both CuPt alloy RD and spiny CuPt alloy RD nanoframes (NFs) were obtained with Pt/Cu ratios of 26/74 and 41/59, respectively. Abundant surface defects render them highly active catalysts due to the open frame structure of both sets of NFs. The spiny RD NFs showed superior specific activity toward the oxygen reduction reaction, 1.3 and 3 times to those of t...

Au-Pd nanocrystals are an intriguing system to study the integrated functions of localized surface plasmon resonance (LSPR) and heterogeneous catalysis. Gold is both durable and can harness incident light energy to enhance the catalytic activity of another metal, such as Pd, via the SPR effect in bimetallic nanocrystals. Despite the superior catalytic performance of icosahedral (IH) nanocrystals compared to alternate morphologies, the controlled synthesis of alloy and core-shell IH is still greatly challenged by the disparate reduction rates of metal precursors and lack of continuous epigrowth on multiply twinned boundaries of such surfaces. Herein, we demonstrate a one-step strategy for the controlled growth of monodisperse Au-Pd alloy and core-shell IH with terraced shells by turning an ionic switch between [Br(-)]/[Cl(-)] in the coreduction process. The core-shell IH nanocrystals contain AuPd alloy cores and ultrathin Pd shells (2 nm). They not only display more than double the activity of the commercial Pd catalysts in ethanol electrooxidation attributed to monatomic step terraces but also show SPR-enhanced conversion of 4-nitrophenol. This strategy holds promise toward the development of alternate bimetallic IH nanocrystals for electrochemical and plasmon-enhanced catalysis.

Geometric modification of Au nanostructures is typically achieved in multistep reactions, where synthesis parameters need to be well-controlled. In this work, we report a facile method using IrCl3 to refine morphologically diverse Au nanostructures and trigger their morphological transformations. The synthesis is accomplished at room temperature by an iterative process of galvanic dissolution and recursive growth. Seeds retrieved after the dissolution of different Au nanostructure archetypes served in the structural recovery and morphological transformation via rapid and slow regrowth, respectively. The rapid regrowth was accomplished by adding ascorbic acid (AA), while the slow regrowth occurred spontaneously. In the structural recovery, the nanostructures regrew back to their original morphologies. Improvements in the shape quality and size distributions were observed for the rapid regrowth case. In the spontaneous slow regrowth transformation, the resulting nanostructures were encased by {111} facets, ...

The creation of hierarchical porosity in metal-organic frameworks (MOFs) could benefit various applications of MOFs such as gas storage and separation. Having single-crystalline microcrystals instead of poly-crystalline composites is critical for these potential applications of MOFs with hierarchical porosity. We developed a room temperature synthetic method to generate uniform hollow and mesoporous zeolitic imidazolate framework-8 (ZIF-8) microcrystals with a single-crystalline structure via overgrowing a ZIF-8 shell in methanol solution on a ZIF-8 core with water adsorbed in the pores. The cavities formed as a result of the different solvent micro-environment. This double-solvent mediated overgrowth method could be applied to prepare other MOFs with hierarchical porosity.

Developing syntheses of more sophisticated nanostructures comprising late transition metals broadens the tools to rationally design suitable heterogeneous catalysts for chemical transformations. Herein, we report a synthesis of Pd-Rh nanoboxes by controlling the migration of metals in a core-shell nanoparticle. The Pd-Rh nanobox structure is a grid-like arrangement of two distinct metal phases, and the surfaces of these boxes are {100} dominant Pd and Rh. The catalytic behaviors of the particles were examined in electrochemistry to investigate strain effects arising from this structure. It was found that the trends in activity of model fuel cell reactions cannot be explained solely by the surface composition. The lattice strain emerging from the nanoscale separation of metal phases at the surface also plays an important role.

We report highly facet-dependent electrical properties of Cu(2)O nanocubes and octahedra and significant enhancement of gold nanocrystal cores to the electrical conductivity of Au-Cu(2)O core-shell octahedra. Cu(2)O nanocubes and octahedra and Au-Cu(2)O core-shell cubes and octahedra were synthesized by following our reported facile procedures at room temperature. Two oxide-free tungsten probes attached to a nanomanipulator installed inside a scanning electron microscope made contacts to a single Cu(2)O nanocrystal for the I-V measurements. Pristine Cu(2)O octahedra bounded by {111} facets are 1100 times more conductive than pristine Cu(2)O cubes enclosed by {100} faces, which are barely conductive. Core-shell cubes are only slightly more conductive than pristine cubes. A 10,000-fold increase in conductivity over a cube has been recorded for an octahedron. Remarkably, core-shell octahedra are far more conductive than pristine octahedra. The same facet-dependent electrical behavior can still be observed on a single nanocrystal exposing both {111} and {100} facets. This new fundamental property may be observable in other semiconductor nanocrystals. We also have shown that both core-shell cubes and octahedra outperform pristine cubes and octahedra in the photodegradation of methyl orange. Efficient photoinduced charge separation is attributed to this enhanced photocatalytic activity. Interestingly, facet-selective etching occurred over the {100} corners of some octahedra and core-shell octahedra during photocatalysis. The successful preparation of Au-Cu(2)O core-shell heterostructures with precise shape control has offered opportunities to discover new and exciting physical and chemical properties of nanocrystals.

Summary The ability to prepare inorganic nanocrystals with well-defined morphologies and sharp faces should facilitate the examination of their facet-dependent surface, catalytic, electrical, and other properties. In this review we cover different synthetic methods for the growth of Cu 2 O nanocrystals with morphological control. Cu 2 O nanocrystals with cubic, cuboctahedral, truncated octahedral, octahedral, and multipod structures have been prepared mainly by wet chemical, electrodeposition, and solvothermal synthesis methods. Methods used for the formation of hollow Cu 2 O nanocubes, octahedra, and truncated rhombic dodecahedra are also presented. Morphology of Cu 2 O nanocrystals can be expanded with the use of gold nanocrystal cores to guide the overgrowth of Cu 2 O shells. Surface properties of Cu 2 O nano- and microcrystals with sharp faces have been examined in a few studies. The {1 1 1} faces were found to interact well with negatively charged molecules, while the {1 0 0} faces are less sensitive to molecular charges. Preferential adsorption of sodium dodecyl sulfate molecules on the {1 1 1} faces of Cu 2 O crystals has been demonstrated via plane-selective deposition of gold nanoparticles on only the {1 0 0} faces. It is expected that the development of improved synthetic methods for Cu 2 O nanocrystals and more knowledge of their facet-dependent properties should lead to their applications in photoactivated energy conversion and catalysis.

We report the growth of core−shell Ga−GaN nanostructures by simple refluxing of a mixture of GaCl3 and lithium bis(trimethylsilyl)amide (LiHMDS) in trioctylamine at 380 °C for 24 h under nitrogen flow. The resulting spherical Ga−GaN nanostructures had diameters of ∼550 nm. By immersing the nanostructures in aqua regia, the gallium cores could be removed, and hollow GaN spheres with thicknesses of 15−25 nm were produced. The shells consisted of connected GaN nanocrystals of both cubic and hexagonal phases. Infrared spectroscopy confirmed the presence of silica or silicate in the GaN shells. The silicon source likely comes from the pyrolysis of LiHMDS. The growth process was studied by examining the intermediate products formed. Gallium metal cores appeared below 380 °C, followed by the slow formation of GaN nanocrystals on the core surfaces. The slow growth of the GaN shells is related to the gradual supply of the nitrogen source from the thermal decomposition of LiHMDS. Thinner shells with a thickness of ...

Here we report the hydrothermal synthesis of octahedral gold nanocrystals from an aqueous solution of HAuCl4, trisodium citrate, and cetyltrimethylammonium bromide (CTAB) surfactant. By heating the mixture at 110 °C for 6, 12, 24, 48, and 72 h, gold octahedra with approximate average sizes of 30, 60, 90, 120, and 150 nm can be obtained. The percent yield of octahedral nanocrystals is more than 90% for all the samples. Products formed at shorter reaction times were also examined. Structural characterization confirmed that the octahedra are bounded by entirely {111} faces. As particle size increases, the surface plasmon resonance (SPR) absorption band red-shifts from 543 to 635 nm. These monodisperse gold octahedra can spontaneously self-assemble into long-range ordered packing structures upon water evaporation. Three types of self-assembled structures with faces, edges, or corners of the octahedra contacting the substrates have been identified. Particle size can affect the type of packing structure they ad...

We report the high yield growth of monodispersed Cu 2 O nanocubes with approximate average sizes of 40, 65, 100, 230, and 420 nm using a seed-mediated synthesis approach in aqueous solution. The nanocubes are formed in 2 hours at room temperature. The standard deviation of the nanocube sizes in each sample is below 10 %. Structural analysis revealed that these nanocubes have six {100} faces, and possess truncated {110} edges and {111} corners. The combination of sodium dodecyl sulfate (SDS) and CuSO 4 was found to be critical to the formation of structurally well-defined Cu 2 O nanocubes. The nanocubes presumably were formed through the controlled aggregation of Cu 2 O seed particles and then surface reconstruction under the influence of SDS capping surfactant and sulfate ions to yield this truncated cubic structure. Optical characterization showed that nanocubes smaller than 100 nm absorb at -490 nm, while nanocubes larger than 200 nm display an absorption band at 515-525 nm. Additional absorption feature was observed in the red and near-infrared regions for the larger Cu 2 O nanocubes due to the light scattering effect. The investigation of the application of these nanocubes for the photodegradation of rhodamine B revealed the {111} crystal surfaces as the active surfaces responsible for the photocatalytic activity of Cu 2 O nanostructures. This simple and rapid synthesis of monodispersed Cu 2 O nanocubes should allow further examination of their various properties as a function of nanocrystal sizes.

We have developed a general synthetic route to encapsulate small molecules in monodisperse zeolitic imid-azolate framework-8 (ZIF-8) nanospheres for drug delivery. Electron microscopy, powder X-ray diffraction, and elemental analysis show that the small-molecule-encapsulated ZIF-8 nanospheres are uniform 70 nm particles with single-crystalline structure. Several small molecules, including fluorescein and the anticancer drug camptothecin, were encapsulated inside of the ZIF-8 framework. Evaluation of fluorescein-encapsulated ZIF-8 nanospheres in the MCF-7 breast cancer cell line demonstrated cell internalization and minimal cytotoxicity. The 70 nm particle size facilitates cellular uptake, and the pH-responsive dissociation of the ZIF-8 framework likely results in endosomal release of the small-molecule cargo, thereby rendering the ZIF-8 scaffold an ideal drug delivery vehicle. To confirm this, we demonstrate that camptothecin encapsulated ZIF-8 particles show enhanced cell death, indicative of internalization and intracellular release of the drug. To demonstrate the versatility of this ZIF-8 system, iron oxide nanoparticles were also encapsulated into the ZIF-8 nanospheres, thereby endowing magnetic features to these nanospheres.

A general synthetic strategy for yolk-shell nanocrystal@ZIF-8 nanostructures has been developed. The yolk-shell nanostructures possess the functions of nanoparticle cores, microporous shells, and a cavity in between, which offer great potential in heterogeneous catalysis. The synthetic strategy involved first coating the nanocrystal cores with a layer of Cu(2)O as the sacrificial template and then a layer of polycrystalline ZIF-8. The clean Cu(2)O surface assists in the formation of the ZIF-8 coating layer and is etched off spontaneously and simultaneously during this process. The yolk-shell nanostructures were characterized by transmission electron microscopy, scanning electron microscopy, X-ray diffraction, and nitrogen adsorption. To study the catalytic behavior, hydrogenations of ethylene, cyclohexene, and cyclooctene as model reactions were carried out over the Pd@ZIF-8 catalysts. The microporous ZIF-8 shell provides excellent molecular-size selectivity. The results show high activity for the ethylene and cyclohexene hydrogenations but not in the cyclooctene hydrogenation. Different activation energies for cyclohexene hydrogenation were obtained for nanostructures with and without the cavity in between the core and the shell. This demonstrates the importance of controlling the cavity because of its influence on the catalysis.

We report a simple approach for the fabrication of cuprous oxide (Cu 2 O) nanocages and nanoframes. An aqueous solution of CuCl 2 , sodium dodecyl sulfate (SDS) surfactant, NH 2 OH·HCl reductant, HCl, and NaOH was prepared with reagents introduced in the order listed. Rapid seed particle aggregation and surface reconstruction of the intermediate structures resulted in the growth of type I nanoframes with just the {110} skeleton faces and empty {100} faces 45 minutes after mixing the reagents. Continued crystal growth for additional 75 min produced the nanocages with filled {100} faces. The nanocages have diameters of 350–400 nm, and their walls are thicker than those of the nanoframes. Selective acidic etching over the {110} faces of the nanocages by HCl via the addition of ethanol and then sonication of the solution led to the formation of type II nanoframes with elliptical pores on the {110} faces. The morphologies of these nanoframes have been carefully examined by electron microscopy. Without adding ethanol, random etching of the nanocages can occur at a slow rate. These composite materials should display interesting properties and functions.

We report a simple approach for the fabrication of cuprous oxide (Cu 2O) nanocages and nanoframes possessing an unusual truncated rhombic dodecahedral structure. An aqueous solution containing CuCl 2, sodium dodecyl sulfate (SDS) surfactant, NH 2OH.HCl reductant, HCl, and NaOH was prepared, with the reagents introduced in the order listed. Rapid seed-particle aggregation and surface reconstruction of the intermediate structure resulted in the growth of type-I nanoframes, which have only {110} skeleton faces and empty {100} faces, 45 min after mixing the reagents. Continued crystal growth for additional 75 min produced nanocages with filled {100} faces. The nanocages have diameters of 350-400 nm, and their walls are thicker than those of the nanoframes. Selective acidic etching over the {110} faces of the nanocages by HCl via the addition of ethanol followed by sonication of the solution led to the formation of type-II nanoframes, which have elliptical pores on the {110} faces. The morphologies of these nanoframes were carefully examined by electron microscopy. Without addition of ethanol, random etching of the nanocages can occur at a slow rate. Octahedral gold nanocrystals and high-aspect-ratio gold nanorods were successfully encapsulated in the interiors of these Cu 2O nanocages by adding the gold nanostructures into the reaction solution. The formation process for such core-cage composite structures was studied. These composite materials should display interesting properties and functions.

The synthesis of gold nanoplates was carried out in an aqueous solution by thermal reduction of HAuCl(4) with trisodium citrate in the presence of cetyltrimethylammonium bromide (CTAB) surfactant in just 5-40 min. The sizes of the gold nanoplates can be varied from as small as tens of nanometers in width, to several hundreds of nanometers, and even a few microns in width by changing the reagent concentrations, solution temperature, and the reaction time. A [CTAB]/[HAuCl(4)] ratio of 6 in the reaction solution was found to be favorable for the formation of gold nanoplates. The nanoplates possess well-defined shapes with sharp edges. The small nanoplates exhibit mainly a triangular shape, while larger nanoplates show a mixture of triangular, hexagonal, truncated triangular, and other symmetrical structures. The nanoplates are composed of essentially (111) lattice planes, as revealed by both XRD and TEM results. Nanoplates with widths from several hundreds of nanometers to a few microns absorb light strongly in the near-infrared region. The growth mechanism of these nanoplates was investigated. The ability to synthesize gold nanoplates with these different size ranges in large scale in aqueous solution using simple CTAB capping surfactant should allow more diverse applications of gold nanoplates.

We have explored the effect of gold nanoparticle (Au NP)-induced surface plasmons on the performance of organic photovoltaic devices (OPVs). The power conversion efficiency of these OPVs was improved after blending the Au NPs into the anodic buffer layer. The addition of Au NPs increased the rate of exciton generation and the probability of exciton dissociation, thereby enhancing the short-circuit current density and the fill factor. We attribute the improvement in device performance to the local enhancement in the electromagnetic field originating from the excitation of the localized surface plasmon resonance.