Zhenchuan Chen

dblp:359/1250 · DBLP profile ↗
← Back
5ranked-venue papers
0as first author
5since 2021 · last 2026
0009-0002-3756-3950ORCID · corroborated

Domains — the database's venue-derived domains; a paper can count in several

Systems, architecture and hardware · 5 · 5 since 2021Software engineering, systems software and programming languages · 1 · 1 since 2021
YearPublicationVenuePosition
2026 SYCL++: A Unified Programming Framework for Heterogeneous Supercomputers at Scale
Zitao Shen, Yuyang Jin 0001, Kinman Lei, Zixuan Ma, Zhenchuan Chen, Di Wei, Fei Wang 0096, Ying Liu 0055, Lin Gan 0001, Jidong Zhai
HPDC8
2025 Qiwu: Exploiting Ciphertext-Level SIMD Parallelism in Homomorphic Encryption Programs
abstract
Fully Homomorphic Encryption (FHE), particularly the CKKS scheme, enables computation on encrypted data, facilitating secure task offloading to untrusted servers. CKKS allows packing multiple complex values into a single ciphertext, crucial for fixed-point arithmetic in machine learning, while leveraging SIMD parallelism at the plaintext level. However, operations such as reductions can degrade performance by creating a large number of bubbles (or gaps) in intermediate ciphertexts, leading to wasted computational resources. We introduce Qiwu, a ciphertext-level vectorization approach that enhances performance by fusing multiple ciphertexts containing bubbles. Qiwu uses a DSL to specify zero bubbles in input ciphertexts and nonzero bubbles in output ciphertexts, employs data-flow analysis to track them, and formulates a fusion plan guided by a cost-benefit assessment. Implemented in an existing FHE compiler, Qiwu was evaluated on four applications (including three machine learning tasks) and three kernels. It achieves speedups of up to 18.0× on CPUs, averaging 3.4× (geometric mean), compared to the state-of-the-art compiler that exploit only plaintext-level parallelism.
Zhongcheng Zhang, Ying Liu 0055, Zhenchuan Chen, Xiaobing Feng 0002, Huimin Cui, Jingling Xue
CGO4
2025 TensorMD: Molecular Dynamics Simulation with Ab Initio Accuracy of 50 Billion Atoms
abstract
Molecular dynamics simulation emerges as an important area that HPC+AI helps to investigate the physical properties, with machine-learning interatomic potentials (MLIPs) being used. General-purpose machine-learning (ML) tools have been leveraged in MLIPs, but they are not perfectly matched with each other, since many optimization opportunities in MLIPs have been missed by ML tools. This inefficiency arises from the fact that HPC+AI applications work with far more computational complexity compared with pure AI scenarios. This paper has developed an MLIP, named TensorMD, independently from any ML tool. TensorMD has been evaluated on two supercomputers and scaled to 51.8 billion atoms, i.e., ~ 3× compared with state-of-the-art.
Yucheng Ouyang, Ying Liu 0055, Honghui Shang, Zhenchuan Chen, Jiahao Shan, Huimin Cui, Xiaobing Feng 0002, Xingyu Gao 0003, Haifeng Song 0003, Xin Chen 0023, Rongfen Lin
PPoPP4
2025 TENSORMD: Accelerating Molecular Dynamics with a High-Performance Machine Learning Interatomic Potential
abstract
AI has been integrated into HPC across various scientific fields, significantly enhancing performance. In molecular dynamics simulations, HPC+AI facilitates the investigation of atomic-scale physical properties using machine-learning interatomic potentials (MLIPs). However, general-purpose ML tools (e.g., TensorFlow) used in MLIPs are not optimally matched, leading to missed optimization opportunities due to the higher computational complexity and greater diversity of HPC+AI applications compared to pure AI scenarios. To address this, we introduce TensorMD, an MLIP independent of existing ML tools, enabling flexible optimizations that standard ML frameworks cannot support. TensorMD outperforms a state-of-the-art MLIP—winner of the 2020 Gordon Bell Prize and built on an ML tool—by 1.88 × on NVIDIA A100 GPU. Additionally, TensorMD was evaluated on two supercomputers with different architectures, achieving significantly reduced time-to-solution and supporting molecular dynamics simulations at scales beyond 50 billion atoms.
Yucheng Ouyang, Ying Liu 0055, Xin Chen 0023, Honghui Shang, Zhenchuan Chen, Rongfen Lin, Xingyu Gao 0003, Jiahao Shan, Haifeng Song 0003, Huimin Cui, Xiaobing Feng 0002, Jingling Xue
SC6
2024 Pushing the Limit of Quantum Mechanical Simulation to the Raman Spectra of a Biological System with 100 Million Atoms
abstract
Raman spectroscopy offers invaluable insights into the chemical composition and structural characteristics of various materials, making it a powerful tool for structural analysis. However, accurate quantum mechanical simulations of Raman spectra for large systems, such as biological materials, have been limited due to immense computational costs and technical challenges. In this study, we developed efficient algorithms and optimized implementations on heterogeneous computing architectures to enable fast and highly scalable ab initio simulations of Raman spectra for large-scale biological systems with up to 100 million atoms. Our simulations have achieved nearly linear strong and weak scaling on two cutting-edge high-performance computing systems, with peak FP64 performances reaching 400 PFLOPS on 96,000 nodes of new Sunway supercomputer and 85 PFLOPS on 6,000 node of ORISE supercomputer. These advances provide promising prospects for extending quantum mechanical simulations to biological systems.
Honghui Shang, Ying Liu 0055, Zhikun Wu, Zhenchuan Chen, Jinfeng Liu 0004, Meiyue Shao, Yingzhou Li, Bowen Kan, Huimin Cui, Xiaobing Feng 0002, Yunquan Zhang, Donald G. Truhlar, Hong An, Xiao He 0004, Jinlong Yang 0003
SC4