High Defect Concentration Research Articles

Die Auswirkungen eines institutionellen Kreuzbandregisters auf Klinik und Wissenschaft: Erfahrungen aus Luxemburg

Breaking the capacity barrier in intercalation-type anode materials for lithium-ion batteries while preserving other essential electrochemical properties remains a significant challenge. Here, using perovskite SrVO3 as a model, we demonstrate the feasibility of employing defect engineering to provide extra active sites for electrochemical reactions. Defective SrxVO3-δ samples with a unique amorphous-crystalline dual-phase structure are successfully prepared by regulating the nonstoichiometric Sr/V ratio and using a non-equilibrium solution combustion strategy to alleviate nucleation. The dual-phase SrxVO3-δ electrodes, which take advantage of both the high defect concentration advantage of amorphous and the high electrical/ionic conductivity of crystalline, give a high specific capacity of 508 mAh/g at a safe potential of 1.0 V vs. Li/Li+, showing a 40% increase over SrVO3 electrodes and outperforming most state-of-the-art intercalation-based anodes. In addition, when coupling with LiFePO4 cathode, the SrxVO3-δ electrodes can operate over 10,000 cycles with 91% capacity retention, overcoming the limited structural stability exhibited in typical defective electrodes. The study demonstrates the viability of modulating the crystallinity in intercalation-based anodes to enhance electrochemical performance and paves the way for the advancement of Li-ion battery technology.

Evaluation of information quality, accuracy and reliability of online videos regarding postoperative rehabilitation and postoperative patient information after arthroscopic rotator cuff repair

Breaking the capacity barrier in intercalation-type anode materials for lithium-ion batteries while preserving other essential electrochemical properties remains a significant challenge. Here, using perovskite SrVO3 as a model, we demonstrate the feasibility of employing defect engineering to provide extra active sites for electrochemical reactions. Defective SrxVO3-δ samples with a unique amorphous-crystalline dual-phase structure are successfully prepared by regulating the nonstoichiometric Sr/V ratio and using a non-equilibrium solution combustion strategy to alleviate nucleation. The dual-phase SrxVO3-δ electrodes, which take advantage of both the high defect concentration advantage of amorphous and the high electrical/ionic conductivity of crystalline, give a high specific capacity of 508 mAh/g at a safe potential of 1.0 V vs. Li/Li+, showing a 40% increase over SrVO3 electrodes and outperforming most state-of-the-art intercalation-based anodes. In addition, when coupling with LiFePO4 cathode, the SrxVO3-δ electrodes can operate over 10,000 cycles with 91% capacity retention, overcoming the limited structural stability exhibited in typical defective electrodes. The study demonstrates the viability of modulating the crystallinity in intercalation-based anodes to enhance electrochemical performance and paves the way for the advancement of Li-ion battery technology.

ADD+Prevention – Entwicklung einer funktionellen Testbatterie zur Erfassung muskuloskelettaler Defizite im Nachwuchsleistungssport

Breaking the capacity barrier in intercalation-type anode materials for lithium-ion batteries while preserving other essential electrochemical properties remains a significant challenge. Here, using perovskite SrVO3 as a model, we demonstrate the feasibility of employing defect engineering to provide extra active sites for electrochemical reactions. Defective SrxVO3-δ samples with a unique amorphous-crystalline dual-phase structure are successfully prepared by regulating the nonstoichiometric Sr/V ratio and using a non-equilibrium solution combustion strategy to alleviate nucleation. The dual-phase SrxVO3-δ electrodes, which take advantage of both the high defect concentration advantage of amorphous and the high electrical/ionic conductivity of crystalline, give a high specific capacity of 508 mAh/g at a safe potential of 1.0 V vs. Li/Li+, showing a 40% increase over SrVO3 electrodes and outperforming most state-of-the-art intercalation-based anodes. In addition, when coupling with LiFePO4 cathode, the SrxVO3-δ electrodes can operate over 10,000 cycles with 91% capacity retention, overcoming the limited structural stability exhibited in typical defective electrodes. The study demonstrates the viability of modulating the crystallinity in intercalation-based anodes to enhance electrochemical performance and paves the way for the advancement of Li-ion battery technology.

Duty factor: A key biomechanical injury risk factor in leisure-time runners

Breaking the capacity barrier in intercalation-type anode materials for lithium-ion batteries while preserving other essential electrochemical properties remains a significant challenge. Here, using perovskite SrVO3 as a model, we demonstrate the feasibility of employing defect engineering to provide extra active sites for electrochemical reactions. Defective SrxVO3-δ samples with a unique amorphous-crystalline dual-phase structure are successfully prepared by regulating the nonstoichiometric Sr/V ratio and using a non-equilibrium solution combustion strategy to alleviate nucleation. The dual-phase SrxVO3-δ electrodes, which take advantage of both the high defect concentration advantage of amorphous and the high electrical/ionic conductivity of crystalline, give a high specific capacity of 508 mAh/g at a safe potential of 1.0 V vs. Li/Li+, showing a 40% increase over SrVO3 electrodes and outperforming most state-of-the-art intercalation-based anodes. In addition, when coupling with LiFePO4 cathode, the SrxVO3-δ electrodes can operate over 10,000 cycles with 91% capacity retention, overcoming the limited structural stability exhibited in typical defective electrodes. The study demonstrates the viability of modulating the crystallinity in intercalation-based anodes to enhance electrochemical performance and paves the way for the advancement of Li-ion battery technology.

Einstellung und Wissen zur Verletzungsprävention im Jugend-Rugby – Eine Querschnittsstudie

Breaking the capacity barrier in intercalation-type anode materials for lithium-ion batteries while preserving other essential electrochemical properties remains a significant challenge. Here, using perovskite SrVO3 as a model, we demonstrate the feasibility of employing defect engineering to provide extra active sites for electrochemical reactions. Defective SrxVO3-δ samples with a unique amorphous-crystalline dual-phase structure are successfully prepared by regulating the nonstoichiometric Sr/V ratio and using a non-equilibrium solution combustion strategy to alleviate nucleation. The dual-phase SrxVO3-δ electrodes, which take advantage of both the high defect concentration advantage of amorphous and the high electrical/ionic conductivity of crystalline, give a high specific capacity of 508 mAh/g at a safe potential of 1.0 V vs. Li/Li+, showing a 40% increase over SrVO3 electrodes and outperforming most state-of-the-art intercalation-based anodes. In addition, when coupling with LiFePO4 cathode, the SrxVO3-δ electrodes can operate over 10,000 cycles with 91% capacity retention, overcoming the limited structural stability exhibited in typical defective electrodes. The study demonstrates the viability of modulating the crystallinity in intercalation-based anodes to enhance electrochemical performance and paves the way for the advancement of Li-ion battery technology.

Sportmedizinische Betreuung im Ultraradsport

Breaking the capacity barrier in intercalation-type anode materials for lithium-ion batteries while preserving other essential electrochemical properties remains a significant challenge. Here, using perovskite SrVO3 as a model, we demonstrate the feasibility of employing defect engineering to provide extra active sites for electrochemical reactions. Defective SrxVO3-δ samples with a unique amorphous-crystalline dual-phase structure are successfully prepared by regulating the nonstoichiometric Sr/V ratio and using a non-equilibrium solution combustion strategy to alleviate nucleation. The dual-phase SrxVO3-δ electrodes, which take advantage of both the high defect concentration advantage of amorphous and the high electrical/ionic conductivity of crystalline, give a high specific capacity of 508 mAh/g at a safe potential of 1.0 V vs. Li/Li+, showing a 40% increase over SrVO3 electrodes and outperforming most state-of-the-art intercalation-based anodes. In addition, when coupling with LiFePO4 cathode, the SrxVO3-δ electrodes can operate over 10,000 cycles with 91% capacity retention, overcoming the limited structural stability exhibited in typical defective electrodes. The study demonstrates the viability of modulating the crystallinity in intercalation-based anodes to enhance electrochemical performance and paves the way for the advancement of Li-ion battery technology.

Primärversorgung von gehunfähigen Schwingern bei einem sportlichen Großanlass

Breaking the capacity barrier in intercalation-type anode materials for lithium-ion batteries while preserving other essential electrochemical properties remains a significant challenge. Here, using perovskite SrVO3 as a model, we demonstrate the feasibility of employing defect engineering to provide extra active sites for electrochemical reactions. Defective SrxVO3-δ samples with a unique amorphous-crystalline dual-phase structure are successfully prepared by regulating the nonstoichiometric Sr/V ratio and using a non-equilibrium solution combustion strategy to alleviate nucleation. The dual-phase SrxVO3-δ electrodes, which take advantage of both the high defect concentration advantage of amorphous and the high electrical/ionic conductivity of crystalline, give a high specific capacity of 508 mAh/g at a safe potential of 1.0 V vs. Li/Li+, showing a 40% increase over SrVO3 electrodes and outperforming most state-of-the-art intercalation-based anodes. In addition, when coupling with LiFePO4 cathode, the SrxVO3-δ electrodes can operate over 10,000 cycles with 91% capacity retention, overcoming the limited structural stability exhibited in typical defective electrodes. The study demonstrates the viability of modulating the crystallinity in intercalation-based anodes to enhance electrochemical performance and paves the way for the advancement of Li-ion battery technology.

Vollständige myofasziale Separation des M. rectus femoris – eine seltene Verletzungsentität

Breaking the capacity barrier in intercalation-type anode materials for lithium-ion batteries while preserving other essential electrochemical properties remains a significant challenge. Here, using perovskite SrVO3 as a model, we demonstrate the feasibility of employing defect engineering to provide extra active sites for electrochemical reactions. Defective SrxVO3-δ samples with a unique amorphous-crystalline dual-phase structure are successfully prepared by regulating the nonstoichiometric Sr/V ratio and using a non-equilibrium solution combustion strategy to alleviate nucleation. The dual-phase SrxVO3-δ electrodes, which take advantage of both the high defect concentration advantage of amorphous and the high electrical/ionic conductivity of crystalline, give a high specific capacity of 508 mAh/g at a safe potential of 1.0 V vs. Li/Li+, showing a 40% increase over SrVO3 electrodes and outperforming most state-of-the-art intercalation-based anodes. In addition, when coupling with LiFePO4 cathode, the SrxVO3-δ electrodes can operate over 10,000 cycles with 91% capacity retention, overcoming the limited structural stability exhibited in typical defective electrodes. The study demonstrates the viability of modulating the crystallinity in intercalation-based anodes to enhance electrochemical performance and paves the way for the advancement of Li-ion battery technology.

Morphological factors and radiological signs for posterior root tears of the lateral meniscus associated with anterior cruciate ligament injuries

Breaking the capacity barrier in intercalation-type anode materials for lithium-ion batteries while preserving other essential electrochemical properties remains a significant challenge. Here, using perovskite SrVO3 as a model, we demonstrate the feasibility of employing defect engineering to provide extra active sites for electrochemical reactions. Defective SrxVO3-δ samples with a unique amorphous-crystalline dual-phase structure are successfully prepared by regulating the nonstoichiometric Sr/V ratio and using a non-equilibrium solution combustion strategy to alleviate nucleation. The dual-phase SrxVO3-δ electrodes, which take advantage of both the high defect concentration advantage of amorphous and the high electrical/ionic conductivity of crystalline, give a high specific capacity of 508 mAh/g at a safe potential of 1.0 V vs. Li/Li+, showing a 40% increase over SrVO3 electrodes and outperforming most state-of-the-art intercalation-based anodes. In addition, when coupling with LiFePO4 cathode, the SrxVO3-δ electrodes can operate over 10,000 cycles with 91% capacity retention, overcoming the limited structural stability exhibited in typical defective electrodes. The study demonstrates the viability of modulating the crystallinity in intercalation-based anodes to enhance electrochemical performance and paves the way for the advancement of Li-ion battery technology.

Is there a tickle-down effect of elite sport on physical activity practice in the general population?

Breaking the capacity barrier in intercalation-type anode materials for lithium-ion batteries while preserving other essential electrochemical properties remains a significant challenge. Here, using perovskite SrVO3 as a model, we demonstrate the feasibility of employing defect engineering to provide extra active sites for electrochemical reactions. Defective SrxVO3-δ samples with a unique amorphous-crystalline dual-phase structure are successfully prepared by regulating the nonstoichiometric Sr/V ratio and using a non-equilibrium solution combustion strategy to alleviate nucleation. The dual-phase SrxVO3-δ electrodes, which take advantage of both the high defect concentration advantage of amorphous and the high electrical/ionic conductivity of crystalline, give a high specific capacity of 508 mAh/g at a safe potential of 1.0 V vs. Li/Li+, showing a 40% increase over SrVO3 electrodes and outperforming most state-of-the-art intercalation-based anodes. In addition, when coupling with LiFePO4 cathode, the SrxVO3-δ electrodes can operate over 10,000 cycles with 91% capacity retention, overcoming the limited structural stability exhibited in typical defective electrodes. The study demonstrates the viability of modulating the crystallinity in intercalation-based anodes to enhance electrochemical performance and paves the way for the advancement of Li-ion battery technology.

Prospective double blinded placebo controlled trial of high energetic magneto transduction therapy in shoulder joint enthesiopathies

Breaking the capacity barrier in intercalation-type anode materials for lithium-ion batteries while preserving other essential electrochemical properties remains a significant challenge. Here, using perovskite SrVO3 as a model, we demonstrate the feasibility of employing defect engineering to provide extra active sites for electrochemical reactions. Defective SrxVO3-δ samples with a unique amorphous-crystalline dual-phase structure are successfully prepared by regulating the nonstoichiometric Sr/V ratio and using a non-equilibrium solution combustion strategy to alleviate nucleation. The dual-phase SrxVO3-δ electrodes, which take advantage of both the high defect concentration advantage of amorphous and the high electrical/ionic conductivity of crystalline, give a high specific capacity of 508 mAh/g at a safe potential of 1.0 V vs. Li/Li+, showing a 40% increase over SrVO3 electrodes and outperforming most state-of-the-art intercalation-based anodes. In addition, when coupling with LiFePO4 cathode, the SrxVO3-δ electrodes can operate over 10,000 cycles with 91% capacity retention, overcoming the limited structural stability exhibited in typical defective electrodes. The study demonstrates the viability of modulating the crystallinity in intercalation-based anodes to enhance electrochemical performance and paves the way for the advancement of Li-ion battery technology.

Etablierung eines Verletzungsüberwachungsystems im Nachwuchs von Snowboard Germany

Breaking the capacity barrier in intercalation-type anode materials for lithium-ion batteries while preserving other essential electrochemical properties remains a significant challenge. Here, using perovskite SrVO3 as a model, we demonstrate the feasibility of employing defect engineering to provide extra active sites for electrochemical reactions. Defective SrxVO3-δ samples with a unique amorphous-crystalline dual-phase structure are successfully prepared by regulating the nonstoichiometric Sr/V ratio and using a non-equilibrium solution combustion strategy to alleviate nucleation. The dual-phase SrxVO3-δ electrodes, which take advantage of both the high defect concentration advantage of amorphous and the high electrical/ionic conductivity of crystalline, give a high specific capacity of 508 mAh/g at a safe potential of 1.0 V vs. Li/Li+, showing a 40% increase over SrVO3 electrodes and outperforming most state-of-the-art intercalation-based anodes. In addition, when coupling with LiFePO4 cathode, the SrxVO3-δ electrodes can operate over 10,000 cycles with 91% capacity retention, overcoming the limited structural stability exhibited in typical defective electrodes. The study demonstrates the viability of modulating the crystallinity in intercalation-based anodes to enhance electrochemical performance and paves the way for the advancement of Li-ion battery technology.

Optimierung der Rückfußbelastung und Laufökonomie mittels orthopädischen Sporteinlagen bei Personen mit Pes valgus

Breaking the capacity barrier in intercalation-type anode materials for lithium-ion batteries while preserving other essential electrochemical properties remains a significant challenge. Here, using perovskite SrVO3 as a model, we demonstrate the feasibility of employing defect engineering to provide extra active sites for electrochemical reactions. Defective SrxVO3-δ samples with a unique amorphous-crystalline dual-phase structure are successfully prepared by regulating the nonstoichiometric Sr/V ratio and using a non-equilibrium solution combustion strategy to alleviate nucleation. The dual-phase SrxVO3-δ electrodes, which take advantage of both the high defect concentration advantage of amorphous and the high electrical/ionic conductivity of crystalline, give a high specific capacity of 508 mAh/g at a safe potential of 1.0 V vs. Li/Li+, showing a 40% increase over SrVO3 electrodes and outperforming most state-of-the-art intercalation-based anodes. In addition, when coupling with LiFePO4 cathode, the SrxVO3-δ electrodes can operate over 10,000 cycles with 91% capacity retention, overcoming the limited structural stability exhibited in typical defective electrodes. The study demonstrates the viability of modulating the crystallinity in intercalation-based anodes to enhance electrochemical performance and paves the way for the advancement of Li-ion battery technology.

Die Polyätiologie der Arthrose und multimodale Therapiemöglichkeiten

Breaking the capacity barrier in intercalation-type anode materials for lithium-ion batteries while preserving other essential electrochemical properties remains a significant challenge. Here, using perovskite SrVO3 as a model, we demonstrate the feasibility of employing defect engineering to provide extra active sites for electrochemical reactions. Defective SrxVO3-δ samples with a unique amorphous-crystalline dual-phase structure are successfully prepared by regulating the nonstoichiometric Sr/V ratio and using a non-equilibrium solution combustion strategy to alleviate nucleation. The dual-phase SrxVO3-δ electrodes, which take advantage of both the high defect concentration advantage of amorphous and the high electrical/ionic conductivity of crystalline, give a high specific capacity of 508 mAh/g at a safe potential of 1.0 V vs. Li/Li+, showing a 40% increase over SrVO3 electrodes and outperforming most state-of-the-art intercalation-based anodes. In addition, when coupling with LiFePO4 cathode, the SrxVO3-δ electrodes can operate over 10,000 cycles with 91% capacity retention, overcoming the limited structural stability exhibited in typical defective electrodes. The study demonstrates the viability of modulating the crystallinity in intercalation-based anodes to enhance electrochemical performance and paves the way for the advancement of Li-ion battery technology.

Patient-specific identification of MPFL isometric femoral footprint on a compressed knee sagittal view using CLASS – MRI sequence

Breaking the capacity barrier in intercalation-type anode materials for lithium-ion batteries while preserving other essential electrochemical properties remains a significant challenge. Here, using perovskite SrVO3 as a model, we demonstrate the feasibility of employing defect engineering to provide extra active sites for electrochemical reactions. Defective SrxVO3-δ samples with a unique amorphous-crystalline dual-phase structure are successfully prepared by regulating the nonstoichiometric Sr/V ratio and using a non-equilibrium solution combustion strategy to alleviate nucleation. The dual-phase SrxVO3-δ electrodes, which take advantage of both the high defect concentration advantage of amorphous and the high electrical/ionic conductivity of crystalline, give a high specific capacity of 508 mAh/g at a safe potential of 1.0 V vs. Li/Li+, showing a 40% increase over SrVO3 electrodes and outperforming most state-of-the-art intercalation-based anodes. In addition, when coupling with LiFePO4 cathode, the SrxVO3-δ electrodes can operate over 10,000 cycles with 91% capacity retention, overcoming the limited structural stability exhibited in typical defective electrodes. The study demonstrates the viability of modulating the crystallinity in intercalation-based anodes to enhance electrochemical performance and paves the way for the advancement of Li-ion battery technology.

Evaluation of a diagnostic-therapeutic algorithm for epiphyseal growth plate stress injuries in adolescent climbers

Breaking the capacity barrier in intercalation-type anode materials for lithium-ion batteries while preserving other essential electrochemical properties remains a significant challenge. Here, using perovskite SrVO3 as a model, we demonstrate the feasibility of employing defect engineering to provide extra active sites for electrochemical reactions. Defective SrxVO3-δ samples with a unique amorphous-crystalline dual-phase structure are successfully prepared by regulating the nonstoichiometric Sr/V ratio and using a non-equilibrium solution combustion strategy to alleviate nucleation. The dual-phase SrxVO3-δ electrodes, which take advantage of both the high defect concentration advantage of amorphous and the high electrical/ionic conductivity of crystalline, give a high specific capacity of 508 mAh/g at a safe potential of 1.0 V vs. Li/Li+, showing a 40% increase over SrVO3 electrodes and outperforming most state-of-the-art intercalation-based anodes. In addition, when coupling with LiFePO4 cathode, the SrxVO3-δ electrodes can operate over 10,000 cycles with 91% capacity retention, overcoming the limited structural stability exhibited in typical defective electrodes. The study demonstrates the viability of modulating the crystallinity in intercalation-based anodes to enhance electrochemical performance and paves the way for the advancement of Li-ion battery technology.

Biochemisches und psychometrisches Beanspruchungsmonitoring im Spitzenhandball

Breaking the capacity barrier in intercalation-type anode materials for lithium-ion batteries while preserving other essential electrochemical properties remains a significant challenge. Here, using perovskite SrVO3 as a model, we demonstrate the feasibility of employing defect engineering to provide extra active sites for electrochemical reactions. Defective SrxVO3-δ samples with a unique amorphous-crystalline dual-phase structure are successfully prepared by regulating the nonstoichiometric Sr/V ratio and using a non-equilibrium solution combustion strategy to alleviate nucleation. The dual-phase SrxVO3-δ electrodes, which take advantage of both the high defect concentration advantage of amorphous and the high electrical/ionic conductivity of crystalline, give a high specific capacity of 508 mAh/g at a safe potential of 1.0 V vs. Li/Li+, showing a 40% increase over SrVO3 electrodes and outperforming most state-of-the-art intercalation-based anodes. In addition, when coupling with LiFePO4 cathode, the SrxVO3-δ electrodes can operate over 10,000 cycles with 91% capacity retention, overcoming the limited structural stability exhibited in typical defective electrodes. The study demonstrates the viability of modulating the crystallinity in intercalation-based anodes to enhance electrochemical performance and paves the way for the advancement of Li-ion battery technology.

Evaluation of anterior cruciate ligament reconstruction methods in pediatric patients: a systematic review

Breaking the capacity barrier in intercalation-type anode materials for lithium-ion batteries while preserving other essential electrochemical properties remains a significant challenge. Here, using perovskite SrVO3 as a model, we demonstrate the feasibility of employing defect engineering to provide extra active sites for electrochemical reactions. Defective SrxVO3-δ samples with a unique amorphous-crystalline dual-phase structure are successfully prepared by regulating the nonstoichiometric Sr/V ratio and using a non-equilibrium solution combustion strategy to alleviate nucleation. The dual-phase SrxVO3-δ electrodes, which take advantage of both the high defect concentration advantage of amorphous and the high electrical/ionic conductivity of crystalline, give a high specific capacity of 508 mAh/g at a safe potential of 1.0 V vs. Li/Li+, showing a 40% increase over SrVO3 electrodes and outperforming most state-of-the-art intercalation-based anodes. In addition, when coupling with LiFePO4 cathode, the SrxVO3-δ electrodes can operate over 10,000 cycles with 91% capacity retention, overcoming the limited structural stability exhibited in typical defective electrodes. The study demonstrates the viability of modulating the crystallinity in intercalation-based anodes to enhance electrochemical performance and paves the way for the advancement of Li-ion battery technology.

Combined effect of anterior cruciate ligament injury and age on knee articular cartilage morphology and quality

Breaking the capacity barrier in intercalation-type anode materials for lithium-ion batteries while preserving other essential electrochemical properties remains a significant challenge. Here, using perovskite SrVO3 as a model, we demonstrate the feasibility of employing defect engineering to provide extra active sites for electrochemical reactions. Defective SrxVO3-δ samples with a unique amorphous-crystalline dual-phase structure are successfully prepared by regulating the nonstoichiometric Sr/V ratio and using a non-equilibrium solution combustion strategy to alleviate nucleation. The dual-phase SrxVO3-δ electrodes, which take advantage of both the high defect concentration advantage of amorphous and the high electrical/ionic conductivity of crystalline, give a high specific capacity of 508 mAh/g at a safe potential of 1.0 V vs. Li/Li+, showing a 40% increase over SrVO3 electrodes and outperforming most state-of-the-art intercalation-based anodes. In addition, when coupling with LiFePO4 cathode, the SrxVO3-δ electrodes can operate over 10,000 cycles with 91% capacity retention, overcoming the limited structural stability exhibited in typical defective electrodes. The study demonstrates the viability of modulating the crystallinity in intercalation-based anodes to enhance electrochemical performance and paves the way for the advancement of Li-ion battery technology.

Analyse der Schmerzverteilung beim Fitness-Breitensportler

Breaking the capacity barrier in intercalation-type anode materials for lithium-ion batteries while preserving other essential electrochemical properties remains a significant challenge. Here, using perovskite SrVO3 as a model, we demonstrate the feasibility of employing defect engineering to provide extra active sites for electrochemical reactions. Defective SrxVO3-δ samples with a unique amorphous-crystalline dual-phase structure are successfully prepared by regulating the nonstoichiometric Sr/V ratio and using a non-equilibrium solution combustion strategy to alleviate nucleation. The dual-phase SrxVO3-δ electrodes, which take advantage of both the high defect concentration advantage of amorphous and the high electrical/ionic conductivity of crystalline, give a high specific capacity of 508 mAh/g at a safe potential of 1.0 V vs. Li/Li+, showing a 40% increase over SrVO3 electrodes and outperforming most state-of-the-art intercalation-based anodes. In addition, when coupling with LiFePO4 cathode, the SrxVO3-δ electrodes can operate over 10,000 cycles with 91% capacity retention, overcoming the limited structural stability exhibited in typical defective electrodes. The study demonstrates the viability of modulating the crystallinity in intercalation-based anodes to enhance electrochemical performance and paves the way for the advancement of Li-ion battery technology.