Dr. Bereket Woldegbreal Taklu is currently work as a postdoctoral research fellow at the NTUST. Area of expertise focuses on lithium battery technology related to interface engineering, solid electrolyte development, and anode materials.
EDUCATION
National Taiwan University of Science and Technology
Wollo University
Bahir Dar University
Gondar University
RESEARCH INTERESTS
Any topics related with
Sulfide solid electrolyte;
Halide solid electrolyte;
Solid electrolyte / Li interface engineering;
Aqueous Zn ion battery;
Anode free lithium metal batteries
Dual-Functional Surface Engineering of Single-Crystal NMC Cathodes via Residue-to-Coating Conversion for Enhanced Interface Stability Shadab Ali Ahmed, Tripti Agnihotri, Ashok Ranjan, Chia‐Yu Chang, Rehbar Hasan, Elango Balaji Tamilarasan, Yosef Nikodimos, Kassie Nigus Shitaw, Tsung‐I Yeh, Bereket Woldegbreal Taklu, Wei‐Sheng Liao, Vinay Boligarla, She‐Huang Wu, Wei‐Nien Su, Bing Joe Hwang Small, 2026 Nickel‐rich layered oxides, such as LiNi 0.83 Mn 0.06 Co 0.11 O 2 (NMC), are among the most promising cathode materials for high‐energy‐density lithium‐ion batteries. However, their practical implementation is limited by surface instability and the presence of residual lithium compounds, which degrade performance and complicate scalability. In this study, a dual‐functional surface modification strategy using lithium dihydrogen phosphate (LiH 2 PO 4 ) is presented. A wet impregnation procedure is used to transform the residual surface contaminants (LiOH, Li 2 CO 3 ) into an advantageous surface coating (Li 3 PO 4 ) on single crystal nickel‐rich (SCNMC) cathode materials rather than directly eliminating them through solvent washing process., as confirmed by titration and in situ Gas Chromotography‐Mas (GC‐MS), while the resulting ≈4 nm Li 3 PO 4 layer enhances structural stability, suppresses nickel migration, and mitigates electrolyte‐induced side reactions. Electrochemical tests reveal significantly improved cycling stability (72.96% capacity retention after 100 cycles at 0.2C compared to 18.25% for pristine SCNMC) and enhanced rate capability, supported by improved Li + diffusion kinetics. Synchrotron X‐ray Absorption Spectroscopy (XAS) and post‐mortem analyses further confirm the preservation of Ni oxidation states and reduced cross‐talk effects.
Structural evolution and stabilities of (CuIn)nTe2 and ((CuIn)nTe2)−(n = 1–8) clusters via DFT study Kidane Goitom Gerezgiher, Bereket Woldegbreal Taklu, Taame Abraha Berhe, Teklay Mezgebe Hagos, Hagos Woldeghebriel Zeweldi Rsc Advances, 2026 CuInTe 2 is a promising semiconductor with a tunable bandgap between 1.0 and 1.2 eV, allowing it to efficiently absorb sunlight and convert it into usable energy.
A signal-processing framework for preemptive detection of soft shorts in lithium-metal batteries Rehbar Hasan, Po-Yi Wu, Tripti Agnihotri, Shadab Ali Ahmed, Ashok Ranjan, Elango Balaji Tamilarasan, Sheng-Chiang Yang, Bereket Woldegebreal Taklu, Liang-Yin Kuo, Wei-Nien Su, She-Huang Wu, Bing Joe Hwang Cell Reports Physical Science, 2025 Lithium-ion batteries are central to sustainable energy systems, yet internal short circuits (ISCs) can trigger catastrophic failures, such as fires and explosions. Current detection methods are based on costly tests, large datasets, or computationally heavy models, which limit their scalability and practical application. Here, we report a physics-based framework for the early detection of soft ISCs by representing the battery as an equivalent resistance-capacitance (RC) circuit with time-varying resistances. Using signal processing, we track periodic resistance fluctuations in charging data to identify the onset of ISCs without any abuse conditions. Fast Fourier transform (FFT) highlights distinct frequency-domain signatures, while Welch's algorithm extracts characteristic power spectral density patterns that serve as detection criteria. Together, these methods provide robust, real-time monitoring of ISC formation. Our results establish a new diagnostic standard that links microscopic ISC dynamics with macroscopic signals, significantly improving battery safety for electric vehicles, consumer electronics, and grid-scale energy storage.
Overcoming Chemo-Mechanical Instability at Silicon-Solid Electrolyte Interfaces in Solid-State Batteries Lammi Terefe Kitaba, Yosef Nikodimos, Semaw Kebede Merso, Bereket Woldegbreal Taklu, Gashahun Gobena Serbessa, Woldesenbet Bafe Dilebo, Tsung-I Yeh, Joshua Alexander Iskandar, Felika Valencia, Chia-Yu Chang, Chia Lung Hsieh, Shawn D. Lin, She-Huang Wu, Wei-Nien Su, Bing Joe Hwang ACS Applied Materials and Interfaces, 2025 Silicon is the preferred choice for lithium-ion battery anodes due to its high theoretical capacity and low lithiation potential. However, achieving high areal capacity with silicon anodes in solid-state batteries (SSBs) is challenging because of poor electronic and ionic conductivity, as well as chemo-mechanical instability at the silicon|solid electrolyte (Si|SE) interfaces. Here, we propose fabricating and testing composite anodes made of nanosized Si powder embedded in partially fluorinated graphene (Si-FG) and Li6PS5Cl (LPSCl) sulfide SE. X-ray photoelectron spectroscopy revealed that the in situ formation of LiF-rich SEI can protect against SE decomposition at the interface in the Si-FG-LPSCl composite anode. FIB-SEM and EIS analyses also indicate a stable structure and low interfacial resistance after one cycle for a composite anode containing FG. The incorporation of partially FG enhances both electronic (through heterojunction formation with Si) and ionic conductivities, buffers significant volume changes, and ensures chemo-mechanical stability in the composite anode. The Si-FG-LPSCl composite anode in SSBs delivered high discharge/charge capacities of 3499/2994 mAh g–1 at a C-rate of C/20 and an ICE of 85.6% in a half cell. This work provides valuable insights for advancing high-capacity Si composite anodes to meet future energy needs.
Unveiling the Chemical Stability and Solvent Compatibility of Halide Solid-State Electrolytes: Insights from Isothermal Calorimetric Titration and Synchrotron Spectroscopy Yosef Nikodimos, Bereket Woldegbreal Taklu, Chia-Yu Chang, Kassie Nigus Shitaw, Teklay Mezgebe Hagos, Zabish Bilew Muche, Siyanand Kumar Chaudhary, Gashahun Gobena Serbessa, Tsung-I Yeh, Semaw Kebede Merso, Shadab Ali Ahmed, Jia-Min Ke, Endalkachew Asefa Moges, Sheng-Chiang Yang, She-Huang Wu, Wei-Nien Su, Bing Joe Hwang Chemistry of Materials, 2025 As interest in next-generation all-solid-state batteries (ASSBs) grows, understanding the impact of solution-based processing on solid-state electrolytes (SSEs) becomes crucial. This study examines the interaction of Li3InCl6 (LIC), a halide SSE, with various solvents, including protic, aprotic polar, and nonpolar types. LIC powder is mixed with ten solvents selected for their diverse physical and chemical properties. Through a series of analytical techniques, this study explores the compatibility of LIC with different solvent environments. The LIC–solvent mixtures are analyzed through color observation, pH measurement, and isothermal calorimetric titration. Moreover, after solvent removal, the dried LIC powder is further characterized using diffraction and various advanced spectroscopic techniques. The findings reveal that LIC is chemically stable in nonpolar solvents but exhibits instability in most polar solvents, with ethanol showing the highest stability among the polar options. It is also observed that indium reacts with highly electronegative elements such as oxygen and nitrogen based on the hard–soft acid–base principle. Furthermore, LIC in protic solvents results in acidic solutions, whereas in aprotic solvents, it exhibits basicity. These results are crucial for the development of ASSBs and underscore the importance of understanding the chemical compatibility of LIC with various solvent systems for advanced energy storage applications.
Potassium Underpotential Deposition for Defect-Free Lithium Deposition in Anode-Free Li-Metal Batteries Kassie Nigus Shitaw, Hailemariam Kassa Bezabh, Yosef Nikodimos, Misganaw Adigo Weret, Teshager Mekonnen Tekaligne, Semaw Kebede Merso, Bereket Woldegbreal Taklu, Shi‐Kai Jiang, Chun‐Ying Li, Hsin‐Yueh Liu, She‐Huang Wu, We‐Nien Su, Bing Joe Hwang Small Methods, 2025 Defects in deposited lithium (Li) severely cause dendrite growth and promote reactions between Li and electrolytes, resulting in active Li loss in anode‐free Li metal batteries (AFLMBs). Herein, potassium underpotential deposition (K‐UPD) is systematically established to heal defective Li and create a K‐Cu bimetallic interface, facilitating uniform bulk Li deposition. The K‐UPD at a potential of ≈1.0 V, higher than the equilibrium potentials of bulk K⁺ (0.1 V) and Li⁺ (0.0 V), significantly lowers the nucleation barrier and mitigates Li dendrite growth due to the better lithiophilicity of K metal compared to Cu. Meanwhile, the higher surface mobility of K atoms than Li atoms enables K metal to heal defects and prevent reactions between Li and electrolytes. The lower adsorption energy (ΔE) of the K atoms (−1.56 eV) than that of Li atoms (0.032 eV) indicates favorable adsorption of the K atom, as confirmed by DFT calculations. As a result, Cu||Li cell containing 1.3 M LiFSI+0.2 M KFSI bimetallic electrolyte reaches >1600 h, while Cu||NMC532 full‐cell achieves a higher average Coulombic efficiency (avg. CE) of 99.6% than the cell with 1.5 M LiFSI electrolyte (≈98.2%) after the 100th cycle. This work offers insights into the K‐UPD mechanism for enhancing interface stability and healing defects in deposited Li.