Photoinduced charge generation of nanostructured carbon derived from human hair biowaste for performance enhancement in polyvinylidene fluoride based triboelectric nanogenerator.

Carbon nanostructures derived from human hair biowaste are incorporated into polyvinylidene fluoride (PVDF) polymer to enhance the energy conversion performance of a triboelectric nanogenerator (TENG). The PVDF filled with activated carbon nanomaterial from human hair (AC-HH) exhibits improved surface charge density and photoinduced charge generation. These remarkable properties are attributed to the presence of graphene-like nanostructures in AC-HH, contributing to the augmented performance of PVDF@AC-HH TENG. The correlation of surface morphologies, surface charge potential, charge capacitance properties, and TENG electrical output of the PVDF composites at various AC-HH loading is studied and discussed. Applications of the PVDF@AC-HH TENG as a power source for micro/nanoelectronics and a movement sensor for detecting finger gestures are also demonstrated. The photoresponse property of the fabricated TENG is demonstrated and analyzed in-depth. The analysis indicates that the photoinduced charge carriers originate from the conductive reduced graphene oxide (rGO), contributing to the enhanced surface charge density of the PVDF composite film. This research introduces a novel approach to enhancing TENG performance through the utilization of carbon nanostructures derived from human biowaste. The findings of this work are crucial for the development of innovative energy-harvesting technology with multifunctionality, including power generation, motion detection, and photoresponse capabilities.

Multiscale Interface Engineering of Sulfur-Doped TiO2 Anode for Ultrafast and Robust Sodium Storage.

Sodium-ion batteries (SIBs) are a promising electrochemical energy storage system; however, their practical application is hindered by the sluggish kinetics and interfacial instability of anode-active materials. Here, to circumvent these issues, we proposed the multiscale interface engineering of S-doped TiO2 electrodes with minor sulfur/carbon inlaying (S/C@sTiO2), where the electrode-electrolyte interface (SEI) and electrode-current collector interface (ECI) are tuned to improve the Na-storage performance. It is found that the S dopant greatly promotes the Na+ diffusion kinetics. Moreover, the ether electrolyte generates much less NaF in the cycled electrode, but relatively richer NaF in the SEI in comparison to fluoroethylene carbonate-contained ester electrolyte, leading to a thin (9 nm), stable, and kinetically favorable SEI film. More importantly, the minor sodium polysulfide intermediates chemically interact with the Cu current collector to form a Cu2S interface between the electrode and the Cu foil. The conductive tree root-like Cu2S ECI serves not only as active sites to boost the specific capacity but also as a 3D "second current collector" to reinforce the electrode and improve the Na+ reaction kinetics. The synergy of S-doping and optimized SEI and ECI realizes large specific capacity (464.4 mAh g-1 at 0.1 A g-1), ultrahigh rate capability (305.8 mAh g-1 at 50 A g-1), and ultrastable cycling performance (91.5% capacity retention after 3000 cycles at 5 A g-1). To the best of our knowledge, the overall SIB performances of S/C@sTiO2 are the best among all of the TiO2-based electrodes.

Microwave-Assisted Synthesis as a Promising Tool for the Preparation of Materials Containing Defective Carbon Nanostructures: Implications on Properties and Applications.

In this review, we focus on a small section of the literature that deals with the materials containing pristine defective carbon nanostructures (CNs) and those incorporated into the larger systems containing carbon atoms, heteroatoms, and inorganic components.. Briefly, we discuss only those topics that focus on structural defects related to introducing perturbation into the surface topology of the ideal lattice structure. The disorder in the crystal structure may vary in character, size, and location, which significantly modifies the physical and chemical properties of CNs or their hybrid combination. We focus mainly on the method using microwave (MW) irradiation, which is a powerful tool for synthesizing and modifying carbon-based solid materials due to its simplicity, the possibility of conducting the reaction in solvents and solid phases, and the presence of components of different chemical natures. Herein, we will emphasize the advantages of synthesis using MW-assisted heating and indicate the influence of the structure of the obtained materials on their physical and chemical properties. It is the first review paper that comprehensively summarizes research in the context of using MW-assisted heating to modify the structure of CNs, paying attention to its remarkable universality and simplicity. In the final part, we emphasize the role of MW-assisted heating in creating defects in CNs and the implications in designing their properties and applications. The presented review is a valuable source summarizing the achievements of scientists in this area of research.

Smart Quantum Tunneling Composite Sensors to Monitor FKM and FFKM Seals.

Operators of industrial machinery relentlessly pursue improving safety, increasing productivity, and minimizing unplanned downtime. Elastomer seals are ubiquitous components of this machinery. In general, static seals are designed to be compressed at a fixed level of compression, taking gland geometry, loading condition, temperature range of operation, fluid media exposure, and other factors into account to ensure the safe operation of equipment. Over time, seals experience compression set, chemical-induced swelling, erosion, and other phenomena which can compromise the compressive force generated by the seal and cause leaking. This is particularly important in critical applications, where high pressure, high temperature, and aggressive media are present, and fluorinated elastomers are common materials for seals. Further, changes in operating conditions at manufacturing plants, either intentional or through regular process variation, create unknown operating conditions for seals. This unknown and variable application environment makes seal performance hard to predict. Therefore, machinery utilizing seals is, at best, serviced preventatively at certain intervals, where seals are removed, and the remaining useful life of the seal is unknown. This leads to unnecessary machinery downtime and increases consumable costs for manufacturers. In the worst case, the seal is run to failure, creating machinery and plant safety concerns. Both scenarios are undesirable for manufacturers using industrial machinery. This paper reports on the development of "smart" intrinsic self-sensing seals, which enable performance monitoring of the compression behavior of seals while in use. In addition, this paper examines quantum tunneling elastomeric composites (QTC) to demonstrate a method of component performance monitoring by modifying the underlying elastomeric material itself. This paper studies QTC sensor-based fluorinated (FKM) and per-fluorinated (FFKM) compositions, which are modified to incorporate varying levels of carbon nanostructure (CNS) material. The resulting seal's resistive properties are shown to be a function of the level of compression, the first time this phenomenon has been demonstrated in high-performing FKM and FFKM seal materials.

An immobilization of aminopropyl trimethoxysilane-phenanthrene carbaldehyde on graphene oxide for toluene extraction and separation in water samples.

A new functionalized Nano graphene with aminopropyl trimethoxysilane-phenanthrene-4-carbaldehyde (NGO@APTMS-PNTCA) as a novel adsorbent was used to extract toluene from water samples by the ultrasound-assisted dispersive solid-phase microextraction procedure (USA-D-SPME). So, 50 mg of NGO@APTMS-PNTCA adsorbent was added to water samples and sonicated for 20 min. After toluene extraction, the NGO@APTMS-PNTCA adsorbent separated from the liquid phase with a Whatman membrane filter (200 nm). Then, the toluene was back-extracted from the adsorbent by 2.0 mL of the acetone/ethanol (1:1, eluent) at 25 °C. Due to the physical properties and structure of toluene, fluorobenzene was used as an internal standard. Finally, the toluene values were measured by a gas chromatography-flame ionization detector (GC-FID). In optimized conditions, the limit of detection (LOD), the working range (WR), and the enrichment factor (EF) were obtained at 2.5 µg L-1, 0.01-1.2 mg L-1, and 9.63, respectively (MRSD% = 3.38). Also, the limit of quantification (LOQ) 10 µg L-1 and extraction recovery of more than 95% was efficiently achieved for toluene. Standard additions of toluene to blank solutions had high recoveries between 95.2% and 104.5% with a relative standard deviation (RSD%) of 0.27-5.2. The absorption capacities of NGO and NGO@APTMS-PNTCA adsorbents for toluene extraction were obtained at 32.8 mg g-1 and 154.9 mg g-1, respectively. The USA-D-SPME method was validated by spiking the standard concentrations of toluene. The proposed method demonstrated relevant and suitable statistical results with high accuracy and precision for toluene extraction by a novel adsorbent synthesis.

Flow Characteristics of Heat and Mass for Nanofluid under Different Operating Temperatures over Wedge and Plate.

BACKGROUND AND PURPOSE: Nanofluids are a new class of heat transfer fluids that are used for different heat transfer applications. The transport characteristics of these fluids not only depend upon flow conditions but also strongly depend on operating temperature. In respect of these facts, the properties of these fluids are modified to measure the temperature effects and used in the governing equations to see the heat and mass flow behavior. Design of Model: Consider the nanofluids which are synthesized by dispersing metallic oxides (SiO2, Al2O3), carbon nanostructures (PEG-TGr, PEG-GnP), and nanoparticles in deionized water (DIW), with (0.025-0.1%) particle concentration over (30-50 °C) temperature range. The thermophysical properties of these fluids are modeled theoretically with the help of experimental data as a function of a temperature and volume fraction. These models are further used in transport equations for fluid flow over both wedge and plate. To get the solution, the equations are simplified in the shape of ordinary differential equations by applying the boundary layer and similarity transformations and then solved by the RK method. RESULTS: The solution of the governing equation is found in the form of velocity and temperature expressions for both geometries and displayed graphically for discussion. Moreover, momentum and thermal boundary layer thicknesses, displacement, momentum thicknesses, the coefficient of skin friction, and Nusselt number are calculated numerically in tabular form. FINDING: The maximum reduction and enhancement in velocity and temperature profile is found in the case of flow over the plate as compared to the wedge. The boundary layer parameters are increased in the case of flow over the plate than the wedge.

A Hybrid Nanocomposite Based on the T-Shaped Carbon Nanotubes and Fullerenes as a Prospect Material for Triple-Value Memory Cells.

Relying on empirical and quantum chemical methods, a hybrid nanocomposite based on the T-shaped carbon nanotube (CNT) junction and internal fullerene C60 is proposed as a potential triple-value memory cell. The T-shaped CNT provides three potential wells where the internal fullerene can be located. The fullerene can move between these wells under the periodic external electric field, whose strength and frequency parameters are identified. The process of the fullerene's motion control corresponds to the memory cell write operation. The read operation can be realized by determining the fullerene's position inside the CNT by estimation of the charge transfer between a fullerene and the CNT's walls. Calculations took into account such external factors as temperature and air environment.

Microporous N-Doped Carbon Obtained from Salt Melt Pyrolysis of Chitosan toward Supercapacitor and Oxygen Reduction Catalysts.

The direct carbonization of low-cost and abundant chitosan biopolymer in the presence of salt eutectics leads to highly microporous, N-doped nanostructures. The microporous structure is easily manufactured using eutectic mixture (ZnCl2-KCl) and chitosan. Potassium ions here can act as an intercalating agent, leading to the formation of lamellar carbon sheets, whereas zinc chloride generates significant porosity. Here, we present an efficient synthetic way for microporous carbon nanostructures production with a total nitrogen content of 8.7%. Preliminary studies were performed to show the possibility of the use of such material as a catalyst for supercapacitor and ORR. The textural properties enhanced capacitance, which stem from improved accessibility of previously blocked or inactive pores in the carbon structure, leading to the conclusion that porogen salts and molten salt strategies produce materials with tailor-made morphologies. The synergistic effect of the eutectic salt is seen in controlled porous structures and pore size, and the micropores boosting adsorption ability.

Bottom-Up Evolution of Diamond-Graphite Hybrid Two-Dimensional Nanostructure: Underlying Picture and Electrochemical Activity.

The diamond-graphite hybrid thin film with low-dimensional nanostructure (e.g., nitrogen-included ultrananocrystalline diamond (N-UNCD) or the alike), has been employed in many impactful breakthrough applications. However, the detailed picture behind the bottom-up evolution of such intriguing carbon nanostructure is far from clarified yet. Here, the authors clarify it, through the concerted efforts of microscopic, physical, and electrochemical analyses for a series of samples synthesized by hot-filament chemical vapor deposition using methane-hydrogen precursor gas, based on the hydrogen-dependent surface reconstruction of nanodiamond and on the substrate-temperature-dependent variation of the growth species (atomic hydrogen and methyl radical) concentration near substrate. The clarified picture provides insights for a drastic enhancement in the electrochemical activities of the hybrid thin film, concerning the detection of important biomolecule, that is, ascorbic acid, uric acid, and dopamine: their limits of detections are 490, 35, and 25 nm, respectively, which are among the best of the all-carbon thin film electrodes in the literature. This work also enables a simple and effective way of strongly enhancing AA detection.

Linking the Defective Structure of Boron-Doped Carbon Nano-Onions with Their Catalytic Properties: Experimental and Theoretical Studies.

Defects are widely present in nanomaterials, and they are recognized as the active sites that tune surface properties in the local region for catalysis. Recently, the theory linking defect structures and catalytic properties of nanocatalysts has been most commonly described. In this study, we prepared boron-doped carbon nano-onions (B-CNOs) by applying an annealing treatment of ultradispersed nanodiamond particles and amorphous boron. These experimental conditions guarantee doping of CNOs with boron atoms in the entire carbon nanostructure, thereby ensuring structural homogeneity. In our research, we discuss the correlations between defective structures of B-CNOs with their catalytic properties toward SO2 and tert-butanol dehydration. We show that there is a close relationship between the catalytic properties of the B-CNOs and the experimental conditions for their formation. It is not only the mass of the substrates used for the formation of B-CNOs that is crucial, that is, the mass ratio of NDs to amorphous B, but also the process, including temperature and gas atmosphere. As it was expected, all B-CNOs demonstrated significant catalytic activity in HSO3- oxidation. However, the subsequent annealing in an air atmosphere diminished their catalytic activity. Unfortunately, no direct relationship between the catalytic activity and the presence of heteroatoms on the B-CNO surface was observed. There was a linear dependence between catalytic activity and Raman reactivity factors for each of the B-CNO materials. In contrast to SO2 oxidation, the B-CNO-a samples showed higher catalytic activity in tert-butanol dehydration due to the presence of Brønsted and Lewis acid sites. The occurence of three types of boron-Lewis sites differing in electron donor properties was confirmed using quantitative infrared spectroscopic measurements of pyridine adsorption.

A low-voltage electro-membrane extraction for quantification of imatinib and sunitinib in biological fluids.

Aim: Hollow-fiber-based supported liquid membrane was modified utilizing nanostructures such as graphite, graphene oxide or nitrogen-doped graphene oxide, for electro-membrane extraction (EME) of imatinib and sunitinib from biological fluids. By applying these conductive nanostructures, a low-voltage EME device (6.0 V) was fabricated. Materials & methods: A response surface methodology through central composite design was used to evaluate and optimize effects of various essential factors that influence on normalized recovery. Results: Optimal extraction conditions were set as, 1-octanol with 0.01 % (w/v) graphene oxide functioning as the supported liquid membrane, an extraction time of 17.0 min, pH of the acceptor and the donor phase of 2.8 and 7.9, respectively. Conclusion: The method was successfully applied to quantify imatinib and sunitinib in biological fluids.

Advanced Carbon-Nickel Sulfide Hybrid Nanostructures: Extending the Limits of Battery-Type Electrodes for Redox-Based Supercapacitor Applications.

Transition-metal sulfides combined with conductive carbon nanostructures are considered promising electrode materials for redox-based supercapacitors due to their high specific capacity. However, the low rate capability of these electrodes, still considered "battery-type" electrodes, presents an obstacle for general use. In this work, we demonstrate a successful and fast fabrication process of metal sulfide-carbon nanostructures ideal for charge-storage electrodes with ultra-high capacity and outstanding rate capability. The novel hybrid binder-free electrode material consists of a vertically aligned carbon nanotube (VCN), terminated by a nanosized single-crystal metallic Ni grain; Ni is covered by a nickel nitride (Ni3N) interlayer and topped by trinickel disulfide (Ni3S2, heazlewoodite). Thus, the electrode is formed by a Ni3S2/Ni3N/Ni@NVCN architecture with a unique broccoli-like morphology. Electrochemical measurements show that these hybrid binder-free electrodes exhibit one of the best electrochemical performances compared to the other reported Ni3S2-based electrodes, evidencing an ultra-high specific capacity (856.3 C g-1 at 3 A g-1), outstanding rate capability (77.2% retention at 13 A g-1), and excellent cycling stability (83% retention after 4000 cycles at 13 A g-1). The remarkable electrochemical performance of the binder-free Ni3S2/Ni3N/Ni@NVCN electrodes is a significant step forward, improving rate capability and capacity for redox-based supercapacitor applications.

Structure Formation and Coupling Reactions of Hexaphenylbenzene and Its Brominated Analog.

The on-surface coupling of the prototypical precursor molecule for graphene nanoribbon synthesis, 6,11-dibromo-1,2,3,4-tetraphenyltriphenylene (C42 Br2 H26 , TPTP), and its non-brominated analog hexaphenylbenzene (C42 H30 , HPB), was investigated on coinage metal substrates as a function of thermal treatment. For HPB, which forms non-covalent 2D monolayers at room temperature, a thermally induced transition of the monolayer's structure could be achieved by moderate annealing, which is likely driven by π-bond formation. It is found that the dibrominated carbon positions of TPTP do not guide the coupling if the growth occurs on a substrate at temperatures that are sufficient to initiate C-H bond activation. Instead, similar one-dimensional molecular structures are obtained for both types of precursors, HPB and TPTP.

Conventional Nanosized Drug Delivery Systems for Cancer Applications.

Clinical responses and tolerability of conventional nanocarriers (NCs) are sometimes different from those expected in anticancer therapy. Thus, new smart drug delivery systems (DDSs) with stimuli-responsive properties and novel materials have been developed. Several clinical trials demonstrated that these DDSs have better clinical therapeutic efficacy in the treatment of many cancers than free drugs. Composition of DDSs and their surface properties increase the specific targeting of therapeutics versus cancer cells, without affecting healthy tissues, and thus limiting their toxicity versus unspecific tissues. Herein, an extensive revision of literature on NCs used as DDSs for cancer applications has been performed using the available bibliographic databases.

Evaluation of the Covalent Functionalization of Carbon Nano-Onions with Pyrene Moieties for Supercapacitor Applications.

Herein, we report the surface functionalization of carbon nano-onions (CNOs) through an amidation reaction that occurs between the oxidized CNOs and 4-(pyren-4-yl)butanehydrazide. Raman and Fourier transform infrared spectroscopy methods were used to confirm the covalent functionalization. The percentage or number of groups in the outer shell was estimated with thermal gravimetric analysis. Finally, the potential applications of the functionalized CNOs as electrode materials in supercapacitors were evaluated by cyclic voltammetry and electrochemical impedance spectroscopy. Functionalization increased the specific capacitance by approximately 138% in comparison to that of the pristine CNOs, while acid-mediated oxidation reduced the specific capacitance of the nanomaterial by 24%.

Synthesis of Three-Dimensional Carbon Nanostructure/Copper Nanowire for Additive Interface Layer of Ionic Polymer Metal Composite.

Additive interface materials for improved ionic polymer metal composite (IPMC) actuator performance are being investigated. In this study, three-dimensional carbon nanostructure/copper nanowire (3DC Cu-NW) with a novel structure was synthesized via low-pressure chemical vapor deposition. An IPMC actuator with a 3DC Cu-NW interface layer was fabricated, which exhibited improved actuation performance, long-term stability, and electrochemical properties. The proposed 3DC consists of carbon nanotubes (CNTs) and graphene, grown using an Fe catalyst and CH4 gas, respectively. We optimized the growth conditions (Fe catalyst: 12.5 mg/L, CH4: 20 sccm) to achieve a 3DC with an appropriate thickness and a large specific surface area. The 3DC Cu-NW benefited from a Cu oxidation prevention property and a large specific surface area. The electrochemical properties and actuation performance of the IPMC actuator improved with an increased 3DC Cu-NW concentration. An IPMC actuator with a 0.6 wt% 3DC Cu-NW interface layer exhibited 1.3- and 5.6-fold electrochemical property and actuation performance improvement, respectively, over an IPMC actuator with no 3DC Cu-NW interface layer. These results show that the proposed 3DC Cu-NW has potential as an IPMC actuator interface material, and that 3DC Cu-NW synthesis and application technology can be applied to future research on sensor, actuator, and flexible devices.

Electrochemical thrombin aptasensor based on using magnetic nanoparticles and porous carbon prepared by carbonization of a zinc(II)-2-methylimidazole metal-organic framework.

A homogeneous electrochemical aptasensor was obtained by modifying a glassy carbon electrode (GCE) with a porous carbon nanomaterial (Z-1000, about 70 nm, deteced by transmission electron microscopic) that was obtained by carbonization of a zinc(II)-2-methylimidazole metal-organic framework. Z-1000 possesses a large specific surface and outstanding electrochemical properties. A thrombin-binding aptamer (CP) was immobilized on the magnetite nanoparticles MNPs by the condensation reaction and further combined with reporter probe (RP) that is functionalized with electroactive methylene blue (MB). In the presence of thrombin, the CP was specifically recognized with it to form the CP/MNP/Thb complex, and the RP was dissociated from MNPs. The released RP was captured by the modified GCE through π-stacking interaction between nucleobases and carbon nanostructure. The electrical signal generated by MB can be monitored by differential pulse voltammetry (DPV). Under the optimized conditions, the DPV peak current at around -0.28 V (vs. SCE) increases with thrombin concentration. The sensor has a detection limit of 0.8 fM of thrombin and a linear range that extends from 10 fM to 100 nM. It was successfully applied to the analysis of spiked serum. The recoveries are 98.1-99.4% and RSDs are 3.9%-4.0%. Conceivably, this aptasensor scheme can be easily extended to other proteins and gives inspiration to manufacture sensitive aptasensor. Graphical abstract A homogeneous electrochemical aptasensor is obtained by modifying a glassy carbon electrode with the MOF-derived porous carbon. The sensor has a detection limit of 0.8 fM and a wide linear range from 10 fM to 100 nM for thrombin detection.

Repression of melanoma tumor in vitro and in vivo by photothermal effect of carbon xerogel nanoparticles.

Nanosized carbonaceous materials are favorable in biomedicine applications including photothermal therapy (PTT) of cancer. Since conventional strategies of cancer treatment have not responded to this serious disease, development of efficient alternative and promising strategies is highly desirable. In this study, carbon xerogel nanoparticles (CX-NPs) were synthesized as a novel photothermal nanomaterial and activated upon laser light of 808-nm wavelength for cancer phototherapy application. The synthesized CX-NPs had a spherical shape with a size of about 16 nm that showed nice photothermal conversion ability. Upon light irradiation with a power density of 1.0 W cm-2 for 15 min, a temperature increment occurred. A concentration-dependent cytotoxicity was also obtained for CX-NPs toward the C540 (B16/F10) cell line upon light irradiation, while CX-NPs presented biocompatibility in the mice model in dark. Photothermal property of CX-NPs efficiently led to reduction in the cell viability. A low-dose of CX-NPs was also applied in PTT of a melanoma tumor-bearing animal model. Based on tumor histopathological evaluations and volume change measurements in mice, a very good control of tumor situations after PTT by CX-NPs was attained. The findings revealed that CX-NPs is a good and novel photoabsorber for PTT of cancer.

In vitro and in vivo tumor annihilation by near-infrared photothermal effect of a NiFe2O4/C nanocomposite.

Nanothechnology-mediated photothermal therapy (PTT) is emerging as one of the inspiring alternative modality of cancer therapy that applies near-infrared radiation. High favorability of this approach is due to its minimum invasiveness, safety of non-targeted area, quick recovery, and capable simultaneous imaging. In this approach, photoabsorbing nanomaterials convert energy of infrared light to vibrational motion and generate heat. In the present study, a nanocomposite comprised nickel ferrite and carbon (NiFe2O4/C) was synthesized, characterized and introduced as a novel photoabsorbing agent in cancer phototherapy. NiFe2O4/C was characterized by field emission scanning electron microscopy, Fourier-transform infrared spectroscopy, and X-ray diffraction patterns. A diode laser of 808 nm with a power density of 1.0 W cm-2 was selected as the light source to evaluate the photothermal property of NiFe2O4/C toward cancer repression in C540 (B16/F10) cell line and melanoma bearing tumor model in male balb/c mice. Temperature enhancement ability of NiFe2O4/C confirmed its photoabsorbing property. While NiFe2O4/C had a concentration dependent cytotoxicity on C540 (B16/F10) cell line, PTT of NiFe2O4/C activated by laser irradiation showed its destroying effect on the C540 (B16/F10) cell line. On the other hand, histological analyses and tumor volume changes were performed for the in vivo PTT of NiFe2O4/C upon intratumoral injection. The results showed that after 24 h, PTT of the nanocomposite cured the tumor properly, whereas NiFe2O4/C injection or laser exposure alone had no treatment effect. Also, 5-day post-treating the melanoma bearing tumor model indicated that the level of necrosis significantly increased during this time in the PTT treated mouse. Therefore, PTT using NiFe2O4/C is proposed as a promising procedure for the melanoma cancer therapy.

Metal-Organic-Framework-Derived Carbon Nanostructure Augmented Sonodynamic Cancer Therapy.

Sonodynamic therapy (SDT) can overcome the critical issue of depth-penetration barrier of photo-triggered therapeutic modalities. However, the discovery of sonosensitizers with high sonosensitization efficacy and good stability is still a significant challenge. In this study, the great potential of a metal-organic-framework (MOF)-derived carbon nanostructure that contains porphyrin-like metal centers (PMCS) to act as an excellent sonosensitizer is identified. Excitingly, the superior sonosensitization effect of PMCS is believed to be closely linked to the porphyrin-like macrocycle in MOF-derived nanostructure in comparison to amorphous carbon nanospheres, due to their large highest occupied molecular orbital (HOMO)-lowest unoccupied molecular orbital (LUMO) gap for high reactive oxygen species (ROS) production. The nanoparticle-assisted cavitation process, including the visualized formation of the cavitation bubbles and microjets, is also first captured by high-speed camera. High ROS production in PMCS under ultrasound is validated by electron spin resonance and dye measurement, followed by cellular destruction and high tumor inhibition efficiency (85%). This knowledge is important from the perspective of understanding the structure-dependent SDT enhancement of a MOF-derived carbon nanostructure.