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Multimodal therapy requires effective drug carriers that can deliver multiple drugs to specific locations in a controlled manner. Here, the study presents a novel nanoplatform constructed using zeolitic imidazolate framework‐8 ( Z IF‐8), a nanoscale metal‐organic framework nucleated under the mediation of silk fibroin ( S F). The nanoplatform is modified with the newly discovered MCF‐7 breast tumor‐targeting peptide, AREYGTRFSLIGGYR ( AR peptide). Indocyanine green ( I CG) and doxorubicin ( D OX) are loaded onto the nanoplatform with high drug encapsulation efficiency (>95%). ICG enables the resultant nanoparticles (NPs), called AR‐ZS/ID‐P, to release reactive oxygen species for photodynamic therapy ( P DT) and heat for photothermal therapy ( P TT) under near‐infrared (NIR) irradiation, promoting NIR fluorescence and thermal imaging to guide DOX‐induced chemotherapy. Additionally, the controlled release of both ICG and DOX at acidic tumor conditions due to the dissolution of ZIF‐8 provides a drug‐targeting mechanism in addition to the AR peptide. When intravenously injected, AR‐ZS/ID‐P NPs specifically target breast tumors and exhibit higher anticancer efficacy than other groups through ICG‐enabled PDT and PTT and DOX‐derived chemotherapy, without inducing side effects. The results demonstrate that AR‐ZS/ID‐P NPs are a promising multimodal theranostic nanoplatform with maximal therapeutic efficacy and minimal side effects for targeted and controllable drug delivery.

Metal–organic framework–derived carbon nanostructures have generated significant interest in electrochemical capacitors and oxygen/hydrogen catalysis reactions. However, they appear to show considerably varied structural properties, and thus exhibit complex electrochemical–activity relationships. Herein, a series of carbon polyhedrons of different sizes, between 50 nm and µm, are synthesized from zeolitic imidazolate frameworks, ZIF‐8 (ZIF‐derived carbon polyhedrons, ZDCPs) and their activity is studied for capacitance and the oxygen reduction reaction (ORR). Interestingly, a well‐correlated performance relationship with respect to the particle size of ZDCPs is evidenced. Here, the identical structural features, such as specific surface area (SSA), microporosity, and its distribution, nitrogen doping, and graphitization are all strictly maintained in the ZDCPs, thus allowing identification of the effect of particle size on electrochemical performance. Supercapacitors show a capacity enhancement of 50 F g−1 when the ZDCPs size is reduced from micrometers to ≤200 nm. The carbonization further shows a considerable effect on rate capacitance—ZDCPs of increased particle size lead to drastically reduced charge transportability and thus inhibit their performance for both the charge storage and the ORR. Guidelines for the capacitance variation with respect to the particle size and SSA in such carbon nanostructures from literature are presented. Carbon‐based nanostructures are indispensable for supercapacitors, fuel cells, and batteries. Advancement in this area requires critical understanding of the form and function. Here, a well‐correlated relationship is demonstrated for the performance of supercapacitors and the oxygen reduction reaction with respect to particle size of metal–rganic frameworks–derived carbon. Surface area, pore‐size distribution, nitrogen doping, and graphitization are all maintained identical.

In article number 1901517, Srinivas Gadipelli and co‐workers present direct evidence of carbon nanoparticle size–dependent electrochemical activity for the supercapacitors and oxygen reduction reaction. For this, the carbon polyhedrons with size between few tens of nanometers to microns are designed from a zeolitic imidazolate framework (ZIF‐8), and all other parameters, such as surface area, microporosity, pore‐size distribution, nitrogen‐doping and graphitization are maintained identically.

Due to the high Brunauer–Emmett–Teller (BET) surface area of zeolitic imidazolate framework (ZIF)-8, a secondary crystallization method was used to prepare a particle electrode of γ-Al2O3@ZIF-8. According to the results from a field emission scanning electron microscope (SEM) and X-ray diffractometer (XRD), the particle electrode of γ-Al2O3 was successfully loaded with ZIF-8, and the BET surface area (1,433 m2/g) of ZIF-8 was over ten times that of γ-Al2O3. The key operation parameters of cell voltage, pH, initial RhB concentration and electrolyte concentration were all optimized. The observed rate constant (kobs) of the pseudo-first-order kinetic model for the electrocatalytic oxidation (ECO) system with the particle electrode of γ-Al2O3@ZIF-8 (15.2 × 10−2 min−1) was over five times higher than that of the system with the traditional particle electrode of γ-Al2O3 (2.6 × 10−2 min−1). The loading of ZIF-8 on the surface of γ-Al2O3 played an important role in improving electrocatalytic activity for the degradation of Rhodamine B (RhB), and the RhB removal efficiency of the three-dimensional (3D) electrocatalytic system with the particle electrode of γ-Al2O3@ZIF-8 was 93.5% in 15 min, compared with 27.5% in 15 min for the particle electrode of γ-Al2O3. The RhB removal efficiency was kept over 85% after five cycles of reuse for the 3D electrocatalytic system with the particle electrode of γ-Al2O3@ZIF-8.